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NCT06270641

Increasing Physical Activity for Adults With Multiple Sclerosis (MS)

Recruiting now NA Last updated 22 February 2024
What this trial tests

NA trial testing ExerciseRx intervention in Multiple Sclerosis (MS) in 106 participants. Currently enrolling.

Timeline
16 February 2024
Primary endpoint
30 April 2025
30 September 2026

Quick facts

Lead sponsorUniversity of Washington
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment106
Start date16 February 2024
Primary completion30 April 2025
Estimated completion30 September 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Washington

Who can join

18 and older, any sex, with Multiple Sclerosis (MS) or Fatigue. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to advance the scientific understanding and potential future implementation of physical activity promotion by testing the efficacy of a phone-based app for increasing activity in insufficiently active patients with multiple sclerosis (MS).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Increasing Physical Activity via Provider Support and Engagement Using a Digital Health Platform in Adults With Multiple Sclerosis: Protocol for a Randomized Controlled Trial.
    Ehde DM, Simmons SB, Alschuler KN, Herring TE, et al · · 2025 · PMID 41268963 · DOI 10.2196/72213

Verify or expand the search:

Other recruiting trials for Multiple Sclerosis (MS)

Currently open trials in the same condition.

Other University of Washington trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06270641.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing