BMJ 2002;325:1082 ( 9 November )

Primary care

Systematic review of mental health interventions for patients with common somatic symptoms: can research evidence from secondary care be extrapolated to primary care?

Rosalind Raine, MRC clinician scientist aAndy Haines, professor of public health and primary care aTom Sensky, reader in psychological medicine bAndrew Hutchings, lecturer in health services research aKirsten Larkin, MRC research assistant aNick Black, professor of health services research a

a Department of Public Health and Policy, London School of Hygiene and Tropical Medicine, London WC1E 7HT, b Department of Psychological Medicine, Imperial College of Science, Technology and Medicine, West Middlesex University Hospital, Middlesex TW7 6AF

Correspondence to: R Raine rosalind.raine{at}lshtm.ac.uk


    Abstract
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

Objectives: To determine the strength of evidence for the effectiveness of mental health interventions for patients with three common somatic conditions (chronic fatigue syndrome, irritable bowel syndrome, and chronic back pain). To assess whether results obtained in secondary care can be extrapolated to primary care and suggest how future trials should be designed to provide more rigorous evidence.
Design: Systematic review.
Data sources: Five electronic databases, key texts, references in the articles identified, and citations from expert clinicians.
Study selection: Randomised controlled trials including participants with one of the three conditions for which no physical cause could be found. Two reviewers screened sources and independently extracted data and assessed quality.
Results: Sixty one studies were identified; 20 were classified as primary care and 41 as secondary care. For some interventions, such as brief psychodynamic interpersonal therapy, little research was identified. However, results of meta-analyses and of randomised controlled trials suggest that cognitive behaviour therapy and behaviour therapy are effective for chronic back pain and chronic fatigue syndrome and that antidepressants are effective for irritable bowel syndrome. Cognitive behaviour therapy and behaviour therapy were effective in both primary and secondary care in patients with back pain, although the evidence is more consistent and the effect size larger for secondary care. Antidepressants seem effective in irritable bowel syndrome in both settings but ineffective in chronic fatigue syndrome.
Conclusions: Treatment seems to be more effective in patients in secondary care than in primary care. This may be because secondary care patients have more severe disease, they receive a different treatment regimen, or the intervention is more closely supervised. However, conclusions of effectiveness should be considered in the light of the methodological weaknesses of the studies. Large pragmatic trials are needed of interventions delivered in primary care by appropriately trained primary care staff.

What is already known on this topic
Patients with functional somatic symptoms are common in primary care and may not receive effective mental health interventions

What this study adds
Research in secondary and primary care shows that cognitive behaviour therapy and behaviour therapy help patients with back pain and that antidepressants benefit patients with irritable bowel syndrome

Effect sizes are larger in secondary care than in primary care

Patients in secondary care with chronic fatigue syndrome may benefit from cognitive behaviour therapy

Future research should focus on large pragmatic trials with longer term follow up and economic evaluation




    Introduction
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

As many as one in five new consultations in primary care are for somatic symptoms for which no specific cause can be found.1 Patients with such symptoms often become frequent attenders, and their management poses considerable challenges for both general practitioners and specialists.2 Although systematic reviews have shown that certain mental health interventions are effective in these patients, the treatments are not always provided.3-6 This may be partly because general practitioners question the quality of the evidence and its relevance for their patients or because the evidence of effectiveness is not widely known.7-9 Much of the research has been carried out in specialist settings, as is often the case when management is shared between primary and secondary care, and findings from specialist settings may not be applicable to primary care.

We did this study to investigate whether there is good evidence that mental health interventions are effective for patients with common somatic symptoms and whether the results of trials in secondary care can be extrapolated to primary care. We selected three common somatic conditions for which general practitioners had indicated they would welcome guidance: chronic fatigue syndrome, irritable bowel syndrome, and chronic back pain.10 In assessing the quality of published research, we also sought to identify how future trials should be designed to provide more rigorous evidence.


    Method
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

We undertook a systematic review of randomised controlled trials, systematic reviews, and meta-analyses of mental health interventions for chronic fatigue syndrome, irritable bowel syndrome, and chronic back pain.

Search strategy
We searched PubMed, the Cochrane Library, PsycLIT, and Embase for English language papers published between 1966 and September 2001. We looked at the references cited in the identified meta-analyses, systematic reviews, and individual studies to find further studies and also searched key texts. 9 11 Six liaison psychiatrists, who were known to have an interest in functional somatic complaints, were asked to cite relevant literature. Box 1 gives the full search strategy


Box 1: Literature search strategy

Step 1: Computer assisted literature searches of the bibliographic databases: PubMed, Cochrane Collaboration database, Embase, and PsychLit for papers published between 1966 and September 2001 using the following search terms:

  • Somati* (and) treatment (or) therapy (or) rehabilitation (or) drug* (or) management (or) intervention
  • Somatoform (and) treatment (or) therapy (or) rehabilitation (or) drug* (or) management (or) intervention
  • Abnormal illness behaviour (and) treatment (or) therapy
  • Medically (near) unexplained symptom* (and) treatment (or) therapy
  • Psychophysiologic (and) treatment
  • Psychogenic (and) treatment
  • (Functional (near) symptom* (or) illness) and (treatment (or) therapy)
  • Unaccounted medical symptoms (and) treatment (or) therapy
  • Pain syndromes (and) treatment

All of the above searches were combined with (or stepwise limits conducted in PubMed): (i)meta-analysis, (ii) review, (iii) randomi*ed control*, (iv) control* trial

Additional searches combined the following key terms:

  • Chronic fatigue (or) irritable bowel (or) chronic back pain
  • Treatment (or) therapy (or) rehabilitation (or) drug* (or) management (or) intervention
  • Randomised controlled (or) RCTKL selected the trials to be included using the broad selection criteria (outlined above) and RR then selected relevant articles using the following criteria:
  • Randomised controlled studies on chronic fatigue syndrome, irritable bowel syndrome, or chronic back pain
  • Mental health interventions
  • Adult study populations (>18 years)
  • Studies reported in English language
  • Patients with symptoms attributable to physical disease were excluded from study

Step 2: The references contained in articles identified in step 1 were examined to identify further relevant studies.

