Skip to content

Robotic Rehabilitation for Stroke Survivors

Robotic Rehabilitation for Stroke Survivors

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05417828
Enrollment
40
Registered
2022-06-14
Start date
2025-12-01
Completion date
2026-12-05
Last updated
2025-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Stroke

Brief summary

Pilot study on the physiological response of robotic rehabilitation therapy for improving the performance of activities of daily living of stroke patients

Detailed description

The purpose of this research is to study the feasibility of the robotic therapy that can train activities of daily living tasks for chronic stroke patients. The participant will be involved in a feasibility study (one-time visit) to prove the efficacy of the robotic device with different force feedback (assistive and resistive force) and other feedback such as VR (virtual reality). We will collect movement data from a motion capture system and sEMG sensors that measure muscle activity to monitor the effect of a robotic rehabilitation device, named Spherical Parallel Instrument for Daily Living Emulation (SPINDLE). We will use a robotic therapy device to practice activities during daily living. This pilot study will be used to understand the effect of SPINDLE to translate the device as a home-based training for chronic stroke patients.

Interventions

DEVICEEmulation of Active Daily Living tasks with a robotic device (SPINDLE)

SPINDLE will provide an assistive and resistive force to aid in rehabilitating the subject's upper limb

Sponsors

Department of Neurology Jacobs School of Medicine and Biomedical Sciences University at Buffalo.
CollaboratorUNKNOWN
State University of New York at Buffalo
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults with chronic stroke, which affected their upper limb motor functions * Adults could able to understand the verbal cues during the training

Exclusion criteria

* Adults with chronic stroke, who did not lose their upper limb motor functions

Design outcomes

Primary

MeasureTime frameDescription
Kinematic change of the upper limb during ADLsimmediately after the interventionThe max and range of motion of shoulder, elbow, and wrist joint for each task
Score of activities of daily living(ADL) tasksimmediately after the interventionWe will use ARM-ULA standard score sheet to measure the performance of ADLs
Muscle activation change of the upper limb during ADLsimmediately after the interventionThe subject will be asked to perform activities of daily living tasks with the passive SPINDLE. Upper limb range of motion and muscle activation will be quantified.

Secondary

MeasureTime frameDescription
Usability measureimmediately after the interventionQuestionnaire will be provided to the user to obtain qualitative feedback

Countries

United States

Contacts

Primary ContactJiyeon Kang
jiyeonk@buffalo.edu7166456063

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026