Evaluating the Anticancer Learning Circle Lifestyle Program in Endometrial Cancer Survivors

NCT ID: NCT06550791

Last Updated: 2025-10-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-09-04
• Study Completion Date: 2025-09-28

Brief 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.

Conditions

Neoplasm, Uterine

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Anticancer Learning Circle Participant

Group Type: EXPERIMENTAL

Anticancer Learning Circle

Intervention Type: BEHAVIORAL

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.

Interventions

Anticancer Learning Circle

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.

Intervention Type: BEHAVIORAL

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

University of Virginia

OTHER

Sponsor Role: lead

Responsible Party

Kari Ring, MD

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kari Ring, MD

Role: PRINCIPAL_INVESTIGATOR

University of Virginia

Locations

University of Virginia

Charlottesville, Virginia, United States

Countries

United States

Other Identifiers

HSR230435

Identifier Type: -

Identifier Source: org_study_id