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Recruiting NCT07565519

NCT07565519 Effects of a Multicomponent Exercise Program in Older Adults Undergoing Cancer Treatment: A Randomized Controlled Trial

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Clinical Trial Summary
NCT ID NCT07565519
Status Recruiting
Phase
Sponsor Federal University of Rio Grande do Sul
Condition Cancer
Study Type INTERVENTIONAL
Enrollment 180 participants
Start Date 2026-03-02
Primary Completion 2027-03-01

Eligibility & Interventions

Sex All sexes
Min Age 60 Years
Max Age N/A
Study Type INTERVENTIONAL
All Conditions
Interventions
Multicomponent exercise

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 180 participants in total. It began in 2026-03-02 with a primary completion date of 2027-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to understand how a home-based exercise program can help improve strength, mobility, and quality of life in older adults receiving cancer treatment. Participants will be randomly divided into two groups: One group will follow a one-year multicomponent exercise program based on the ViviFrail model, done safely at home. The other group will continue with usual care. We will include men and women aged 60 or older treated at Hospital Conceição in Porto Alegre. Assessments will take place at the beginning and after 12, 24, and 48 weeks. We will measure walking speed, balance, muscle strength, and ask about quality of life, symptoms, and daily activity. The goal is to see whether home-based exercise can help older adults with cancer stay stronger, more independent, and feel better during treatment.

Eligibility Criteria

Inclusion Criteria: Men and women aged 60 years or older who are undergoing cancer treatment at Hospital Conceição in Porto Alegre, who have the cognitive ability to understand the exercises, are able to walk (even with assistance), and have medical clearance to participate in physical exercise will be included in the study. \- Exclusion Criteria: Participants who miss more than two assessments will be excluded. \-

Contact & Investigator

Central Contact

Eduardo L Cadore, PhD

✉ edcadore@yahoo.com.br

📞 +555191193651

Principal Investigator

Eduardo L Cadore, PhD

PRINCIPAL INVESTIGATOR

Federal University of Rio Grande do Sul

Frequently Asked Questions

Who can join the NCT07565519 clinical trial?

This trial is open to participants of all sexes, aged 60 Years or older, studying Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07565519 currently recruiting?

Yes, NCT07565519 is actively recruiting participants. Contact the research team at edcadore@yahoo.com.br for enrollment information.

Where is the NCT07565519 trial being conducted?

This trial is being conducted at Porto Alegre, Brazil, Porto Alegre, Brazil.

Who is sponsoring the NCT07565519 clinical trial?

NCT07565519 is sponsored by Federal University of Rio Grande do Sul. The principal investigator is Eduardo L Cadore, PhD at Federal University of Rio Grande do Sul. The trial plans to enroll 180 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology