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

University of Michigan logo

University of Michigan

Status

Active, not recruiting

Conditions

Multiple Sclerosis

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05252195
HUM00199732
5R01HD102337-04 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Enrollment

300 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Are able to fluently converse and read in English.
  2. Multiple Sclerosis (MS) diagnosis (confirmed from neurologist, all relapsing and progressive subtypes included)
  3. 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

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

Trial design

300 participants in 1 patient group

Participants
Description:
Participants with Multiple Sclerosis who meet eligibility criteria.

Trial contacts and locations

3

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Central trial contact

Kristi Pickup

Data sourced from clinicaltrials.gov

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