Yoga program to help cancer survivors manage stress

Influence of Yoga on Cancer-Related Stress in Cancer Survivors

Not applicable Interventional Roswell Park Cancer Institute · NCT04754529

This study is trying out a 12-week online yoga program to see if it can help cancer survivors manage stress and improve their quality of life.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment30 (estimated)
Ages18 Years and up
SexAll
SponsorRoswell Park Cancer Institute Academic / other
Locations1 site (Buffalo, New York)
Trial IDNCT04754529 on ClinicalTrials.gov

What this trial studies

This clinical trial develops and tests a 12-week online hatha yoga intervention aimed at improving cancer-related stress in cancer survivors. Participants will engage in weekly sessions that include restorative poses, breathing techniques, and guided meditation. The study will assess the feasibility of the intervention and evaluate its impact on self-reported stress levels and quality of life. Additionally, the trial will explore the collection of biological samples to measure stress biomarkers before and after the intervention.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 and older who have completed cancer treatment and have been cleared for physical activity.

Not a fit: Patients who are pregnant, nursing, or have significant skeletal or cardio-pulmonary comorbidities may not benefit from this study.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce stress levels and enhance the overall quality of life for cancer survivors.

How similar studies have performed: Other studies have shown promising results with yoga interventions for stress management in cancer survivors, indicating potential for success in this approach.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age \>= 18 years of age
* Have been diagnosed with a cancer and have finished treatment
* Have been cleared for physical activity by a physician or nurse practitioner (physician or nurse practitioner name and date clearance received)
* Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

Exclusion Criteria:

* Unwilling or unable to complete the assessment in English
* Are pregnant or nursing
* Are unwilling or unable to follow protocol requirements
* Have skeletal instabilities and/or cardio-pulmonary comorbidities
* Have any condition which in the investigator's opinion deems the subject an unsuitable candidate to participate in this study

Where this trial is running

Buffalo, New York

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Hematopoietic and Lymphoid Cell NeoplasmMalignant Solid Neoplasm
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.