- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05708378
Comparison of Rocker Board and Stable Surface Training on Postural Stability, Balance and Gait (ACAMCAOAMMSE)
Comparison of Rocker Board and Stable Surface Training on Postural Stability, Balance and Gait in Stroke
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Khyber Pakhtunkhwa
-
Abbottabad, Khyber Pakhtunkhwa, Pakistan, 22020
- Chinnar Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both genders
- Age: between 40-60 years.
- Unilateral hemiplegia.
- ACA and MCA lesions only.
- Subacute and chronic stroke patients.
- First time affected.
- No visual and sensory deficits.
- Ambulatory stroke patients scoring 21 to 40 on Berg Balance Scale.
- Scoring > 21 on MMSE.
Exclusion Criteria:
● Any other neurological deficits as multiple sclerosis, Parkinsons disease etc.
- Any musculoskeletal disorders like OA, ligament injury etc.
- Non-ambulatory patients
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Rocker board training
Stretching Exercises (Heel drop, heel raises, Hamstring stretch, quad stretch, half kneel, IT band stretch, half squats). Hold the stretch for 20 seconds and repeat 10 times. Isometric Strengthening Exercises of calves, hamstrings, quads, hip flexors, gluteus, dorsiflexors and plantarflexors. Hold for 20 seconds and repeat 10 times. Pelvic Bridging Exercises. Trunk control exercises on Rocker Board in standing position first in medio-lateral direction for 10 min and then in anterio-posterior direction for 10 min with breaks in between. |
Patients will perform 24 sessions (4 times per week over 6 weeks) and effects will be measured before treatment, at 3rd and after 6th week.
Other Names:
|
Other: Stable surface training
Stretching Exercises (Heel drop, heel raises, Hamstring stretch, quad stretch, half kneel, IT band stretch, half squats). Hold the stretch for 20 seconds and repeat 10 times. Strengthening Exercises calves, hamstrings, quads, hip flexors, gluteus, dorsiflexors and plantarflexors. Hold for 20 seconds and repeat 10 times. Pelvic Bridging Exercises. Trunk balance exercise (flexion, extension of lower and upper trunk, rotation of lower and upper trunk, forward and lateral reach) on plain surface. |
Patients will perform 24 sessions (4 times per week over 6 weeks) and effects will be measured before treatment, at 3rd and after 6th week.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Beg Balance Scale
Time Frame: 6 weeks
|
It is used to assess balance.
, "Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Trunk Impairment Scale
Time Frame: 6 weeks
|
It is used to measure motor impairment of the trunk after stroke.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Postural Assessment Scale for Stroke Patients
Time Frame: 6 weeks
|
It is used for the assessments of postural control in stroke patients.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Timed Up and Go Test
Time Frame: 6 weeks
|
It is for the assessment of lower extremity function, mobility and fall risk.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Functional Gait Assessment
Time Frame: 6 weeks
|
It is for assessment of postural stability during walk.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Timed Walking Test
Time Frame: 6 weeks
|
It is used for assessing functional status or fitness.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroke Self-Efficacy Questionnaire
Time Frame: 6 weeks
|
It evaluate self-efficacy as a result of being able to successfully perform a specific action in stroke patients.
"Change will be measured from Baseline to 6 weeks"
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aruba Saeed, PhD*, Riphah International University Pakistan
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/01489 Zarafshann
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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