Micro-Clinic Obesity and Metabolic Risk Prevention Program
- Conditions
- Diabetes Mellitus, Type IIObesityHeart DiseaseHypertensionDyslipidemia
- Interventions
- Behavioral: ControlBehavioral: Microclinic Diabetes Education Program
- Registration Number
- NCT01651065
- Lead Sponsor
- Microclinic International
- Brief Summary
The purpose of this randomized trial is to study the efficacy of a novel social propagation intervention which integrates social network induction with health education for weight and metabolic control among patients with type 2 diabetes, BMI of 25-30+, and cardiovascular disease. The intervention takes place in the form of a community health program, where participants who enroll in this program will be asked if they would like to take part in the study to evaluate its efficacy. Thus, the investigators will study the efficacy of social networks in propagating changes in lifestyle factors for diabetes and chronic disease management
- Detailed Description
The potential to harness the propagating power of social networks for chronic disease treatment and management, such as for diabetes and obesity, is an emerging area in epidemiology and clinical research. Social induction for disease management has been effectively leveraged for disease management, but we have not carefully disaggregated of different layers and modalities of social network effects in this context. This study will test and demonstrate this through a novel randomized trial.
The randomized design is comprised of 2 arms. 1) Intervention Group: This arm takes part in a 10-month (9-month for Phase 2, cycles 1 and 2) diabetes, weight, and cardiovascular disease education and management program in combination with the microclinic social support model. A microclinic is a support group of 2-6 individuals from the same social network who learn how to manage their disease together. 2) Control Group: This is a control arm with observational parallel assessments of metabolic and lifestyle risk factors alone (implemented in Phase 1 and 2, cycles 1 and 2). Each arm will take part in a 6-month follow-up. The investigators also aim to study the intervention effects of social networks in improving lifestyle risk factors on a small sample of Phase 1 controls in a repeated measures design. Observational controls with 7 repeated measures in Phase 1 (pre-intervention) will receive the 9-month diabetes, weight, and cardiovascular disease education and management program with microclinic social support model condensed in a 4-6 months program. The controls in this cycle will also receive 17 medical screenings during the intervention, and 6-month follow-up (post-intervention).
Aim 1- (Phase 1 and 2, Cycles 1 \& 2)
To evaluate the efficacy of the microclinic intervention group versus observational control in improving lifestyle factors and metabolic outcome.
Aim 2- (Phase 2, Cycle 3)
To examine the effect of the microclinic intervention by comparing pre- and post measures among those who were first controls in Phase 1 and then participated in the microclinic intervention Phase 2, Cycle 3.
AIM 3- (Phases 1 \& 2, cycles 1, 2, and 3)
To differentiate the modalities of social network effects: direct causal induction versus homophilly, and to determine the extent of long-term temporal cross-propagating effects between-persons in a microclinic group.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 494
- Must be enrolled in our community health program.
- Over the age of 18
- BMI of 30 or higher, or
- BMI of 25 or higher AND must be diagnosed with at least one additional risk factor 1) type 2 diabetes, 2) high blood pressure, and/or 3) high cholesterol
- For those who will be participating in the cross-over sub-sample, they must have previously participated in Phase 1 as subject of the control group, or
- Patients who are not enrolled in the our community health education program (applies to Phase 1 only)
- Are not able to provide informed consent for themselves
- Under the age of 18
- Has undergone weight loss surgery
- Pregnant women*
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Active Controls Control Individuals will receive screening by clinical staff. Control group subjects are offered standard of care from local health department, but will not participate in program activities, other than offered option to join open-community health events. Microclinic Social Network Program Microclinic Diabetes Education Program Subjects will be receiving a 10/9-month Microclinic Diabetes Education Program (Team Up 4 Health) and 6 months of follow up. In the intervention these subjects will engage in the Microclinic Program support groups. The intervention program consists of 25 event sessions. Sessions are offered weekly the first month, and biweekly thereafter.
- Primary Outcome Measures
Name Time Method Weight From baseline until end of intervention period (9-10 months), and 6 months post-intervention Change in weight over time
- Secondary Outcome Measures
Name Time Method Waist circumference From baseline until end of intervention period (9-10 months), and 6 months post-intervention Change in waist measurement over time
Blood pressure From baseline until end of intervention period (9-10 months), and 6 months post-intervention Change in systolic/diastolic blood pressure over time
HDL From baseline until end of intervention period (9-10 months), and 6 months post-intervention Change in HDL over time
Hemoglobin A1c (%, HbA1c) From baseline until end of intervention period (9-10 months), and 6 months post-intervention Change in HbA1c over time
Trial Locations
- Locations (1)
Bell County Health Department
🇺🇸Pineville, Kentucky, United States