Characteristics and quality of reporting of cluster randomized trials in children: reporting needs improvement

被引:24
作者
Walleser, Silke
Hill, Suzanne R. [2 ]
Bero, Lisa A. [1 ]
机构
[1] Univ Calif San Francisco, Dept Clin Pharm, Inst Hlth Policy Studies, San Francisco, CA 94118 USA
[2] WHO, Dept Essential Med & Pharmaceut Policies, CH-1211 Geneva 27, Switzerland
关键词
Cluster randomized trial; Randomized trial; Children; Research reporting; Quality appraisal; Research methods; Bias; CONSORT STATEMENT; CLINICAL-TRIALS; HEALTH; PREVENTION; PROGRAM; DESIGN;
D O I
10.1016/j.jclinepi.2011.04.006
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objective: To describe the characteristics and quality of reporting of cluster randomized trials (CRTs) in children published from 2004 to 2010. Study Design and Setting: Four databases were searched for reports of CRTs in children (0-18 years). Characteristics of the studies were summarized and the quality of reporting assessed using consolidated standards of reporting trial-CRT (CONSORT-CRT). Results: Of 1,949 identified references, 106 were included. The number of published CRTs in children increased since 2004. The greatest proportion of CRTs was undertaken in Europe (29%), whereas 40% was conducted in low- and middle-income countries. Most studies were of complex rather than simple interventions (83%); were preventive rather than treatment interventions (76%); and most frequently addressed infectious disease (21%), diet/physical activity interventions (19%), health-risk behaviors (15%), and undernutrition (13%). The majority used schools as units of randomization (72%) and enrolled 1,000-10,000 children per study (51%). Reporting was generally poor, with 34% of CRTs inadequately reporting on more than half of the CONSORT-CRT criteria. Although 85% of CRTs reported that they had ethics approval for the study, consent or assent was not obtained from children in most studies. Conclusion: Children-specific elements of reporting are needed to improve the quality of reporting of CRTs and consequently their planning and implementation. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1331 / 1340
页数:10
相关论文
共 28 条
[1]   Considerations in the rational design and conduct of phase I/II pediatric clinical trials: Avoiding the problems and pitfalls [J].
Abdel-Rahman, S. M. ;
Reed, M. D. ;
Wells, T. G. ;
Kearns, G. L. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 81 (04) :483-494
[2]  
[Anonymous], CLUST RAND TRIALS ME
[3]  
[Anonymous], PREVENTIVE MED
[4]   A systematic review of paediatric randomised controlled drug trials published in 2007 [J].
Aripin, Khairun N. B. Nor ;
Choonara, Imti ;
Sammons, Helen M. .
ARCHIVES OF DISEASE IN CHILDHOOD, 2010, 95 (06) :469-473
[5]   The YouthMood Project: A Cluster Randomized Controlled Trial of an Online Cognitive Behavioral Program With Adolescents [J].
Calear, Alison L. ;
Christensen, Helen ;
Mackinnon, Andrew ;
Griffiths, Kathleen M. ;
O'Kearney, Richard .
JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 2009, 77 (06) :1021-1032
[6]   Framework for design and evaluation of complex interventions to improve health [J].
Campbell, M ;
Fitzpatrick, R ;
Haines, A ;
Kinmonth, AL ;
Sandercock, P ;
Spiegelhalter, D ;
Tyrer, P .
BRITISH MEDICAL JOURNAL, 2000, 321 (7262) :694-696
[7]   CONSORT statement: extension to cluster randomised trials [J].
Campbell, MK ;
Elbourne, DR ;
Altman, DG .
BMJ-BRITISH MEDICAL JOURNAL, 2004, 328 (7441) :702-708
[8]   Assessment of Risk of Bias Among Pediatric Randomized Controlled Trials [J].
Crocetti, Michael T. ;
Amin, Diane D. ;
Scherer, Roberta .
PEDIATRICS, 2010, 126 (02) :298-305
[9]   Internal and external validity of cluster randomised trials: systematic review of recent trials [J].
Eldridge, Sandra ;
Ashby, Deborah ;
Bennett, Catherine ;
Wakelin, Melanie ;
Feder, Gene .
BMJ-BRITISH MEDICAL JOURNAL, 2008, 336 (7649) :876-880
[10]  
Eldridge Sandra M, 2004, Clin Trials, V1, P80, DOI 10.1191/1740774504cn006rr