Skip to content

Study on the Safety and Efficacy of Brain-Computer Interface Combined with Functional Electrical Stimulation in the Treatment of Parkinson's Disease

Study on the Safety and Efficacy of Brain-Computer Interface Combined with Functional Electrical Stimulation in the Treatment of Parkinson's Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124148
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-12
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Parkinson's disease

Interventions

Treatment group:Brain-computer interface training equipment (LSR-A? BCI Rehabilitation Training System) combined with functional electrical stimulation therapy: 20 min/day for the upper extremities an
Control group:Functional electrical stimulation therapy: 20 min/day for the upper extremities and 20 min/day for the lower extremities, for a total of 12 treatment days within two weeks.

Sponsors

Binzhou Medical University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 40–80 years, male or female; 2.Meet the diagnostic criteria for Parkinson’s disease formulated by the United Kingdom Parkinson’s Disease Society Brain Bank and the Movement Disorder Society (MDS) in 2015; 3.Have received stable doses of levodopa and benserazide tablets, dopamine receptor agonists, or monoamine oxidase type B inhibitors for one month prior to study enrollment; 4.Subjects and their family members understand the clinical trial protocol, volunteer to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Various secondary Parkinsonian syndromes, Parkinson-plus syndromes, and other non-primary Parkinson's disease (PD); 2.Presence of intracranial metal implants, cardiac pacemakers, or incomplete skull; 3.Skin lesions, damage, infection at the electrode contact sites, or allergies to electrodes; 4.History of stroke or thrombosis within one year; 5.Severe cognitive impairment or comorbidity with other serious mental disorders, resulting in inability to comply with the study protocol; 6.Other conditions deemed inappropriate for enrollment by the researchers.

Design outcomes

Primary

MeasureTime frame
mds unified-parkinson disease rating scale-?;

Secondary

MeasureTime frame
Fractional Anisotropy,Mean Diffusivity;Glutamate;Diffusion Tensor Imaging Analysis along the Perivascular Space; Amplitude of Low-Frequency Fluctuation, Regional Homogeneity;The Non-Motor Symptoms Scale for Parkinson’s Disease;Pittsburgh Sleep Quality Index score;Hoehn-Yahr;Montreal Cognitive Assessment score;Parkinson's Disease Questionnaire-39;Parkinson's Disease Sleep Scale-2 score;Hamilton Anxiety Rating Scale score;Hamilton Depression Rating Scale-17 score;Fatigue Scale-14 score;Autonomic Nervous System Symptom Self-Rating Scale score;Patient Assessment of Constipation-Symptoms score;

Countries

China

Contacts

Public ContactHongcai Wang

Binzhou Medical University Hospital

whc2891@126.com+86 139 5433 5445

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026