Badanie skuteczności programu HOBSCOTCH-MS - ćwiczenia poznawcze dla osób ze stwardnieniem rozsianym

ClinicalTrials.gov➕ 03.11.2026Status: Trwa rekrutacjaFaza: Nie dotyczy

HOBSCOTCH-MS-Efficacy Trial

W skrócie

Badanie sprawdza, czy program ćwiczeń prowadzonych przez internet może poprawić pamięć, myślenie i jakość życia u osób ze stwardnieniem rozsianym oraz zmniejszyć obciążenie ich opiekunów. Pacjenci biorą udział w 9 sesjach z certyfikowanym coachem, gdzie uczą się technik radzenia sobie ze stresem i ćwiczeń na rozluźnienie, a także prowadzą dziennik postępów. Badanie trwa około 6 miesięcy i skierowane jest do żołnierzy, weteranów i cywilów ze stwardnieniem rozsianym, którzy mają problemy z pamięcią i myśleniem.

Oryginalny opis (angielski)

The purpose of this study is to assess the ability of the home-based intervention, HOBSCOTCH-MS to improve the quality of life and cognitive function in Service Members, Veterans and civilians who have multiple sclerosis with cognitive and memory problems (MS participants). This study will also assess the ability of the HOBSCOTCH-MS program to improve quality of life in caregivers of patients with multiple sclerosis and to reduce caregiver burden. Enrolling with a Caregiver is optional for MS participants. Investigators will compare two groups of MS participants and their Caregiver (enrolling with a Caregiver is optional): one who receives HOBSCOTCH-MS immediately (Group 1) and another group that will receive HOBSCOTCH-MS (Group 2) after a 3-month waiting period. Participants will be in the study for about 6 months total. HOBSCOTCH-MS 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. MS participants are asked to do short homework assignments and both MS and Caregiver participants are asked to 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). After completing the intervention, MS Participants and their Caregivers may also participate in an optional one-time Key Informant Interview for qualitative analysis in an effort to further adapt and improve the HOBSCOTCH-MS in the future.

Metadane badania

NCT ID
NCT06951919
Status
Trwa rekrutacja
Faza
Nie dotyczy
Sponsor
Dartmouth-Hitchcock Medical Center
Data startu
09.09.2025
Choroby
Multiple Sclerosis, Cognitive Dysfunction, Memory Disorders, Memory Impairment, Memory Dysfunction
Kraje
United States