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Active (not recruiting) Not applicable NCT06880627

Brain Boost Program to Improve Cognitive Function in People With Systemic Sclerosis

No applicable phase (e.g. observational)
Conditions: Scleroderma

Sponsor: University of Michigan

trial.available_in: БГ
Overview
The purpose of this study is to examine whether an 8-week online educational group-based program tailored to people with systemic sclerosis can help improve cognitive function and well-being. The study team hypothesize that participants that receive the intervention will have better improvements immediately after treatment at week 8 in all cognitive function measures, non-cognitive symptoms, and self-management compared to those in the waitlist control.
Who can participate
Inclusion Criteria: * Have physician-diagnosis of Systemic sclerosis (SSc) (any subtype) * A score of ≥ 10 on the Perceived Deficits Questionnaire * A score of ≤ 7 on the 6-Item Cognitive Impairment Test * Have access to a reliable, internet-connected device (e.g. computer, smartphone, tablet) * Visual acuity with correction sufficient to work on a computer, smartphone, tablet or screen * Be able to read, speak, and understand English Exclusion Criteria: * Diagnosis of dementia or head injury * Other neurological disorders that might impact cognition * Have major psychiatric disorder such as major depression and schizophrenia * Complex, unstable health issues that would preclude full participation in the study (like a planned surgery or active cancer treatment)
Interventions
Brain Boost group
BEHAVIORAL
Waitlist group
OTHER
Locations 1
United States (1)
University of Michigan
Ann Arbor , Michigan
Technical details
Status
Active (not recruiting)
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
70 Years
Healthy volunteers
No
Start date
16.04.2025
Completion date
01.12.2026
Registry ID
NCT06880627
Source
clinicaltrials.gov
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