NCT06550791Completed
Evaluating the Anticancer Learning Circle Lifestyle Program in Endometrial Cancer Survivors
A Prospective Feasibility Study Evaluating the Implementation of the Anticancer Lifestyle Program in Endometrial Cancer Survivors
Source: ClinicalTrials.gov · Last updated 24 Oct 2025
Brief summary (registry, in English)
The purpose of this study is to promote positive lifestyle change among endometrial cancer survivors by using a group-based intervention. Endometrial cancer survivors are at an increased risk of other health conditions like heart disease, diabetes, and other cancers. The study team at the University of Virginia wants to explore new ways to lower these risks. This study will be evaluating the Anticancer Lifestyle program, which takes a more holistic approach and uses web-based learning modules along with weekly group sessions to discuss each topic of the web-based learning modules.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 23 (actual)
- First submitted
- 29 Jul 2024
- Start date
- 4 Sept 2024
- Primary completion date
- 24 Mar 2025
- Lead sponsor
- University of Virginia
- Diseases
- Endometrial cancer
- NCT number
- NCT06550791
What you commit to
- Study type: Interventional
- Participants enrolled: 23
- From 4 Sept 2024 to the primary completion date, 24 Mar 2025
- 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
- Pregnant women
- Prisoners
- Subject is blind
Who the study is looking for
- History of stage I-IV endometrial cancer, any histologic subtype
- Completed cancer treatment, and in surveillance
- Have no evidence of endometrial cancer as determined by primary oncologist
- Be at least 18 years of age
- Be able to read and communicate in English
- Have a smartphone with access to cellular service or computer access with internet service
- Must have technological competency/proficiency to use their Smartphone and/or computer, as self-reported by potential subject
- Stated willingness to comply with all study procedures and availability for the duration of the study.
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 Virginia Coordinator of this site? Confirm its status | Charlottesville | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.