Breast Cancer Survivors Clinical Trial
Official title:
Evaluation of an Ayurvedic Whole Systems-based Lifestyle Protocol for Quality of Breast Cancer Survivorship: A Randomized Controlled Pilot Study
Verified date | February 2023 |
Source | Maharishi International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a pilot study to assess the feasibility and effectiveness of a 12-week intervention of personalized diet and lifestyle protocol based on the principles of Ayurveda's whole systems approach to achieving improvement in a) quality of life, b) digestive health, c) sleep among women breast cancer survivors.
Status | Active, not recruiting |
Enrollment | 15 |
Est. completion date | June 1, 2023 |
Est. primary completion date | April 1, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - A breast cancer survivor in remission (Females = 18 years) - Diagnosis of stage I-IV breast cancer - Three months or more after receiving conventional treatment (chemotherapy, radiation therapy, and/or surgery) - Willing to comply with the study intervention recommendations for 12 weeks - English speaking - Have access to technology to participate in zoom visits Exclusion Criteria: - Male responders - Inability to provide informed consent - Physiological or psychological debility that would interfere with the ability to participate in the study fully - Active metastatic or recurrent disease (to avoid early withdrawal from the study) - Anticipates undergoing surgery during the duration of the intervention - Substance abuse (to avoid early withdrawal from the study) |
Country | Name | City | State |
---|---|---|---|
United States | Maharishi International University | Richmond | California |
Lead Sponsor | Collaborator |
---|---|
Robert Schneider, MD |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Quality of life | Assess change from baseline quality of life to 6 and 12 weeks.
Researchers will use the following Self-reported outcome measure instruments: Quality of life: Quality of Life instrument (cancer patient/cancer survivor version) developed by the City of Hope National Medical Center in California. |
0, 6 weeks, and 12 weeks | |
Primary | Change in Digestive health | Assess change from baseline digestive health to 6 and 12 weeks.
Researchers will use the following Self-reported outcome measure instruments: Ayurvedic assessment of digestive strength questionnaire and Gastrointestinal Symptoms Rating Scale (GSRS) for the gut health assessment. |
0, 6 weeks, and 12 weeks | |
Primary | Change in Sleep disturbance | Assess change from baseline sleep disturbance to 6 and 12 weeks.
Researchers will use the following Self-reported outcome measure instruments: Assessment using the General Sleep Disturbance Scale (GSDS). |
0, 6 weeks and 12 weeks |
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