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AI app aims to boost arm recovery after stroke

NCT ID NCT06190795

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested a new AI-powered smartphone app designed to help people who recently had a stroke improve arm function through guided exercises at home. Researchers compared the app to a standard paper manual in 38 participants over four weeks. The goal was to see if the app was easy to use and improved arm recovery and exercise adherence.

What this could mean

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

Active substance
AMPLIFY Smartphone Application
What this could lead to
If it works, this could offer a convenient, AI-guided way for stroke survivors to improve arm function at home without frequent clinic visits.
What could go wrong
This is a small, early feasibility study with only 38 participants. The app may not prove more effective than a simple paper manual, and results may not apply to all stroke survivors.

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

38 people

The number who actually took part.

Started

Mar 2024

Finished

Mar 2025

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 90 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: * Diagnosis of stroke (confirmed by CT/MRI scans) * ≤four weeks post-stroke * Montreal Cognitive Assessment (MOCA)\>=21 * Finger extension Medical Research Council (MRC) \>=1 * Fugl Meyer Upper Limb score \<60 or NIHSS Motor Arm section score\>=2 * Potential discharge to home (able to do tele-rehabilitation for review) Exclusion Criteria: * Bilateral stroke * Montreal Cognitive Assessment (MOCA)\<21 * Paretic upper limb numeric pain rating scale (NPRS)\>5 * Reduced paretic upper limb use prior to stroke episode (e.g. frozen shoulder, fracture, etc) * Reduced paretic upper limb use due to orthopaedic problems such as fracture in existing stroke episode * Medically unstable * Neglect as ascertained by treatment team * Severe behavioural disturbance or agitation or epilepsy or untreated depression or psychiatric conditions * Pregnancy or lactation states

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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.

Contacts and locations

Locations

  • Lay Fong Chin

    Singapore, Singapore, 307382, Singapore

More trials for these conditions

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