- A O'Cathain, research fellow ()a,
- S J Walters, lecturera,
- J P Nicholl, professora,
- K J Thomas, senior research fellowa,
- M Kirkham, professorb
- a School of Health and Related Research, University of Sheffield, Regent Court, Sheffield S1 4DA
- b Women's Informed Childbearing and Health Research Group, School of Nursing and Midwifery, University of Sheffield, Sheffield S3 7ND
- Correspondence to: A O'Cathain
- Accepted 5 October 2001
Objective: To assess the effect of leaflets on promoting informed choice in women using maternity services.
Design: Cluster trial, with maternity units randomised to use leaflets (intervention units) or offer usual care (control units). Data collected through postal questionnaires.
Setting: 13 maternity units in Wales.
Participants: Four separate samples of women using maternity services. Antenatal samples: women reaching 28 weeks' gestation before (n=1386) and after (n=1778) the intervention. Postnatal samples: women at eight weeks after delivery before (n=1741) and after (n=1547) the intervention.
Intervention: Provision of 10 pairs of Informed Choice leaflets for service users and midwives and a training session for staff in their use.
Main outcome measures: Change in the proportion of women who reported exercising informed choice. Secondary outcomes: changes in women's knowledge; satisfaction with information, choice, and discussion; and possible consequences of informed choice.
Results: There was no change in the proportion of women who reported that they exercised informed choice in the intervention units compared with the control units for either antenatal or postnatal women. There was a small increase in satisfaction with information in the antenatal samples in the intervention units compared with the control units (odds ratio 1.40, 95% confidence interval 1.05 to 1.88). Only three quarters of women in the intervention units reported being given at least one of the leaflets, indicating problems with the implementation of the intervention.
Conclusion: In everyday practice, evidence based leaflets were not effective in promoting informed choice in women using maternity services.
What is already known on this topic
Decision aids can help patients to participate in their care
Ten evidence based leaflets (Informed Choice) are used by maternity services in the United Kingdom to promote informed choice in women using these services
What this paper adds
The leaflets did not help to promote informed choice in maternity care
Decision aids may not be effective in the real world
There is a growing consensus that people should be informed about, and able to influence, decisions about their own health care. 1 2 Decision aids, which present the options available to patients with evidence from research on their effects, can help people to participate in decisions about their care.3 Midwives Information and Resource Service (MIDIRS) and the NHS Centre for Reviews and Dissemination have produced a set of 10 leaflets on informed choice in maternity care. The leaflets summarise evidence on 10 decisions that women face in pregnancy and childbirth to encourage their involvement in decisions about their own care. Many maternity units buy the leaflets, yet little is known about their effectiveness.
We investigated whether the leaflets promoted informed choice and led to increased levels of knowledge, satisfaction with information, satisfaction with the way choices were made, and discussion with health professionals. We also examined whether they changed the actions women took or the services they used.
We tested the hypotheses in a cluster randomised controlled trial, with maternity units as clusters, in everyday practice. Qualitative research was undertaken alongside the trial to explore the use of the leaflets in practice and is reported separately.4
We randomised maternity units rather than individual women because of the risk of women sharing the leaflets in an individual level trial. Units were included if they had not already purchased the leaflets and had over 1000 deliveries annually. Twelve of the 15 large maternity units in Wales had not already purchased the leaflets and agreed to participate in the study. We also included a small unit under the managerial control of one of the 12 larger units. Maternity units were grouped into 10 clusters because some shared management or clinicians. Clusters were paired on the basis of their annual numbers of deliveries to ensure balance in the two arms of the trial. Members of pairs were randomly assigned by tossing a coin to receive the set of leaflets (five intervention units) or to continue with usual care (five control units). The intervention is described in the box.
Ten pairs of Informed Choice leaflets:
Support in labour
Listening to your baby's heartbeat during labour
Ultrasound scans—should you have one?
Alcohol and pregnancy
Positions in labour and delivery
Epidurals for pain relief in labour
Feeding your baby—breast or bottle?
Looking for Down's syndrome and spina bifida in pregnancy
Breech baby: What are your choices?
Where will you have your baby - hospital or home?
