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

Roswell Park Cancer Institute27 enrolled

Overview

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.

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Hematopoietic and Lymphoid Cell Neoplasm Malignant Solid Neoplasm

Interventions

Quality-of-Life AssessmentOTHER

Ancillary studies

Survey AdministrationOTHER

Ancillary studies

YogaOTHER

Receive yoga intervention

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Roswell Park Cancer Institute

Buffalo, New York, United States

Outcomes

Primary Outcomes

Proportion of subjects who participate or show high adherence to the intervention

Will be presented as observed proportion and 95% Clopper-Pearson confidence intervals (CIs).

Time frame: Up to 12 weeks

Secondary Outcomes

Efficacy of the intervention in stress-reduction

Serum cortisol and norepinephrine levels will be measured by blood collection

Time frame: Up to 3 months post-intervention

Efficacy of the intervention in stress-reduction

Self report stress

Time frame: Up to 3 months post intervention

Efficacy of the intervention in stress reduction

salivary cortisol will be measured by saliva collection

Time frame: Up to 3 months post intervention

Data from ClinicalTrials.gov

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