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SMARTHealth Diabetes in China Using Lay Family Health Promoters

Primary Purpose

Diabetes Mellitus, Type 2, Hypertension, Dyslipidemias

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
SMARTHealth Diabetes
Sponsored by
The George Institute for Global Health, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Diabetes Mellitus, Type 2 focused on measuring Telemedicine, Diabetes Mellitus, Type 2, Decision Support Systems, Clinical, Family Health Promoter, Primary Health Care

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Hebei Medical University
  • Center of Disease Control and Prevention, Luquan

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention arm

Control arm

Arm Description

Participants in intervention communities will receive the SMARTHealth Diabetes intervention that connects community health service centers and family health providers for diabetes management. Medical staff and FHPs in the intervention communities will be provided with an initial training session on the installation and use of the platform.

Control group doesn't use SMARTHealth Diabetes.The "usual-care" in our study will be conducted in a standard way which is defined in the Guidance of National Essential Public Health Service. All the relevant doctors in control group will be trained and required to record the activities defined in the guidance.

Outcomes

Primary Outcome Measures

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

The proportion of patients achieving the "A" goal
The proportion of patients achieving HbA1c <7.0% at 24 months
The proportion of patients achieving the "B" goal
The proportion of patients achieving blood pressure (BP) <140/80mmHg at 24 months
The proportion of patients achieving the "C" goal
The proportion of patients achieving LDL cholesterol <100mg/dl or 2.6mmol/L at 24 months
The proportion of patients achieving FPG<7.0 mmol/L
The proportion of patients achieving FPG<7.0 mmol/L at 24 months
Mean change in HbA1c level
Mean change in HbA1c level from baseline to 24 months
Mean changes in systolic and diastolic blood pressure levels
Mean changes in systolic and diastolic blood pressure levels from baseline to 24 months
Mean change in LDL cholesterol level
Mean change in LDL cholesterol level from baseline to 24 months
Mean change in FPG level
Mean change in FPG level from baseline to 24 months
Mean change in the Summary of Diabetes Self-Care Activities (SDSCA) from baseline to 24 month
The Summary of Diabetes Self-Care Activities is a scale to measure patients' self-management. The minimum value of each scale item is 0 and the maximum value is 7. Higher scores mean a better outcome.

Full Information

First Posted
March 22, 2016
Last Updated
March 11, 2021
Sponsor
The George Institute for Global Health, China
Collaborators
Global Alliance for Chronic Diseases (GACD), National Health and Medical Research Council, Australia
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1. Study Identification

Unique Protocol Identification Number
NCT02726100
Brief Title
SMARTHealth Diabetes in China Using Lay Family Health Promoters
Official Title
Systematic Medical Assessment, Referral and Treatment for Diabetes Care in China Using Lay Family Health Promoters
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
October 19, 2019 (Actual)
Study Completion Date
February 28, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The George Institute for Global Health, China
Collaborators
Global Alliance for Chronic Diseases (GACD), National Health and Medical Research Council, Australia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Hypertension, Dyslipidemias
Keywords
Telemedicine, Diabetes Mellitus, Type 2, Decision Support Systems, Clinical, Family Health Promoter, Primary Health Care

