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Research Plan for Multimodal Intelligent Early Screening of Parkinson's Disease and NIDBS Intervention

Research Plan for Multimodal Intelligent Early Screening of Parkinson's Disease and NIDBS Intervention

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114398
Enrollment
Unknown
Registered
2025-12-11
Start date
2025-12-25
Completion date
Unknown
Last updated
2025-12-15

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(Sham Stimulation Group):Sham stimulation + conventional drug treatment
Electrical stimulation group:Transcranial electrical stimulation + conventional drug therapy

Sponsors

The Third Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. All cases meet the diagnostic criteria for Parkinson's disease (PD) of the UK Brain Bank Parkinson's Disease Society. 2. Aged between 40 and 75. 3. Parkinson's disease patients with Hoehn-Yahr (HY) stage 1 to 2.5, who can walk independently. 4. At the time of the experiment, the subjects had stable condition, clear consciousness, no language communication barriers, and could communicate fluently. 5. Before the start of the study, they received a stable dose of anti-Parkinson's medication for at least 2 weeks and maintained this dose during the treatment period. 6. No transcranial electrical stimulation (tDCS, tACS) was used within 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of stroke, head trauma, hydrocephalus, brain tumor, increased intracranial pressure, and intracranial surgery; 2. Patients with metal foreign bodies, pacemakers, heart stents, cochlear implants, etc. in their bodies; 3. Those who cannot cooperate with the rs-fMRI scan and the exercise intervention program; 4. Patients with alcohol dependence or central nervous system drug dependence; 5. Patients with alcohol dependence or central nervous system drug dependence.

Design outcomes

Primary

MeasureTime frame
Unified Parkinson's disease rating scale III, UPDRS III;electroencephalogram signal;Olfactory detection results;

Secondary

MeasureTime frame
Magnetic resonance data;Hamilton Anxiety;Electromyographic signal;Gait parameter;Hamilton Depression;King Parkinson's Pain Scale, KPPS;Pittsburgh Sleep Quality Index, PSQI;Parkinson's Disease Sleep Scale-2, PDSS-2;Scales for Outcomes in Parkinson’s Disease-Autonomic Dysfunction, SCOPA-AUT;

Countries

China

Contacts

Public ContactHongxia Xin

The Third Affiliated Hospital of Xinxiang Medical University

xhxwh02@163.com+86 135 9871 6007

Outcome results

None listed

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