Study Results
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View full resultsBasic Information
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COMPLETED
NA
590 participants
INTERVENTIONAL
2019-03-01
2023-04-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Teleconference
Teleconference Intervention arm
Teleconference
This intervention arm will be a 6-week, group-based course involving weekly 80-min teleconference sessions. It will be delivered in small groups (6-12 participants) to maximize participants' opportunities for interaction. A program manual divided into 6 sections, 1 for each week that includes worksheets and homework activities will be given to the participants. Occupational therapists will facilitate the sessions. Participants and the OT will dial into 1-800 conference call line on the designated date and time.
Internet
Internet Intervention arm
Internet
The internet course is similar to the teleconference format. It will occur in a 6-week period and be group based; i.e., 8-12 participants will begin the intervention at the same time and interact with each other during the 6-week period. Participants will be given a username and a password to view a different session each week at a time convenient for them. Each session will include completing practice activities and sharing information (e.g., offering advice and support to one another through the discussion forum). OTs will facilitate the discussions by responding to entries, asking questions, and providing encouragement to complete sessions.
I-to-1, in-person or videoconference
1-to-1, in-person or videoconference intervention arm
1-to-1, in-person or videoconference
Unlike the teleconference and internet courses, the number and length of sessions for the 1-to-1, in-person or videoconference course will vary over the 6-week period. The OT will cover all 6 topics, but the pace will be tailored to the participants' needs and preferences. Thus, although the topics are consistent, OTs are able to spend more time on topics that participants find pertinent to their situations. The participant and OT will be instructed to meet at least 3 times with at least 7 days between each session.
Interventions
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Teleconference
This intervention arm will be a 6-week, group-based course involving weekly 80-min teleconference sessions. It will be delivered in small groups (6-12 participants) to maximize participants' opportunities for interaction. A program manual divided into 6 sections, 1 for each week that includes worksheets and homework activities will be given to the participants. Occupational therapists will facilitate the sessions. Participants and the OT will dial into 1-800 conference call line on the designated date and time.
Internet
The internet course is similar to the teleconference format. It will occur in a 6-week period and be group based; i.e., 8-12 participants will begin the intervention at the same time and interact with each other during the 6-week period. Participants will be given a username and a password to view a different session each week at a time convenient for them. Each session will include completing practice activities and sharing information (e.g., offering advice and support to one another through the discussion forum). OTs will facilitate the discussions by responding to entries, asking questions, and providing encouragement to complete sessions.
1-to-1, in-person or videoconference
Unlike the teleconference and internet courses, the number and length of sessions for the 1-to-1, in-person or videoconference course will vary over the 6-week period. The OT will cover all 6 topics, but the pace will be tailored to the participants' needs and preferences. Thus, although the topics are consistent, OTs are able to spend more time on topics that participants find pertinent to their situations. The participant and OT will be instructed to meet at least 3 times with at least 7 days between each session.
Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years
* Fatigue Severity Scale score ≥ 4
* Ability to speak English
Exclusion Criteria
* Unable to access the internet or unable to travel to in-person sessions
18 Years
ALL
No
Sponsors
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Patient-Centered Outcomes Research Institute
OTHER
University of Illinois at Chicago
OTHER
University of Minnesota
OTHER
Queen's University, Kingston, Ontario
OTHER
Dalhousie University
OTHER
The Cleveland Clinic
OTHER
Case Western Reserve University
OTHER
Responsible Party
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Matthew Plow
Assistant Professor
Principal Investigators
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Matthew Plow, PhD
Role: PRINCIPAL_INVESTIGATOR
Case Western Reserve University
Locations
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University of Illinois at Chicago
Chicago, Illinois, United States
University of Minnesota
Minneapolis, Minnesota, United States
Case Western Reserve University
Cleveland, Ohio, United States
Countries
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References
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Plow M, Packer T, Mathiowetz VG, Preissner K, Ghahari S, Sattar A, Bethoux F, Finlayson M. REFRESH protocol: a non-inferiority randomised clinical trial comparing internet and teleconference to in-person 'Managing Fatigue' interventions on the impact of fatigue among persons with multiple sclerosis. BMJ Open. 2020 Aug 16;10(8):e035470. doi: 10.1136/bmjopen-2019-035470.
Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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MS-1610-37015
Identifier Type: -
Identifier Source: org_study_id
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