Remotely-Delivered Cognitive Behavioral Stress Management for Breast Cancer (R-CBSM)
Recruiting now · Not applicable
Conditions studied: Breast Cancer
In brief
The purpose of this research study to find out if a program called Remotely-delivered Cognitive Behavioral Stress Management (R-CBSM) can help women with breast cancer in the period of survivorship after they have completed treatment. This is a group stress management program done from home using technology, like Zoom to conduct video calls to conduct group-based training in stress management techniques (e.g., relaxation, cognitive behavioral therapy, coping skills training) in a supportive environment. It is for women aged 50 or older who have finished their main breast cancer treatments (like surgery, radiation, or chemo) and are undergoing hormone treatment. This study is important because many breast cancer survivors still feel stress, even after treatment ends. Teaching stress management may help the body and mind work better and may slow down the effects of aging caused by cancer and stress.
Key facts
- Study ID
- NCT07502352
- Run by
- University of Miami
- People needed
- 192
- Starts
- 2026-07-01
- Expected to finish
- 2029-08-01
- Last updated by the study team
- 2026-07-10
Who can join
Age: 50 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 50 yrs or older
- Speaks and reads English or Spanish at 6th grade level
- Diagnosed and completed primary treatment for Stage I-III HR + estrogen/ progesterone + (ER/PR)
- Human Epidermal Growth Factor Receptor 2 (Her2neu)- breast cancer 3 - 12 months prior
- Post-menopausal (> 12 months since last menstrual cycle)
- Elevated distress (Impact of Event Scale-intrusive thoughts [IES-I] > 14 or elevated distress based on assessment of PI
- If prescribed anti-depressants or anxiolytics on similar regimen > 2 months.
- Undergoing treatment with Adjuvant Endocrine Therapy (AET)
- Participants may or may not have received chemotherapy or radiation during primary treatment
You may not qualify if…
- Unable or unwilling to provide informed consent
- Diagnosis with metastatic disease, HER2neu+ or Triple Negative breast cancer
- Prior cancer diagnosis (with the exception of non-melanoma skin cancer) in the 2 years prior to the current breast cancer diagnosis
- Active untreated major mental illness (e.g., schizophrenia, psychosis, bi-polar, substance abuse, panic disorder, PTSD diagnosis),
- Acute or chronic co-morbid medical condition with known effects on the immune system (e.g., HIV infection, autoimmune diseases such as Lupus, Rheumatoid Arthritis, Acute or Chronic Hepatitis, and Multiple Sclerosis, Graves' Disease, Chronic Fatigue Syndrome, Fibromyalgia etc.). example: history of heart disease, e.g., past stroke, myocardial infarction (MI), or congestive heart failure are not exclusionary.
- Significant cognitive impairment, <32 on the Telephone Interview for Cognitive Status (TICS)
- Receipt of immunotherapy as part of treatment
Where it is running
- University of Miami — Coral Gables, Florida, United States (enrolling)
Full record on ClinicalTrials.gov
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