Stroke Clinical Trial
Official title:
The Effects of Standardized Physical Therapy and Functional Strength Training on Upper Limb Function and Neuromuscular Weakness After Stroke: a Pilot Study
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.
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 pilot clinical trial (Phase II). Subjects will be within 3
months of first stroke with some voluntary movement in the paretic upper limb.
A Research Physiotherapist, blinded to measurement, will recruit subjects, allocate subjects
to one of three intervention groups using sequentially numbered sealed envelopes containing
previously allocated intervention cards and provide interventions. Ten participants will be
recruited to each group therefore the trial will recuit 30 participants. The Research
Assessor, 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, five 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 the Action Research Arm Test (ARAT)and the Nine
Hole Peg Test (9HPT). The secondary outcomes are peak torque around the elbow joint in elbow
flexion and extension, grip force, pinch force, smoothness of movement during turning a
cranked wheel and reciprocal inniveration of biceps and triceps during turning of a cranked
wheel.
Data will be analysed using descriptive statistics and the estimation of standard deviations
will be used to inform a power calculation to estimate sample size for a Phase II randomised
controlled trial.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
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