Step 3: Relevant references in the Department of Health Report Treatment Choice in Psychological Therapies and Counselling: Evidence Based Clinical Practice Guideline, and in Mayou et al were identified.11

Step 4: Six liaison psychiatrists who have a special interest in this area were asked to cite relevant literature.

Inclusion criteria
We identified published studies of cognitive behaviour, cognitive, behaviour, brief interpersonal psychodynamic, and antidepressant therapy. For analysis of the randomised controlled trials, we pooled cognitive behaviour and cognitive therapy because there is no practical distinction between them and the studies gave insufficient details about the interventions to validate any distinction. Studies that included subjects whose symptoms were attributable to physical disease were excluded.

Data extraction and assessment of study quality
One of us (RR) extracted data from the identified papers and a second reviewer checked them (KL). Discrepancies were resolved by referring to the original studies. We extracted data on the source of the patient sample; patient characteristics; the intervention and comparison treatment and who carried them out; outcomes; and study dropouts and reasons for withdrawal. Studies were defined as primary care studies if they included patients who were recruited from the community or through their primary care physician. Ten studies included a mixture of primary and secondary care patients, and these were classified as primary care studies.12-21

Both reviewers independently noted methodological details using a checklist including randomisation, blinding of those assessing outcomes, and handling of attrition in the analysis. The methodological quality of much of this literature has been previously systematically assessed using quality scales.3-5 However, the scales vary in the dimensions covered and their complexity. We therefore assessed the relevant methodological aspects individually rather than use a composite score.22

Outcome measures and analysis
For all studies, we compared the findings of research from each setting by tabulating the reported health status and functional outcomes (tables 1-3). We compared initial disease severity of patients and treatment effect sizes between settings when studies used similar interventions and the same health status measures. In the limited number of cases in which we could compare primary and secondary care patients using the same outcome measure, the severity in each study was calculated by combining patients from all treatment arms. We calculated treatment effect sizes with 95% confidence intervals from the difference in mean health status after treatment and standardised them using Cohen's d.23 We combined treatment effects using fixed effects meta-analysis when two or more studies from the same setting used the same health status measure. A random effects meta-analysis was used if there was significant heterogeneity (P<0.05) of study effect sizes.


                              
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Table 1. Literature review of mental health interventions for chronic fatigue syndrome


                              
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Table 2. Literature review of mental health interventions for irritable bowel syndrome


                              
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Table 3. Literature review of mental health interventions for chronic back pain




    Results
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

We identified 61 randomised controlled studies 12-21 24-81 and two meta-analyses: one on the effectiveness of behaviour therapy for chronic back pain, and one on the effectiveness of antidepressants for irritable bowel syndrome. 3 4 One third (20) of the randomised controlled studies were defined as primary care studies (table 4). This included eight studies of patients who had been recruited solely through their primary care physician. 13 17 18 21 25 40 60 68 A further eight studies included patients who were recruited in two ways within the same trial: either by their primary care physician or self referred after media publicity. 12 14-16 19 20 37 41 The authors did not distinguish the source of referral when presenting their results. A further four studies recruited volunteers, but the inclusion criteria of two of these studies specified that participants must have had sick leave for their somatic symptom, and in the third study, the general practitioner was contacted to exclude organic disease. 39 41 77 The conclusions are summarised in box 2.


                              
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Table 4. Number of comparisons conducted in each treatment setting


Box 2: Summary of research findings for effectiveness of mental health interventions for patients with somatic symptoms in primary and secondary care

Chronic fatigue syndrome

Cognitive behaviour therapy---Seems to be effective in secondary care patients. One study suggests a lack of supremacy of cognitive behaviour therapy over counselling in primary care patients

Behavioural therapy---Some evidence of effectiveness of graded exercise in secondary care patients

Brief psychodynamic interpersonal therapy---No trials identified

Antidepressants---No evidence for sustained symptomatic improvement in primary or secondary care patients

Irritable bowel syndrome

Cognitive behaviour therapy---Mixed results. In studies that showed effectiveness (in both settings), this may reflect the training and experience of the therapist, rather than the efficacy of the intervention.

