Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06919874

Dyadic Yoga Program for Patients Undergoing Thoracic Radiotherapy and Their Family Caregivers: The Testing of a Mobile Application Delivery

Led by M.D. Anderson Cancer Center · Updated on 2026-01-09

60

Participants Needed

1

Research Sites

189 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of the trial is to test the usability, feasibility and acceptability of an unsupervised, appbased yoga program for participants undergoing thoracic RT and their caregivers.

CONDITIONS

Official Title

Dyadic Yoga Program for Patients Undergoing Thoracic Radiotherapy and Their Family Caregivers: The Testing of a Mobile Application Delivery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with non-small cell lung cancer or esophageal cancer and planned to receive at least 24 fractions of thoracic radiotherapy
  • Have an ECOG performance status less than 2
  • Have a family caregiver (spouse, sibling, adult child) willing to participate
  • Both patient and caregiver are over 18 years old
  • Both patient and caregiver can read and speak English
  • Both patient and caregiver can provide informed consent
  • Both patient and caregiver have regular access to Wi-Fi or high-speed internet
Not Eligible

You will not qualify if you...

  • Cognitive deficits that prevent completing self-report questionnaires as judged by the attending oncologist
  • Medical contraindications to exercise as determined by the clinical team
  • Regular participation in a yoga program in the year before diagnosis
  • Participation in Part 1 of this study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

K

Kathrin Milbury, MA,PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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