The effect of game-based in comparison to conventional circuit exercise on functions, motivation level, self-efficacy and quality of life among stroke survivors

Not Applicable

Recruiting

• Conditions: Stroke; Stroke - Haemorrhagic; Stroke - Ischaemic

• Registration Number: ACTRN12621001489886
• Lead Sponsor: Assoc. Prof Dr Nor Azlin binti Mohd Nordin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-11-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 82

Inclusion Criteria

Participants who are; 1) diagnosed either hemorhagic or ischemic by a Neurology physician who could be referred as early as 2 weeks after stroke which stable clinically, 2) able to perform basic instrumental activities of daily living such as walking, stepping up and turning with or without walking, hold a glass full of water with the non-affected hand, 3) an average Montreal Cognitive Assessment (MoCA) score of 22.1 and more will be recruited in this trial.

Exclusion Criteria

Participants had, 1) Having other therapy such as home physiotherapy and traditional therapy; 2) Modified Rankin Scale score 4 to 6; 3) More than one stroke or had other neurologic disorders such as Parkinson’s Disease; 4) Severe medical illness such uncontrolled hypertension, diabetes and severe asthma; 5) Musculoskeletal conditions such as severe osteoarthritis and rheumatoid arthritis; 6) Visual field defects will be excluded

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ower limb strength assessed using the 30-second Chair Rise test[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement];Postural stability assessed using the Dynamic Gait Index[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement];Aerobic endurance assessed using the 6-Minute Walk test[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement]

Secondary Outcome Measures

Name	Time	Method
Motivation level assessed using the Intrinsic Motivation Inventory Questionnaire[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement];Self-efficacy assessed using the Stroke Self-Efficacy Questionnaire[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement];Quality of life assessed using the SF-36 Quality of Life Questionnaire[Baseline, at 12 weeks, 24 weeks and 36 weeks after intervention commencement]