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Recruiting NCT07390045

NCT07390045 Exercise and Cognitive Rehabilitation Interventions for Older Cancer Survivors

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Clinical Trial Summary
NCT ID NCT07390045
Status Recruiting
Phase
Sponsor University of Rochester
Condition Cancer
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-07-31
Primary Completion 2028-03-31

Eligibility & Interventions

Sex All sexes
Min Age 65 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
EXCAPMAATECO

Eligibility Fast-Check

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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 40 participants in total. It began in 2026-07-31 with a primary completion date of 2028-03-31.

⚠ 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

The objective of this study is to assess the preliminary effects of an integrated exercise and cognitive rehabilitation intervention (ECO), an exercise intervention (EXCAP), and a cognitive rehabilitation intervention (MAAT) as compared to usual care on objective cognition (Trail Making Test).

Eligibility Criteria

Inclusion criteria: * Age ≥65 years (from date of consent, confirmed on the electronic medical record) * A diagnosis of any cancer * Have completed curative intent treatments * Patients on endocrine therapies are allowed to enroll * Patients with hematologic malignancies after autologous or allogeneic stem cell transplant are allowed to enroll if they have completed curative-intent treatment * Answered "yes" to the verbal question "Do you have concerns about memory or other thinking abilities following your cancer treatment?" * Able to speak English (interventions are available in English only) * Eastern Cooperative Oncology Group (ECOG) performance status of 0-3# * No medical contraindications to exercise# * Able to walk 4 meters# * Able to provide informed consent# * Confirmed through eligibility confirmation with the patient's oncologist or their designee Exclusion criteria: * Any physical, psychological, or social impairments that would interfere with a patient's ability to participate in the study as determined by the patient's oncologist or their designee * Unwilling to complete study procedures

Contact & Investigator

Central Contact

Kah Poh Loh

✉ Kahpoh_Loh@URMC.Rochester.edu

📞 585-276-4353

Principal Investigator

Kah Poh Loh

PRINCIPAL INVESTIGATOR

University of Rochester

Frequently Asked Questions

Who can join the NCT07390045 clinical trial?

This trial is open to participants of all sexes, aged 65 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 NCT07390045 currently recruiting?

Yes, NCT07390045 is actively recruiting participants. Contact the research team at Kahpoh_Loh@URMC.Rochester.edu for enrollment information.

Where is the NCT07390045 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT07390045 clinical trial?

NCT07390045 is sponsored by University of Rochester. The principal investigator is Kah Poh Loh at University of Rochester. The trial plans to enroll 40 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: July 2026  ·  Data Methodology