This randomized clinical trial will occur at Bahawal Victoria Hospital, Bahawalpur within 7 months after the approval of synopsis. The sample size for this trial will be 40 participants. Participants fulfilling the inclusion criteria will be recruited by using the convenience sampling randomly allocated into two groups by computer generator method. 20 participants will be assigned to Group A receiving gaze stability exercises and 20 to the Group B receiving optokinetic exercises, both alongside routine physical therapy. Each group will undergo 5 weekly sessions of treatment for 4 weeks.The assessment tools include Dizziness Handicap Inventory for dizziness; Mini-BESTest and modified-Clinical Test of Sensory Interaction of Balance for balance assessment while Vestibular Disorders Activities of Daily Living Scale for daily activities.
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Dizziness Handicap Inventory
Timeframe: At Baseline, 2nd week and 4th week
Mini-Bestest
Timeframe: At Baseline, 2nd week and 4th week.
Modified-Clinical Test of Sensory Interaction on Balance
Timeframe: At Baseline, 2nd week and 4th week.
Vestibular Disorders Activities of Daily Living Scale
Timeframe: At Baseline, 2nd week and 4th week.