SuspendedNot applicableNCT07234799

Feasibility Testing of a Dyadic Exercise Program for Patients Undergoing Thoracic Radiotherapy and Their Family Caregivers

The goal of this study is to examine the feasibility and acceptability of an exercise intervention for patients undergoing thoracic radiation and their family caregivers.

Checked against the public recordLast updated Aug 3, 2026 · Source: ClinicalTrials.gov

StatusSuspended
PhaseNot applicable
U.S. locations1
SponsorM.D. Anderson Cancer Center
01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Not applicable
Sponsor
M.D. Anderson Cancer Center
Interventions being studied
Other: Exercise
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Be diagnosed with a non-small cell lung cancer or esophageal cancer and going to receive at least 24 fractions thoracic RT * Have an ECOG performance status of ≤2 * Have a family caregiver (e.g., spouse, sibling, adult child) willing and able (self-identified) to participate in the exercise program Both patient and caregiver must meet all the following criteria: * Be ≥18 years old * Be able to read and speak English * Be able to provide informed consent Exclusion Criteria: * A patient who meets the following criteria will be excluded from participating in this study: * Cognitive deficits noted in the medical records and/or cognitive deficits that would impede the completion of self-report instruments as deemed by the patient's attending radiation oncologist. * Experiences contraindications to exercise as determined by the clinical team * Regularly (self-defined) participates in an exercise program in the year prior to diagnosis A patient and caregiver who is pregnant (medical notes and/or self-identified, respectively) will be excluded.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • The University of Texas M. D. Anderson Cancer CenterHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 3, 2026. Always confirm current availability with the study team.

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