Cancer Clinical Trial
Official title:
Developing a Yoga Intervention During Cancer Chemotherapy
Verified date | November 2019 |
Source | University of California, San Francisco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This proposal aims to expand non-pharmacologic options for the control of symptoms during chemotherapy using yoga practices. It is particularly focused on sleep disturbance with a secondary focus on fatigue.
Status | Completed |
Enrollment | 73 |
Est. completion date | October 1, 2019 |
Est. primary completion date | October 1, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 and older - Have a Karnofsky Performance Status Score of 60 or above - Diagnosed with any cancer except acute leukemia - Self-reported poor quality of sleep - Receiving Chemotherapy - Able to read, write, and understand English - Ability to give informed consent Exclusion Criteria: - Diagnosed with brain metastasis - Diagnosed with severe Chronic Obstructive Pulmonary Disease (COPD) or emphysema - Have New York Heart Association class II or greater congestive heart failure - Requiring chronic home oxygen therapy - Diagnosed with a sleep disorder (e.g., sleep apnea or narcolepsy) - Have received more than 3 prior chemotherapy regimens - Receiving radiation therapy - Has a less than 6 month life expectancy - Regular yoga practice within the last 2 months |
Country | Name | City | State |
---|---|---|---|
United States | UCSF | San Francisco | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Francisco | National Center for Complementary and Integrative Health (NCCIH) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Quality of Life as measured by the Multidimensional Quality of Life Scale--Cancer | 6 weeks | ||
Other | Depressive Symptoms as measured by the CES-D | 6 weeks | ||
Other | Anxiety as measured by the Spielberger State Anxiety Inventory | 6 weeks | ||
Other | Pain as measured by the modified Brief Pain Inventory | 6 weeks | ||
Other | Hot Flashes as measured by the Hot Flash Related Daily Interference Scale | 6 weeks | ||
Other | Mindfulness as measured by the Five Facet Mindfulness Questionnaire | 6 weeks | ||
Other | Body Awareness as measured by the Multidimensional Assessment of Interoceptive Awareness | 6 weeks | ||
Other | Coping and Self Efficacy as measured by the Coping and Self Efficacy Scale | 6 weeks | ||
Other | Social Support as measured by single items on social support | 6 weeks | ||
Primary | Sleep Disturbance as measured by the General Sleep Disturbance Scale | 6 weeks | ||
Secondary | Fatigue as measured by the Lee Fatigue Scale | 6 weeks |
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