Behavioural therapy---Limited evidence for the effectiveness of relaxation training in primary care patients

Brief psychodynamic interpersonal therapy---Some evidence of effectiveness in secondary care refractory patients

Antidepressants---Seems to be effective in primary and secondary care patients

Chronic back pain

Cognitive behaviour therapy---Seems to be effective in primary and secondary care patients

Behavioural therapy---Seems to be effective in primary and secondary care patients

Brief psychodynamic interpersonal therapy---No trials identified

Antidepressants---Insufficient evidence to allow conclusions to be drawn

Treatments evaluated in primary and secondary care

Back pain
The effectiveness of cognitive behaviour therapy and behaviour therapy has been measured in both primary and secondary care patients. Of 16 studies of cognitive behaviour therapy for patients with back pain, seven were in primary care (891 patients) and nine in secondary care (625 patients). Patients from both settings reported sustained improvements in pain, disability, and depression. 17 19 20 24-36 A meta analysis of the effectiveness of behaviour therapy found a moderate positive effect on intensity of pain and a small positive effect on behavioural outcomes in patients, regardless of setting.3 Behaviour therapy also seems to be effective in both primary and secondary care. Eight out of nine primary care studies on 659 patients and five out of six secondary care studies with a total of 398 patients reported improvements in symptoms. 17 19 20 26 28 29 37-43 There was some evidence from both settings that these improvements were sustained at one year follow up. 18 39 41 The initial health status of secondary care patients was poorer than that of patients in primary care (table 5) but they reported greater improvements (figs 1 and 2, table 6).


                              
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Table 5. Health state before treatment in patients in primary care and secondary care studies (higher scores indicate greater severity for all measures except coping skills questionnaire)


                              
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Table 6. Standardised treatment effect sizes immediately after treatment for studies comparing intervention against control for back pain. Negative effect sizes indicate a benefit of treatment over control. Effect sizes with two or more references (shown in superscript) are aggregated



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Fig 1.    Standardised treatment effects and 95% confidence intervals for cognitive behaviour therapy versus control interventions in patients with back pain (negative effect sizes indicate a benefit for cognitive behaviour therapy)



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Fig 2.    Standardised treatment effects and 95% confidence intervals for behaviour therapy versus control interventions in patients with back pain (negative effect sizes indicate a benefit for behaviour therapy)

Chronic fatigue syndrome
Antidepressants in patients with chronic fatigue syndrome produced no sustained improvement. 12 44-46

Irritable bowel syndrome
A meta-analysis of the effect of antidepressants, regardless of setting, reported a moderate improvement in symptoms.4 Antidepressants seem to be effective in both primary and secondary care: improvements in physical symptoms and depression were reported in the study that included primary care patients and 10 out of 11 studies of 444 secondary care patients.21-55 We could compare treatment effect sizes in two of these studies, and these suggest that improvement in pain relief was far greater among secondary than primary care patients (table 7). 21 51 The two studies in which we could directly compare initial pain severity suggested that secondary care patients reported only slightly more severe pain than their counterparts in primary care, and patients in all these studies were similar in terms of symptom chronicity and age (table 5). 21 51


                              
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Table 7. Treatment effect sizes for chronic fatigue syndrome and irritable bowel syndrome in studies comparing intervention against control immediately after treatment and follow up. Positive effect sizes indicate a benefit of treatment over control

Treatments with uncertain effectiveness in primary care patients
The effectiveness of cognitive behaviour therapy in patients with chronic fatigue syndrome and irritable bowel syndrome has been measured in patients in both primary and secondary care but differences in treatment regimens limit the conclusions that can be drawn. Cognitive behaviour therapy has been effective in patients with chronic fatigue syndrome in secondary care, although brief cognitive behaviour therapy was ineffective.56-59 In primary care patients, there was no difference in effectiveness between brief therapy and counselling (table 7).60

Three studies of 169 primary care or community patients and five studies of 171 secondary care patients examined the effectiveness of cognitive behaviour therapy for irritable bowel syndrome. 13 14 16 61-65 All the secondary care studies reported significant improvements with cognitive behaviour therapy in symptoms and in coping.61-65 The two smaller primary care studies reported greater symptomatic improvement with cognitive behaviour therapy than in controls, but in the largest study cognitive behaviour therapy was no better than placebo. There were insufficient data to draw conclusions about treatment effectiveness in primary care for behaviour therapy in patients with chronic fatigue syndrome (promising results were reported in secondary care) and for behaviour therapy and brief psychodynamic therapy in patients with irritable bowel syndrome. 15 45 66-74




    Discussion
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

We found little or no research on the effectiveness of some interventions, such as brief psychodynamic interpersonal therapy. However, meta-analyses suggest that behaviour therapy is effective for chronic back pain and that antidepressants are effective for irritable bowel syndrome. Analysis of individual studies indicates that cognitive behaviour therapy and behaviour therapy for patients with back pain is more effective in patients in secondary care than those in primary care; antidepressant treatment for irritable bowel syndrome may also be more effective in secondary care. It should not, therefore, be assumed that interventions which are effective in secondary care will produce the same magnitude of effect in primary care. Instead, these findings need to be replicated independently in primary care patients.

Limitations of the evidence
For most treatments, we could draw only qualified conclusions because of methodological weaknesses in the research conducted. A major limitation of all the studies is that they evaluated the effect of interventions delivered by specialist therapists rather than primary care staff (box 3). Yet the main burden of disease occurs in primary care, and patients are unlikely to be referred to specialists because many would find it unacceptable and there is often a shortage of specialist resources.


Box 3: Randomised trials of mental health interventions for somatic conditions: methodological shortcomings and how they should be overcome.

