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Clinical study on the effect of progressive inspiratory resistance training combined with swallowing exercise on swallowing function patients Parkinson's disease

Clinical study on the effect of progressive inspiratory resistance training combined with swallowing exercise on swallowing function patients Parkinson's disease

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060790
Enrollment
Unknown
Registered
2022-06-11
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Parkinson's disease

Interventions

intervention group:Progressive inspiratory resistance training
control group:Mendelson

Sponsors

Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The diagnostic criteria were in accordance with the 2016 Chinese Parkinson's Disease Guidelines issued by the Chinese Society of Neurology; 2. A certain degree of dysphagia as assessed by the scale (e.g., cough during meals and prolonged eating time); 3. Aged 50-80 years; 4. Hoehn-yahr grading was stage II-IV; 5. MMSE 24 or more; 6. Continued stable medication regimen (dose and drug type) during the study; 7. Patients gave informed consent and voluntarily participated in the study.

Exclusion criteria

Exclusion criteria: 1. Other neurodegenerative diseases or serious cerebrovascular diseases; 2. Severe digestive, respiratory and cardiovascular diseases; 3. Associated with head and neck tumor or nasal septum foreign body; 4. Smoking history in recent 3 years; 5. Compliance difficulties caused by severe mental and psychological diseases; 6. It is difficult to maintain proper oral seal or avoid air leakage in lung function test; 7. Taking other investigational drugs or participating in other clinical trials within 3 months prior to study inclusion; 8. For any reason not suitable for the study or not suitable for inclusion in the study as considered by the researcher.

Design outcomes

Primary

MeasureTime frame
Fiberoptic Endoscopic Evaluation of Swallowing;Water swallow scale;swallowing quality of life questionaire;unified Parkinson disease ration scale;Pulmonary function test;

Secondary

MeasureTime frame
modified water swallow test;Parkinson disease quality;activities of daily living;Mini-mental state Examination;Hamilton Depression Scale;Borg index;10-meter walk test;Tinetti balance and gait analysis;

Countries

China

Contacts

Public ContactLi Qin

Second Affiliated Hospital of Army Medical University

liqin8311@yeah.net+86 13696418919

Outcome results

None listed

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