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Social Determinants and a Diabetes Prevention Program Tailored for African Americans (FIT4ALL)

Primary Purpose

PreDiabetes, Overweight and Obesity

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Culturally Tailored Diabetes Prevention Program
Culturally Tailored DPP Enhanced with Socioeconomic Supports
Diabetes Prevention Program
Sponsored by
University of Missouri, Kansas City
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for PreDiabetes focused on measuring African American, Prediabetes, Diabetes Prevention Program, Cultural tailoring, Linkage to care, Weight loss, Class attendance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Black/African American
  • Overweight ([BMI> 24); and
  • Diagnosed with prediabetes OR pre-diagnosed with gestational diabetes OR high risk result on prediabetes risk test

Exclusion Criteria:

  • Diagnosed with diabetes
  • Pregnant
  • Not fluent in English
  • Currently pregnant, planning a pregnancy in the next year, currently breastfeeding or have given birth in the last 6 months
  • Currently participating in a weight loss program
  • Currently have a medical condition that causes drastic weight loss
  • Bariatric weight loss surgery in last year
  • Cannot walk a 1-block distance without assistance and without stopping due to pain, tightness, or pressure in the chest
  • Had heart failure
  • Not willing to use a fitness tracker, wi-fi scale, and the internet
  • Not available in the evening one day each week to participate in a class

Sites / Locations

  • University Health
  • University of Missouri-Kansas CityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Standard

Culturally Tailored DPP

Culturally Tailored DPP Enhanced with Socioeconomic Supports

Arm Description

Standard Diabetes Prevention Program (DPP)

DPP culturally tailored for African Americans

Culturally tailored DPP plus promotions for class attendance, hybrid attendance (in-person and virtual), and linkage to care services provided by a community health worker

Outcomes

Primary Outcome Measures

Percent Weight Loss
Percentage of weight loss from initial baseline weight
Percent Weight Loss
Percentage of weight loss from initial baseline weight
DPP Class Attendance
Number and proportion of the classes attended
DPP Class Attendance
Number and proportion of the classes attended

Secondary Outcome Measures

Physical Activity
Self-reported hours/minutes of physical activity in past week
Physical Activity
Self-reported hours/minutes of physical activity in past week
Blood pressure
Systolic and diastolic blood pressure will be measured
Blood pressure
Systolic and diastolic blood pressure will be measured
Blood glucose
Hemoglobin A1C
Blood glucose
Hemoglobin A1C
Office/clinic visits
Proportion of participants with a physician office/clinic visit

Full Information

First Posted
March 9, 2022
Last Updated
May 1, 2023
Sponsor
University of Missouri, Kansas City
Collaborators
University of Massachusetts, Amherst, University of Kansas, Children's Mercy Hospital Kansas City, University Health
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1. Study Identification

Unique Protocol Identification Number
NCT05301413
Brief Title
Social Determinants and a Diabetes Prevention Program Tailored for African Americans
Acronym
FIT4ALL
Official Title
Addressing Social Determinants of Health to Improve Diabetes Prevention Program Outcomes Among Underserved African Americans (FIT4ALL Project)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 20, 2022 (Actual)
Primary Completion Date
July 25, 2025 (Anticipated)
Study Completion Date
July 25, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri, Kansas City
Collaborators
University of Massachusetts, Amherst, University of Kansas, Children's Mercy Hospital Kansas City, University Health

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
African Americans (AAs) have rates of diabetes mellitus (DM) twice that of Whites and are disproportionately affected by leading risk factors for DM - obesity and low-income. A critical strategy in the battle against DM is the Diabetes Prevention Program (DPP), an evidence-based intervention that significantly delays or prevents Type 2 diabetes through the promotion of diet change, exercise and modest weight loss. However, weight loss from the DPP among AAs is about half that of White participants, and suboptimal AA attendance is a critical contributor. The investigators propose to conduct a study that will address social determinants (SD) that challenge DPP attendance with underserved African Americans from a safety net hospital. The investigators will examine DPP attendance and weight loss with participants randomized to 3 groups: standard DPP, a culturally-tailored DPP to address acceptability, and a culturally-tailored DPP enhanced to address socioeconomic-related barriers to DPP participation. This novel study is the first to tailor the DPP to address SD cultural and socioeconomic barriers that limit DPP attendance and reduce its effectiveness on outcomes. The proposed multidimensional, SD tailored DPP has great potential to be a feasible and scalable model to reduce DM risks among urban, African Americans and ultimately reduce DM disparities.
Detailed Description
African Americans (AAs) are disproportionately burdened by diabetes mellitus (DM) with rates twice as high as Whites (13% vs 7.5%), and increased rates of DM-related complications and comorbidities (e.g. amputations, cardiovascular disease). A key pre-DM risk factor is overweight/obesity. Nearly 70% of AAs are overweight or obese, with higher rates among AAs with low-income. A critical component of national efforts to reduce growing obesity rates and prevent DM is the Diabetes Prevention Program (DPP), a lifestyle intervention proven to reduce or delay DM onset with diet change, exercise, and modest weight loss (5-7%) in a rigorously evaluated national trial. A group-based version of the DPP has been widely disseminated and numerous community-based trials support its efficacy. In spite of these successes, there are significant health disparities in DPP attendance and outcomes and considerable room exists for improving success rates among AAs, a population that tends to experience half the amount of DPP weight loss compared to Whites. The investigators aim to build on our promising pilot studies by tailoring the DPP via a social determinants (SD) of health lens to achieve optimal DPP attendance and clinically meaningful weight loss with pre-DM AAs. This includes tailoring on cultural and socioeconomic SD mechanisms that are associated with improving health outcomes and align with predisposing needs among AAs who are primarily of low-income and live in low-resource AA communities. The investigators propose a randomized controlled trial of 360 pre-DM AA patients from a safety net hospital (SNH) to test a standard DPP (S-DPP) against a culturally tailored DPP (TC-DPP; e.g., tailoring of language, foods, values, religiosity, norms, values) alone and a culturally tailored DPP enhanced to address access and support related economic barriers (TCE-DPP; hybrid group/online/text DPP; community health worker support to improve access to DPP classes, healthy food, exercise, and other community and health resources; and class promotions) over 12 months. The investigators will: 1) examine effects of TC-DPP and TCE-DDP on percent weight loss and attendance (primary outcomes) and on secondary outcomes (physical activity, completion of physician follow-up visit, hbA1c, and blood pressure) at 6 and 12 months with SNH AAs, 2) evaluate potential mediators/ moderators related to weight loss and attendance among AA SNH patients at 6 and 12 months to determine modifiable facilitators and barriers, and 3) conduct a process evaluation to examine TCE-DPP acceptability, feasibility, and fidelity, and relationships between delivery dose, exposure, costs, and outcomes to identify and improve essential intervention components. Our multidimensional DPP interventions are guided by our past pilots, and based on components that, all together, were used to help drive clinically important outcomes in the original DPP trial - and are certainly needed to achieve similar outcomes with AA primarily of low-income. To our knowledge this is the first study to test multidimensional tailoring via an SD lens to truly impact DPP attendance and outcomes, and has potential to be a feasible, scalable model to reduce DM disparities among at-risk AA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes, Overweight and Obesity
Keywords
African American, Prediabetes, Diabetes Prevention Program, Cultural tailoring, Linkage to care, Weight loss, Class attendance