1. Dearth of studies in primary care settings, with intervention provided by members of the primary care team ( doctor, nurse, counsellor) or lay person

right-arrow Identify elements of interventions which can be conducted in primary care and conduct pragmatic trials in primary care, by primary care professionals, on unselected patients

2. Inadequate information about the content and quality of the intervention and the comparison group

right-arrow Use treatment manual and quality checks

3. Lack of data on characteristics of the patient sample

right-arrow Conduct exploratory phase to assess illness attributions. Use results to increase recruitment and to reduce drop outs, and to tailor intervention to the beliefs and attitudes of the patients

right-arrow Collect data on participants, non-eligible patients and drop outs

4. Limited assessment of outcome: short term only, no cost effectiveness data

right-arrow Measure long term health outcomes in each group

right-arrow Conduct economic analyses as part of trial

5. Studies commonly not powerful enough to detect clinically important differences with high precision.

right-arrow Undertake power calculations to enable clinically important differences to be detected and measured with high precision

6. Great diversity of measurement instruments used

right-arrow Limit the use of health outcome measures to validated instruments. Use generic and symptom or disease specific measures

7. Problems of internal validity

right-arrow Address causes of selection, performance, detection and attrition bias

There was sometimes insufficient detail for us to be sure how the intervention was implemented and whether it was provided in a standardised way. Only eight studies stated that a treatment manual was used, and only two studies (by the same author) monitored adherence to the protocol. 16 17 20 25 26 36 37 42 Quality checks were hardly ever mentioned; at best there was rating by an independent assessor to check that the intervention and control condition were distinct and intervention credibility checks. 13 56 60 63 68 There was also a lack of data on characteristics of the patients. Age and symptom duration were usually the only data provided. Dropout rates and their causes were rarely given. 12 16 19 28 29 44 46 48 52-54 56 67 71 75

There were few studies of long term outcome. Most studies (79%) measured only immediate outcome. Longer term outcome studies would provide evidence of sustained effectiveness and reduce the possibility of non-specific effects such as those due to therapist attention or patient expectations.82 Cost effectiveness is likely to be an important motivator for changing practice, but only one study examined this.83

Patients with the conditions we studied characteristically have symptoms for many years, and such patients are likely to be frequent attenders in primary care. If, as shown for patients with other conditions, the effect of cognitive behaviour therapy continues to improve with time, it could be a highly cost effective intervention.84

Another methodological shortcoming was that studies were commonly not powerful enough to detect clinically important differences. Sample sizes were often less than 20 patients. 14 30 46 50 64 68 75 76 77 80 In addition, many different outcome measures were used, which limited the number of comparisons that could be made between settings. Finally, the studies commonly had problems of internal validity---for example, the absence of strict randomisation and of blind assessment of observer rated outcomes. 18 28-35 39 40 43 50 52 53 55 59 61-63 70 71 75 73 74 78

Explanations for findings
We identified four factors that may contribute to the greater improvements seen in secondary care than primary care. The first factor relates to differences between patients in the two settings. Patients in secondary care were more severely ill than their primary care counterparts (for cognitive behaviour therapy and behaviour therapy in back pain). Other unaccounted patient differences may explain the greater improvement in secondary care than primary care for patients with irritable bowel syndrome taking antidepressants. The second factor concerns differences in the treatment regimen. In the two studies of antidepressants in irritable bowel syndrome for which we could compare treatment effect sizes, the minimum therapeutic dose was used in the primary care study, whereas a dose exceeding the recommended maximum dose was used in the secondary care study. 46 50 Similarly, primary care patients with chronic fatigue syndrome received just four hours of cognitive behaviour therapy whereas secondary care patients received 16 hours of treatment. 58 60 The third factor concerns differences in treatment provision: for cognitive behaviour therapy in irritable bowel syndrome, studies that reported an improvement used fewer therapists, most of whom were supervised by doctors, than studies that found no effect. The final factor is concerned with differences in study design. In the studies of behaviour therapy for back pain, the control group in the secondary care setting was assigned to the waiting list, whereas in the primary care study they were provided with an educational package that could be regarded as an active treatment. 38 43

Implications
Pragmatic studies of the effectiveness of psychological interventions in primary care and on unselected patients are needed to provide a basis for decisions about healthcare provision.85 Studies should identify which elements of an intervention require specialist training and which require specialist intervention. They should also measure the effectiveness of interventions carried out by primary care staff after a realistic amount of training and with the aid of standard manuals for patients and practitioners.86

The standards of reporting of trials need to be improved and harmonised to ensure that sufficient information is provided. The revised CONSORT criteria provide general guidance on trial reporting but more detailed directions are required when describing complex mental health interventions (box 4).87 As well as precise details of the intervention, baseline clinical data and data about participants deemed ineligible should be provided to inform decisions about the extrapolation of the findings to other people with the condition.


Box 4: Checklist of items to include when reporting randomised trials of mental health interventions for somatic conditions

Give precise details of the interventions intended for each group, including:

  • How, when, and by whom they are administered (including the nature and level of training of therapist, and details of the terms used to describe the intervention to the patient)
  • Provision of treatment manual (including frequency, timing, content of interventions)
  • Description of quality checks (such as adherence to protocol, independent assessors of quality of intervention)
  • Additional resources required (including equipment, space, support staff)
  • Also give clear information on
  • Characteristics of eligible v ineligible patients, recruited v not recruited patients, and those who completed study v dropouts
  • Baseline demographic and clinical characteristics (including age, sex, comorbidity, baseline severity, duration, illness attributions by patient (these may be difficult to specify but are useful, particularly in developing the intervention)
  • Reasons for dropout

Trials of mental health interventions should measure cost effectiveness and long term outcomes. Although outcomes and illness presentations are multifaceted and often difficult to encapsulate in one or two rating scales, this does not negate the need to rationalise the use of outcome instruments. Where possible, well tested instruments should be used and a primary outcome measure salient to both patients and clinicians should be selected. The use of both generic instruments, such as the SF-36, and of disease and symptom specific instruments should be considered.88 Trials of effectiveness should be accompanied by qualitative research on the health beliefs and attitudes of participants and non-participants. This will enable interventions to be tailored to improve recruitment and dropout rates.

