Surveying Patient's Interest in Robotic Rehabilitation Device

NCT ID: NCT05417802

Last Updated: 2025-03-21

Study Results

Results pending

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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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-12-08

Study Completion Date

2026-12-07

Brief Summary

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This is a survey study to understand the stroke survivor's interest in robotic training. Investigators will use a questionnaire and show a video of robotic therapy to ask questions on their interest.

Detailed Description

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The purpose of this research is to investigate the interest of individuals with recent stroke in robotic therapy. Investigators will introduce a novel robotic platform to train ADLs of stroke patients. Investigators will examine the usability of this device as a home trainer for training rotational hand manipulation tasks such as opening a pickle jar, turning a key, missing a pot with a ladle, etc. The device will especially target stroke patients with ischemic stroke to enhance the performance of ADL. Also, investigators will examine the frequency and dosage of the current occupational therapy, followed by the satisfaction of the current therapy. Participant's participation will contribute to the development of a new therapy method using a robotic device for home-based training.

Conditions

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Stroke, Acute

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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 stroke
* Adults with no cognitive difficulties

Exclusion Criteria

* Adults with pregnancy,
* Adults with other neurological disorders than stroke
* Adults with hemorrhagic stroke
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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State University of New York at Buffalo

OTHER

Sponsor Role lead

Responsible Party

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Amit Kandel, MD, MBA

Principal Investigator

Responsibility Role 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

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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STUDY00004756

Identifier Type: -

Identifier Source: org_study_id

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