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Confirmatory Trial for Alleviating Fatigue in Multiple Sclerosis
NCT06441617 · Accelerated Cure Project for Multiple Sclerosis
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
CAFE-MS will assess the effectiveness of two online programs for fatigue in multiple sclerosis (MS). Although they differ, both of these online programs contain information about MS and fatigue intended to help people with MS understand and manage their fatigue.
This large-scale, decentralized clinical trial is projected to enroll 2,000 people with MS. The collaboration between iConquerMS and 5 Veterans Affairs (VA) sites in the MS Centers of Excellence is designed to ensure sufficient representation of people with MS from populations traditionally under-represented in MS clinical trials.
The study is a 3-arm, randomized controlled clinical trial with study participation lasting 1 year. Two of the trial arms will include one of two online programs for managing fatigue in MS added to the trial participants' usual MS treatment, and the third arm will include usual MS treatment alone. The online program phase of the trial lasts for 6 months after randomization followed by a final study visit at 12 months. Participants in the usual MS treatment alone arm for the first 6 months will have an opportunity to choose one of the online programs for the final 6 months of the trial.
Eligibility criteria
Inclusion Criteria:
* Informed consent by person with MS
* Living in the US
* Age ≥ 22
* Confirmed diagnosis of MS by a physician, who is a neurologist or has access to a neurologist's statement of diagnosis
* Fatigue Severity Scale score at or above eligibility threshold
* Fluent in English
* Willingness to engage in self-administration of an online intervention for 24 weeks and complete follow-up assessments
* Access to the internet and e-mail with a compatible device (smartphone, computer, or tablet)
* No MS relapse / no steroid treatment in the 4 weeks prior to answering the screening questionnaire (self-reported)
* No disease-modifying therapeutic (DMT) started in the 4 weeks prior to answering the screening questionnaire (self-reported)
Exclusion Criteria:
* Unwilling or unable to consent
* Refusal to saving, processing and forwarding of pseudonymized data
* Concurrent participation in another interventional trial
Study design
Enrollment target: 2000 participants
Allocation: randomized
Masking: double
Age groups: adult, older_adult
Timeline
Starts: 2024-12-05
Estimated completion: 2027-09-14
Last updated: 2026-04-15
Interventions
Device: Online Program for Fatigue
Primary outcomes
- • Chalder Fatigue Scale (Day 180)
Sponsor
Accelerated Cure Project for Multiple Sclerosis · other
With: Congressionally Directed Medical Research Programs, United States Department of Defense, Charite University, Berlin, Germany, University Medical Center Goettingen, US Department of Veterans Affairs
Contacts & investigators
ContactGrace Okafor · contact · cafe-ms@iconquerms.org · 781-487-0008
All locations (6)
Washington VA Medical CenterRecruiting
Washington D.C., District of Columbia, United States
Baltimore VA Medical CenterRecruiting
Baltimore, Maryland, United States
iConquerMSRecruiting
Waltham, Massachusetts, United States
Portland VA Medical CenterRecruiting
Portland, Oregon, United States
Nashville VA Medical CenterRecruiting
Nashville, Tennessee, United States
Seattle VA Medical CenterRecruiting
Seattle, Washington, United States