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Liuzijue Qigong vs. traditional breathing training for patients with post-stroke dysarthria complicated with abnormal respiratory control

Liuzijue Qigong vs. traditional breathing training for patients with post-stroke dysarthria complicated with abnormal respiratory control

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010215
Enrollment
Unknown
Registered
2016-12-21
Start date
2017-01-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

dysarthria

Interventions

control group:traditional breathing training combined with basic articulation training
study group:Liuzijue qigong combined with basic articulation training

Sponsors

Central Hospital of Shanghai Xuhui
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) meet the diagnostic criteria of cerebral infarction or hemorrhage; 2) meet the traditional Chinese medicine (TCM) diagnostic criteria of apoplexy; 3) had the first brain stroke with dysarthria; 4) was diagnosed with a < 27 score of FDS and dysarthria combined with = b scale of pulmonary function during speech according to the FDA criteria (revised by the Rehabilitation Center of Hebei Provincial Peoples Hospital; 5) in a phase 2 weeks to 6 months after stroke; 6) have enough physical strength to complete 40-minute speech training; 7) have a sitting balance ranking =3; 8) have at least normal unilateral upper-limb movement function or = Brunnstrom stage 4; 9) have normal and stable vital signs and 10) have willingness and ability to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1) unconsciousness and severe cognitive impairment; 2) combined with aphasia; 3) incapable of completing 40-minute speech breathing training; 4) complicated with acute disease in major organs such as heart, brain and kidney; 5) serious psychological disorders.

Design outcomes

Primary

MeasureTime frame
the speech breathing level assessed by the modified FDA ;

Secondary

MeasureTime frame
the comprehensive evaluation of dysarthria using modified FDA;Maximum counting ability;S/Z Ratio;Loudness rating scale;MPT(%);

Countries

China

Contacts

Public Contactzhang Ying

Central Hospital of Shanghai Xuhui

2397538826@qq.com+86 18918520980

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 6, 2026