Breast Cancer Clinical Trial
Official title:
Mindful Movement Program for Breast Cancer Survivors
Verified date | June 2015 |
Source | City of Hope Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
RATIONALE: Mindful movement is a self-directed activity of mindfulness (intention,
attention, and attitude) and physical movement. A mindful movement program may be effective
in improving well-being in older women who are breast cancer survivors.
PURPOSE: This randomized clinical trial is studying how well a mindful movement program
works in improving quality of life in older female breast cancer survivors.
Status | Completed |
Enrollment | 49 |
Est. completion date | April 2010 |
Est. primary completion date | April 2010 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 50 Years and older |
Eligibility |
DISEASE CHARACTERISTICS: - Breast cancer survivor - At least 12 months since completion of treatment (chemotherapy, biotherapy [e.g., trastuzumab], or radiotherapy) - No evidence of metastatic disease PATIENT CHARACTERISTICS: - English speaking - Not under acute psychological distress - Not using an assistive device (cane, walker, or wheelchair) - Able to participate in the Mindful Movement Program by a medical release from the patient's physician - Pregnancy allowed PRIOR CONCURRENT THERAPY: - See Disease Characteristics - Concurrent selective estrogen-receptor modulator permitted - No other concurrent treatment |
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
United States | City of Hope Comprehensive Cancer Center | Duarte | California |
Lead Sponsor | Collaborator |
---|---|
City of Hope Medical Center | National Cancer Institute (NCI) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effects of the Mindful Movement Program on psychological well-being, distress, fear of recurrence, physical well-being, upper-body symptom bother, social well-being, body image, and spiritual well-being at baseline and weeks 12 and 18 | 6 months after study entry | No | |
Primary | Effects of this program on attention and attitude | 6 months after study entry | No | |
Primary | Differences of attention and attitude between the experimental group and the control group | 6 months after study entry | No | |
Primary | Perceptions of the program as described by the experimental group | 6 months after entry | No |
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