Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06545604

Comprehensive Yoga Therapy Based Lifestyle Prehabilitation Program for Women With Ovarian Cancer

Led by M.D. Anderson Cancer Center · Updated on 2025-11-26

40

Participants Needed

1

Research Sites

107 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To provide a comprehensive yoga therapy (CYT) program to patients with ovarian, fallopian tube, or primary peritoneal cancer who are scheduled to receive chemotherapy and then undergo surgery. Researchers want to learn about the effects of the program on patients' quality of life and other outcomes described below.

CONDITIONS

Official Title

Comprehensive Yoga Therapy Based Lifestyle Prehabilitation Program for Women With Ovarian Cancer

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with stage III-IV epithelial ovarian, fallopian tube, or primary peritoneal cancer recommended for neoadjuvant chemotherapy and interval debulking surgery
  • Able to read, write, and speak English
  • 18 years of age or older
  • Oriented to person, place, and time
  • Access to internet connection
  • Access to a tablet, laptop, computer, or smartphone
  • Ability to participate in virtual sessions
  • Planned surgical intervention at MD Anderson Cancer Center
  • Performance status 0-2
Not Eligible

You will not qualify if you...

  • Completed chemotherapy prior to the study
  • Presence of major thought disorders such as schizophrenia or dementia
  • Major communication barriers like significant visual or hearing impairment
  • Severe mobility issues preventing unassisted movement in and out of a chair
  • Regular practitioner of mind-body or yoga practices

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

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

L

Lois Ramondetta, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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