NCT02774759Active, not recruiting
Feasibility of the NEXT Steps Weight Loss Intervention +/- Resistance Training for Endometrial Cancer Survivors: Effect on Lean Mass & Biomarkers
Source: ClinicalTrials.gov · Last updated 18 Sept 2026
Brief summary (registry, in English)
The goal of this research study is to learn if a home-based physical activity program is feasible and can help endometrial cancer survivors lose weight.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 15 (actual)
- First submitted
- 11 May 2016
- Start date
- Oct 2016
- Primary completion date
- Dec 2026
- Lead sponsor
- M.D. Anderson Cancer Center
- Diseases
- Obesity, Endometrial cancer
- NCT number
- NCT02774759
What you commit to
- Study type: Interventional
- Participants enrolled: 15
- From Oct 2016 to the primary completion date, Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Recurrent disease
Other
- Unmanaged lymphedema
- Medical contraindications to home-based exercise or low-fat, high fruit and vegetable diet
- Functional limitations requiring a walker/scooter/wheelchair for daily activities
- Vigorous exercise \> or = 60 min/week or moderate exercise \> or = 150 min/week. If a combination of moderate and vigorous exercise are preformed, the minutes of moderate exercise/week plus 2 x minutes of vigorous exercise/week \> or = 150 min/week.
- Resistance training on \> or = 2 days/week accounting for more than 30 minutes of strength training per week
- Enrollment in a structured weight loss program in the past 6 months
Who the study is looking for
- Diagnosed with Stage I-II endometrial cancer
- Six to 36 months post treatment
- Body mass index (BMI) 30-\<45 kg/m2
- Age of at least 18 years
- Access to a telephone for coaching sessions and access to a computer, smartphone, or tablet for syncing Fitbit devices
- Can speak and read English
- Can provide informed consent
- Willing to travel to MD Anderson's main campus for 2 visits (baseline and 6 months post-baseline)
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Texas - MD Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.