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Yoga Breathing for Fatigue in Patients Undergoing Chemotherapy

Effects of Pranayama on Fatigue Among Patients Undergoing Chemotherapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00982748
Enrollment
25
Registered
2009-09-23
Start date
2008-10-31
Completion date
2009-12-31
Last updated
2011-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Fatigue, Chemotherapy, Yoga, Breathing, Cancer, Anxiety, Pranayama, Stress, Fatigue-associated symptoms in chemotherapy patients, Quality of life in chemotherapy patients

Brief summary

The purpose of this study is to determine the feasibility and efficacy of yoga breathing techniques to manage fatigue and other cancer-related side effects, in cancer patients undergoing chemotherapy.

Detailed description

Fatigue is the most common complaint among cancer patients. This pilot study will evaluate the effects of pranayama (ancient yoga breathing techniques) on fatigue and quality of life among 30 patients undergoing chemotherapy, on an every 2, 3, or 4 week schedule, with a fatigue score of at least 4 on a scale of 0 (none) to 10 (most). Patients will be randomized to either pranayama or wait-list control. The pranayama group will learn and practice 3 breathing techniques on a daily basis. The study period will occur during 2 consecutive cycles of chemotherapy (cycle A and Cycle B), and the wait-list control patients will crossover to the treatment arm at the beginning of his/her Cycle B. Fatigue will be measured using the revised Piper Fatigue Scale along with quality of life measures. These study measures will be conducted at baseline, at the end of cycle A, and at the end of cycle B. We hypothesize that pranayama will improve clinical symptoms of fatigue and quality of life among patients undergoing chemotherapy.

Interventions

BEHAVIORALPranayama (Yoga Breathing) Techniques

1-hour long yoga breathing classes, taught once per week for 2-8 consecutive weeks. Dose (Number of classes) administered is dependent on randomization arm and individuals' chemotherapy cycle length.

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* A diagnosis of cancer that requires at least 2 further cycles of chemotherapy on an every 14, 21, or 28 day schedule * A score of at least 4/10 on a 0-10 (0-none, 10-most) visual analog scale for fatigue at the time of enrollment * Able to read, write and understand English * Karnofsky Performance Status greater than 60 * Ability to give informed consent

Exclusion criteria

* Severe COPD * Receiving chronic oxygen therapy * Congestive heart failure: NYHA class 3 or greater * Transfusion dependent anemia * Uncontrolled thyroid disease * Advance kidney disease requiring dialysis * Advance liver disease * More than three previous chemotherapy regimens * Current, ongoing yoga breathing practice

Design outcomes

Primary

MeasureTime frameDescription
FeasibilityBaseline and second cycle of chemotherapyFeasibility will be evaluated based on recruitment, retention, completion of study classes and home practice, and completion of study measures

Secondary

MeasureTime frameDescription
Cancer associated symptoms and quality of lifebaseline and final cycle of chemotherapyfatigue, sleep, stress, anxiety and depression quality of life

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026