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Completed Not applicable Interventional Accepts healthy volunteers Results available

Enhanced DPP-GLB to Promote Weight Loss Among Nonresponders in a Community-Based Lifestyle Intervention.

ClinicalTrials.gov ID: NCT04757519

Public ClinicalTrials.gov record NCT04757519. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 11:24 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Enhancing the Diabetes Prevention Program to Promote Weight Loss Among Nonresponders in a Community-Based Lifestyle Intervention.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study seeks to establish the efficacy of identifying weight loss nonresponders early in a Diabetes Prevention Program (DPP) intervention in 20 community settings (primarily churches and community centers) and providing them with individual-level, enhanced treatment through telephone contacts and access to additional resources. Additionally, potential mediators and moderators of the relationship between intervention status and weight loss response at 6 months in both nonresponders and responders will be examined and a cost-effectiveness analysis to evaluate the cost of the intervention will be conducted. This study addresses key gaps in the literature about the weight loss effects of identifying nonresponders early and characterizing individuals who need more intense personalized strategies. The investigators hypothesize that changes between baseline and 3 months will be more pronounced among the nonresponders in the intervention group compared to the nonresponders in the active control group.

Study identification

NCT ID
NCT04757519
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Lovoria Williams
Other
Enrollment
403 participants

Conditions and interventions

Conditions

Interventions

Behavioral

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 17, 2021
Primary completion
Dec 3, 2024
Completion
Apr 16, 2026
Last update posted
Jun 23, 2026

2021 – 2026

United States locations

U.S. sites
21
U.S. states
1
U.S. cities
5
Facility City State ZIP Site status
First Corinthian Baptist Church Frankfort Kentucky 40601
Heavenly Outpour Frankfort Kentucky 40601
Consolidated Baptist Church Lexington Kentucky 40505
Historic St. Paul AME Church Lexington Kentucky 40507
First African Baptist Church Lexington Kentucky 40508
Pilgrim Baptist Church Lexington Kentucky 40508
Shiloh Baptist Church Lexington Kentucky 40508
Redeemed Christian Church of God Lexington Kentucky 40509
First Baptist Church Brackstown Lexington Kentucky 40511
Lima Drive Seventh Day Adventist Church Lexington Kentucky 40511
Kingdom Fellowship Louisville Kentucky 40202
Bates Memorial Baptist Church Louisville Kentucky 40203
St. Stephen Baptist Church Louisville Kentucky 40210
Greater Gaililee CDC Louisville Kentucky 40211
Historic Calvary MBC Louisville Kentucky 40211
Spirit Filled New Life Church Louisville Kentucky 40214
Forest Baptist Church Louisville Kentucky 40218
Burnett Ave BC Louisville Kentucky 40291
Marnel C. Moorman Family Life Center Shelbyville Kentucky 40065
New Mt. Zion Baptist Church Shelbyville Kentucky 40065
First Baptist Winchester Winchester Kentucky 40391

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04757519, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04757519 live on ClinicalTrials.gov.

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