TY - JOUR
T1 - Supporting people with type 2 diabetes in effective use of their medicine through mobile health technology integrated with clinical care (SuMMiT-D Feasibility)
T2 - a randomised feasibility trial protocol
AU - Farmer, Andrew
AU - Allen, Julie
AU - Bartlett, Kiera
AU - Bower, Peter
AU - Chi, Yuan
AU - French, David
AU - Gudgin, Bernard
AU - Holmes, Emily A
AU - Horne, Robert
AU - Hughes, Dyfrig A
AU - Kenning, Cassandra
AU - Locock, Louise
AU - McSharry, Jenny
AU - Miles, Lisa
AU - Newhouse, Nikki
AU - Rea, Rustam
AU - Riga, Evgenia
AU - Tarassenko, Lionel
AU - Velardo, Carmelo
AU - Williams, Nicola
AU - Williams, Veronika
AU - Yu, Ly-Mee
AU - SuMMiT-D Collaborative Group
N1 - The SUpport through Mobile Messaging and digital health Technology for Diabetes research team acknowledge the support of the National Institute for Health Research (NIHR) through the Clinical Research Networks (AF: NIHR Senior Investigator and AF and RR: funding from NIHR Oxford Biomedical Research Consortium).
All trial data will be entered on electronic case report forms. The clinical database is built on Research Electronic Data Capture, a secure, web-based application designed to support data capture for research studies
PY - 2019/12/29
Y1 - 2019/12/29
N2 - INTRODUCTION: Type 2 diabetes is common, affecting over 400 million people worldwide. Risk of serious complications can be reduced through use of effective treatments and active self-management. However, people are often concerned about starting new medicines and face difficulties in taking them regularly. Use of brief messages to provide education and support self-management, delivered through mobile phone-based text messages, can be an effective tool for some long-term conditions. We have developed messages aiming to support patients' self-management of type 2 diabetes in the use of medications and other aspects of self-management, underpinned by theory and evidence. The aim of this trial is to determine the feasibility of a large-scale clinical trial to test the effectiveness and cost-effectiveness of the intervention, compared with usual care.METHODS AND ANALYSIS: The feasibility trial will be a multicentre individually randomised, controlled trial in primary care recruiting adults (≥35 years) with type 2 diabetes in England. Consenting participants will be randomised to receive short text messages three times a week with messages designed to produce change in medication adherence or non-health-related messages for 6 months. The aims are to test recruitment methods, retention to the study, the feasibility of data collection and the mobile phone and web-based processes of a proposed definitive trial and to refine the text messaging intervention. The primary outcome is the rate of recruitment to randomisation of participants to the trial. Data, including patient reported measures, will be collected online at baseline and the end of the 6-month follow-up period. With 200 participants (100 in each group), this trial is powered to estimate 80% follow-up within 95% CIs of 73.8% to 85.3%. The analysis will follow a prespecified plan.ETHICS AND DISSEMINATION: Ethics approval was obtained from the West of Scotland Research Ethics Committee 05. The results will be disseminated through conference presentations, peer-reviewed journals and will be published on the trial website: www.summit-d.org (SuMMiT-D (SUpport through Mobile Messaging and digital health Technology for Diabetes)).TRIAL REGISTRATION NUMBER: ISRCTN13404264.
AB - INTRODUCTION: Type 2 diabetes is common, affecting over 400 million people worldwide. Risk of serious complications can be reduced through use of effective treatments and active self-management. However, people are often concerned about starting new medicines and face difficulties in taking them regularly. Use of brief messages to provide education and support self-management, delivered through mobile phone-based text messages, can be an effective tool for some long-term conditions. We have developed messages aiming to support patients' self-management of type 2 diabetes in the use of medications and other aspects of self-management, underpinned by theory and evidence. The aim of this trial is to determine the feasibility of a large-scale clinical trial to test the effectiveness and cost-effectiveness of the intervention, compared with usual care.METHODS AND ANALYSIS: The feasibility trial will be a multicentre individually randomised, controlled trial in primary care recruiting adults (≥35 years) with type 2 diabetes in England. Consenting participants will be randomised to receive short text messages three times a week with messages designed to produce change in medication adherence or non-health-related messages for 6 months. The aims are to test recruitment methods, retention to the study, the feasibility of data collection and the mobile phone and web-based processes of a proposed definitive trial and to refine the text messaging intervention. The primary outcome is the rate of recruitment to randomisation of participants to the trial. Data, including patient reported measures, will be collected online at baseline and the end of the 6-month follow-up period. With 200 participants (100 in each group), this trial is powered to estimate 80% follow-up within 95% CIs of 73.8% to 85.3%. The analysis will follow a prespecified plan.ETHICS AND DISSEMINATION: Ethics approval was obtained from the West of Scotland Research Ethics Committee 05. The results will be disseminated through conference presentations, peer-reviewed journals and will be published on the trial website: www.summit-d.org (SuMMiT-D (SUpport through Mobile Messaging and digital health Technology for Diabetes)).TRIAL REGISTRATION NUMBER: ISRCTN13404264.
U2 - 10.1136/bmjopen-2019-033504
DO - 10.1136/bmjopen-2019-033504
M3 - Article
C2 - 31888938
VL - 9
JO - BMJ Open
JF - BMJ Open
SN - 2044-6055
IS - 12
M1 - e033504
ER -