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Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents

Background In the evaluation of childhood obesity interventions, few researchers undertake a rigorous feasibility stage in which the design and procedures of the evaluation process are examined. Consequently, phase III studies often demonstrate methodological weaknesses. Purpose Our aim was to condu...

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Autores principales: Bryant, Maria, Farrin, Amanda, Christie, Deborah, Jebb, Susan A, Cooper, Ashley R, Rudolf, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724279/
https://www.ncbi.nlm.nih.gov/pubmed/22024104
http://dx.doi.org/10.1177/1740774511424766
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author Bryant, Maria
Farrin, Amanda
Christie, Deborah
Jebb, Susan A
Cooper, Ashley R
Rudolf, Mary
author_facet Bryant, Maria
Farrin, Amanda
Christie, Deborah
Jebb, Susan A
Cooper, Ashley R
Rudolf, Mary
author_sort Bryant, Maria
collection PubMed
description Background In the evaluation of childhood obesity interventions, few researchers undertake a rigorous feasibility stage in which the design and procedures of the evaluation process are examined. Consequently, phase III studies often demonstrate methodological weaknesses. Purpose Our aim was to conduct a feasibility trial of the evaluation of WATCH IT, a community obesity intervention for children and adolescents. We sought to determine an achievable recruitment rate; acceptability of randomisation, assessment procedures, and dropout rate; optimal outcome measures for the definitive trial; and a robust sample size calculation. Method Our goal was to recruit 70 participants over 6 months, randomise them to intervention or control group, and retain participation for 12 months. Assessments were taken prior to randomisation and after 6 and 12 months. Procedures mirrored those intended for a full-scale trial, but multiple measures of similar outcomes were included as a means to determine those most appropriate for future research. Acceptability of the research and impact of the research on the programme were ascertained through interviewing participants and staff. Results We recruited 70 participants and found that randomisation and data collection procedures were acceptable. Self-referral (via media promotion) was more effective than professional referral. Blinding of assessors was sustained to a reasonable degree, and optimal outcome measures for a full-scale trial were identified. Estimated sample size was significantly greater than sample sized reported in published trials. There was some negative impact on the existing programme as a result of the research, a lesson for designers of future trials. Limitations We successfully recruited socially disadvantaged families, but the majority of families were of White British nationality. The composition of the participants was an added valuable lesson, suggesting that recruitment strategies to obtain a more heterogeneous ethnic sample warrant consideration in future research. Conclusions This study provided us with confidence that we can run a phase III multi-centre trial to test the effectiveness of WATCH IT. Importantly, it was invaluable in informing the design not only of that trial but also of future evaluations of childhood obesity treatment interventions.
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spelling pubmed-37242792013-07-30 Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents Bryant, Maria Farrin, Amanda Christie, Deborah Jebb, Susan A Cooper, Ashley R Rudolf, Mary Clin Trials Recruitment and Retention Background In the evaluation of childhood obesity interventions, few researchers undertake a rigorous feasibility stage in which the design and procedures of the evaluation process are examined. Consequently, phase III studies often demonstrate methodological weaknesses. Purpose Our aim was to conduct a feasibility trial of the evaluation of WATCH IT, a community obesity intervention for children and adolescents. We sought to determine an achievable recruitment rate; acceptability of randomisation, assessment procedures, and dropout rate; optimal outcome measures for the definitive trial; and a robust sample size calculation. Method Our goal was to recruit 70 participants over 6 months, randomise them to intervention or control group, and retain participation for 12 months. Assessments were taken prior to randomisation and after 6 and 12 months. Procedures mirrored those intended for a full-scale trial, but multiple measures of similar outcomes were included as a means to determine those most appropriate for future research. Acceptability of the research and impact of the research on the programme were ascertained through interviewing participants and staff. Results We recruited 70 participants and found that randomisation and data collection procedures were acceptable. Self-referral (via media promotion) was more effective than professional referral. Blinding of assessors was sustained to a reasonable degree, and optimal outcome measures for a full-scale trial were identified. Estimated sample size was significantly greater than sample sized reported in published trials. There was some negative impact on the existing programme as a result of the research, a lesson for designers of future trials. Limitations We successfully recruited socially disadvantaged families, but the majority of families were of White British nationality. The composition of the participants was an added valuable lesson, suggesting that recruitment strategies to obtain a more heterogeneous ethnic sample warrant consideration in future research. Conclusions This study provided us with confidence that we can run a phase III multi-centre trial to test the effectiveness of WATCH IT. Importantly, it was invaluable in informing the design not only of that trial but also of future evaluations of childhood obesity treatment interventions. SAGE Publications 2011-12 /pmc/articles/PMC3724279/ /pubmed/22024104 http://dx.doi.org/10.1177/1740774511424766 Text en © The Society for Clinical Trials 2011 http://creativecommons.org/licenses/by-nc/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Recruitment and Retention
Bryant, Maria
Farrin, Amanda
Christie, Deborah
Jebb, Susan A
Cooper, Ashley R
Rudolf, Mary
Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title_full Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title_fullStr Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title_full_unstemmed Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title_short Results of a feasibility randomised controlled trial (RCT) for WATCH IT: a programme for obese children and adolescents
title_sort results of a feasibility randomised controlled trial (rct) for watch it: a programme for obese children and adolescents
topic Recruitment and Retention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724279/
https://www.ncbi.nlm.nih.gov/pubmed/22024104
http://dx.doi.org/10.1177/1740774511424766
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