How Frequently and in What Format Are Research Trial Results Disseminated to Participants (ResponseQT)
ResponseQT
1 other identifier
interventional
1,198
1 country
1
Brief Summary
Questionnaires are frequently used in online research, however recruiting, and completion rates of online participants from a variety of cultures and demographic backgrounds can be challenging. The challenge is greater in an online cohort because there is no way to observe the participant beyond what is contributed online. Poor recruiting and completion can result in underpowered research that may not be representative of the sample population. This can trigger an increase in costs as the recruitment period may have to be extended until sample size is reached. When recruiting and completion rates are inadequate studies may have to be terminated and the answer to the research question can remain unknown. To mitigate these challenges, reminder emails are sent to questionnaire respondents. There is uncertainty about how the tone of the email reminder affects the proportion of recruitment rates. A nested randomized trial will be used to test the intervention of tone delivery in survey email reminders to establish an evidence base. This study (ResponseQT) proposes to link with the anticipated 20,000 person international cohort study, (How Frequently and in What Format are Research Trial Results Disseminated to Participants: A Survey of Trialists (ResponseQT) to explore the evidence of effect for the research question, "Does the tone of a survey email reminder affect the proportion of survey participants recruited. The population will consist of researchers who have published a clinical trial indexed in Pub Med in 2014-15.The intervention is the tone of questionnaire email reminders and the outcomes will be the proportion of participants recruited after invitation (partial plus complete responses) following reminder 1 and 2.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2017
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 11, 2017
CompletedStudy Start
First participant enrolled
January 15, 2017
CompletedFirst Posted
Study publicly available on registry
January 16, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2019
CompletedMarch 22, 2021
March 1, 2021
1.5 years
January 11, 2017
March 18, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Recruitment
Proportion of sample recruited
Duration of study up to 60 days
Study Arms (9)
Group A Reminder
ACTIVE COMPARATORTone of reminder email (duty 14 days followed by duty for non-responders 28 days)
Group B Reminder
ACTIVE COMPARATORTone of reminder email (encouragement 14 days followed by encouragement for non-responders 28 days)
Group C Reminder
ACTIVE COMPARATORTone of reminder email (encouragement 14 days followed by duty for non-responders 28 days)
Group D Reminder
ACTIVE COMPARATORTone of reminder email (duty 14 days followed by encouragement for non-responders 28 days)
Group E Reminder
ACTIVE COMPARATORTone of reminder email (generic reminders at 14 days followed by generic for non-responders 28 days)
Group F Reminder
ACTIVE COMPARATORTone of reminder email (generic 14 days followed by duty for non-responders 28 days)
Group G Reminder
ACTIVE COMPARATORTone of reminder email (generic 14 days followed by encouragement for non-responders 28 days)
Group H Reminder
ACTIVE COMPARATORTone of reminder email (duty 14 days followed by generic for non-responders 28 days)
Group I Reminder
ACTIVE COMPARATORTone of reminder email (encouragement 14 days followed by generic for non-responders 28 days)
Interventions
Tone of reminder email (duty 14 days followed by duty 28 days for non-responders)
Tone of reminder email (encouragement 14 days followed by encouragement 28 days for non-responders)
Tone of reminder email (encouragement 14 days followed by duty for non-responders 28 days)
Tone of reminder email (duty 14 days followed by encouragement for non-responders 28 days)
Tone of reminder email (generic reminders 14 days followed by 28 days for non-responders)
Tone of reminder email (generic 14 days followed by duty for non-responders 28 days)
Tone of reminder email (generic 14 days followed by encouragement for non-responders 28 days)
Tone of reminder email ( duty14 days followed by generic for non-responders 28 days)
Tone of reminder email (encouragement 14 days followed by generic non-responders 28 days)
Eligibility Criteria
You may qualify if:
- reports of clinical trials with human participants indexed in PubMed 2014-15
You may not qualify if:
- reports of laboratory or animal studies,
- reports of preclinical trials,
- reports of trials where there were no study participants
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- ThinkWelllead
- University of Oxfordcollaborator
- The BMJcollaborator
- Queen's University, Belfastcollaborator
Study Sites (1)
ThinkWell
Oxford, Oxfordshire, OX4 4DN, United Kingdom
Related Publications (7)
Wilson PM, Petticrew M, Calnan MW, Nazareth I. Disseminating research findings: what should researchers do? A systematic scoping review of conceptual frameworks. Implement Sci. 2010 Nov 22;5:91. doi: 10.1186/1748-5908-5-91.
PMID: 21092164BACKGROUNDTetroe JM, Graham ID, Foy R, Robinson N, Eccles MP, Wensing M, Durieux P, Legare F, Nielson CP, Adily A, Ward JE, Porter C, Shea B, Grimshaw JM. Health research funding agencies' support and promotion of knowledge translation: an international study. Milbank Q. 2008 Mar;86(1):125-55. doi: 10.1111/j.1468-0009.2007.00515.x.
PMID: 18307479BACKGROUNDFelix LM, Burchett HE, Edwards PJ. Factorial trial found mixed evidence of effects of pre-notification and pleading on response to Web-based survey. J Clin Epidemiol. 2011 May;64(5):531-6. doi: 10.1016/j.jclinepi.2010.06.001. Epub 2010 Sep 17.
PMID: 20850270BACKGROUNDFang J, Shao P, Lan G. Effects of innovativeness and trust on web survey participation. Comput Human Behav 2009;25:144-52. doi:10.1016/j.chb.2008.08.002
BACKGROUNDFan W, Yan Z. Factors affecting response rates of the web survey: A systematic review. Comput Human Behav 2010;26:132-9. doi:10.1016/j.chb.2009.10.015
BACKGROUNDCook DA, Wittich CM, Daniels WL, West CP, Harris AM, Beebe TJ. Incentive and Reminder Strategies to Improve Response Rate for Internet-Based Physician Surveys: A Randomized Experiment. J Med Internet Res. 2016 Sep 16;18(9):e244. doi: 10.2196/jmir.6318.
PMID: 27637296BACKGROUNDBaruch Y, Holtom BC. Survey response rate levels and trends in organizational research. Hum Relations 2008;61:1139-60. doi:10.1177/0018726708094863
BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Amy I Price, PhD
ThinkWell
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 11, 2017
First Posted
January 16, 2017
Study Start
January 15, 2017
Primary Completion
June 30, 2018
Study Completion
September 30, 2019
Last Updated
March 22, 2021
Record last verified: 2021-03
Data Sharing
- IPD Sharing
- Will share
De-Identified, aggregated data upon request to investigators due to data protection laws