- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03039400
Physiotherapist-guided Home Exercise in Moderate to Severe MS
7. april 2021 opdateret af: Katherine Knox, University of Saskatchewan
Physiotherapist-guided Home Exercise in Moderate to Severe Multiple Sclerosis
Physical activity is a crucial component to wellness and is associated with multiple health benefits.
Persons with MS may find it challenging to participate in regular physical activity or exercise, which is activity done to improve health and/or fitness.
This research will test an innovative web-based intervention to help persons with moderate-to-severe disability manage their condition through a maintenance exercise program with specialized physiotherapist guidance and support.
The researchers will examine adherence to the web-based physiotherapy program compared to standard physiotherapy care.
Forty-five people with MS will be randomly assigned to the web group or standard care group at a rate of 2:1.
Participants in the web group will receive supported and individualized web-based physiotherapy.
Participants in the standard care group will receive a written exercise program.
Regular participation (adherence) in the exercise programs will be evaluated in both groups over six months.
The research will also examine participant satisfaction with the programs, safety, MS symptoms, and physical function.
A web-based approach may be widely accessible to persons with MS in their own homes and could support long-term participation in physical activity important to wellness.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
48
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Saskatchewan
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Saskatoon, Saskatchewan, Canada, S7K 0M7
- Department of Physical Medicine & Rehabilitation, University of Saskatchewan
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- diagnosed with MS
- moderate to severe disability (PDDS 2-7)
- able to access the internet in your current living environment
Exclusion Criteria:
- already doing structured exercise more than once per week
- residing >300km from Saskatoon (unless able to travel to Saskatoon for the appointments)
- unable to understand the intent and process of this study
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Web-based physio group
Those in the web-based physio group will have an individual exercise program set up by a treating physiotherapist on webbasedphysio.com
after an initial face-to-face assessment.
They will be encouraged to undertake their exercise program at least twice per week and diarize their work.
Participants will receive a weekly phone call from their treating physiotherapist for the first two weeks.
The treating physiotherapist will review the exercise diary of each participant every two weeks, and remotely alter the participant's exercise program as appropriate, by changing exercises, level of difficulty or number of repetitions.
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Those in the web-based physio group will access their exercise program online and will be able to leave messages for their physiotherapist on the platform.
Physiotherapists will monitor usage and respond to messages every two weeks.
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Aktiv komparator: Standard care group
Those in the standard care group will have their exercise program explained to them at an initial face-to-face assessment with a treating physiotherapist as per usual care.
They will receive a written, home-based exercise program.
Participants in the usual care group will also be encouraged to undertake their exercise program at least twice per week, and will be asked to keep an exercise diary, in paper format.
Participants in the usual care group will also receive a weekly phone call from the physiotherapist for the first two weeks to check on progress.
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Those in the standard care group will receive a written, home-based exercise program.
Participants in the usual care group will be asked to keep an exercise diary, in paper format.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Adherence to prescribed exercise program
Tidsramme: 6 months
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Measured by number of completed exercise sessions on exercise diary
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6 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Injury or fall
Tidsramme: 6 months
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Participants will be asked to contact their treating physiotherapist in the event of new pain, injury, or fall.
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6 months
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Multiple Sclerosis Impact Scale (MSIS29 v.2)
Tidsramme: 6 months
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6 months
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Godin Leisure Time Exercise Questionnaire (GLTEQ)
Tidsramme: 6 months
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6 months
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Grip strength measured on hand dynamometer
Tidsramme: 6 months
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6 months
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Timed 25-Foot Walk Test
Tidsramme: 6 months
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6 months
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Timed Up and Go
Tidsramme: 6 months
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6 months
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FIM (R) instrument
Tidsramme: 6 months
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The FIM (R) instrument, data set and impairment codes referenced herein are the property of Uniform Data System for Medical Rehabilitation, a division of UB Foundation Activities, Inc.
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6 months
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Hospital Anxiety and Depression Scale
Tidsramme: 6 months
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6 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Katherine Knox, MD, University of Saskatchewan
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Donkers SJ, Nickel D, Paul L, Wiegers SR, Knox KB. Adherence to Physiotherapy-Guided Web-Based Exercise for Persons with Moderate-to-Severe Multiple Sclerosis: A Randomized Controlled Pilot Study. Int J MS Care. 2020 Sep-Oct;22(5):208-214. doi: 10.7224/1537-2073.2019-048. Epub 2020 Jan 8.
- Knox KB, Nickel D, Donkers SJ, Paul L. Physiotherapist and participant perspectives from a randomized-controlled trial of physiotherapist-supported online vs. paper-based exercise programs for people with moderate to severe multiple sclerosis. Disabil Rehabil. 2022 Mar 28:1-7. doi: 10.1080/09638288.2022.2055159. Online ahead of print.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
6. marts 2017
Primær færdiggørelse (Faktiske)
11. oktober 2018
Studieafslutning (Faktiske)
11. oktober 2018
Datoer for studieregistrering
Først indsendt
20. december 2016
Først indsendt, der opfyldte QC-kriterier
30. januar 2017
Først opslået (Skøn)
1. februar 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
13. april 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
7. april 2021
Sidst verificeret
1. april 2021
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Bio 16-280
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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