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Living Well With Brain Cancer: A Group-Based Intervention to Promote Whole-Person Well-Being

Recruiting

Pilot Study of the Living Well With Brain Cancer Intervention

Who can join

Ages 18 and older · All sexes

Full eligibility 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

About the study

The goal of this clinical trial is to learn if the newly designed group self-management program is feasible to conduct and improves mental and behavioral health outcomes compared to a control group in people diagnosed with brain cancer. The main questions it aims to answer are:

* Is it feasible to conduct this program? * Does the new group self-management program improve behavioral health outcomes more than in the control group that will not be in a group setting?

What is being tested

Sponsor: University of Colorado, Denver · Participants: 64 · Started: Jun 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07628647

Locations in the U.S.

ColoradoUniversity of Colorado Anschutz, Aurora
OhioUniversity Hospitals Cleveland Medical Center, Cleveland

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.