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
360 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard
Arm Type
Active Comparator
Arm Description
Standard Diabetes Prevention Program (DPP)
Arm Title
Culturally Tailored DPP
Arm Type
Experimental
Arm Description
DPP culturally tailored for African Americans
Arm Title
Culturally Tailored DPP Enhanced with Socioeconomic Supports
Arm Type
Experimental
Arm Description
Culturally tailored DPP plus promotions for class attendance, hybrid attendance (in-person and virtual), and linkage to care services provided by a community health worker
Intervention Type
Behavioral
Intervention Name(s)
Culturally Tailored Diabetes Prevention Program
Other Intervention Name(s)
Culturally Tailored DPP
Intervention Description
This intervention includes a culturally tailored DPP curriculum, class procedures, and handouts
Intervention Type
Behavioral
Intervention Name(s)
Culturally Tailored DPP Enhanced with Socioeconomic Supports
Other Intervention Name(s)
FIT4ALL
Intervention Description
This intervention includes the culturally tailored DPP curriculum, class procedures, and handouts along with promotional items for class participation, opportunities to attend class in-person or virtually through a digital platform, and assistance from a community health worker to provide linkage to health care services and community resources
Intervention Type
Behavioral
Intervention Name(s)
Diabetes Prevention Program
Other Intervention Name(s)
DPP
Intervention Description
This is the CDC TD2 evidence-based Diabetes Prevention Program
Primary Outcome Measure Information:
Title
Percent Weight Loss
Description
Percentage of weight loss from initial baseline weight
Time Frame
6 months
Title
Percent Weight Loss
Description
Percentage of weight loss from initial baseline weight
Time Frame
12 months
Title
DPP Class Attendance
Description
Number and proportion of the classes attended
Time Frame
6 months
Title
DPP Class Attendance
Description
Number and proportion of the classes attended
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Physical Activity
Description
Self-reported hours/minutes of physical activity in past week
Time Frame
6 months
Title
Physical Activity
Description
Self-reported hours/minutes of physical activity in past week
Time Frame
12 months
Title
Blood pressure
Description
Systolic and diastolic blood pressure will be measured
Time Frame
6 months
Title
Blood pressure
Description
Systolic and diastolic blood pressure will be measured
Time Frame
12 months
Title
Blood glucose
Description
Hemoglobin A1C
Time Frame
6 months
Title
Blood glucose
Description
Hemoglobin A1C
Time Frame
12 months
Title
Office/clinic visits
Description
Proportion of participants with a physician office/clinic visit
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Black/African American Overweight ([BMI> 24); and Diagnosed with prediabetes OR pre-diagnosed with gestational diabetes OR high risk result on prediabetes risk test Exclusion Criteria: Diagnosed with diabetes Pregnant Not fluent in English Currently pregnant, planning a pregnancy in the next year, currently breastfeeding or have given birth in the last 6 months Currently participating in a weight loss program Currently have a medical condition that causes drastic weight loss Bariatric weight loss surgery in last year Cannot walk a 1-block distance without assistance and without stopping due to pain, tightness, or pressure in the chest Had heart failure Not willing to use a fitness tracker, wi-fi scale, and the internet Not available in the evening one day each week to participate in a class
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christopher Winders
Phone
18162355370
Email
windersc@umkc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Carole Bowe Thompson
Phone
8162356062
Email
bowethompsonc@umkc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jannette Y Berkley-Patton, PhD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Betty Drees, M.D.
Phone
816-404-4070
Email
dreesb@umkc.edu
First Name & Middle Initial & Last Name & Degree
Betty Drees
Facility Name
University of Missouri-Kansas City
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jannette Berkley-Patton, PhD
Phone
816-235-6362

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Social Determinants and a Diabetes Prevention Program Tailored for African Americans

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