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Supportive Psychoeducational Intervention for Patients With Brain Tumors (Acceptance and Commitment Therapy-based Supportive Intervention for Patients With Central Nervous System Tumors)

Recruiting

An ACT-Based Supportive Intervention for Patients With Central Nervous System Tumors

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age ≥ 18
* Massachusetts General Hospital Cancer Center Patient
* Diagnosed with a malignant primary Central Nervous System (CNS) tumor
* English speaking

Exclusion Criteria:

* Inability to provide informed consent as assessed by the study team (e.g., due to severe cognitive impairment/dementia)
* Moderate to severe receptive aphasia (Quick Aphasia Battery sentence comprehension subscale \< 8)
* Deemed by treating team to have less than 6 month life expectancy, including patients with current or imminent hospice enrollment
* Current participant in the NeuroTransitions (23-574) or NeuroPathways (23-178) studies at Massachusetts General Hospital
* Diagnosis of Primary CNS Lymphoma

About the study

The goal of this study is to refine and test a psychosocial intervention called ASCENT (ACT-based Supportive intervention for patients with CENTral nervous system tumors). This intervention was developed to help patients after being diagnosed with a brain tumor. The main question this study aims to answer is whether this intervention is feasible (i.e., possible to carry out) and acceptable (i.e., considered helpful) to patients. Participants will be asked to take part in 6 coaching sessions and complete short surveys at four different time points. Some participants will be asked to share feedback via interviews.

What is being tested

Sponsor: Massachusetts General Hospital · Participants: 100 · Started: May 15, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT06099743

Locations in the U.S.

MassachusettsMassachusetts General Hospital Cancer Center, Boston

Conditions

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