Leaflets were in pairs—a women's leaflet, designed to be accessible and give information about the benefits and risks of options available, and a more detailed professionals' leaflet, with references for the research on which it is based, which could be accessed by women through the midwife. The leaflets were designed to be given by health professionals to women at different stages of pregnancy
Each intervention unit received sets of leaflets in May 1998 for an eight month period. A two hour training session was provided for staff. Training material was left with managers for cascade training
Women in the intervention arm of the trial received the leaflets relevant to early pregnancy at their first booking appointment (10-12 weeks' gestation) and the other leaflets at 34-36 weeks' gestation
We identified two samples of women. The first sample was all women who reached 28 weeks' gestation during a six week period and were receiving antenatal care in any setting (antenatal sample). Women were identified through hospital computer systems and the records of midwives and clerks in hospital and community antenatal clinics. The second sample was all women who delivered during a six week period (postnatal sample). Women were identified through child health computer records and hospital and home delivery registers. Women were excluded if they lived outside the catchment area of the hospital or in areas where antenatal care was provided by midwives from other hospitals, were under 16 years old, or had miscarried or if their baby had died or was seriously ill.
We identified an antenatal sample and a postnatal sample before the introduction of the leaflets and again nine months after they were introduced. We assessed outcomes using a postal questionnaire sent to women in these four different samples (figure). Women in the antenatal samples received the questionnaire at 28 weeks' gestation, and women in the postnatal samples received the questionnaire eight weeks after delivering their babies. Up to two reminders were sent at intervals of three weeks. The second reminder for the women in the antenatal samples was a shorter questionnaire that covered only key questions.
The primary outcome was the proportion of women who answered “yes” to the question “Have you had enough information and discussion with midwives or doctors to make a choice together about all the things that happened during maternity care?” with the options “yes,” “partly,” “no,” “there was no choice,” and “did not apply.” As informed choice is a difficult concept to measure2 we also asked women about the role they took when choices were made, with six options ranging from “active” to “passive.”5
Secondary outcomes were the “components” and the “consequences” of informed choice. The components measured were women's levels of knowledge of the 10 topics covered by the leaflets; satisfaction with information and with how choices had been made; and views of whether they had had sufficient discussion with health professionals. The consequences measured were the actions taken or services used by women. We also collected data on sociodemographic factors, parity, and women's preferences for involvement in decision making.5
Validation and quality assurance
We developed and piloted some measures specifically for the study on the basis of interviews with women in three maternity units not involved in this trial.6 Other measures were modified from published sources. The questionnaires were piloted by post outside the study area. Ethical approval was obtained for the study in each area.
Sample size and statistical analysis
Assuming an intraclass correlation coefficient of 0.007 and an average cluster size of 200 we calculated we would need a sample size of 925 in the intervention units and 925 in the control units for each of the antenatal and postnatal samples. This would give us an 80% chance of detecting an increase from 50% to 60% in the proportion of women reporting that they made informed choices in the intervention units compared with no change in the control units, at a two tailed significance level of 5%. We paired maternity units to ensure balance and undertook an unmatched analysis.7 We compared sociodemographic variables of respondents in all four antenatal samples and in all four postnatal samples at the individual level using analysis of variance and χ2 tests. We compared any changes in the intervention units with changes over the same period in the control units using multilevel modelling. 8 9 Analysis was by intention to treat. We adjusted for women's age, age at leaving full time education, parity, and preference for involvement in decision making in the analyses. Intraclass correlation coefficients were 0.01 and 0.002 for the change in informed choice in antenatal and postnatal samples respectively.
Response rates—The overall response rate to the questionnaires was 64% (6452/10 070), with a rate of 65% (3164/4835) for the antenatal sample and 63% (3288/5235) for the postnatal sample. Response rates were lower in women with manual occupations and from ethnic minorities but did not differ by type of delivery, type of pain relief, parity, or age.6
Comparison of intervention and control groups—Sociodemographic variables of respondents in all four antenatal samples were similar (table 1). Women's age was different in the four postnatal samples, with respondents after the intervention an average of about seven months younger than respondents before.
Impact on informed choice—Before the intervention about half of women in both intervention and control units reported exercising informed choice “overall” in their maternity care. After the intervention, this proportion increased slightly in both groups (table 2) but with no significant difference in the change between groups. Results were similar for the proportion of women reporting active involvement in decision making. In the antenatal samples there were increases in knowledge, discussion, and satisfaction with information and with the way choices were made in intervention units (tables 2 and 3). They were not significant, however, with the exception of satisfaction with information. For this variable the difference in change was less than the minimum important difference of 10 percentage points. There was only one change in postnatal samples, with an increase of 0.24 points on a 10 point knowledge score, which was no longer significant after adjustment for covariates (table 3).
