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Multi-mode Stroke Rehabilitation System: Development and Validation of Clinical Efficacy

NCT04441190 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2021-11-26

No results posted yet for this study

Summary

The specific study aims will be:

1. To develop the novel, digital, and interactive MSR system of arm and hand with integrated digital action observation therapy (AOT) and mirror therapy (MT).
2. To pilot usability testing for examining the feasibility of this new MSR system from the users' experiences and feedback.
3. To examine the treatment effects of digital AOT, digital MT and a control intervention in patients with stroke by conducting a randomized controlled trial.
4. To identify who will be the possible good responders to digital AOT and MT based on their baseline motor function and mental imagery abilities.

Conditions

Interventions

BEHAVIORAL

Digital Action Observation Therapy (Digital AOT)

The participants will be asked to observe videos and then practice what the participants observed.

BEHAVIORAL

Digital Mirror Therapy (Digital MT)

The participants will observe the real-time self-recorded visual illusion, and move their upper limbs as could as possible.

BEHAVIORAL

Conventional Occupational Therapy

The participants will receive upper-limb training without providing videos for observing neither providing them mirror illusions of movements.

Sponsors & Collaborators

  • Chang Gung Memorial Hospital

    lead OTHER

Principal Investigators

  • Yu-Wei Hsieh, PhD · Department of Occupational Therapy, College of Medicine, Chang Gung University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-03
Primary Completion
2021-05-11
Completion
2021-07-31

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04441190 on ClinicalTrials.gov