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RECRUITING
NCT07641361
NA

Hydration Intervention to Decrease Side Effects Associated With GLP - 1 RA Therapy

Sponsor: State University of New York at Buffalo

View on ClinicalTrials.gov

Summary

This is a 17 - week study consisting of a one - week run - in period and a 16 - week intervention. The 16 - week pilot interventions aims to increase hydration in those beginning GLP - 1 RA therapy. Investigators aim to increase hydration to potentially decrease side effect severity, amount of side effects, and drug discontinuation associated with GLP - 1 RA therapy. The investigators are piloting to assess feasibility and preliminary efficacy of the intervention through examining participant retention, participant feedback, researcher and participant adherence to protocols, impact on hydration biomarkers, and participant reported GLP - 1 RA side effects.

Official title: Hydration Intervention to Address Dehydration Associated With Use of GLP-1 Based Medications

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-06-15

Completion Date

2027-02-01

Last Updated

2026-06-11

Healthy Volunteers

No

Interventions

BEHAVIORAL

Hydration Plus

The hydration plus intervention aims to increase hydration through employing the following behavior change strategies/techniques: coaching (consisting of goal setting, making a plan, and coping planning), positive feedback, and utilize a contingency management payment schedule wherein participant earned amount hinges on them meeting their goal.

BEHAVIORAL

Control

Participants randomly assigned to the control group will receive information on hydration and will receive prompts to drink.

Locations (1)

State University of New York at Buffalo, South Campus

Buffalo, New York, United States