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NCT Number: NCT07698522

Digital Technology-Informed Stroke Rehabilitation

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?

Recruiting

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Key information

Age range

30 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kennecott Mechanical Engineering Building

Salt Lake City, Utah, 84112, United States

Location status: Recruiting

Location contact

Scott Uhlrich, PhD

CONTACT

About this study

The study is a randomized, controlled feasibility trial investigating rehabilitation to improve movement patterns after stroke. The study will recruit participants who have had a stroke that led to upper-extremity impairment. Individuals will be assigned to one of two digital technology-guided groups. One group will be guided through exercises in a home-based setting, the other will be lab-based.

Participants will engage in training sessions multiple days a week for up to 6 weeks, either in-lab or at home. Both groups will visit the lab weekly for movement assessments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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.
  • Diagnosis of neurological disorders other than stroke.
  • Orthopedic/musculoskeletal conditions (e.g., severe arthritis) affecting the upper extremity.
  • Currently or planning to become pregnant.
  • Participation in concurrent occupational therapy.
  • Unilateral neglect, defined as failure of the Line Bisection Task
  • Upper extremity pain >= 7/10 on Numeric Rating Scale

Treatment and study plan

Lab-based movement guidance

Other

Participants will receive computer-generated guidance on how to perform different activities of daily living efficiently. The guidance will be delivered using lab-based sensing and feedback technology.

Home-based movement guidance

Other

Participants will receive computer-generated guidance on how to perform different activities of daily living efficiently. This guidance will be delivered using home-based technologies, such as a computer or tablet.

Primary outcomes

  1. Kinematic movement quality score

    Time frame: From enrollment to the end of treatment at 3 weeks.

    A score based on subject kinematics during a daily task (like reaching), comparing the subject's reaching kinematics to normative kinematics.

Secondary outcomes

  1. FMA-UE Score

    Time frame: From enrollment to the end of treatment at 3 weeks.

    Upper Extremity Fugl-Meyer Score

Study contacts

Contact information is provided by the study sponsor or research team.

Samantha McNeill

CONTACT

[email protected]

(385) 215-9146‬

Sponsors and collaborators

Lead sponsor

University of Utah

Other

Registry information

Important dates

Study start
2026
Primary completion
2033
Study completion
2033
First posted
Jul 13, 2026
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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