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he effect and mechanism of iTBS on non-motor symptoms in Parkinson's disease: an fNIRS study

The effect and mechanism of iTBS on non-motor symptoms in Parkinson's disease: an fNIRS study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095922
Enrollment
Unknown
Registered
2025-01-15
Start date
2025-02-01
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

Non motor symptoms including depression and cognitive impairment in Parkinson' s disease

Interventions

Real-iTBS group:intermittent theta-burst stimulation (iTBS)

Sponsors

Xi'an Jiaotong University Second Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patients with Parkinson's disease (PD) who have been diagnosed according to the PD diagnostic criteria established by MDS in 2018, with Hoehn and Yahr (H-Y) stage 2-4 and aged 18-85 years; 2.Have good cooperation and demonstrate a certain level of compliance; 3.With normal vision, hearing, and language comprehension and expression abilities; 4.PD patients included in the experiment are receiving standard anti-Parkinson's medication treatment; 5.Commit to adhering to the research procedures, cooperating throughout the entire research process, and are willing to sign the informed consent form for the study.

Exclusion criteria

Exclusion criteria: 1.Patients with severe cognitive or emotional disorders that prevent them from completing the experiment; 2.Patients with other organic lesions in the central nervous system, such as cerebrovascular diseases, encephalitis, tumors, or a history of severe epilepsy; 3.Patients with other diseases that affect cognitive function, such as Parkinsonism; 4.Patients with a history of other mental illnesses or a family history of mental illnesses, such as schizophrenia, bipolar disorder, or autism; 5.Patients with metal objects in the head, such as cerebrovascular stents, cochlear implants, or other metallic implants; 6.Patients with cardiac pacemakers, heart stents, etc; 7.Patients with severe visual or hearing impairments; 8.Patients who are currently participating in another clinical trial; 9.Patients for whom the researcher deems there may be any conditions that could harm the subject or render them unable to meet or perform the requirements of the study;

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Rating Scale-17 score;

Secondary

MeasureTime frame
The Montreal Cognitive Assessment score;The number of words during Verbal Fluency Task;Boston Naming Test score;Animal Verbal Fluency Test score;Parameters of Oxyhemoglobin;Functional Connectivity;The shortest path length;Clustering coefficient;Small-Worldness s;modularity statistic;Global Efficiency;Local Efficiency;Trail Making Test-A/B score;Clock Drawing Test score;Parkinson’s Disease Questionnaire-39 score;Latency of Event-Related Potentials P300;Hamilton Anxiety Scale score;Auditory Verbal Learning Test score;

Countries

China

Contacts

Public Contactlibo li

Xi'an Jiaotong University Second Affiliated Hospital

liboli@xjtu.edu.cn+86 15339099431

Outcome results

None listed

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