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Behavioural Intervention

Supportive Care (home-based exercise program) for Endometrial Adenocarcinoma

N/A
Waitlist Available
Led By Amanika A Kumar, M.D.
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 50+
Stage IA-IB endometrial cancer
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 2 years
Awards & highlights

Study Summary

This trial is studying how a home-based exercise program can help improve the health of endometrial cancer survivors who have limited access to cancer survivorship resources. Many cancer survivors in rural areas face challenges in

Who is the study for?
This trial is for endometrial cancer survivors living in rural areas, especially those who face challenges accessing supportive care. It aims to include individuals from underserved communities such as historically black, Hispanic, and Native populations. Participants should be able to engage in a home-based exercise program delivered remotely.Check my eligibility
What is being tested?
The study tests a remote exercise program designed for strength training at home. It examines if this approach can improve the quality of life and physical performance for endometrial cancer survivors with limited access to traditional survivorship care.See study design
What are the potential side effects?
Since the intervention involves an exercise program, potential side effects may include typical workout-related issues like muscle soreness or strain. However, these are generally mild and manageable with proper guidance.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 50 years old or older.
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My condition is early-stage endometrial cancer.
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My condition is considered mild to moderate in severity.
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My cancer has not come back after treatment.
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It has been 1 to 5 years since my surgery.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Feasibility of intervention
Retention of participants
Satisfaction with program - self-reported
Secondary outcome measures
Change in physical function

Trial Design

1Treatment groups
Experimental Treatment
Group I: Supportive Care (home-based exercise program)Experimental Treatment7 Interventions
Participants participate in a home-based exercise program with an exercise prescription that will include resistance band and body weight exercises targeting the 5 major large muscle groups along with 3 booklets about exercise and exercise training and attend weekly exercise coaching sessions to report on exercise adherence and to progress exercise over 10 weeks on study.

Find a Location

Who is running the clinical trial?

Mayo ClinicLead Sponsor
3,227 Previous Clinical Trials
3,771,588 Total Patients Enrolled
Amanika A Kumar, M.D.Principal InvestigatorMayo Clinic in Rochester

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are prospective patients still eligible to participate in this ongoing medical study?

"According to the information available on clinicaltrials.gov, this particular trial is not currently seeking participants. Its initial posting was made on March 1st, 2024 and the most recent update occurred on January 10th, 2024. However, it's worth noting that there are currently a total of 1067 active clinical trials actively enrolling patients at present."

Answered by AI
~53 spots leftby May 2026