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Delfa

← All trials/NCT07702461

Recruiting

Determination of Resistance Training Status for Patients on Glucagon-Like Peptide-1 Receptor Agonists

Assets

Dulaglutide / Exenatide / Liraglutide / Semaglutide / Tirzepatide

Listed sites

1

Recruiting sites

1

Estimated enrollment

300

Study population

Obesity / overweight

Eligibility highlights

-

Primary endpoint

-

Registered trial locations

Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT07702461
Org study IDSTUDY20260750

Timeline

Milestones

Study start2026-06-12actual
Study first posted2026-07-14actual
Last update posted2026-07-24actual
Primary completion2026-10estimated (month precision)
Study completion2027-01estimated (month precision)

Assets

Investigational agents

Who this study enrolls

Obesity / overweight

Who can enroll

Minimum age18 Years
SexAll
Healthy volunteersNot accepted
Sampling methodNon probability sample

Study population text

Adults residing in the United States who are current users of GLP-1 receptor agonist medications for type 2 diabetes, overweight or obesity, and/or weight management. Participants are recruited from community and online settings rather than from a single physical site. Sources include: IRB-approved flyers and posters displayed in relevant clinical settings (e.g., endocrinology, primary care) and community locations; social media outreach (posts and advertisements) directed at adults using GLP-1 receptor agonist medications; and clinic-based outreach in which participating clinic staff post handouts in waiting areas or distribute them to potentially interested patients during routine visits. Interested individuals self-refer by accessing an anonymous online Qualtrics survey link. The study team does not pre-screen, identify, or contact patients directly, and does not access medical records or protected health information at any point.

Inclusion criteria

Adult aged 18 years or older
Currently taking a GLP-1 receptor agonist medication
On the GLP-1 receptor agonist for at least 3 months
Using the GLP-1 receptor agonist for type 2 diabetes, overweight or obesity, and/or weight management (self-reported)
Stable GLP-1 receptor agonist dose for the past 4 to 8 weeks
Able to read and respond to the survey in English
Willing and able to provide informed consent electronically

Exclusion criteria

Currently or planning to become pregnant
Planned bariatric surgery within the next 3 months
Recent bariatric surgery (within the past 3 months) or other conditions that substantially alter resistance training capacity (e.g., advanced cancer cachexia, severe mobility-limiting conditions)
Unable to read or respond to the survey in English

Endpoints (0)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

No endpoints recorded for this trial.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 6, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 6, 2026 snapshot.