NCT05737745Completed
FitEx for Endometrial Cancer Survivors: Initial Efficacy
The Initial Efficacy of FitEx for Endometrial Cancer Survivors: A Pilot Randomized Controlled Trial of a Walking Promotion Program With or Without Yoga
Source: ClinicalTrials.gov · Last updated 9 May 2025
Brief summary (registry, in English)
The goal of this clinical trial is to compare physical activity outcomes between endometrial cancer survivors randomized to 1 of 3 conditions: 1) usual care, 2) FitEx, 3) FitEx+yoga. Survivors randomized to FitEx groups will recruit \~3 support team members to complete the intervention with them. The main question\[s\] it aims to answer are: * Do FitEx groups undertake more physical activity than the usual care group? * Are there differences in quality of life, self-compassion, flourishing, self-efficacy, social support, habit formation, and fruit /vegetable consumption Participants will: * Wear a Fitbit * Complete surveys * Participate in 30 minute weekly virtual meetings (FitEx groups only) * Receive weekly newsletters (FitEx groups only)
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 111 (actual)
- First submitted
- 1 Feb 2023
- Start date
- 1 Feb 2023
- Primary completion date
- 30 Nov 2023
- Lead sponsor
- Carilion Clinic
- Diseases
- Obesity, Endometrial cancer
- NCT number
- NCT05737745
What you commit to
- Study type: Interventional
- Participants enrolled: 111
- From 1 Feb 2023 to the primary completion date, 30 Nov 2023
- 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 endometrial cancer
- Meeting physical activity guidelines set forth by the American Cancer Society at screening (greater than 150 minutes/week of moderate physical activity, or greater than 75 minutes/week of vigorous physical activity)
Other
- SURVIVOR
- SUPPORT TEAM: Have functional limitations requiring a walker, wheelchair, scooter, or other walking aid which limits their capacity to engage in the intervention safely
Who the study is looking for
- SURIVIVOR
- Diagnosed with early stage (I-II) endometrial cancer, any histology
- Received cancer care at Carilion Clinic after 1/1/2010
- At least 18 years of age
- Have adequate comprehension (reading and writing) of the English language
- Have a BMI ≥ 30 kg/m\^2 at screening
- Have stable internet access or access to a smartphone with internet capabilities
- Meet the requirements of the Physical Activity Readiness Questionnaire(PARQ)
- Have the capacity to provide informed consent and are willing to provide informed consent
- SUPPORT TEAM--
- Were identified by a participant with endometrial cancer as a member of their support system
- Are at least 18 years of age
- Have adequate comprehension (reading and writing) of the English language
- Have stable internet access or access to a smartphone with internet capabilities
- Meet the requirements of the Physical Activity Readiness Questionnaire (PARQ)
- Have the capacity to provide informed consent and are willing to provide informed consent
Age in the registry: 18 years to - · Sex: All · 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 |
|---|---|---|---|
| Carilion Clinic Coordinator of this site? Confirm its status | Roanoke | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.