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Heart Health Assessment Tool for Endometrial Cancer Survivors
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Waitlist Available
Led By Kathryn E Weaver, PhD, MPH
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This trial aims to improve heart health for cancer patients by asking them to use an electronic tool. Researchers hope to learn how to better help patients manage their heart health. #HeartHealth #CancerCare
Who is the study for?
This trial is for endometrial cancer survivors who are at least 18 years old, can read medical information in English, have an email address, and are more than 3 months post-cancer treatment. They should be scheduled for a routine check-up but not currently receiving cancer treatments or expected to live less than six months.Check my eligibility
What is being tested?
The study tests a digital tool called the PREVENT Cardiovascular Health Assessment Tool along with surveys and interviews about heart health. It aims to understand how this tool might help manage heart health for cancer survivors outside of clinical settings.See study design
What are the potential side effects?
Since this trial involves using an assessment tool and providing feedback rather than testing a drug or medical procedure, there are no direct physical side effects associated with participating in this study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants to Complete Heart Health Assessment - Feasibility
Secondary outcome measures
Number of Participants Stating Satisfaction with PREVENT Tool
Number of Participants to Report Initiating Discussions Regarding Cardiovascular Health with Health Care Providers
Trial Design
1Treatment groups
Experimental Treatment
Group I: PREVENT - Cardiovascular Health Assessment ToolExperimental Treatment3 Interventions
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).
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Who is running the clinical trial?
Wake Forest University Health SciencesLead Sponsor
1,239 Previous Clinical Trials
1,004,141 Total Patients Enrolled
1 Trials studying Endometrial Cancer
112 Patients Enrolled for Endometrial Cancer
National Cancer Institute (NCI)NIH
13,654 Previous Clinical Trials
40,933,111 Total Patients Enrolled
74 Trials studying Endometrial Cancer
73,332 Patients Enrolled for Endometrial Cancer
Kathryn E Weaver, PhD, MPHPrincipal InvestigatorWake Forest Baptist Comprehensive Cancer Center
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 years old or older.I am currently undergoing treatment for endometrial cancer.My endometrial cancer has come back.I have a working email address.I have a confirmed diagnosis of endometrial cancer and am scheduled for a routine check-up.It has been over 3 months since my last cancer treatment aimed at curing me.
Research Study Groups:
This trial has the following groups:- Group 1: PREVENT - Cardiovascular Health Assessment Tool
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there current openings for participants in this research project?
"As noted on clinicaltrials.gov, the timelines for this medical trial indicate that it is not currently open to new patients. This study was first posted June 1st 2023 and the last update took place March 21st 2023. Additionally, there are 340 other studies actively seeking participants at present."
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