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Randomised controlled trial of community based speech and language therapy in preschool children

Margaret Glogowska, research assistant ^a, Sue Roulstone, clinical research director ^a, Pam Enderby, professor of community rehabilitation ^b, Tim J Peters, reader in medical statistics ^c. 

^a Speech and Language Therapy Research Unit, Frenchay Hospital, Bristol BS16 1LE, ^b Centre for Ageing and Rehabilitation Studies, School of Health and Related Studies, University of Sheffield, Northern General Hospital, Sheffield S5 7AU, ^c Department of Social Medicine, University of Bristol, Canynge Hall, Bristol BS8 2PR

Correspondence to: S Roulstone sue{at}speech-therapy.org.uk

	Abstract

Top Abstract Introduction Subjects and methods Results Discussion References

Objective: To compare routine speech and language therapy in preschool children with delayed speech and language against 12 months of "watchful waiting."
Design: Pragmatic randomised controlled trial.
Setting: 16 community clinics in Bristol.
Participants: 159 preschool children with appreciable speech or language difficulties who fulfilled criteria for admission to speech and language therapy.
Main outcome measures: Four quantitative measures of speech and language, assessed at 6 and 12 months; a binary variable indicating improvement, by 12 months, on the trial entry criterion.
Results: Improvement in auditory comprehension was significant in favour of therapy (adjusted difference in means 4.1, 95% confidence interval 0.5 to 7.6; P=0.025). No significant differences were observed for expressive language (1.4, 2.1 to 4.8; P=0.44); phonology error rate (4.4, 12.0 to 3.3; P=0.26); language development (0.1, 0.4 to 0.6; P=0.73); or improvement on entry criterion (odds ratio 1.3, 0.67 to 2.4; P=0.46). At the end of the trial, 70% of all children still had substantial speech and language deficits.
Conclusions: This study provides little evidence for the effectiveness of speech and language therapy compared with watchful waiting over 12 months. Providers of speech and language therapy should reconsider the appropriateness, timing, nature, and intensity of such therapy in preschool children. Continued research into more specific provision to subgroups of children is also needed to identify better treatment methods. The lack of resolution of difficulties for most of the children suggests that further research is needed to identify effective ways of helping this population of children.

	Introduction

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Of the impairments presenting in early childhood, speech or language delay may be the most common.¹ At any one time a fifth of parents in Britain are concerned about their young child's language development.² Although there has been a shift to providing early intervention for these children, this has not been based on research evidence. Yet provision of therapy to children is estimated to consume 70% of the NHS budget for speech and language therapy in the United Kingdom.²

A systematic review has shown short term efficacy of speech and language therapy for young children in an experimental environment.³ No clear evidence exists, however, on the long term effectiveness of therapy in the context of service provision or on the natural course of early speech and language delays. In particular, the longer term course of early difficulties seems to vary for different groups of children. Some studies have suggested that 40% to 60% of children with only expressive language delay outgrow their difficulties ^{4 5} ; others have shown that those with a range of language problems have more persistent linguistic, literacy, and social difficulties.^6-8

We investigated in a pragmatic randomised controlled trial the effectiveness of speech and language therapy for preschool children as delivered in community clinics.

	Subjects and methods

Top Abstract Introduction Subjects and methods Results Discussion References

Subject selection and baseline assessment
We considered for inclusion all children presenting to 16 NHS community clinics from December 1995 to March 1998. Box 1 shows the selection criteria; box 2 shows the three clinical criteria. Local research ethics committees for the three participating healthcare trusts gave approval for the trial; informed parental consent was obtained by therapists.

Assignment
Eligible children were randomised to receive therapy or to "watchful waiting." Randomisation was stratified by the 16 clinics and by the three clinical criteria (general language, expressive language, and phonology). The sequence of random numbers was generated before the trial independently of the therapists. The allocation was implemented by the therapists opening sealed opaque envelopes in the presence of the parents.

Blinding
The same assessments were used at 6 and 12 months as at baseline, with the exception of the Bristol language development scales and the Vineland scales, which were measured only at 12 months. Assessors were blind to previous results, and every attempt was made to maintain blindness in terms of allocation.

Outcome measures
The five primary outcomes were auditory comprehension and expressive language scores, phonology error rate, the score for the Bristol language development scales, and a binary variable indicating whether the child, by 12 months, had improved sufficiently on the single clinical measure on which he or she had entered the study to no longer satisfy that particular criterion. The 11 secondary outcomes were four therapy outcome measures¹⁵; attention and play ratings; the Vineland socialisation domain; three separate binary variables indicating improvement or no deterioration over 12 months in auditory comprehension, expressive language, and phonology; and a fourth binary variable reflecting whether, at the 12 month follow up, the child satisfied any of the clinical criteria (a reassessment of eligibility for the trial irrespective of the initial clinical criterion on which the child entered the trial).

