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Clinical study of the efficacy of nurse-led stepped swallowing function training on dysphagia in patients with Parkinson's disease

Clinical study of the efficacy of nurse-led stepped swallowing function training on dysphagia in patients with Parkinson's disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102605
Enrollment
Unknown
Registered
2025-05-16
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Parkinson's disease

Interventions

Stepped Swallowing Function Training Group:Stepped Swallowing Function Training
Routine swallowing instruction group:Routine swallowing instruction

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Stable condition and diagnosis of Parkinson's disease by the attending physician with reference to the 2016 updated Diagnostic Criteria for Parkinson's Disease in China (2016 edition); (2) Puddle Field Drinking Water Test level 3 or higher; (3) Basic communication and cooperation ability to complete the assessment; (4) Patients and their immediate family members voluntarily participated in the study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Diagnosis of non-Parkinson's disease such as secondary Parkinson's syndrome and Parkinson's superimposed syndrome; (2) Previous or existing other diseases that can lead to dysphagia, such as stroke, esophageal tumors, and postoperative radiotherapy, myasthenia gravis, and other diseases; (3) Accompanied by obvious cognitive disorders, psychiatric disorders, and aphasia that cannot be cooperated with; (4) Combined with severe cardio-pulmonary, hepatic, and renal dysfunctions, and accompanied by pulmonary infections (5) patients with oral delivery time >60s; (6) those who have participated in other clinical trials at the same time or within 3 months.

Design outcomes

Primary

MeasureTime frame
Improvement in swallowing function;

Secondary

MeasureTime frame
Nutritional status;Caregiver burden;Activities of daily living;

Countries

China

Contacts

Public ContactLiang Yan

West China Hospital of Sichuan University

179050526@qq.com+86 189 8060 6113

Outcome results

None listed

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