Living Well With Brain Cancer: A Group Program to Support Whole-Person Health
Official title: Pilot Study of the Living Well With Brain Cancer Intervention
Run by University of Colorado, Denver · NCT07628647 · Data updated 2026-11-12
This program tests a group self-management approach to improve mental and behavioral health for adults with malignant brain tumors.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 64 (estimated) |
| Sponsor | University of Colorado, Denver Academic / other |
| Locations | 2 sites (Aurora, Colorado and 1 other locations) |
| Status | Recruiting |
| Started | June 10, 2026 |
| Main results expected | October 31, 2027 |
| Study ends | October 31, 2027 |
| Registry record updated | November 3, 2026 |
| Trial ID | NCT07628647 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years and older with a confirmed malignant brain tumor (including gliomas) who are under the care of a treating provider and reside in the United States.
✕Probably not a fit
Individuals with very advanced disability, cognitive impairment that prevents participation, or those not fluent in English may be less likely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study is designed to determine if a newly developed group self-management program is feasible to run and whether it can improve behavioral health outcomes compared with a control group not in a group setting. Participants are adults 18 and older with malignant brain tumors living in the United States, enrolled with a treating provider, and not currently in hospice or receiving psychiatric treatment for a serious mental illness. The intervention consists of group self-management sessions and educational materials, with outcomes assessed against a control condition. The study is led by the University of Colorado, Denver, with collaboration from University Hospitals Cleveland Medical Center, the U.S. Army Medical Research and Development Command, and Case Western Reserve University, and sites in Colorado and Ohio.
Why it matters
Potential benefit: If successful, participants may experience improved mental and behavioral health and better overall well-being while managing brain cancer.
How similar studies have gone: Previous work in group-based self-management for cancer patients has shown benefits in behavioral health, though the exact brain cancer population and approach are specific to this study.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Currently living in the United States * Aged 18 years or older * Confirmed diagnosis of a malignant brain tumor including diffuse gliomas, World Health Organization (WHO) grades II, III, and IV (either by directly sharing their pathology report or confirmation from their prescribing treating provider) * Treating prescribing provider who follows regularly with participant Exclusion Criteria: * \<1 month since initial diagnosis and/or \<1 month since surgical resection * Enrollment in hospice * Significant physical or cognitive disabilities that prohibit involvement using our clinician's judgement as a self-management expert, with consultation with personal clinician if needed * Currently receiving psychiatric treatment for a serious mental illness (e.g., schizophrenia) * Not able to communicate in English at a conversational level
Where it's running
-
University of Colorado Anschutz
Aurora, Colorado, United States Recruiting -
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States Recruiting
Study contacts
- Principal investigator: Bethany M Kwan, PhD, MSPH — University of Colorado, Denver
- Study coordinator: Research Services Professional
- Email: lwbc@cuanschutz.edu
- Phone: 303-724-1723
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.