No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 60
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
State University of New York at Buffalo · Other
Who this trial is looking for
This trial is looking for adults aged 18-60 who have recently started a GLP-1 RA medication for type 2 diabetes. Participants will help test if increasing hydration can reduce side effects from the medication over 16 weeks.
Are You a Good Fit for This Trial?
You may be able to join if
I am an adult aged 18-60
I have been prescribed a GLP-1 RA medication within the last week
I can speak and understand English
I am willing to follow the study guidelines
You may not be able to join if
I am over 60 years old
I am not taking a GLP-1 RA medication
I have been on a GLP-1 RA for more than a week
I am not fluent in English
I am pregnant or plan to become pregnant during the study
I am not willing to follow the study guidelines
I have a cardiac implant
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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…
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.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Adults aged 18-60
* Recently prescribed a GLP-1RA (within one week of prescription)
* Fluent in English
* Willing to complete the study protocol
Exclusion Criteria:
* Children and adults \> 60 years of age
* Those not taking a GLP-1RA
* Those who have been on a GLP-1RA longe…
Inclusion Criteria:
* Adults aged 18-60
* Recently prescribed a GLP-1RA (within one week of prescription)
* Fluent in English
* Willing to complete the study protocol
Exclusion Criteria:
* 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
Contacts
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