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Trial Title:
Evaluating the Anticancer Learning Circle Lifestyle Program in Endometrial Cancer Survivors
NCT ID:
NCT06550791
Condition:
Neoplasm, Uterine
Conditions: Official terms:
Endometrial Neoplasms
Uterine Neoplasms
Conditions: Keywords:
Endometrial Cancer
Holistic Cancer Treatment
Lifestyle Change
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Supportive Care
Masking:
None (Open Label)
Intervention:
Intervention type:
Behavioral
Intervention name:
Anticancer Learning Circle
Description:
All participants will partake in the Anticancer Learning Circle, a lifestyle modification
program. All participants will complete web-based learning modules focused on improving
diet, lowering stress, increasing fitness, and reducing exposure to toxins in the home
environment. Each week, all participants will meet as a group to discuss the learning
topic of the web-based learning module for the week.
Arm group label:
Anticancer Learning Circle Participant
Summary:
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.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Pregnant women
- Prisoners
- Subject is blind
Gender:
Female
Gender based:
Yes
Gender description:
Person born with a uterus
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
University of Virginia
Address:
City:
Charlottesville
Zip:
22903
Country:
United States
Status:
Recruiting
Contact:
Last name:
Tam Le
Phone:
434-924-6872
Email:
ttl3gnw@uvahealth.org
Contact backup:
Last name:
Kathryn Dryer, MD
Phone:
763-370-5543
Email:
hfk5rb@uvahealth.org
Investigator:
Last name:
Kari Ring, MD
Email:
Principal Investigator
Start date:
September 4, 2024
Completion date:
May 2025
Lead sponsor:
Agency:
University of Virginia
Agency class:
Other
Source:
University of Virginia
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06550791