Consequences of informed choice—Given that there was no change in the proportion of women who reported that they exercised informed choice we would not expect changes in choices made. The one significant difference, which was in the proportion of women having screening tests for Down's syndrome and spina bifida, was due in part to an increase in reported uptake in the control units (table 4).
Uptake of leaflets—During the intervention period there was a significant increase in the proportion of women who reported that they had been given any of the Informed Choice leaflets in the intervention units compared with the control units, which showed little change (table 5). However, it was difficult to assess the uptake of the intervention leaflets with any precision. A large minority of women in the intervention units (44%) reported that they had been given at least one of the Informed Choice leaflets before the intervention had taken place (table 5). It is possible that a few Informed Choice leaflets were distributed in all the maternity units before the trial. However, most of this reported use probably relates to leaflets other than those under study because women had difficulty in distinguishing the intervention leaflets from other leaflets available in the maternity units.
In this randomised controlled trial the use of Informed Choice leaflets did not change the proportion of women who reported exercising informed choice, or components or consequences of informed choice, in maternity care. This is surprising as a recent systematic review concluded that decision aids improve knowledge and increase the proportion of people who assume a more active role in decision making.3
Limitations in design
Possible limitations of this study are response bias, poor definition of “informed choice,” and lack of power. The response rate of 64% may have introduced some bias, with under-representation of non-white women and women with manual occupations in both intervention and control groups. The pilot study of two of the leaflets suggested that women with manual occupations might benefit more from the leaflets,10 suggesting that we may have underestimated the true effect of the leaflets. However, the main study found no relation between social class and effect of the leaflets.6
The question used to measure informed choice may have been insensitive. However, we used two different questions and neither showed change. Additionally, we found little change in the components of informed choice, which was consistent with a genuine lack of change in informed choice. Although we recruited fewer women than planned, the analysis for postnatal women was adequately powered due to a smaller intraclass correlation coefficient than estimated for the sample size calculation. The analysis for antenatal women had a power of about 65%. However, observed changes were small, and, although low power can explain the lack of significance, it cannot explain the size of the observed effect. Overall, it is unlikely that the study failed to detect any important change.
We carried out this trial in everyday practice. We included thousands of women who might have received the 10 leaflets, but only 70% reported receiving one of them. Studies reported in the systematic review of decision aids were explanatory trials, with the implicit assumption that all patients received the intervention.3 One conclusion might be that the systematic review showed that decision aids can be effective under certain circumstances but that our study showed that they are not necessarily effective in the real world. The pragmatic nature of our design may have affected the outcome, but that outcome represents a true picture of the impact of introducing the leaflets into clinical practice.
Quality of implementation
There is some evidence from the trial that there were difficulties with the implementation of the intervention. The accompanying qualitative study shows that the Informed Choice leaflets were not introduced to women as special and different from other leaflets.4 Additionally, not all women reported that they had been given any of the leaflets during the intervention. This limited implementation of decision aids is by no means unique to either the Informed Choice leaflets or maternity care.11
Generalisability of findings
The results are generalisable to maternity units that use Informed Choice leaflets to promote informed choice but not to health professionals purchasing the leaflets to guide evidence based practice or individual enthusiastic health professionals purchasing the leaflets to help meet the information needs of their clients.
We thank midwives, managers, and administrative staff in the maternity units in Wales (unnamed to ensure confidentiality of participating units), who worked so hard to help us with data collection. We thank the thousands of women who completed our questionnaires at such an important time in their lives.
Contributors: AO'C contributed to the design of the study, designed the questionnaire, coordinated data collection, contributed to data analysis, wrote the paper, and is guarantor for the paper. SJW contributed to the design of the study, undertook the data analysis, and contributed to the writing of the paper. JPN and KJT contributed to design of the study and the questionnaire, interpretation of the data, and writing of the paper. MK contributed to the design of the study and the questionnaire and writing of the paper. Helen Stapleton contributed to the design and piloting of the questionnaire. Heather Rothwell helped to establish data collection systems. Andrea Shippam and April Dagnell undertook data administration. Donna Mead, Laurence Moseley, Barbara Bale, Gwenan Thomas, and Sandy Kirkman were members of the research team for the wider study, of which the randomised controlled trial forms a part.
Funding This work was commissioned by the NHS Centre of Reviews and Dissemination and funded by the Department of Health. The views expressed here are those of the authors and not necessarily those of the Department of Health.
Competing interests None declared.