Surveying Patient's Interest in Robotic Rehabilitation Device
NCT ID: NCT05417802
Last Updated: 2025-03-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
88 participants
OBSERVATIONAL
2021-12-08
2026-12-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Stroke with acute stroke
Inclusion criteria
* Episode of single stroke within the past twelve weeks
* Individuals' age over 18 years old.
Exclusion criteria
* Pregnant women , neurological disorders other than stroke (i.e. Parkinson's), non-ischemic stroke
* Individuals with severe cognitive impairments (demonstrating difficulty to understand, read, and answer the questions in writing)
* Individuals with difficulties to listen the instruction and video of the robotic device
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Adults with no cognitive difficulties
Exclusion Criteria
* Adults with other neurological disorders than stroke
* Adults with hemorrhagic stroke
18 Years
ALL
No
Sponsors
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State University of New York at Buffalo
OTHER
Responsible Party
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Amit Kandel, MD, MBA
Principal Investigator
Principal Investigators
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Jiyeon Kang
Role: PRINCIPAL_INVESTIGATOR
University at Buffalo
Locations
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Buffalo General Hospital
Buffalo, New York, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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STUDY00004756
Identifier Type: -
Identifier Source: org_study_id
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