Purpose

The primary objective of the STRIVE study is to compare two implementation strategies for Diabetes Prevention Program delivery: an in-person health coach strategy (standard 24 in-person sessions at WIC clinics) vs. a multifaceted technology-assisted health coach implementation strategy (12 in-person sessions at WIC clinics supplemented by technology support) on implementation and health-related outcomes in postpartum women.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
Female
Accepts Healthy Volunteers
Yes

Criteria


Inclusion Criteria for Clinics:

- Serve a large number of WIC postpartum participants

- Willing and able to provide space for the study

Inclusion Criteria for Participants:

- Age 18 or older

- Gave birth in the past 6 weeks to 12 months

- Obesity or history of gestational diabetes mellitus (Current BMI ≥30 kg/m², OR
Medical-record documented history of gestational diabetes mellitus and BMI ≥25 kg/m²)

- No self-reported diabetes (other than gestational diabetes)

- Hemoglobin A1c <6.5%

- Not currently pregnant or planning to become pregnant in the next 6 months

- No plans to move outside of the study region in the next 12 months

- Access to a smartphone

- Willing and able to participate in the intervention and provide consent

- Not an immediate family member of the staff at the WIC clinic

- Other concerns regarding ability to meet trial requirements, at the discretion of the
principal investigator or study coordinator

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Cluster-randomization of 36 Women, Infants, and Children (WIC) clinics
Primary Purpose
Prevention
Masking
None (Open Label)
Masking Description
Due to the nature of the cluster design and intervention program, the study participants, health coaches, DPP Coordinators, WIC clinic staff, and research staff who collect clinical outcome data will not be blinded.

Arm Groups

ArmDescriptionAssigned Intervention
Active Comparator
In-person health coach strategy
Delivery of 24 health coaching sessions in-person by health coaches over 1 year. Standard delivery of 24-sessions of the Group Lifestyle Balance (GLB) behavioral intervention in WIC clinics. The GLB was adapted from the original Lifestyle Balance behavioral intervention used in the original Diabetes Prevention Program trial for use in community translation and group settings. It focuses on improving diet and physical activity and promoting moderate weight loss through health coaching on behavioral change, including self-monitoring of food intake, physical activity, and weight.
  • Behavioral: In-person health coach delivery of the GLB
    Delivery of 24 health coaching sessions in-person by health coaches over 1 year. Standard delivery of 24-sessions of the Group Lifestyle Balance (GLB) behavioral intervention in WIC clinics. The GLB was adapted from the original Lifestyle Balance behavioral intervention used in the original Diabetes Prevention Program trial for use in community translation and group settings. It focuses on improving diet and physical activity and promoting moderate weight loss through health coaching on behavioral change, including self-monitoring of food intake, physical activity, and weight.
Active Comparator
Multifaceted technology-assisted health coach implementation strategy
Delivery of 12 health coaching GLB sessions in-person by health coaches over one year; supplemental technology support, including tools for self-monitoring, health coach monitoring, asynchronous delivery of intervention materials, and asynchronous coach and group connection. The GLB was adapted from the original Lifestyle Balance behavioral intervention used in the original Diabetes Prevention Program trial for use in community translation and group settings. It focuses on improving diet and physical activity and promoting moderate weight loss through health coaching on behavioral change, including self-monitoring of food intake, physical activity, and weight.
  • Behavioral: Technology-assisted health coach delivery of the GLB
    Delivery of 12 health coaching GLB sessions in-person by health coaches over one year; supplemental technology support, including tools for self-monitoring, health coach monitoring, asynchronous delivery of intervention materials, and asynchronous coach and group connection. The GLB was adapted from the original Lifestyle Balance behavioral intervention used in the original Diabetes Prevention Program trial for use in community translation and group settings. It focuses on improving diet and physical activity and promoting moderate weight loss through health coaching on behavioral change, including self-monitoring of food intake, physical activity, and weight.

Recruiting Locations

Tulane University School of Public Health and Tropical Medicine
New Orleans, Louisiana 70112
Contact:
Tara Dobson, BA
504-988-9922
tdobson@tulane.edu

More Details

Status
Recruiting
Sponsor
Tulane University

Study Contact

Tara Dobson, BA
504.988.9922
tdobson@tulane.edu

Detailed Description

The overall objective of this project is to study the implementation, effectiveness, and sustainability of implementing the Diabetes Prevention Program (DPP) in postpartum women who receive services from WIC. In this effectiveness-implementation type III cluster-randomized trial, we will compare two implementation strategies for DPP delivery: an in-person health coach-led implementation strategy (standard 24 in-person sessions) vs. a multifaceted technology-assisted health coach implementation strategy (12 in-person sessions supplemented by technology tools). Eighteen clinics will be randomized to the multifaceted technology-assisted health coach strategy and 18 to the in-person health coach-led strategy. A total of 900 postpartum participants (25 per clinic) will be recruited into the study and followed for 12 months for implementation and effectiveness outcomes. A post-intervention study visit will take place 6 months after the end of the 12-month intervention to evaluate the sustainability of the implementation strategies.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.