Multiple Sclerosis Clinical Trial

Optimizing Detection and Prediction of Changes in Cognitive Function in Multiple Sclerosis (MS)

Summary

The researchers will use technology-assisted ambulatory assessment techniques to examine cognitive dysfunction in people with Multiple Sclerosis (MS).

The researchers will determine if ambulatory assessments are sensitive to subtle declines in cognitive functioning. They will also explore the impact of modifiable factors, such as sleep, physical activity, mood, and somatic symptoms on cognitive function. These efforts will uncover behavioral and medical intervention methods. Finally, they will explore whether variability in cognitive functioning predicts short- and long-term changes in other patient-centered functional domains, social participation and physical functioning.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Are able to fluently converse and read in English.
Multiple Sclerosis (MS) diagnosis (confirmed from neurologist, all relapsing and progressive subtypes included)
Ambulate either independently or with the use of a cane or walker (or similar device) for at least 50% of the time at baseline

Exclusion Criteria:

MS relapse within the past 30 days (may become eligible after 30 days; criteria used at T1, T2, and T3).
Inability to use study data collection tools (i.e., ActiGraph wrist-worn activity watch, smart phone app).

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

300

Study ID:

NCT05252195

Recruitment Status:

Active, not recruiting

Sponsor:

University of Michigan

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There are 3 Locations for this study

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University of Michigan
Ann Arbor Michigan, 48109, United States
Wayne State University
Detroit Michigan, 48202, United States
University of Washington
Seattle Washington, 98195, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

300

Study ID:

NCT05252195

Recruitment Status:

Active, not recruiting

Sponsor:


University of Michigan

How clear is this clinincal trial information?

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