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Not Yet Recruiting
NCT05676255
The Breast Cancer Survivors and Partners Online Research Together (SUPORT) Project
Conditions: Breast Cancer Female, Psychological Distress
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: PHASE2
Enrollment: 452
Sponsor: University of Arizona
Location: United States
Summary
Many breast cancer survivors (estimated 70% in some studies) experience clinically significant depression and/or anxiety in the months and years after finishing cancer treatments.
This research will build on the rigor of prior research to reduce breast cancer survivor depression and anxiety with a compassion meditation intervention called CBCT (Cognitively-Based Compassion Training) for online synchronous delivery that is also inclusive of informal caregivers (i.e., adult family members who live with and typically provide half the care for survivors, aka supportive partners).
Eligibility Criteria
Breast cancer survivors:Inclusion Criteria:biological sex: womanable to speak and understand Englishhave a diagnosis of a breast cancerhave completed primary curative cancer treatments (i.e., surgery, radiation, chemotherapy) except for hormonal therapies (e.g., aromatase inhibitors) or trastuzumab a minimum of 3 months and a maximum of 5 years before starting CBCT or the controlhave a supportive partner (aka caregiver) who can participate with themExclusion Criteria:nursing home residenthave ongoing (1 or more meditation sessions per week) or past regular meditation experience in the last 4 years (i.e., more than two meditation sessions [completed or attempted] per year, either with a group or individually, to be evaluated by the Principal Investigator)Supportive partners (aka informal caregivers)Inclusion Criteria:named by the survivorlive in the same household as the survivorable to speak and understand EnglishExclusion Criteria:have ongoing (1 or more meditation sessions per week) or past regular meditation experience in the last 4 years (i.e., more than two meditation sessions [completed or attempted] per year, either with a group or individually, to be evaluated by the Principal Investigator)
Source: ClinicalTrials.gov (NCT05676255). StuddyBuddy aggregates publicly available trial information.