- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05894330
Perception About Upper Limb Functional Recovery, Barriers & Use of Training Devices Among Indian Stroke Survivors.
Perception About Upper Limb Functional Recovery, Barriers & Use of Training Devices Among Stroke Survivors- A Cross-Sectional Survey
The goal of this observational study is to evaluate perceptions regarding affected arm and hand function and their willingness to use devices to enhance upper limb functions among stroke survivors. The main question[s] it aims to answer are:
- what will the stroke survivor's perception of interventions and device development in his/her arm recovery?
- Wheather he is willing to use it for his arm recovery?
Study Overview
Status
Detailed Description
Individuals with stroke will be recruited from MGM Hospital and other hospitals from Aurangabad. Participants will be adults (age >30) with stroke and with the capacity to provide written or verbal informed consent, and the ability to communicate verbally/online/phone. Participants will be contacted via phone or email by a member of the research team. If needed personal interviews of the patients will be taken. The research team will consist of the author and one helper Physical Therapy student and the guide. All team members participating in the training will ensure consistency in communications with participants. All the participants will be provided with information about the study objectives and procedures and will be asked if they are willing to participate. If they consent, they will be given one of three options:
- Complete the survey via phone immediately
- Complete the survey online. In this case, they will be sent a link to their email to complete an online survey.
- Complete the survey via personal interview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Maharashtra
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Aurangabad, Maharashtra, India, 431003
- MGM's Institute of Physiotherapy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
- Inclusion Criteria:
- First-ever stroke
- All stages of stroke
- Onset of a stroke at least 1 year ago
- Age group: 30 to 75
- Both genders included
- Patients diagnosed with MCA (Middle Cerebral Artery) stroke
- Exclusion Criteria:
- Aphasia
- Patients who are unable to follow commands
- Patients with other neurological disorders such as Multiple sclerosis and Parkinson's disease
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self Structured Marathi language translated Version Questionnaire
Time Frame: One Month
|
It's a 69 item questionnaire to obtain the responses from the stroke survivors about their Upper limb recovery and use of devices for the same.
The Obtained responses will be used for the analyze the willingness of stroke clients for use of devices for his/her upper limb arm recovery
|
One Month
|
Collaborators and Investigators
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
- Ischemia
- Pathologic Processes
- Necrosis
- Cardiovascular Diseases
- Vascular Diseases
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Brain Ischemia
- Brain Infarction
- Cerebral Arterial Diseases
- Intracranial Arterial Diseases
- Cerebral Infarction
- Infarction
- Stroke
- Infarction, Middle Cerebral Artery
Other Study ID Numbers
- MGM-ECRHS/2021/39
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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-
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