Yoga Intervention for the Improvement of Cancer-Related Stress in Cancer Survivors

Roswell Park Comprehensive Cancer Center

Status

Completed

Conditions

Hematopoietic and Lymphoid Cell Neoplasm

Malignant Solid Neoplasm

Treatments

Other: Quality-of-Life Assessment

Other: Survey Administration

Other: Yoga

Study type

Interventional

Funder types

Other

Identifiers

NCT04754529

I 891720 (Other Identifier)

NCI-2021-00698 (Registry Identifier)

Details and patient eligibility

About

This clinical trial develops and test a yoga intervention in improving cancer-related stress in cancer survivors. The online hatha yoga intervention of breathing and movement incorporates both restorative poses, breathing techniques, guided meditation and may reduce stress levels and improve overall quality of health in cancer survivors.

Full description

PRIMARY OBJECTIVE:

I. To develop and test the feasibility of a standardized 12-week online hatha yoga intervention (n=30) of breathing and movement incorporating both restorative poses, breathing techniques, guided meditation.

SECONDARY OBJECTIVES:

I. To evaluate the yoga intervention in relation to self-reported levels of stress and quality of life in cancer survivors (n=30).

II. Feasibility of collecting blood and saliva at baseline and post-intervention for stress biomarkers, including cortisol and norepinephrine.

EXPLORATORY OBJECTIVE:

I. To determine how behavior change, quality of life (QoL), and biomarkers of adrenergic stress, inflammation, and immunosuppression are affected by a 12-week online yoga program completed by cancer survivors.

OUTLINE:

Patients receive online yoga intervention once a week (QW) for 12 weeks.

After completion of study, patients are followed up at 3 months.

Enrollment

27 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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