MedPath

Transforming Robot-mediated Telerehabilitation: Citizen Science for Rehabilitation

Not Applicable
Recruiting
Conditions
Hemiparesis
Stroke
Interventions
Behavioral: Output-Focus Condition
Behavioral: Input-Focus Condition
Registration Number
NCT03096262
Lead Sponsor
Johns Hopkins University
Brief Summary

The purpose of this study is to advance upper limb robot-mediated tele-rehabilitation for patients recovering from stroke by empowering them through active science participation. By varying the tasks' features and affordances of a platform that combines a low-cost haptic device on one hand, and an online citizen science platform on the other, investigators will evaluate different strategies for social telerehabilitation. the two fundamental modes of social interaction - competition and cooperation - in addition to a control condition. Specifically, citizen science activities will be performed by competing, cooperating, or isolated users, and their rehabilitation effectiveness examined. Such effectiveness will be measured by (i) participants' rehabilitation performance (inferred from sensorimotor data acquired through the platform and directly quantified by a supervising therapist); (ii) participants' motivations to contribute (measured through surveys administered online); and (iii) participants' emotional well-being and sense of self-esteem (measured through online surveys).

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria

For treatment group:

  • post-stroke hemiparesis >3 months
  • ability to stand or sit independently
  • sufficient cognitive skills to perform the exercises as demonstrated
  • full passive range of motion in the affected arm but limited active movement as determined by a upper extremity Fugl-Meyer score of <50/66
  • technical savvy and interest to use an internet platform

For control group:

(ii) no history of learning disabilities (iii) technical savvy and interest to use an internet platform

Exclusion Criteria

For treatment group:

  • visual deficit such as deficit in visual acuity, eye movements, visual field cut, or neglect
  • medical comorbidity such as other neurological conditions (e.g. Parkinson's disease, brain tumor, epilepsy), or previous injury to the upper limb
  • pain in the upper limbs that prevents full passive range of motion to perform the exercises.

For control group:

  • visual deficit such as deficit in visual acuity, eye movements, visual field cut, or neglect
  • any previous injury or medical condition that prevents full passive range of motion to perform the exercises.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy ControlsInput-Focus Condition-
Stroke PatientsInput-Focus Condition-
Stroke PatientsOutput-Focus Condition-
Healthy ControlsOutput-Focus Condition-
Primary Outcome Measures
NameTimeMethod
assessment of tone using Ashworth scale1 Month

this scale measures resistance during passive soft-tissue stretching and is used as a simple measure of spasticity.

Video-based motion analysis1 Month

Passive and active range-of-motion measurements of the affected and unaffected arm using video-based motion analysis

Fugl-Meyer scale1 Month

Stroke-specific, performance-based impairment index. It is designed to assess motor functioning, balance, sensation and joint functioning in patients with post-stroke hemiplegia.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Matthew Bird

🇺🇸

Baltimore, Maryland, United States

© Copyright 2025. All Rights Reserved by MedPath