Mindfulness-based Intervention for Depressive Symptoms Sent Via Text (MINDSET)

Starting soon · Not applicable

Conditions studied: Depression, Cancer, Stage III Breast Cancer, Stage II Breast Cancer, Stage I Breast Cancer, Stage III Prostate Cancer, Stage II Prostate Cancer, Stage I Prostate Cancer, Stage III Colorectal Cancer, Stage II Colorectal Cancer, Stage I Colorectal Cancer

In brief

The purpose of this study is to develop and test a new intervention to reduce depressive symptoms in post-treatment cancer participants.

Key facts

Study ID

NCT06811454

Run by

Case Comprehensive Cancer Center

People needed

76

Starts

2026-08-03

Expected to finish

2029-03-31

Last updated by the study team

2026-01-23

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Self-reported mild to moderately-severe symptoms of depression (score 5-19 on PHQ-9).
• A diagnosis of stage 0-III breast, prostate, or colorectal cancer.
• Completion of primary cancer treatment within 2 years (excludes hormone therapy).
• An ability to provide informed consent.
• An ability to read and speak English.
• Access to a web-enabled device (phone, tablet, computer).

You may not qualify if…

• Self-reported minimal and severe depressive symptoms (<4 and > 20 on PHQ-9).
• Self-reported suicidal ideation (>1 on item 9 PHQ-9).
• Another psychological, medical, or other condition/issue determined that necessitates priority treatment and/or that would interfere with participation (e.g., schizophrenia, borderline personality disorder)
• Current or recent substance abuse/dependence.
• Stage IV cancer diagnosis.
• A cancer recurrence actively requiring treatment.
• Self-reported active mindfulness practice.
• Prior participation in a formal mindfulness program (e.g., MBCT, Mindfulness-Based Stress Reduction Program, Mindfulness-Based Cancer Recovery

Where it is running

• Case Comprehensive Cancer Center, Cleveland Clinic Foundation — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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