Tight fit, better touch? stroke trial tests pressure garments for hand recovery

NCT ID NCT07725744

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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 Results may not be published yet.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

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Status unknown
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First seen Jul 24, 2026 · Last updated Jul 24, 2026

Summary

This trial tests whether different types of pressure garments can improve touch sensation in the hand after a stroke. Adults aged 21 to 60 with hand stiffness will wear one of three garment designs for at least 12 hours daily over four weeks. Researchers will measure how the pressure changes over time, how well participants stick with wearing them, and whether the garments help them identify shapes and textures by touch.

What this could mean

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

Active substance
compression garments with varying circumferential reduction and layering
What this could lead to
If one garment design works best, it could point toward a simple, low-cost way to improve hand sensation and recovery after stroke.
What could go wrong
This is a small, early-stage trial with only 33 participants, so results may not apply to all stroke survivors. Garments may cause discomfort or skin issues.

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 33 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

Mar 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

21 to 60 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: * adults aged between 21 years to 60 years old * a history of stroke (no restrictions on the stroke type) * Modified Ashworth Scale of 1, 1+ or 2 when hand performing flexion and extension * no cognitive impairment (Montreal Cognitive Assessment (MoCA ⩾ 21) Exclusion Criteria: * skin lesions, infections or other skin problems * serious circulatory problems such as deep vein thrombosis * hypersensitive to Lycra materials * behavioural disturbances or motor impairments caused by other orthopaedic or neurological conditions other than stroke

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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  1. The official record

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