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Clinical Trials/NCT00322192
NCT00322192
Completed
Phase 2

The Effects of Functional Strength Training on Weakness and Function of the Lower Limb After Stroke

St George's, University of London4 sites in 1 country300 target enrollmentJanuary 2004
ConditionsStroke

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Stroke
Sponsor
St George's, University of London
Enrollment
300
Locations
4
Primary Endpoint
Maximum torque around the knee joint
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to test the hypothesis that adding functional strength training to UK conventional therapy improves muscle function and walking than either UK conventional therapy alone or increased intensity of UK conventional therapy

Detailed Description

Neuromuscular weakness occurs frequently after stroke and the processes underlying recovery are still poorly understood. Accepted practice in UK physiotherapy is to avoid training of muscle strength after stroke but there is preliminary evidence that it might be effective. An observer-blind randomised clinical trial. Subjects will be within 3 months of first stroke with some voluntary movement in the paretic lower limb. A power calculation estimated the sample size as 300. Research Physiotherapists, blinded to measurement, will recruit subjects, allocate subjects to one of the three intervention groups using sequentially numbered sealed envelopes containing previously randomised allocated intervention cards and provide interventions. The Research Assessors, blinded to intervention allocation will undertake all measurements. Conventional therapy (control) will be provided as normal for the clinical setting, the additional conventional therapy (experimental 1) or functional strength training (experimental 2) will be provided for one hour, four times a week, for six weeks. Subjects in the two experimental groups will also receive the conventional therapy standard in their clinical setting. Blinded measurement will be made before randomisation, at the end of intervention and 12-weeks thereafter. Primary outcomes are maximum torque around the knee joint, and gait velocity. The secondary outcomes include movement analysis, functional ability, corticospinal transmission (transcranial magnetic stimulation) and health related quality of life (Euroqol). The primary analysis will be analysis of covariance. A multiple comparison procedure (Gabriel's test) will be used to compare each pair of treatments. Euroqol data will be used to estimate the relative costs of the interventions and to calculate the incremental cost per QUALY gained. Every effort will be made to invite patients for assessment at outcome and follow-up even if they have withdrawn from therapy to allow the intention-to-treat principle to be applied.

Registry
clinicaltrials.gov
Start Date
January 2004
End Date
December 2006
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Subjects in this study will:
  • be aged over 50 years.
  • be between one week and three months after stroke when recruited to the study;
  • have been independently mobile indoors, with or without aids, before the stroke;
  • have some voluntary movement in the paretic lower limb i.e. score above 28/100 on the lower limb section of the Motricity Index43;
  • demonstrate adequate orientation and communication (be able to complete a one-stage command using the non-paretic upper limb e.g. point at the ceiling).
  • In addition those who agree to participate in TMS measurement will have no contraindications to TMS.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Maximum torque around the knee joint

gait velocity

Secondary Outcomes

  • Lower limb kinematics during walking
  • timing and pattern of muscle activation during functional activity
  • Modified Rivermead Mobility Index
  • Lower limb kinematics during standing up
  • Lower limb kinematics during sitting down
  • EuroQuol for health related quality of life
  • Transmission in the corticospinal pathways for suitable subjects who provide additional written informed consent for TMS

Study Sites (4)

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