Study designs should include an appropriate randomisation method, blind assessment of outcomes, and consistent handling of dropouts from each group. Whenever possible, the only difference in care between study groups should be the intervention being studied.




    Conclusion
Top
Abstract
Introduction
Method
Results
Discussion
Conclusion
References

Research from both primary and secondary care suggests that that cognitive behaviour therapy and behaviour therapy may help patients with back pain and that patients with irritable bowel syndrome may improve with antidepressants but effect sizes tend to be larger in secondary care. Thus, it cannot be assumed that results from secondary care can be extrapolated to primary care. The quality and amount of evidence on mental health interventions for back pain, chronic fatigue syndrome, and irritable bowel syndrome is sometimes poor.

    Acknowledgments

This study is part of a research programme examining the methods of group decision making for developing clinical guidelines. This research programme is overseen by a steering committee comprising three of the authors (A Haines, NB, and TS) and T Marteau and S Carter.

Contributors: RR and NB were awarded the grant that funded this work. A Haines suggested comparing findings in primary and secondary care. RR and KL identified, reviewed, and tabulated the studies. TS advised on the classification of interventions. A Hutchings analysed the data. RR wrote the first draft of the paper and all authors contributed to later drafts. RR is the guarantor.

    Footnotes

Funding: RR and KEL are funded by the Medical Research Council.

Competing interests: None declared.


    References
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Abstract
Introduction
Method
Results
Discussion
Conclusion
References

