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Evaluating the Anticancer Learning Circle Lifestyle Program in Endometrial Cancer Survivors

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University of Virginia

Status

Completed

Conditions

Neoplasm, Uterine

Treatments

Behavioral: Anticancer Learning Circle

Study type

Interventional

Funder types

Other

Identifiers

NCT06550791
HSR230435

Details and patient eligibility

About

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.

Enrollment

23 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

23 participants in 1 patient group

Anticancer Learning Circle Participant
Experimental group
Treatment:
Behavioral: Anticancer Learning Circle

Trial contacts and locations

1

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Central trial contact

Kathryn Dryer, MD; Tam Le

Data sourced from clinicaltrials.gov

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