The Breast Cancer Survivors and Partners Online Research Together (SUPORT) Project
University of Arizona · with National Cancer Institute (NCI) · NCT05676255
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 2
- Target enrollment
- 452
- US sites recruiting
- 1
- Study start
- March 20, 2023
- Record last updated
- October 8, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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).
Being studied: Cognitively-Based Compassion Training for Survivors; Cognitively-Based Compassion Training for Dyads; Health Education
Conditions: Breast Cancer Female; Psychological Distress
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Breast cancer survivors
Inclusion Criteria
- biological sex: woman
- able to speak and understand English
- have a diagnosis of a breast cancer
- have 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 control
- have a supportive partner (aka caregiver) who can participate with them
Exclusion Criteria
- nursing home resident
- 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)
Supportive partners (aka informal caregivers)
Inclusion Criteria
- named by the survivor
- live in the same household as the survivor
- able to speak and understand English
Exclusion 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)
Recruiting US locations
University of Arizona
Tucson, AZ 85721
Site contact: Jacquelyn Martin · 520-621-1930 · UArizona-SUPORT@email.arizona.edu
Study contacts (from the official record)
- Jacquelyn Martin · 520-621-1930 · UArizona-SUPORT@email.arizona.edu
Similar studies in Arizona
All healthy volunteers studies in Arizona →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
Developing Biomarkers of Dietary Intake: Dose Dependent Measurement of Sugar Intake
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Location
- Phoenix, AZ
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A Phase I Study to Investigate the Effect of Hepatic Impairment of AZD9550 and AZD6234
AstraZeneca
- Location
- Chandler, AZ + 2 other US sites
- Eligibility basics
- Ages 18–85
- RecruitingHealthy volunteersPhase 1
A Phase 1 Relative Bioavailability Study of a VX-581 Tablet Formulation
Vertex Pharmaceuticals Incorporated
- Location
- Tempe, AZ
- Eligibility basics
- Ages 18–55 · Men only
- RecruitingHealthy volunteersPhase 1
A Single and Multiple Ascending Dose Study of EPX-100 in Healthy Adult Participants
Epygenix
- Location
- Tempe, AZ
- Eligibility basics
- Ages 18–55