1. Bridges KW, Goldberg DP. Somatic presentation of DSM-III psychiatric disorders in primary care. J Psychosom Res 1985; 29: 563-569[CrossRef][Web of Science][Medline].
2. Jyvasjarvi S, Joukamaa M, Vaisanen E, Larivaara P, Kivela S, Keinanen-Kiukaanniemi S. Somatising frequent attenders in primary health care. Psychosom Res 2001; 50(4): 185-192.
3. Van Tulder M, Ostelo R, Vlaeyen J, Linton S, Morley S, Assendelf W. Behavioural treatment for chronic low back pain. Cochrane Database Syst Rev 2000;(2):CD002014.
4. Jackson J, O'Malley P, Tomkins G, Lalden E, Santoro J, Kroenke K. Treatment of functional gastrointestinal disorders with antidepressants: a meta-analysis. Am J Med 2000; 108: 65-72[CrossRef][Web of Science][Medline].
5. Whiting P, Bagnall A-M, Sowden A, Cornell J, Mulrow C, Ramirez G. Interventions for the treatment and management of chronic fatigue syndrome. JAMA 2001; 286: 1360-1368[Abstract/Free Full Text].
6. Raine R, Lewis L, Sensky T, Hutchings A, Hirsch S, Black N. Patient determinants of mental health interventions in primary care. Br J Gen Pract 2000; 50: 620-625[Web of Science][Medline].
7. Haines A, Jones R. Implementing the findings of research. BMJ 1994; 308: 1488-1492[Free Full Text].
8. Whitford DL, Jelley D, Gandy S, Southern A, van Zwanenberg T. Making research relevant to the primary health care team. Br J Gen Pract 2000; 50: 573[Web of Science][Medline].
9. Black N. Evidence based policy: proceed with care. BMJ 2001; 323: 275-279[Free Full Text].
10. Department of Health. Treatment choice in psychological therapies and counselling: evidence based clinical practice guideline. London: Department of Health, 2001.
11. Mayou R, Bass C, Sharpe M. Treatment of somatic symptoms. Oxford: Oxford University Press, 1995.
12. Vercoulen J, Swanink C, Zitman F, Vreden S, Hoofs M, Fennis J, et al. Randomised, double-blind, placebo-controlled study of fluoxetine in chronic fatigue syndrome. Lancet 1996; 347: 858-861[CrossRef][Web of Science][Medline].
13. Payne A, Blanchard E. A controlled comparison of cognitive therapy and self-help support groups in the treatment of irritable bowel syndrome. J Consult Clin Psychol 1995; 63: 779-786[CrossRef][Web of Science][Medline].
14. Greene B, Blanchard E. Cognitive therapy for irritable bowel syndrome. J Consult Clin Psychol 1994; 62: 576-582[CrossRef][Web of Science][Medline].
15. Blanchard E, Green B, Scharff L, Schwartz-McMorris S. Relaxation training as a treatment for irritable bowel syndrome. Biofeedback Self Regul 1993; 18(3): 125-132[CrossRef][Web of Science][Medline].
16. Blanchard E, Schwarz, Suls J, Gerardi M, Scharff L, Greene B, et al. Two controlled evaluations of multi-component psychological treatment of irritable bowel syndrome. Behav Res Ther 1992; 30: 175-189[CrossRef][Web of Science][Medline].
17. Newton-John T, Spence S, Schotte D. Cognitive-behavioural therapy versus EMG biofeedback in the treatment of chronic low back pain. Behav Res Ther 1995; 33(6): 691-697[CrossRef][Web of Science][Medline].
18. Rose M, Reilly J, Pennie B, Bowen-Jones K, Stanley I, Slade P. Chronic low back pain rehabilitation programs. Spine 1997; 22: 2246-2253[CrossRef][Web of Science][Medline].
19. Turner J, Jensen M. Efficacy of cognitive therapy for chronic low back pain. Pain 1993; 52: 169-177[CrossRef][Web of Science][Medline].
20. Turner J, Clancy S. Comparison of operant behavioral and cognitive-behavioral group treatment for chronic low back pain. J Consult Clin Psychol 1988; 56: 261-266[CrossRef][Web of Science][Medline].
21. Myren J, Lovland B, Larssen S-E, Larsen S. A double-blind study of the effect of trimipramine in patients with the irritable bowel syndrome. Scand J Gastroenterol 1984; 19: 835-843[Web of Science][Medline].
22. Juni P, Altman DG, Egger M. Assessing the quality of controlled clinical trials. BMJ 2001; 323: 42-46[Free Full Text].
23. Deeks J, Altman D, Bradburn M. Statistical methods for examining heterogeneity and combining results from several studies in meta-analysis. In: Egger M, Smith GD, Altman DG, eds. Systematic reviews in health care: meta-analysis in context. 2nd ed. London: BMJ Books, 2001.
24. Strong J. Incorporating cognitive-behavioral therapy with occupational therapy: A comparative study with patients with low back pain. J Occup Rehabil 1998; 8: 61-71.
25. Moore J, Von Korff M, Cherkin D, Saunders K, Lorig K. A randomized trial of a cognitive-behavioral program for enhancing back pain self care in a primary care setting. Pain 2000; 88: 145-153[CrossRef][Web of Science][Medline].
26. Kole-Snijders A, Vlaeyen J, Goossens M, Rutten-van Molken M, Heuts P, Breukelen G. Chronic low-back pain: what does cognitive coping skills training add to operant behavioral treatment? Results of a randomized clinical trial. J Consult Clin Psychol 1999; 67: 931-944[CrossRef][Web of Science][Medline].
27. Goossens M, Rutten-van Molken M, Kole-Snijiders A, Vlaeyen J, Breukelen G, Leidl R. Health economic assessment of behavioural rehabilitation in chronic low back pain: a randomised clinical trial. Health Econ 1998; 7: 39-51[CrossRef][Web of Science][Medline].
28. Vlaeyen J, Haazen I, Schuerman J, Kole-Snijders A, van Eek H. Behavioural rehabilitation of chronic low back pain: comparison of an operant treatment, an operant-cognitive treatment and an operant-respondent treatment. Br J Clin Psychol 1995; 34: 95-118.
29. Nicholas M, Wilson P, Goyen J. Operant-behavioural and cognitive-behavioural treatment for chronic low back pain. Behav Res Theapy 1991; 29: 225-238.
30. Nicholas M, Wilson P, Goyen J. Comparison of cognitive-behavioral group treatment and an alternative non-psychological treatment for chronic low back pain. Pain 1992; 48: 339-347[CrossRef][Web of Science][Medline].
31. Altmaier E, Lehmann T, Russell D, Weinstein J, Kao C. The effectiveness of psychological interventions for the rehabilitation of low back pain: a randomised controlled trial evaluation. Pain 1992; 49: 329-335[CrossRef][Web of Science][Medline].
