The Construction and Application Study of Salivary Intervention Plan Based on Symptom Management Theory for Parkinson's Disease Patients

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500096034

Enrollment

Unknown

Registered

2025-01-16

Start date

2025-01-23

Completion date

Unknown

Last updated

2025-01-27

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

Conditions

Parkinson's disease

Interventions

control group:Parkinson's disease patients in control group received standardized anti-Parkinson's drug treatment, oral rehabilitation training, psychological nursing, health education and other non-d

experimental group:On the basis of receiving standardized anti-Parkinson's disease drug treatment, the experimental group implemented an intervention program for salivation symptoms of Parkinson's dis

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) According to the 2016 edition of "Diagnostic Criteria for Parkinson's Disease in China", the clinician diagnosed Parkinson's disease; (2) Unified Parkinson's Disease Rating Scale (UPDRS), Part II (UPDRS-II) item 6, score >=1 indicates the presence of salivation; (3) Informed consent and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: (1) Patients with secondary PD or PD plus syndrome; (2) Patients with severe cognitive impairment, mental illness, and severe visual or hearing impairment.

Design outcomes

Primary

Measure	Time frame
swallowing function;Salivation severity;	—

Secondary

Measure	Time frame
self-management;living quality;	—

Countries

China

Contacts

Public ContactHeng Liu

Qingdao University

liuheng516@163.com+86 150 2006 7060

Outcome results

None listed

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