Dehydration Clinical Trials

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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• Adults aged 18-60

• Recently prescribed a GLP-1RA (within one week of prescription)

• Fluent in English

• Willing to complete the study protocol

Locations
United States
New York
State University of New York at Buffalo, South Campus
RECRUITING
Buffalo
Time Frame
Start Date: 2026-06-15
Estimated Completion Date: 2027-02-01
Participants
Target number of participants: 30
Treatments
Active_comparator: Control
Participants assigned to the control group will receive all information as the Hydration Plus (experimental) group, but will not receive any behavior change strategies or technique training/materials.
Experimental: Hydration Plus
The hydration plus group will receive the following behavior change strategies/techniques: coaching (consisting of goal setting, making a plan, and coping planning), positive feedback, and follow a contingency management payment schedule.
Sponsors
Leads: State University of New York at Buffalo
Collaborators: National Institutes of Health (NIH)

This content was sourced from clinicaltrials.gov