Breast Cancer Clinical Trial
Compass Course: Efficacy Study
Summary
The Compass Course is an 8-session progressive structure that was developed based on theoretical and scientific evidence from psychology and occupational therapy. The goal of the intervention is to provide participants with information, tools, and support that help them move towards reclaiming a sense of self-grounded purpose in daily life. The study will use a convenience sample of breast cancer survivors to evaluate the efficacy of the Compass Course intervention.
Eligibility Criteria
Inclusion criteria:
25 years of age or older
Completed treatment (such as chemotherapy, radiation, surgery) for Stage 0, 1, 2, or 3 breast cancer at least 2 months prior to participating in the Compass Course intervention
English speaking
High school diploma or GED
Able to see, hear, speak (with or without assistive devices)
Able to provide own transportation to sessions
Willing and able to commit to attend all 8 intervention sessions
Exclusion criteria (all self-reported):
Stage 4 breast cancer or any other stage 4 cancer
Actively receiving chemotherapy or radiation treatments for cancer. (However, patients may be on Herceptin and/or endocrine treatment and participate in the study.)
History of neurologic disorder (such as stroke or brain injury) with residual impairments that likely interfere with learning
Any medical condition (physical or mental health) that interferes with the performance of everyday activities and roles.
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There are 3 Locations for this study
Golden Valley Minnesota, 55422, United States
Minneapolis Minnesota, 55407, United States
Shoreview Minnesota, 55126, United States
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