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Can combined brain and body training speed recovery after a brain bleed?

NCT ID NCT06648187

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This pilot study tested a new rehabilitation approach called early motor-cognitive integrative training (e-MCIT) in 6 patients recovering from a brain aneurysm bleed. The training combines thinking exercises with physical movement in 30-minute sessions, done 4-5 times a week until hospital discharge. The main goal was to see if this approach is feasible and safe, and to gather initial data on thinking and movement skills.

What this could mean

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

Active substance
early motor-cognitive integrative training (e-MCIT)
What this could lead to
If successful, this could lead to a new rehabilitation approach that helps patients recover thinking and movement skills faster after a brain aneurysm bleed.
What could go wrong
This is a very small pilot study with only 6 participants, so results may not apply to everyone. It is designed to test feasibility, not to prove the training works.

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

6 people

The number who actually took part.

Started

Nov 2024

Finished

Dec 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

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: * Diagnosis of spontaneous SAH resulting from aneurysm rupture confirmed by either CT scan or angiography. * Onset of stroke occurring in the acute phase, specifically 2-7 days after medical intervention. * Participants must be over 18 years old. * WFNS: 1-3. * Able to stand without support above 30 seconds. * Montreal Cognitive Assessment (MoCA)\<26. Exclusion Criteria: * unstable vital sign (e.g., heart rate (HR): 40- 100bpm, mean arterial pressure (MAP)\> 80mmHg, respiratory rate (RR): 12-20, oxygen saturation (SpO2) \> 95%, intracranial pressure (ICP) \< 20mmHg and cerebral perfusion pressure (CPP) \> 70mmHg) * patients evaluated as unsuitable by their attending physician * those with other neurological diseases that might interfere with the experiment * with less than 12 years of education

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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

  • School and Graduate Institute of Physical Therapy, College of Medicine, National Taiwan University

    Taipei, 100, Taiwan

More trials for these conditions

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