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临床试验/NCT07641361
NCT07641361招募中不适用

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

State University of New York at Buffalo1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年6月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged 18-60
  • Recently prescribed a GLP-1RA (within one week of prescription)
  • Fluent in English
  • Willing to complete the study protocol

排除标准

  • Children and adults > 60 years of age
  • Those not taking a GLP-1RA
  • Those who have been on a GLP-1RA longer than one week
  • Not fluent in English
  • Those who are pregnant or planning on becoming pregnant during the duration of the study
  • Unwilling to comply with study protocol
  • People with cardiac implants

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Katherine Balantekin

Principal Investigator

State University of New York at Buffalo

研究点 (1)

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