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A Comparative Study on the Efficacy of Cross-Resistance Training for Respiratory Function in Patients with Severe Stroke Complicated by Tracheotomy

A Comparative Study on the Efficacy of Cross-Resistance Training for Respiratory Function in Patients with Severe Stroke Complicated by Tracheotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126506
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Stroke

Interventions

Experimental group:Combined cross-resistance training
Contral group:Regulate rehabilitation training

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with cerebral infarction or intracerebral hemorrhage in accordance with the 2019 Chinese Diagnostic Criteria for Major Cerebrovascular Diseases , confirmed by cranial CT or MRI; first-ever onset with disease duration = 3 months. 2.Underwent tracheotomy with a plastic tracheostomy tube in place; 3.Aged 18–75 years with stable vital signs; 4.Fully conscious without significant cognitive dysfunction; Mini-Mental State Examination (MMSE) score = 24; 5.Unilateral limb dysfunction with Brunnstrom stage I–II; 6.The patients and their families were fully informed of the study protocol, volunteered to participate, and signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Patients with post-stroke disturbance of consciousness, hearing impairment, cognitive dysfunction or other conditions leading to poor cooperation; 2.Patients with a history of spinal cord lesions, neurological disorders, vestibular or cerebellar lesions; 3.Patients with bilateral limb dysfunction; 4.Patients with severe cardiopulmonary diseases who cannot tolerate training or complete pulmonary function tests; 5.Patients with severely limited joint motion, intractable pain, severe osteoporosis, severe traumatic diseases or other conditions interfering with exercise training;

Design outcomes

Primary

MeasureTime frame
Diaphragm thickness(DT) and Diaphragm thickening fraction(DTF);

Secondary

MeasureTime frame
Physical function assessment, including muscle strength(MMT), Brunnstrom stage and modified Barthel Index.;Pulmonary function tests including maximal inspiratory pressure (MIP), maximal expiratory pressure (MEP), forced expiratory volume in one second (FEV?) and forced vital capacity (FVC).;

Countries

China

Contacts

Public ContactSu Guodong

Beijing Bo'ai Hospital

13911289198@163.com+86 10 87569510

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026