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Can a tablet guide stroke recovery at home?

NCT ID NCT07698522

Disease control Sponsor: University of Utah Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 13, 2026 · Last updated Jul 21, 2026 · Updated 3 times

Summary

This study explores whether computer-generated guidance can help people who have had a stroke improve their movement patterns. Participants practice daily tasks like reaching, either in a lab with advanced sensors or at home using a tablet. The goal is to see if home-based technology can be as effective as lab-based training for stroke rehabilitation.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
computer-generated movement guidance delivered via lab sensors or home tablet
What this could lead to
If successful, this could point toward effective home-based rehabilitation tools for stroke survivors, reducing the need for frequent clinic visits.
What could go wrong
This is a small early-stage study with only 60 participants, so results may not apply to all stroke survivors. The technology may not work as well at home as in the lab.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2033

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 85 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Stroke

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Kennecott Mechanical Engineering Building

    RECRUITING

    Salt Lake City, Utah, 84112, United States

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