Sample size considerations
A total of 146 to 166 children was needed to detect a 20% difference between the two arms (that is, 15% v 35%) at a two sided 5% significance level, for 80% to 85% power. This sample size range had 80% to 85% power to detect differences between the trial groups of 0.43 to 0.50 standard deviations for the continuous outcome measures.

Analysis
The trial arms were compared on an "intention to treat" basis. The continuous outcome measures were analysed by using simple or repeated measures analysis of covariance, with adjustment for the baseline assessment of the outcome measurement. The binary outcome measures were analysed by using ² tests and logistic regression. In addition, for the two primary outcomes that were not age standardised (the Bristol language development scales and the phonology error rate), the relevant regression models were repeated after adjustment for age. All analyses were performed with the SPSS statistical package (version 10.0), and a two sided 5% significance level was used throughout.

	Results

Top Abstract Introduction Subjects and methods Results Discussion References

In all, 507 children aged under 31/2 years were referred to the participating speech and language therapy clinics, and 159 eligible children were subsequently randomised (figure). The children in both trial arms were closely similar for a broad range of baseline characteristics (table 1).

Therapy provided in the study tended to focus on several areas of language simultaneously. Therapy techniques included Derbyshire language scheme tasks, as well as everyday play and games used as contexts for modelling language for the child. Goals covered a wide range of language stagesfor example, understanding and building single words, using narratives, and identifying consonants in words.

Although all of the observed comparisons for the primary outcome measures were in favour of the therapy group, only one was statistically significant namely, auditory comprehension (table 2). For this outcome, the difference of 4.1 points corresponds to about 0.3 SD, with the upper confidence limit being about 0.5 SD.

For the 11 secondary outcomes none of the seven continuous variables was significant and all of the observed differences were very close to zero, with narrow confidence intervals in most cases. Of the four binary outcomes, however, two were significant, with a greater proportion of children in the therapy group improving their phonology and no longer satisfying the original eligibility criteria for the trial. Of the 71 children in the therapy group, 27 (38%) were no longer eligible by the end of the trial, compared with 19 (23%) of the 84 children followed up in the watchful waiting group. Overall, 109 (70%) children still satisfied the eligibility criteria at the 12 month follow up.

	Discussion

Top Abstract Introduction Subjects and methods Results Discussion References

This trial is by far the largest to date investigating the effectiveness of speech and language therapy in preschool children. Improvement in the therapy group was significant (compared with the watchful waiting group) for only one of the five primary outcomesauditory comprehension. Moreover, the two secondary outcomes for which the results were significant measure different aspects. The two possible explanations are, firstly, that the statistically significant findings may simply be due to chance, and, secondly, that there may be a therapeutic benefit across a range of measures, with differential sensitivity resulting in only a small number of (different) outcomes yielding statistical significance. Table 2 supports this latter interpretation, given the direction of the estimates for the primary outcomes and that their confidence intervals generally include large effects in favour of the therapy group but rule out clinically significant differences in favour of the watchful waiting group. The sizeable minority of parents in the watchful waiting group who requested therapy at the 6 month follow up shows that some parents found it difficult to accept a 12 month period of monitoring.

View larger version (25K): [in this window] [in a new window]   Progress of children through trial

Limitations of trial
Overall, the impact of therapy in this trial was small, perhaps because of the relatively low level of therapy providedconsiderably lower than levels reported in previous studies. ^{3 17} On the other hand, this trial aimed to evaluate routine therapy rather than a prescribed regimen.

Relation to literature
Although the level of therapy in this trial was lower than in smaller scale, more explanatory trials, the present study was a relatively large and randomised trial and it had considerably longer follow up (12 months) than other studies.^18-20

Conclusions
Most children in this study still had important clinical difficulties at 12 months, regardless of trial allocation; indeed, many remained eligible for the trial, with little evidence of "spontaneous resolution." This study provides little evidence for the effectiveness of speech and language therapy when compared with "watchful waiting" over 12 months. In clinical terms, these findings suggest that speech and language therapy for preschool children should be reconsidered in terms of appropriateness, timing, nature, and intensity. Further research into more specific types of provision with subgroups of children is required to identify better treatment methods.

	Acknowledgments

We thank the speech and language therapists from Frenchay and United Bristol Healthcare Trusts for their hard work and the families and their health visitors for support and cooperation. The department of social medicine at the University of Bristol is the lead centre of the MRC Health Services Research Collaboration.

Contributors: The original trial design was formulated by PE and TJP, with all authors contributing to its subsequent development. The trial was implemented by SR and MG, with support and advice from TJP and PE. Data management and analysis were carried out by MG, SR, and TJP, under the overall supervision of TJP. MG produced the first draft of the paper, with substantial redrafting by TJP and SR and additional input and academic support from PE. All authors will act as guarantors for the paper.

	Footnotes

Funding: Research and development directorate of the South and West regional office of the NHS Executive.

Competing interests: None declared.

The full version of this paper appears on the BMJ's website

	References

Top Abstract Introduction Subjects and methods Results Discussion References

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(Accepted 14 June 2000)