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
2073 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention arm
Arm Type
Experimental
Arm Description
Participants in intervention communities will receive the SMARTHealth Diabetes intervention that connects community health service centers and family health providers for diabetes management. Medical staff and FHPs in the intervention communities will be provided with an initial training session on the installation and use of the platform.
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Control group doesn't use SMARTHealth Diabetes.The "usual-care" in our study will be conducted in a standard way which is defined in the Guidance of National Essential Public Health Service. All the relevant doctors in control group will be trained and required to record the activities defined in the guidance.
Intervention Type
Behavioral
Intervention Name(s)
SMARTHealth Diabetes
Intervention Description
SMARTHealth Diabetes is an interactive mobile health platform to promote improved self-management for people with T2DM.
Primary Outcome Measure Information:
Title
The proportion of patients achieving at least two "ABC" goals
Description
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
Time Frame
24 months
Secondary Outcome Measure Information:
Title
The proportion of patients achieving the "A" goal
Description
The proportion of patients achieving HbA1c <7.0% at 24 months
Time Frame
24 months
Title
The proportion of patients achieving the "B" goal
Description
The proportion of patients achieving blood pressure (BP) <140/80mmHg at 24 months
Time Frame
24 months
Title
The proportion of patients achieving the "C" goal
Description
The proportion of patients achieving LDL cholesterol <100mg/dl or 2.6mmol/L at 24 months
Time Frame
24 months
Title
The proportion of patients achieving FPG<7.0 mmol/L
Description
The proportion of patients achieving FPG<7.0 mmol/L at 24 months
Time Frame
24 months
Title
Mean change in HbA1c level
Description
Mean change in HbA1c level from baseline to 24 months
Time Frame
24 months
Title
Mean changes in systolic and diastolic blood pressure levels
Description
Mean changes in systolic and diastolic blood pressure levels from baseline to 24 months
Time Frame
24 months
Title
Mean change in LDL cholesterol level
Description
Mean change in LDL cholesterol level from baseline to 24 months
Time Frame
24 months
Title
Mean change in FPG level
Description
Mean change in FPG level from baseline to 24 months
Time Frame
24 months
Title
Mean change in the Summary of Diabetes Self-Care Activities (SDSCA) from baseline to 24 month
Description
The Summary of Diabetes Self-Care Activities is a scale to measure patients' self-management. The minimum value of each scale item is 0 and the maximum value is 7. Higher scores mean a better outcome.
Time Frame
24 months
Other Pre-specified Outcome Measures:
Title
Mean change in body mass index (BMI)
Description
Mean change in body mass index (BMI) from baseline to 24 months
Time Frame
24 months
Title
Mean change in waist circumstance (WC)
Description
Mean change in waist circumstance (WC) from baseline to 24 months
Time Frame
24 months
Title
Mean change in the European quality of life 5 dimensions 3 levels scale (EQ-5D-3L) index value
Description
Mean change in the European quality of life 5 dimensions 3 levels scale (EQ-5D-3L) index value from baseline to 24 months. The minimum value of the scale is 0 and the maximum value is 1. Higher scores mean a better outcome.
Time Frame
24 months
Title
Mean change in the European quality of life overall self-rated visual analogue scale (EQ-VAS)
Description
Mean change in the European quality of life overall self-rated visual analogue scale (EQ-VAS) from baseline to 24 months. The minimum value of the scale is 0 and the maximum value is 100. Higher scores mean a better outcome.
Time Frame
24 months
Title
Mean change in The Summary of Diabetes Self-Care Activities (SDSCA) from baseline to 24 months
Description
Pending
Time Frame
24 months
Title
Mean change in urine albumin creatinine ratio (ACR)
Description
Mean change in urine albumin creatinine ratio (ACR) from baseline to 24 months
Time Frame
24 months
Title
Mean change in estimated glomerular filtration rate (GFR)
Description
Mean change in estimated glomerular filtration rate (GFR) from baseline to 24 months
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Puhong Zhang, PhD
Organizational Affiliation
The George Institute for Global Health at Peking University Health Science Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Peiris, PhD
Organizational Affiliation
The George Institute for Global Health, University of Sydney
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hebei Medical University
City
Shijiazhuang
State/Province
Hebei
ZIP/Postal Code
050017
Country
China
Facility Name
Center of Disease Control and Prevention, Luquan
City
Shijiazhuang
State/Province
Hebei
ZIP/Postal Code
050200
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data are only accessed by investigators.
Citations:
PubMed Identifier
27535128
Citation
Peiris D, Sun L, Patel A, Tian M, Essue B, Jan S, Zhang P. Systematic medical assessment, referral and treatment for diabetes care in China using lay family health promoters: protocol for the SMARTDiabetes cluster randomised controlled trial. Implement Sci. 2016 Aug 17;11(1):116. doi: 10.1186/s13012-016-0481-8.
Results Reference
derived

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SMARTHealth Diabetes in China Using Lay Family Health Promoters

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