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Observation on the Efficacy of Respiratory Exercise Training in Stroke-Associated Sarcopenia

Observation on the Efficacy of Respiratory Exercise Training in Stroke-Associated Sarcopenia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111452
Enrollment
Unknown
Registered
2025-10-31
Start date
2022-07-30
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Post-stroke Sarcopenia

Interventions

Observation group:Breathing exercise training and Routine rehabilitation training
Control group:Routine rehabilitation training

Sponsors

Jiangbin Hospital of Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis is made by experienced clinicians based on medical history and auxiliary examinations, following the sarcopenia diagnosis process in large general hospitals or specialized hospitals and the stroke diagnosis criteria, in accordance with the "Expert Consensus on the Diagnosis and Treatment of Sarcopenia in Elderly Chinese People (2021)"; 2. Disease course of 14 days to 6 months, aged 18-80 years, in generally good condition, conscious, without hearing or comprehension impairment. 3. Able to independently cooperate with rehabilitation training.

Exclusion criteria

Exclusion criteria: 1. Does not meet the diagnostic criteria; prior to this stroke, the self-screening SARC-F score was >=4 points; 2. The patient has unstable vital signs, suffers from severe underlying diseases, has dysfunction or failure of major organs such as the heart, lungs, liver, or kidneys, and cannot cooperate with related rehabilitation training; 3. There are contraindications for body composition analysis, such as having metal or electronic devices on the body: cochlear implants, cardiac pacemakers, medical pumps, fixed steel pins, etc.; or being unable to complete the examination independently.

Design outcomes

Primary

MeasureTime frame
Modified Barthel Index;Appendicular skeletal muscle mass;Calf circumference measurement;Grip strength measurement;

Secondary

MeasureTime frame
Fugl-Meyer assessment;

Countries

China

Contacts

Public ContactZhou Muhua

Jiangbin Hospital of Guangxi Zhuang Autonomous Region

1009766256@qq.com+86 157 7811 7017

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 25, 2026