Literature DB >> 16317812

Reasons for high retention in pediatric clinical trials: comparison of participant and staff responses in the Correction of Myopia Evaluation Trial.

Lynette Dias1, Elinor Schoenfeld, Jennifer Thomas, Catherine Baldwin, Jennifer McLeod, Justin Smith, Robert Owens, Leslie Hyman.   

Abstract

BACKGROUND: The Correction of Myopia Evaluation Trial (COMET), a randomized, multicenter clinical trial of myopia progression in children, had an exceptionally high retention rate of 98.5% (462/469) at three years of follow-up. The present investigation was designed to evaluate and compare the reasons for COMET's high retention rate according to participating families and clinical center staff.
METHODS: Families (n = 411) and staff (n = 35) completed a confidential 19-item questionnaire by indicating families' levels of preference for each item, and rating its importance in keeping families in the study. The questionnaire evaluated study features in four categories: staff characteristics, operational aspects, specific study elements, and incentives.
RESULTS: Results showed that most families viewed the study very favorably. Features that appealed to 90% or more families and promoted continued study participation included staff attributes such as friendliness, responsiveness and encouragement, and aspects pertaining to standard of care such as completeness of eye exam, quality of eye care and free eyeglasses. Compared to families, staff tended to underestimate the importance of the following features for retention: seeing the same staff at each visit, appointment reminders, center location, newsletters, commitment to the study, being part of a nationwide study, length of the study, association with a college of optometry, completeness of eye exam, and eye drops (p < 0.05 by chi-square analyses). However, staff responses also revealed less preferred components of the study protocol (e.g., eye drops), to which families might have been reluctant to respond unfavorably.
CONCLUSIONS: Our findings highlight the importance of intangible factors such as staff attributes and participants' study commitment in maintaining high retention rates, and the usefulness of surveying both families and staff.

Entities:  

Mesh:

Year:  2005        PMID: 16317812     DOI: 10.1191/1740774505cn113oa

Source DB:  PubMed          Journal:  Clin Trials        ISSN: 1740-7745            Impact factor:   2.486


  11 in total

Review 1.  Interventions to slow progression of myopia in children.

Authors:  Jeffrey J Walline; Kristina Lindsley; Satyanarayana S Vedula; Susan A Cotter; Donald O Mutti; J Daniel Twelker
Journal:  Cochrane Database Syst Rev       Date:  2011-12-07

2.  Participant characteristics and study features associated with high retention rates in a longitudinal investigation of type 1 diabetes mellitus.

Authors:  John R Kramer; Margaret L Bayless; Gayle M Lorenzi; Georgia K Ziegler; Mary E Larkin; Mary E Lackaye; Judith Harth; Lisa J Diminick; Karen L Anderson; Barbara H Braffett; Patricia A Cleary
Journal:  Clin Trials       Date:  2012-10-01       Impact factor: 2.486

3.  Experiences of families with a child, adolescent, or young adult with neurofibromatosis type 1 and plexiform neurofibroma evaluated for clinical trials participation at the National Cancer Institute.

Authors:  Staci Martin; Andrea Gillespie; Pamela L Wolters; Brigitte C Widemann
Journal:  Contemp Clin Trials       Date:  2010-10-14       Impact factor: 2.226

4.  Predictors of web-based follow-up response in the Prevention Of Low Back Pain In The Military Trial (POLM).

Authors:  John D Childs; Deydre S Teyhen; Joshua J Van Wyngaarden; Brett F Dougherty; Bryan J Ladislas; Gary L Helton; Michael E Robinson; Samuel S Wu; Steven Z George
Journal:  BMC Musculoskelet Disord       Date:  2011-06-13       Impact factor: 2.362

5.  Interventions to slow progression of myopia in children.

Authors:  Jeffrey J Walline; Kristina B Lindsley; S Swaroop Vedula; Susan A Cotter; Donald O Mutti; Sueko M Ng; J Daniel Twelker
Journal:  Cochrane Database Syst Rev       Date:  2020-01-13

6.  Community Willingness to Participate in a Dengue Study in Aceh Province, Indonesia.

Authors:  Harapan Harapan; Samsul Anwar; Aslam Bustaman; Arsil Radiansyah; Pradiba Angraini; Riny Fasli; Salwiyadi Salwiyadi; Reza Akbar Bastian; Ade Oktiviyari; Imaduddin Akmal; Muhammad Iqbalamin; Jamalul Adil; Fenni Henrizal; Darmayanti Darmayanti; Rovy Pratama; Jonny Karunia Fajar; Abdul Malik Setiawan; Allison Imrie; Ulrich Kuch; David Alexander Groneberg; R Tedjo Sasmono; Meghnath Dhimal; Ruth Müller
Journal:  PLoS One       Date:  2016-07-12       Impact factor: 3.240

Review 7.  Trials need participants but not their feedback? A scoping review of published papers on the measurement of participant experience of taking part in clinical trials.

Authors:  Claire Planner; Peter Bower; Ailsa Donnelly; K Gillies; Katrina Turner; Bridget Young
Journal:  Trials       Date:  2019-06-24       Impact factor: 2.279

8.  Reasons for Staying as a Participant in the Environmental Determinants of Diabetes in the Young (TEDDY) Longitudinal Study.

Authors:  Barbro Lernmark; Kristian Lynch; Lori Ballard; Judith Baxter; Roswith Roth; Tuula Simell; Suzanne Bennett Johnson
Journal:  J Clin Trials       Date:  2012

Review 9.  Duration of Pediatric Clinical Trials Submitted to the US Food and Drug Administration.

Authors:  Kanecia O Zimmerman; P Brian Smith; Ann W McMahon; Jean Temeck; Debbie Avant; Dianne Murphy; Susan McCune
Journal:  JAMA Pediatr       Date:  2019-01-01       Impact factor: 26.796

10.  A feasibility study of a randomised controlled trial to examine the impact of the ABCDE bundle on quality of life in ICU survivors.

Authors:  Kellie Sosnowski; Marion L Mitchell; Hayden White; Lynette Morrison; Joanne Sutton; Jessica Sharratt; Frances Lin
Journal:  Pilot Feasibility Stud       Date:  2018-01-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.