RecruitingNCT06877572

Weight Loss Management in Endometrial Cancer Survivors

Enacting Active Survivorship: Implementation of Weight Management Strategies in Endometrial Cancer Survivors


Sponsor

University of Kansas Medical Center

Enrollment

50 participants

Start Date

Mar 25, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

This study is being done to understand how oncologists can engage a multidisciplinary team to help endometrial cancer survivors with obesity to engage in a weight management program and potentially start a weight loss medication. Obesity often impacts the future health and longevity of early-stage endometrial cancer survivors more than their cancer diagnosis. Patients will be referred to the KUMC OB/Gyn weight management clinic to discuss weight management options. * If patients decide to use medications for weight loss, then the study will collect data from their chart that is recorded as part of routine monitoring for patients on weight loss medications. * If patients decide not to use any medications, the study will monitor physical exam and lab data collected as part of their routine medical care. The study will also try to understand reasons why patients did or did not start using a weight loss medication.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a structured weight loss program for survivors of early-stage endometrial cancer (uterine cancer) who are overweight, to see if losing weight improves outcomes and reduces cancer recurrence risk. **You may be eligible if...** - You are 18 or older - You have a BMI of 30 or higher (clinically obese) - You have been diagnosed with stage 1 endometrioid endometrial cancer (a specific type of uterine cancer) with a normal p53 gene - You have completed surgical staging with no remaining evidence of disease - You are on active surveillance, with or without brachytherapy (a type of internal radiation) - Your general health is good to moderate (ECOG 0-2) **You may NOT be eligible if...** - You are unable to participate in a behavioral weight loss program - You have had a stroke, heart attack, end-stage liver disease, or end-stage kidney disease in the past 6 months - You are already taking a GLP-1 agonist (such as semaglutide/Ozempic) or insulin Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALWeight loss with pharmacotherapy

Patients will meet with a weight management specialist and discuss their options for weight loss including medications (GLP-1 agonist, naltrexone/bupropion, orlistat, or phentermine/topiramate) or bariatric surgery.

BEHAVIORALWeight loss without pharmacotherapy

Participants not on medications will have their weight recorded at subsequent cancer surveillance or other routine medical visits


Locations(1)

University of Kansas Medical Center

Kansas City, Kansas, United States

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NCT06877572


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