32. Bendix A, Bendix T, Vægter, Lund C, Frolund L, Holm L. Multidisciplinary intensive treatment for chronic low back pain: a randomized prospective study. Cleve Clin J Med 1996; 63: 62[Web of Science][Medline].
33. Bendix A, Bendix T, Lund C, Kirbak S, Ostenfeld S. Comparison of three intensive programs for chronic back pain patients: a prospective, randomized, observer-blinded study with one-year follow-up. Scand J Rehab Med 1997; 29: 81-89[Web of Science][Medline].
34. Bendix A, Bendix T, Hæstrup C, Busch E. A prospective, randomized 5-year follow-up study of functional restoration in chronic low back pain patients. Eur Spine J 1998; 7: 111-119[CrossRef][Medline].
35. Bendix A, Bendix T, Labriola M, Boekgaard P. Functional restoration for chronic low back pain. Spine 1998; 23: 717-725[CrossRef][Web of Science][Medline].
36. Basler H-D, Jakle C, Kroner-Herwig B. Incorporation of cognitive-behavioural treatment into the medical care of chronic low back patients: a controlled randomized study in German pain treatment centres. Patient Educ Counselling 1997; 31: 113-124[CrossRef][Web of Science][Medline].
37. Turner J, Clancy S, McQuade J, Cardenas D. Effectiveness of behavioral therapy for chronic low back pain: A component analysis. J Consult Clin Psychol 1990; 58: 573-579[CrossRef][Web of Science][Medline].
38. Donaldson S, Romney D, Donaldson M, Skubick D. Randomized study of the application of single motor unit biofeedback training to chronic low back pain. J Occup Rehab 1994; 4: 23-27.
39. Bru E, Mykletun R, Berge W, Svebak S. Effects of different psychological interventions on neck, shoulder and low back pain in female hospital staff. Psychology and Health 1994; 9: 371-382.
40. Lindstrom I, Ohlund C, Eek C, Wallin L, Peterson L-E, Fordyce W, et al. The effect of graded activity on patients with subacute low back pain: a randomised prospective clinical study with an operant-conditioning behavioral approach. Physical Therapy 1992; 72: 279-290[Abstract/Free Full Text].
41. Linton S, Bradley L, Jenson I, Spangfort E, Sundell L. The secondary prevention of low back pain: a controlled study with follow-up. Pain 1989; 36: 197-207[CrossRef][Web of Science][Medline].
42. Philips H. The effects of behavioural treatment on chronic pain. Behav Res Ther 1987; 25: 365-377[CrossRef][Web of Science][Medline].
43. Turner J. Comparison of group progressive-relaxation training and cognitive-behavioral group therapy for chronic low back pain. J Consult Clin Psychol 1982; 50: 757-765[CrossRef][Web of Science][Medline].
44. Hickie I, Wilson A, Wright M, Bennett B, Wakefield D, Lloyd A. A randomized, double-blind, placebo-controlled trial of moclobemide in patients with chronic fatigue syndrome. J Clin Psychiatry 2000; 61: 643-648[Web of Science][Medline].
45. Wearden A, Morriss R, Mullis P, Strickland D, Pearson D, Appleby L, et al. Randomised, double-blind, placebo-controlled treatment trial of fluoxtine and graded exercise for chronic fatigue syndrome. Br J Psychiatry 1998; 172: 485-490[Abstract/Free Full Text].
46. Natelson BCJ, Pareja J, Policastro T, Findley T. Randomized, double blind, controlled placebo-phase trial of low dose phenelzine in the chronic fatigue syndrome. Psychopharmacology 1996; 124: 226-230[CrossRef][Medline].
47. Myren J, Groth H, Larssen S-E, Larsen S. The effect of trimipramine in patients with the irritable bowel syndrome. Scand J Gastroenterol 1982; 17: 871-875[Web of Science][Medline].
48. Vji J, Jiloha R, Kumar N, Madhu S, Malika V, Anand B. Effect of antidepressant drug (Doxepin) on irritable bowel syndrome patients. Indian J Psychiatry 1991; 33: 243-246.
49. Rajagopalan M, Kurian G, John J. Symptom relief with amitriptyline in the irritable bowel syndrome. J Gastroenterol Hepatol 1998; 13: 738-741[Web of Science][Medline].
50. Mertz H, Fass R, Kodner A, Yan-Go F, Fullerton S, Mayer E. Effect of amitryptiline on symptoms, sleep and visceral perception in patients with functional dyspepsia, Am J Gastroenterol 1998; 93: 160-164[CrossRef][Web of Science][Medline].
51. Tanum L, Malt U. A new pharmacologic treatment of functional gastrointestinal disorder: a double blind placebo controlled study with mianserin. Scand J Gastroenterol 1996; 31: 318-325[Web of Science][Medline].
52. Alevizos B, Christodoulou C, Ioannidis A, Voulgari A, Mantidis A, Spiliadis C. The efficacy of amineptine in the treatment of depressive patients with irritable bowel syndrome. Clin Neuropharmacol 1989; 12: S66-S76.
53. Greenbaum D, Mayle J, Vanegeren L, Jerome J, Mayor J, Greenbaum R, et al. Effects of desipramine on irritable bowel syndrome compared with atropine and placebo. Digest Dis Sci 1987; 32: 257-266.
54. Heffner J, Wilder R, Wilson D. Irritable colon and depression. Psychosomatics 1978; 19: 540-547[Free Full Text].
55. Tripathi B, Misra N, Gupta A. Evaluation of tricyclic compound (trimipramine) vis-a-vis placebo in irritable bowel syndrome (double blind randomised study). J Assoc Physicians India 1983; 31: 201-203[Medline].
56. Prins J, Bleijenberg G, Bazelmans E, Elving L, de Boo T, Severns J, et al. Cognitive behaviour therapy for chronic fatigue syndrome: a multi-centre randomised controlled trial. Lancet 2001; 357: 841-847[CrossRef][Web of Science][Medline].
57. Deale A, Chalder T, Marks I, Wessely S. Cognitive behaviour therapy for chronic fatigue syndrome: a randomized controlled trial. Am J Psychiatry 1997; 154: 408-414[Abstract].
58. Sharpe M, Hawton K, Simkin S, Surawy C, Hackmann A, Klimes I, et al. Cognitive behaviour therapy for the chronic fatigue syndrome: a randomised controlled trial. BMJ 1996; 312: 22-26[Abstract/Free Full Text].
59. Lloyd A, Hickie I, Brockman A, Hickie C, Wilson A, Dwyer J, et al. Immunologic and psychologic therapy for patients with chronic fatigue syndrome: a double blind, placebo controlled trial. Am J Med 1993; 94: 197-203[CrossRef][Web of Science][Medline].
