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3D-Printed splints could boost stroke arm recovery

NCT ID NCT07243314

Symptom relief Sponsor: King Saud University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares 3D-printed dynamic splints to traditional ones for improving arm function in people who have had a stroke. One hundred adults with chronic stroke and mild to moderate arm weakness will receive 20 sessions of task-oriented therapy over four weeks, using either a 3D-printed or conventional splint. The goal is to see which splint leads to better movement, dexterity, and satisfaction.

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 100 people

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

Expected to start

Nov 2025

An estimate. Start dates often move.

Expected to finish

Sep 2027

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

18 years and older

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: 1. Over 18 years old. 2. Chronic stroke 3. Upper limb hemiparalysis 4. Ability to understand and follow orders and able to provide informed consent (Mini-Mental State Exam (MMSE) \> 24) 5. Upper-limb mild to moderate spasticity (Modified Ashworth Scale 1+ to 3 at the wrist). 6. Not participating in other clinical or research studies at the same time Exclusion Criteria: 1. Had deficits in language or cognitive impairments that were likely to interfere with their cooperation in the study 2. Deformity or presented with severe upper-limb contractures 3. Inability to commit to the time requirement of the protocol. 4. Unilateral neglect

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Conditions

The condition(s) this trial relates to.

Hemorrhagic Stroke Ischemic Stroke Paresis stroke disorder

As listed by the trial registrant

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

Hemiparesis of the upper limb following stroke Stroke Stroke rehabilitation

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

  • Sultan Bin Abdulaziz Humanitarian City

    Riyadh, Riyadh Region, 13571, Saudi Arabia

More trials for these conditions

Other studies related to the condition(s) this trial covers.