No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Supportive Care
Participants needed
452 (estimated)
Sponsor
University of Arizona · Other
Who this trial is looking for
This trial is looking for women who have survived breast cancer and experience feelings of anxiety or depression after treatment. Participants will take part in a compassion meditation program online, along with a supportive partner who lives with them.
Are You a Good Fit for This Trial?
You may be able to join if
I am a woman.
I can speak and understand English.
I have been diagnosed with breast cancer.
I completed my main cancer treatments at least 3 months ago and no more than 5 years ago.
I have a supportive partner who can join me.
You may not be able to join if
I live in a nursing home.
I have practiced meditation regularly in the last 4 years.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 syn…
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).
Trial Locations
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City
State
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Status
Eligibility 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) …
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)
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