NCT07313384

Brief Summary

The DINE-GLP1 study aims to understand how people on GLP-1 therapy change their eating habits and what kind of dietary support they need. As more people use GLP-1 medications, there's not much guidance on what they should eat, mostly just focusing on managing symptoms and cutting calories. Since these medications reduce food intake, it's important to ensure the diet is nutritious even with fewer calories to help with long-term weight control and health. Most research has looked at how the body responds to the medication and whether patients take it as prescribed, but not much is known about what patients actually experience, what they think they need, or how they could use additional support. Understanding patients' views can help create better lasting solutions. Note that this study does not provide free GLP-1 medication.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
6mo left

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress42%
Feb 2026Dec 2026

First Submitted

Initial submission to the registry

December 1, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 31, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

February 11, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

February 19, 2026

Status Verified

February 1, 2026

Enrollment Period

9 months

First QC Date

December 1, 2025

Last Update Submit

February 17, 2026

Conditions

Keywords

GLP-1 TherapyNutrition SupportObesityWeight loss therapy

Outcome Measures

Primary Outcomes (1)

  • Change in Healthy Eating Index

    The Healthy Eating Index (HEI) is a scoring metric developed by the U.S. Department of Agriculture (USDA) and the NCI to assess how well a person's diet conforms to the Dietary Guidelines for Americans. It evaluates the consumption of 13 dietary components, including both adequacy (foods to increase) and moderation (foods to decrease). The scores range from 0 to 100. An ideal overall HEI score of 100 reflects that the set of foods aligns with key dietary recommendations and dietary patterns published in the Dietary Guidelines.

    Baseline and 12-weeks

Secondary Outcomes (1)

  • Change in Body Weight

    Baseline and 12 weeks

Study Arms (1)

GLP-1 Therapy

Individuals prescribed with GLP-1 Therapy for obesity or T2DM management.

Drug: GLP-1 Therapy

Interventions

Exposure to GLP-1 Therapy for obesity or T2DM management.

GLP-1 Therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The recruitment will be conducted at the Prisma Health Weight Management Institute in Greenville, South Carolina, with support from the on-site research team. A total of 50 patients will be enrolled. Eligible individuals will be adults aged 18 years or older who have recently been prescribed GLP-1 therapy for the treatment of obesity or T2DM but have not yet initiated the medication.

You may qualify if:

  • Adults aged 18 and older
  • Recently has been prescribed GLP-1 therapy for the treatment of obesity or T2DM but have not yet initiated the medication
  • Has regular access to a smartphone and internet to complete short surveys and food recalls online
  • Willing to sign informed consent.

You may not qualify if:

  • Already began the GLP-1 medication
  • Have medical concerns making participation unsafe

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

University South Carolina

Columbia, South Carolina, 20208, United States

ENROLLING BY INVITATION

Prisma Health Weight Management Institute

Greenville, South Carolina, 29607, United States

RECRUITING

MeSH Terms

Conditions

Obesity

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
12 Weeks
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Posdoctoral Fellow

Study Record Dates

First Submitted

December 1, 2025

First Posted

December 31, 2025

Study Start

February 11, 2026

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

February 19, 2026

Record last verified: 2026-02

Locations