60. Ridsdale L, Godfrey E, Chalder T, Seed P, King M, Wallace T, et al. Chronic fatigue in general practice: is counselling as good as cognitive behaviour therapy? A UK randomised trial. Br J Gen Pract 2001; 51: 19-24[Web of Science][Medline].
61. Van Dulmen A, Fennis J, Blenijenberg G. Cognitive-behavioural group therapy for irritable bowel syndrome: effects and long term follow up. Psychosom Med 1996; 58: 508-514[Abstract/Free Full Text].
62. Rumsey N. Group stress management programmes v pharmacological treatment in the treatment of irritable bowel syndrome. In: Heaton K, Goeting N, eds. Towards confident management of irritable bowel syndrome: current approaches. London: Duphar Medical Relations, 1991.
63. Lynch P, Zamble E. A controlled behavioral treatment study of irritable bowel syndrome. Behav Ther 1989; 20: 509-523[CrossRef].
64. Neff D, Blanchard E. A multi-component treatment for irritable bowel syndrome. Behav Ther 1987; 18: 70-83[CrossRef].
65. Bennett P, Wilkinson S. A comparison of psychological and medical treatment of irritable bowel syndrome. Br J Clin Psychol 1985; 24: 215-216.
66. Fulcher K, White P. Randomised controlled trial of graded exercise in patients with the chronic fatigue syndrome. BMJ 1997; 314: 1647-1652[Abstract/Free Full Text].
67. Powell PBR, Nye F, Edwards R. Randomised controlled trial of patient education to encourage graded exercise in chronic fatigue syndrome. BMJ 2001; 322: 387-390[Abstract/Free Full Text].
68. Keefer L, Blanchard E. The effects of relaxation response meditation on the symptoms of irritable bowel syndrome: results of a controlled treatment study. Behav Res Ther 2001; 39: 801-811[CrossRef][Web of Science][Medline].
69. Shaw G, Srivastava E, Saldier M, Swann P, James J, Rhodes J. Stress management for irritable bowel syndrome: a controlled trial. Digestion 1991; 50: 36-42[CrossRef][Web of Science][Medline].
70. Corney R, Stanton R, Newell R, Clare A, Fairclough P. Behavioural psychotherapy in the treatment of irritable bowel syndrome J Psychosom Res 1990; 35: 461-469.
71. Guthrie E, Creed F, Dawson D, Tomenson B. A randomised controlled trial of psychotherapy in patients with refractory irritable bowel syndrome. Br J Psychiatry 1993; 163: 315-321[Abstract/Free Full Text].
72. Guthrie E, Creed F, Dawson D, Tomenson B. A controlled trial of psychological treatment for the irritable bowel syndrome. Gastroenterology 1991; 100: 450-457[Web of Science][Medline].
73. Svedlund J, Sjodin I, Ottosson J-O, Dotevall G. Controlled study of psychotherapy in irritable bowel syndrome. Lancet 1983; ii: 589-592.
74. Svedlund J, Sjodin I. A psychosomatic approach to treatment in the irritable bowel syndrome and peptic ulcer disease with aspects of the design of clinical trials. Scand J Gastroenterol 1985; 20 (suppl 109): 147-151[CrossRef][Web of Science].
75. Loldrup D, Langemark M, Hansen H, Olesen J, Bech P. Clomipramine and mianserin in chronic idiopathic pain syndrome: a placebo controlled study. Psychopharmacology 1989; 99: 1-7[CrossRef][Medline].
76. Pheasant H, Bursk A, Goldfarb J, Azen S, Weiss J, Borelli L. Amitriptyline and chronic low-back pain: a randomized double-blind crossover study. Spine 1983; 8: 552-557[CrossRef][Web of Science][Medline].
77. Nouwen A. EMG biofeedback used to reduce standing levels of paraspinal muscle tension in chronic low back pain. Pain 1983; 17: 353-360[CrossRef][Web of Science][Medline].
78. Lancaster-Smith M, Pinto P, Anderson J, Schiff A. Influence of drug treatment on the irritable bowel syndrome and its interaction with psychoneurotic morbidity. Acta Psychiatr Scand 1982; 66: 33-41[Web of Science][Medline].
79. Deale A, Husain K, Chalder T, Wessely S. Long term outcome of cognitive behavior therapy versus relaxation therapy for chronic fatigue syndrome: a five year follow up study. Am J Psych 2001; 158: 2038-2042[Abstract/Free Full Text].
80. Steinhart M, Wong P, Zarr M. Therapeutic usefulness of amitriptyline in spastic colon syndrome. Int J Psychiatry Med 1981; 11: 45-57[Web of Science][Medline].
81. Linton S, Andersson T. Can chronic disability be prevented? A randomized trial of a cognitive-behaviour intervention and two forms of information for patients with spinal pain. Spine 2000; 25: 2825-2831[CrossRef][Web of Science][Medline].
82. Chilvers C, Dewey M, Fielding K, Gretton V, Miller P, Palmer B, et al. Antidepressant drugs and generic counselling for treatment of major depression in primary care: randomised trial with patient preference arms. BMJ 2001; 322: 772-775[Abstract/Free Full Text].
83. Chisholm D, Godfrey E, Ridsdale L, Chalder T, King M, Seed P, et al. Chronic fatigue in general practice: economic evaluation of counselling versus cognitive behaviour therapy. Br J Gen Pract 2001; 51: 15-18[Web of Science][Medline].
84. De Rubeis R, Crits-Christoph P. Empirically supported individual and group psychological treatments for adult mental disorders. J Consult Clin Psychol 1998; 66: 37-52[CrossRef][Web of Science][Medline].
85. Shwartz D, Lellouch J. Explanatory and pragmatic attitudes in therapeutic trials. J Chron Dis 1976; 20: 637-648.
86. Evans K, Tryer P, Catalan J, Schmidt U, Davidson K, Dent J, et al. Manual-assisted cognitive-behaviour therapy (MACT): a randomised controlled trial of a brief intervention with bibliotherapy in the treatment of recurrent deliberate self-harm. Psychol Med 1999; 29: 19-25[CrossRef][Web of Science][Medline].
87. Moher D, Schulz KF, Altman DG, for the CONSORT group. The CONSORT statement: revised recommendations for improving the quality of parallel-group randomised trials Lancet 2001; 357: 1191-1194[CrossRef][Web of Science][Medline].
88. Ware J, Sherbourne C. The MOS 36-item short form health survey (SF-36): I. Conceptual framework and item selection. Med Care 1992; 30: 473-483[Web of Science][Medline].

(Accepted 23 May 2002)


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