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NCT03096262Completed

Transforming Robot-mediated Telerehabilitation: Citizen Science for Rehabilitation

Feasibility of a Kinect-Based Citizen Science Telerehabilitation Platform

Source: ClinicalTrials.gov · Last updated 11 Jul 2025

Brief summary (registry, in English)

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).

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
24 Mar 2017
Start date
Apr 2021
Primary completion date
May 2025
Lead sponsor
Johns Hopkins University
Diseases
Stroke
NCT number
NCT03096262

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From Apr 2021 to the primary completion date, May 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • medical comorbidity such as other neurological conditions (e.g. Parkinson's disease, brain tumor, epilepsy), or previous injury to the upper limb
  • any previous injury or medical condition that prevents full passive range of motion to perform the exercises.

Other

  • For treatment group:
  • visual deficit such as deficit in visual acuity, eye movements, visual field cut, or neglect
  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Matthew Bird
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.