Confirmatory Trial for Alleviating Fatigue in Multiple Sclerosis

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:

• 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)

Locations
United States
Washington, D.c.
Washington VA Medical Center
RECRUITING
Washington D.c.
Massachusetts
iConquerMS
RECRUITING
Waltham
Maryland
Baltimore VA Medical Center
RECRUITING
Baltimore
Oregon
Portland VA Medical Center
RECRUITING
Portland
Tennessee
Nashville VA Medical Center
RECRUITING
Nashville
Washington
Seattle VA Medical Center
RECRUITING
Seattle
Contact Information
Primary
Grace Okafor
cafe-ms@iconquerms.org
781-487-0008
Time Frame
Start Date: 2024-12-05
Estimated Completion Date: 2027-09-14
Participants
Target number of participants: 2000
Treatments
Experimental: Fatigue Program A added to Treatment as Usual
An MS-specific fatigue management program, delivered as a stand-alone, fully automated intervention via an internet-browser.
Active_comparator: Fatigue Program B added to Treatment as Usual
Fatigue Program B will use a web-based interface with similar design and functionality as Fatigue Program A.
No_intervention: Treatment as Usual
Related Therapeutic Areas
Sponsors
Collaborators: United States Department of Defense, Congressionally Directed Medical Research Programs, Charite University, Berlin, Germany, US Department of Veterans Affairs, University Medical Center Goettingen
Leads: Accelerated Cure Project for Multiple Sclerosis

This content was sourced from clinicaltrials.gov