Clinical trial · Interventional
Cognitive Intervention After a Brain Tumor
NCT02489071CI-TRIAL-00035064completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study evaluates the feasibility and utility of two behavioural programs designed to reduce cognitive impairments secondary to brain tumors and/or their treatment. One-third of participants will complete training in either program, with the remaining third a wait-list control group.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain Tumors | Brain Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Brain Health Program | Behavioral | — | UNRESOLVED |
| Brain Training Program | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Brain Training
- description
- 8-session cognitive training program
- interventionNames
- Behavioral: Brain Training Program
- type
- EXPERIMENTAL
- label
- Brain Health
- description
- 8-session cognitive education program
- interventionNames
- Behavioral: Brain Health Program
- type
- NO_INTERVENTION
- label
- Control
- description
- Wait-list control group
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. age 18 or older 2. fluent in English 3. able to provide informed consent to all procedures 4. diagnosis of a brain tumor 5. indication of lasting post-treatment cognitive deficits (e.g., from clinical presentation, prior neuropsychological assessment, and/or self-report) 6. sufficient motor and sensory functioning to complete study activities 7. availability to complete all study activities 8. for patients treated with cranial radiation, at least 3 months post-radiation Exclusion Criteria: (1) comorbid neurological or psychiatric disorder or other medical condition suspected to influence cognition
References
Publications (1)
- DERIVEDRichard NM, Bernstein LJ, Mason WP, Laperriere N, Maurice C, Millar BA, Shultz DB, Berlin A, Edelstein K. Cognitive rehabilitation for executive dysfunction in brain tumor patients: a pilot randomized controlled trial. J Neurooncol. 2019 May;142(3):565-575. doi: 10.1007/s11060-019-03130-1. Epub 2019 Mar 7. PMID 30847839