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Study on the effect of remote breathing training on respiratory function in acute stroke survivors

Study on the effect of remote breathing training on respiratory function in acute stroke survivors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088647
Enrollment
Unknown
Registered
2024-08-22
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

experimental group:Conventional physiotherapy+Breathing training based on Telerehabilitation App

Sponsors

Sichuan Mianyang 404 Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnostic criteria for stroke established by the Fourth Academic Conference on Cerebrovascular Disease and confirmed by cranial CT or MRI; 2. Within 2 weeks of onset, aged 18-80 years old, currently in stable condition; 3. Mini-Mental State Examination (MMSE) =27 points; 4. Presence of reduced respiratory function, with a Maximal Inspiratory Pressure(MIP) of <80 cmH2O or a Maximal Expiratory Pressure (MEP)of <90 cmH2O; 5. Have an Internet mobile terminal capable of logging in to the tele-rehabilitation App; 6. Participate in the study voluntarily, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment (MMSE assessment score of stroke patients, illiteracy <17 points, primary education <20 points, junior high school and above <24 points) or mental illness and other reasons can not understand the instructions of the researcher, unable to cooperate with the research subjects; 2. the existence of other diseases that may interfere with the respiratory function of the rehabilitation training, surgical and traumatic injury history, such as severe lung infection, tracheotomy intubation, myasthenia gravis phrenic nerve paralysis, facial paralysis, abnormalities of oropharyngeal structure, and history of thoracic and abdominal surgery and rib fracture within the last one year; 3. Patients with unstable vital signs and/or with serious complications, such as serious heart, liver, kidney, lung and other organ diseases and history of malignant diseases; 4. Refusal or termination of this study.

Design outcomes

Primary

MeasureTime frame
Maximal Inspiratory Pressure;Maximal Expiratory Pressure;Forced Vital Capacity;Forced expiratory volume in one second;Peak expiratory flow;The Borg Rating of Perceived Exertion(RPE)Category Ratio CR-10 Scale;Activity of daily living ;

Secondary

MeasureTime frame
Balance;Trunk function;Posture control ability;Rivermead mobility;

Countries

China

Contacts

Public ContactMa Zongke

Sichuan Mianyang 404 Hospital

Horusmzk@126.com+86 199 8173 7818

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026