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Feasibility of a Patient Directed Tool to Assess Heart Health Among Endometrial Cancer Survivors

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Completed

Conditions

Endometrial Cancer
Survivorship

Treatments

Other: Survey
Other: Interview Regarding Heart Health
Other: PREVENT Cardiovascular Health Assessment Tool

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05796518
P30CA012197 (U.S. NIH Grant/Contract)
WFBCCC 99123 (Other Identifier)
IRB00095005

Details and patient eligibility

About

Investigators are conducting this study to find out more about what heart health means to participants and how healthcare providers can best help to manage heart health. Participants will be asked to view an electronic tool designed to promote heart health awareness and help to manage heart health outside of the clinic. This study will provide important information to help investigators develop future programs that improve cancer patient's heart health after they complete their treatment.

Full description

Primary Objective: The primary objective of this pilot study is to assess the feasibility of enrolling and completing the heart health assessment among endometrial cancer patients scheduled for routine follow-up care.

Secondary Objectives:

  • To assess patient satisfaction with the tool.
  • To identify the proportion of patients with non-ideal cardiovascular health scores who report initiating discussions regarding cardiovascular health during their routine oncology appointment.

Enrollment

44 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Scheduled for a routine surveillance visit for pathologically confirmed stages I-IV endometrial cancer
  • Greater than or equal to 3 months post-potentially curative cancer treatment
  • Patients must be at least 18 years of age
  • Have a working email address
  • Comfortable reading medical information in English, as per self-report

Exclusion criteria

  • Currently receiving treatment (e.g. radiation, chemotherapy, immunological treatments for endometrial cancer)
  • Have a history of endometrial cancer recurrence
  • Enrolled in hospice care or documentation of life expectancy < 6 months

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

44 participants in 1 patient group

PREVENT - Cardiovascular Health Assessment Tool
Experimental group
Description:
An adapted version of the PREVENT tool for endometrial cancer survivors will be used collect data during routine follow-up care for endometrial cancer that will yield a cardiovascular health score based on the Simple 7 risk factors (current smoking habits, body mass index, physical activity, diet, cholesterol, blood pressure and fasting plasma glucose).
Treatment:
Other: Interview Regarding Heart Health
Other: PREVENT Cardiovascular Health Assessment Tool
Other: Survey

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Study Coordinator

Data sourced from clinicaltrials.gov

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