๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-08

Hydration Intervention to Decrease Side Effects Associated With GLP - 1 RA Therapy (NCT07641361)

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

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿง  Behavioral & Psychological Program Sponsor: State University of New York at Buffalo

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: State University of New York at Buffalo, South Campus โ€” Buffalo, New York

Age range: 18 Years to 60 Years

๐Ÿงช Interventions in This Study

  • Hydration Plus (BEHAVIORAL)
  • Control (BEHAVIORAL)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • State University of New York at Buffalo, South Campus โ€” Buffalo, New York

๐Ÿ“ž Contact the Study Coordinator

Phone: (716) 829-5820

Email: hkolpack@buffalo.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—