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The effect of Baduanjin on motor symptoms and non-motor symptoms of Parkinson's disease

The effect of Baduanjin on motor symptoms and non-motor symptoms of Parkinson's disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069360
Enrollment
Unknown
Registered
2023-03-14
Start date
2023-03-15
Completion date
Unknown
Last updated
2023-05-29

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:Cnventional drugs
Baduanjin group:Conventional drugs and Baduanjin

Sponsors

The Third Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of MDS-UPDRS Parkinson's disease; 2. Parkinson's disease patients with Hoehn-Yahr (HY) grade of 1-2.5 who could walk independently; 3. Sign informed consent; 4. Mini-mental state examination (MMSE) >= 24; 5. To receive a stable dose of anti-Parkinson drugs for at least 2 weeks before the start of the study, and to maintain this dose during treatment; 6. At least 1 year without regular physical exercise (3 months, 3 to 4 times a week, 30 minutes each time is regarded as the minimum standard of regular physical exercise).

Exclusion criteria

Exclusion criteria: 1. Secondary Parkinson's disease syndrome and other superimposed syndromes; 2. Patients with stroke, head trauma, hydrocephalus, brain tumors, increased intracranial pressure and history of intracranial surgery; 3. Patients with metal foreign bodies, cardiac pacemakers, cardiac stents, cochlear implants, etc.; 4. Those who could not cooperate with resting-state functional magnetic resonance scanning and exercise intervention program; 5. Patients with alcohol dependence and central nervous system drug dependence; 6. There were serious organic lesions in heart, liver, kidney and other organs.

Design outcomes

Primary

MeasureTime frame
Unified Parkinson's disease rating scale III, UPDRS III;Berg balance scale, BBS;Parkinson's sleep scale 2, PDSS-2;Interleukin-6, IL-6;Interleukin-1 beta, IL-1ß;

Secondary

MeasureTime frame
Non-motor symptoms scale, NMSS;Minimum mental state examination, MMSE;Montreal cognitive assessment, MoCA;Hamilton depression scale, HAMD;Hamilton anxiety scale, HAMA;King's PD pain scale, KPPS;Pittsburgh sleep quality index, PSQI;The scale for outcomes in PD for au tonomic symptoms, SCOPA-AUT;The 39-Item Parkinson's disease questionnaire, PDQ-39;Olfactory detection results;Gait parameter;Resting-state funetional magnetic resonance imaging;Brain-derived neurotrophic factor, BDNF;5-hydroxytryptamine, 5-HT;Dopamine, DA;

Countries

China

Contacts

Public ContactHongxia Xing

The Third Affiliated Hospital of Xinxiang Medical University

xhxwh02@163.com+86 13598716007

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 24, 2026