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Clinical Trials/NCT02726100
NCT02726100
Completed
Not Applicable

Systematic Medical Assessment, Referral and Treatment for Diabetes Care in China Using Lay Family Health Promoters

The George Institute for Global Health, China2 sites in 1 country2,073 target enrollmentAugust 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
The George Institute for Global Health, China
Enrollment
2073
Locations
2
Primary Endpoint
The proportion of patients achieving at least two "ABC" goals
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

It's a community-based parallel-arm cluster Randomized Controlled Trial (RCT). An interactive mobile health management system will be developed to support lay family health promoters and healthcare staff to improve clinical outcomes for family members with Type 2 Diabetes Mellitus (T2DM). 2,000 participants from 80 sites will be chosen from urban (40 communities) and rural (40 villages) settings in Shijiazhuang City, Hebei Province.

Detailed Description

Study design and Settings: Cluster randomised controlled trial involving 80 sites (40 communities in urban Shijiazhuang and 40 villages in rural Shijiazhuang) and 2,000 people with T2DM. Hypothesis: An interactive mobile health management system can support lay family health promoters (FHP) and healthcare staff to improve clinical outcomes for family members with T2DM Intervention: SMARTHealth Diabetes is an interactive mobile health platform to promote improved self-management for people with T2DM. It comprises the following core features: * Management support based on best practice clinical guidelines * Self-management tools and resources for family members * Password protected registration of patients and their nominated FHP to access this information * Population of key clinical information into a desktop application used by health care providers when applicable Community eligibility: * 40 urban communities and 40 rural villages from geographically dispersed regions will be selected * Each community/ village must have at least one community health station providing services to ≥1,000 adult residents * Staff at the community health station must be willing to participate in the intervention Statistical power: 80 clusters and a mean community cluster size of 25 participants (2,000 total) will provide 90% power to detect an absolute improvement of 10% in the primary outcome. This assumes 20% of people in the control arm will achieve ≥2 'ABC' diabetes goals ((HbA1C\<7%; Blood Pressure \<140/80 mmHg, LDL cholesterol \<100mg/dl or 2.6mmol/L) at end of study; an intra-class correlation coefficient of 0.05, a 20% loss to follow-up, and a 2-sided significance level of 0.05. This translates to a mean reduction of 0.35% for HbA1C, 0.14 mmol/L for LDL cholesterol and 3.4mmHg for systolic BP. Primary analyses will be conducted at the patient level. Secondary analyses will be conducted at the cluster level. Sub-group analyses will be conducted at the community level (based on size and health service characteristics) and patient level (based on demographic factors (co-habitation with FHP) and clinical factors (control rate of 'ABC' risk factors at baseline). Significance: The Chinese government has placed prevention and treatment of diabetes as one of 11 National Basic Public Health Services. Despite great promise for mobile health (mHealth) interventions to improve access to effective healthcare, there remains uncertainty about how this can be successfully achieved. These uncertainties pose substantial dilemmas for health system planners. The findings are likely to inform policy on a scalable strategy to overcome sub-optimal access to effective health care in China.

Registry
clinicaltrials.gov
Start Date
August 1, 2017
End Date
February 28, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
The George Institute for Global Health, China
Responsible Party
Principal Investigator
Principal Investigator

Puhong Zhang

Associate Director

The George Institute for Global Health, China

Eligibility Criteria

Inclusion Criteria

  • Established T2DM
  • HbA1C \>= 7%
  • Nominated family member with mobile internet access who agrees to be a family health promoter (FHP)
  • Able to provide informed consent

Exclusion Criteria

  • Psychologically or physically unable to participate the trials.

Outcomes

Primary Outcomes

The proportion of patients achieving at least two "ABC" goals

Time Frame: 24 months

The proportion of patients achieving at least two "ABC" goals defined as any two of the following: HbA1c \<7.0%, blood pressure (BP) \<140/80mmHg and LDL cholesterol \<100mg/dl or 2.6mmol/L) at 24 months

Secondary Outcomes

  • The proportion of patients achieving the "B" goal(24 months)
  • The proportion of patients achieving the "C" goal(24 months)
  • The proportion of patients achieving FPG<7.0 mmol/L(24 months)
  • Mean changes in systolic and diastolic blood pressure levels(24 months)
  • The proportion of patients achieving the "A" goal(24 months)
  • Mean change in HbA1c level(24 months)
  • Mean change in LDL cholesterol level(24 months)
  • Mean change in FPG level(24 months)
  • Mean change in the Summary of Diabetes Self-Care Activities (SDSCA) from baseline to 24 month(24 months)

Study Sites (2)

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