TRIal to slow the Progression Of Diabetes (TRIPOD): study protocol for a randomized controlled trial using wireless technology and incentives

被引:3
作者
Lim, Robyn Su May [1 ]
Gardner, Daphne Su Lyn [2 ]
Bee, Yong Mong [2 ]
Cheung, Yin Bun [1 ,3 ]
Bairavi, Joann [1 ]
Gandhi, Mihir [3 ,4 ]
Goh, Su-Yen [2 ]
Ho, Emily Tse Lin [2 ]
Lin, Xinyi [3 ,5 ]
Tan, Ngiap Chuan [6 ]
Tay, Tunn Lin [7 ]
Finkelstein, Eric Andrew [1 ]
机构
[1] Duke NUS Med Sch, Hlth Serv & Syst Res, 8 Coll Rd, Singapore 169857, Singapore
[2] Singapore Gen Hosp, Dept Endocrinol, Outram Rd, Singapore 169608, Singapore
[3] Duke NUS Med Sch, Ctr Quantitat Med, 8 Coll Rd, Singapore 169857, Singapore
[4] Singapore Clin Res Inst, Dept Biostat, 31 Biopolis Way, Singapore 138669, Singapore
[5] ASTAR, Singapore Inst Clin Sci, 30 Med Dr, Singapore 117609, Singapore
[6] SingHlth Polyclin, Dept Res, 167 Jalan Bukit Merah, Singapore 150167, Singapore
[7] Changi Gen Hosp, Dept Endocrinol, 2 Simei St 3, Singapore 529889, Singapore
基金
英国医学研究理事会;
关键词
Diabetes; Smartphone apps; mHealth; Behavior change; Physical activity; Weight monitoring; Blood glucose monitoring; Medication adherence; Financial incentive; FINANCIAL INCENTIVES; COST-EFFECTIVENESS; DISEASE RISK; WEIGHT-LOSS; HEALTH; ADULTS; METAANALYSIS; MANAGEMENT; WISEWOMAN; NORMS;
D O I
10.1186/s13063-019-3749-x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background The outcomes for those with type 2 diabetes mellitus (T2DM) in Singapore are poor. In this TRIal to slow the Progression Of Diabetes (TRIPOD), we will evaluate the effectiveness and cost-effectiveness of a comprehensive diabetes management package (DMP), with or without a financial incentives program, M-POWER Rewards, in efforts to improve HbA(1c) levels for individuals with T2DM. Methods/design TRIPOD is a randomized, open-label, controlled, multi-center, superiority trial with three parallel arms: (1) usual care only, (2) usual care with DMP, and (3) usual care with DMP plus M-POWER Rewards. A total of 339 adults with sub-optimally controlled T2DM (self-reported HbA(1c) 7.5-11.0%) will be block randomized according to a 1:1:1 allocation ratio to the three arms. The primary outcome is mean change in HbA(1c) level at Month 12 from baseline. Secondary outcomes include mean change in HbA(1c) level at Months 6, 18, and 24; mean changes at Months 6, 12, 18, and 24 in weight, blood pressure, and self-reported physical activity, weight monitoring, blood glucose monitoring, medication adherence, diabetes self-management, sleep quality, work productivity and daily activity impairment, and health utility index; and proportion of participants initiating insulin treatment by Months 6, 12, 18, and 24. Incremental cost-effectiveness ratios will be computed based on costs per improvement in HbA(1c) at Month 12 and converted to cost per quality-adjusted life year gained. Discussion The TRIPOD study will present insights about the long-term cost-effectiveness and financial viability of the interventions and the potential for integrating within usual care.
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页数:16
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