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A Preliminary Investigation Into The Effect Of Home Standing Programs On Lower Limb Spasticity, Spasm, Pain and Well-being For Individuals With Progressive Multiple Sclerosis (MS)
Source of recordUK Clinical Trials Gateway
ISRCTNISRCTN34844778
Date ISRCTN assigned30/09/2005
Local reference number(s)N0515143146
Public titleA Preliminary Investigation Into The Effect Of Home Standing Programs On Lower Limb Spasticity, Spasm, Pain and Well-being For Individuals With Progressive Multiple Sclerosis (MS)
Scientific title
AcronymN/A
Disease/condition/study domainNervous System Diseases: Multiple sclerosis (MS)
Study hypothesisThe principal research questions are that daily standing in a frame will:
1. Decrease passive resistance to movement in lower limb (lower limb stiffness know as hyper tonicity)
2. Enhance range of motion at ankles.
3. Decrease frequency of lower limb spasms.
4. Lead to self-reported decrease in pain.
5. Lead to self-reported improvement in well-being.
Design/methodologyRandomised controlled trial
Research ethics reviewNot provided at time of registration
Countries of trialUnited Kingdom
Participants - inclusion criteriaParticipants are to be identified from clinical team members (physiotherapists) working in either Harrow PCT, Northwick Park Hospital or Harrow MS Therapy Centre.
Participants - exclusion criteriaNot provided at time of registration
Patient information material
Anticipated start date01/05/2004
Anticipated end date01/05/2005
Status of trialCompleted
Target number of participants6
InterventionsThe study proposed to use a cross over design of a minimum of six participants with primary or secondary MS these participants will be randomly selected to either a three-week exercise group or a three week standing group. The participants in the standing group will stand daily in a Standing Frame for 30 minutes if able. These participants will be shown how to use and stand in the frame, given exercises to perform whilst standing and show how to correctly position themselves in the frame. Preliminary research results will be feedback to the participants at the end of the six week study period. They will also be informed that final results will be available from the researchers , and the local MS society will also be made aware of the results. Measurements will be taken at assessment, three and six weeks, with the groups crossing over after three weeks.
Primary outcome measure(s)Not provided at time of registration
Secondary outcome measure(s)See Primary outcome measures
Sources of fundingNorth West London Hospitals NHS Trust
Unfunded
NHS R&D Support Funding
Sponsor nameRecord Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)
Sponsor detailsThe Department of Health, Richmond House, 79 Whitehall
London
United Kingdom
SW1A 2NL
Sponsor telephone+44 (0)20 7307 2622
Sponsor emaildhmail@doh.gsi.org.uk
Sponsor websitehttp://www.dh.gov.uk/Home/fs/en
Contact nameMiss Karen Baker
Contact detailsPhysical Disability Support Team
North West London Hospitals NHS Trust
P Block Northwick Park Hospital
Watford Road
Harrow
United Kingdom
HA1 3UJ
Contact telephone+44 (0)20 8869 3636
Contact fax+44
Contact emailkaren_baker73@yahoo.co.uk
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN34844778
Date last extracted from ISRCTN register17/04/2008
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