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NCT07698522Recruiting

Digital Technology-Informed Stroke Rehabilitation

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

The goal of this study is to determine the effects of lab and home-based technology guidance during movement training post-stroke. The study will compare movement training informed by lab-based technology to training delivered with technology at home. The main questions it aims to answer are: * How well do lab and home-based technologies help individuals post-stroke improve their movement patterns? * Is there a difference in improvement between the in-lab and at-home training groups? * Which technologies lead to the most improvement?

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
6 Jul 2026
Start date
27 Jul 2026
Primary completion date
31 Dec 2033
Lead sponsor
University of Utah
Diseases
Stroke
NCT number
NCT07698522

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 27 Jul 2026 to the primary completion date, 31 Dec 2033
  • 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

  • Participation in concurrent occupational therapy.

Other illness

  • Diagnosis of neurological disorders other than stroke.
  • Orthopedic/musculoskeletal conditions (e.g., severe arthritis) affecting the upper extremity.
  • Unilateral neglect, defined as failure of the Line Bisection Task

Other

  • Presence of severe aphasia preventing the ability to follow 1-step directions at least 80% of the time.
  • Excessive spasticity of the wrist, elbow, and shoulder, defined as a Modified Ashworth Score \>2.
  • Currently or planning to become pregnant.
  • Upper extremity pain \>= 7/10 on Numeric Rating Scale

Who the study is looking for

  • Age between 30-85 years.
  • Diagnosis of stroke.
  • Stroke onset of at least six months prior to the time of participation.
  • Fugl Meyer Upper Extremity between 30-50 (mild-moderate)
  • Cognitive skills to consent and actively participate, as indicated by scores of ≥ 24 on the Mini- Mental Status Examination
  • Able to visit lab up to 5x per week for 3 weeks

Age in the registry: 30 years to 85 years · Sex: All · Does not accept 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
Kennecott Mechanical Engineering Building
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesRecruiting

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