- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05008822
Effect of Motor Imaginary Training on Upper Limb Functions in Stroke
Effect of Motor Imaginary Training on Upper Limb Functions in Stroke Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Motor imagery is a technique for inducing motor activity in response to a certain motor output by producing a mental image of the action without intending to conduct it. It is a cognitive technique that, rather than making a patient to pick up new procedures, promotes neural alterations in order enable the patient to re-acquire motor skills mastered before the CVA or copy the actions of others. Motor imaging training is a sort of therapy in which the patient imagines a gesture or movement in order to learn, reinforce, or improve the movement's performance. A study done in South Korea, published in 2015, revealed that Motor imagery training has a good impact on UL performance by refining functional mobility during stroke rehabilitation. The results suggest that motor imagery training is viable and helpful for improving UL function in CVA patients.
Meta-analysis done in Australia in the year 2013, was supportive of Motor imaginary techniques further convincing that Mental imagery can be a possible intervention for stroke patients given that it being, safe cost-effective & unlimited practice opportunities. Study done in China in 2017, suggested that clinicians should consider the use of MI in addition to treatment currently used to improve upper extremity functions after stroke as no evidence of side effects or harm was noted . RCT done in year 2006 in USA indicated that for patients with chronic, moderate upper limb impairment after CVA, program of CIMT with mental practice only resulted in decrease impairment, with functional enhancement.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Khyber Pakhtunkha
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Peshawar, Khyber Pakhtunkha, Pakistan, 25000
- Physical therapy department of Rehman Medical Institute, Peshawar, Pakistan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- MCA stroke
- Chronic stroke patients
- Mini-Mental State Examination (MMSE) score >24 points
- Spasticity grade II and III on Modified Ashworth scale
Exclusion Criteria:
- Severe cognitive disability such as depression, unilateral neglect, seizure, dementia,
- Any MSK disorder including muscle contracture
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Motor Imaginary Training Group
After the baseline assessment, the participant will receive Motor Imaginary Program
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After the baseline assessment, the participant will receive Motor Imaginary Program
|
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Active Comparator: Task oriented Training Group
After the baseline assessment, the participant will receive MRP and CIMT training
|
After the baseline assessment, the participant will receive MRP and CIMT training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
wolf motor function
Time Frame: Change from Baseline to 4th Weeks
|
The Wolf Motor Function Test (WMFT) is a timed and functional test that assesses upper extremity motor skills in a quantitative manner.
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Change from Baseline to 4th Weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Misbah ghous, MS, Riphah International University Islamabad
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/0832 Zulfiqar Ali
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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