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Influence of providing information to participants about development of trial outcomes on response rates and attitudes to questionnaire completion: Protocol for a study within a trial.
Griffin, Charlotte; Toomey, Elaine; Queally, Michelle; Hayes, Catherine; Kearney, Patricia M; Matvienko-Sikar, Karen.
Affiliation
  • Griffin C; School of Public Health, University College Cork, Cork, T12 XF62, Ireland.
  • Toomey E; School of Psychology, National University of Ireland, Galway, Galway City, H91 EV56, Ireland.
  • Queally M; Discipline of Economics, National University of Ireland, Galway, Galway, H91 EV56, Ireland.
  • Hayes C; School of Medicine, Trinity College Dublin, Dublin, D06 W226, Ireland.
  • Kearney PM; School of Public Health, University College Cork, Cork, T12 XF62, Ireland.
  • Matvienko-Sikar K; School of Public Health, University College Cork, Cork, T12 XF62, Ireland.
HRB Open Res ; 2: 2, 2019.
Article in En | MEDLINE | ID: mdl-32002511
ABSTRACT

Background:

Issues with questionnaire completion introduce bias and limit examinations in trials. Improving communication with participants about trial processes, such as outcome and questionnaire development, may improve questionnaire completion and response rates. Providing information about the involvement of stakeholders in the development of core outcome sets (COS) measured in trials may improve responding by tapping into subjective norms and behaviour change mechanisms. The aim of this Study Within a Trial (SWAT) is to examine if questionnaire response rates and participants' attitudes towards questionnaire completion are impacted by providing information about COS use in a trial of a complex intervention.

Methods:

This is a randomised, single-blinded, parallel group intervention SWAT, embedded within a feasibility trial of an infant feeding intervention to prevent childhood obesity. The SWAT intervention consisting of a brief written description and explanation about the development and use of a COS of infant feeding outcomes to prevent childhood obesity, used in the trial. Participants are parents or caregivers of infants aged two months at questionnaire completion. Participants will be randomly assigned to receive the SWAT intervention prior to questionnaire completion (I1 condition), or to receive the information following completion of all questionnaires (I2 condition). The SWAT will be assessed using closed-ended and an open-ended question to evaluate participants' attitudes about questionnaire completion. Response rates will be measured as proportion of full questionnaire completion and individual item response rates.

Discussion:

 We hypothesise that providing information about development and use of a COS will increase questionnaire response rates and attitudes toward questionnaire completion relative to the control condition. Findings will indicate the potential usefulness of this strategy for improving participant attitudes and response rates in trials.  Trial Registration This SWAT is registered on the Northern Ireland Hub for Trials

Methodology:

Research SWAT Repository ( SWAT57).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: HRB Open Res Year: 2019 Type: Article Affiliation country: Ireland

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: HRB Open Res Year: 2019 Type: Article Affiliation country: Ireland