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Effectiveness of carer-mediated game-based circuit exercise on functions and quality of life among stroke survivors: A protocol for randomized controlled trial

Not Applicable
Conditions
Stroke
Stroke - Haemorrhagic
Stroke - Ischaemic
Registration Number
ACTRN12621000727842
Lead Sponsor
niversiti Kebangsaan Malaysia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
82
Inclusion Criteria

Participants who are; 1) diagnosed at least 2 months after stroke either hemorhagic or ischemic by a Neurology physician, 2) able to walk continuously for 10 meters independently with or without walking aid, 3) able to perform basic instrumental activities of daily living such as walking, stepping up and turning with or without walking aid, 4) able to hold a glass full of water with the non-affected hand and 5) able to follow 3 steps command and 6) physically healthy without disability based on Nagi’s concepts (Pope & Tarlov 1991) will be recruited in this trial.

Exclusion Criteria

Participants had, 1) more than one stroke, 2) other neurologic disorders such as Parkinson’s Disease and traumatic brain injury, 3) an average Montreal Cognitive Assessment score of 22.1 and less, 4) severe orthopedic conditions such as joint deformities, osteoarthritis and rheumatoid, 5) visual field defects or 6) currently on medications which can caused giddiness such as anti-hypertensive (alpha-blockers) and medicine to lower hypercholesterol (amlodipine/atorvastatin) will be excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ower limb strength assessed using the 30-second Chair Rise test<br><br>[Baseline and at 12 weeks after intervention commencement];Postural stability assessed using the Dynamic Gait Index <br><br>[Baseline and at 12 weeks after intervention commencement];Aerobic endurance assessed using the S6-Minute Walk test <br><br>[Baseline and at 12 weeks after intervention commencement]
Secondary Outcome Measures
NameTimeMethod
Quality of life assessed using the SF-36 Quality of Life Questionnaire[Baseline and at 12 weeks after intervention commencement]
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