Breathing new life: could targeted muscle training speed stroke recovery?
NCT ID NCT07770776
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This trial tests whether a high-intensity breathing exercise program, started within days of an acute stroke, can strengthen the muscles used for breathing and speech. Hospitalized stroke patients will be randomly assigned to either this new training or conventional diaphragmatic breathing exercises. Researchers will measure changes in inspiratory and expiratory muscle strength, chest expansion, and breath-holding capacity to see if the new approach offers greater early benefits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- High-intensity interval inspiratory and expiratory muscle training using a breathing device
- What this could lead to
- If effective, this training could become a standard early rehabilitation approach to improve breathing and speech endurance in stroke patients.
- What could go wrong
- This is a small, early-phase trial with only 24 participants, so results may not apply broadly. The training is intense and may be challenging for some patients.
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
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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
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24 people
The number who actually took part.
- Started
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Apr 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Male or female participants aged 18 years or older. * First-ever acute ischemic stroke, with stroke onset 2 to 14 days before enrollment, confirmed by computed tomography (CT) or magnetic resonance imaging (MRI). * National Institutes of Health Stroke Scale (NIHSS) score ≥5, with the presence of hemiparesis. * Baseline maximal inspiratory pressure (MIP) \<80 cmH₂O. * Baseline maximal expiratory pressure (MEP) \<68 cmH₂O. * Able to understand instructions and participate in the respiratory muscle training program. * Willing to comply with the study protocol and provide written informed consent. Exclusion Criteria: * Resting blood pressure \>160/100 mmHg. * Resting peripheral oxygen saturation (SpO₂) \<92%. * Resting heart rate \<40 beats/min or \>110 beats/min. * Fever, defined as body temperature ≥37.5°C. * Previous participation in or experience with a respiratory muscle training program. * Presence of chronic pulmonary disease. * Presence of a tracheostomy tube. * Presence of unstable cardiac disease. * Presence of another neurological disorder associated with respiratory dysfunction. * Presence of an orthopedic or musculoskeletal condition that significantly interferes with respiratory function or the ability to perform respiratory muscle training. * History of major thoracic or abdominal surgery within the previous 3 months.
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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
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Prof. R. D. Kandou General Hospital
Manado, North Sulawesi, Indonesia
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Correlation of visual and motor deficits in stroke patients
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study
- Determination of efficacy of sustained motor contraction generated using StimWave peripheral nerve stimulator
- Glenzocimab in anterior stroke with large ischemic core eligible for endovascular therapy