Condition: Brain Cancer · Brain Tumor · Brain Neoplasms · Sponsor: Dartmouth-Hitchcock Medical Center
The purpose of this study is to assess the ability of the home-based intervention, HOBSCOTCH-CA, to improve the quality of life and cognitive function in Service Members, Veterans and civilians who are survivors of brain cancer or a brain tumor (CA participants). This study will also assess the ability of the HOBSCOTCH-CA program to improve quality of life in caregivers of patients with brain cancer/tumor and to reduce caregiver burden. Enrolling with a Caregiver is optional for CA participants. Investigators will compare two groups of CA participants and their Caregiver (enrolling with a Caregiver is optional): one who receives HOBSCOCTCH-CA immediately (Group 1) and another group that will receive HOBSCOTCH-CA (Group 2) after a 3-month waiting period. Participants will be in the study for about 6 months total. HOBSCOTCH-CA involves 45 to 60 minute one on one virtual sessions with a certified Cognitive Coach including a "pre" program session and 8 weekly sessions thereafter. Participants will learn about problem solving therapy and mindfulness or relaxation training. CA participants are asked to do short homework assignments and keep a brief daily diary on a smart phone app. All participants complete study questionnaires or surveys at enrollment, 3 months later and at 6 months (at the end of the study).
This description comes directly from the study's public registry record.
Sarah J. Kaden, BA · 603-650-4225 · sarah.j.kaden@hitchcock.org
Trina K Dawson, BA · 603-650-4205 · trina.k.dawson@hitchcock.org
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| Dartmouth-Health Lebanon | Lebanon, New Hampshire, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06930846