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Study on the efficacy and mechanism of transcranial temporal interference electrical stimulation on motor function in children with dyskinetic cerebral palsy

Study on the efficacy and mechanism of transcranial temporal interference electrical stimulation on motor function in children with dyskinetic cerebral palsy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090107
Enrollment
Unknown
Registered
2024-09-24
Start date
2024-10-10
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Cerebral palsy

Interventions

1 group (sham stimulation group):1 group (sham stimulation group) selected pseudo-stimulation, and the treatment frequency was 20 min/time/side, 1 time/side/day, and the washout time was 20 min, 5 day
2 group (GPi target):MRI imaging and simulation algorithm were used to locate the medial target of the GPi. The product conducts multiple high-frequency sinusoidal pulse currents (2.00kHz and 2.01kHz)
3 groups (putamen targets):MRI imaging and simulation algorithm were used to locate the medial target of the putamen.The product conducts multiple high-frequency sinusoidal pulse currents (2.00kHz and

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: ? Meet the diagnosis of DCP, age between 2-12 years old, regardless of gender; ? Family members understand the purpose and procedures of this study, can comply with the requirements of the study protocol and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? Those with a history of epileptic seizures or previous epileptic convulsions; ? Those with skull defects, malignant tumors, etc.; ? Those with other neurological diseases that can cause dystonia; ? Those with metal implants in the body such as cochlear implants, pacemakers, medical pumps, etc.; ? Those who have received botulinum toxin injection treatment within the past 6 months (=180 days); ? Those who have used drugs to control muscle tension or have undergone surgical procedures including selective posterior rhizotomy and Achilles tendon lengthening in the past; ? Those who are considered by the researchers to be unsuitable for participation in this study due to other factors.

Design outcomes

Primary

MeasureTime frame
Gross Motor Function Measure;Fine Motor Function Measure;

Secondary

MeasureTime frame
Pediatric Balance Scale;Wee function independent measurement;Gait analysis;Electroencephalogram;MRRI"Magnetic Resonance Imaging;

Countries

China

Contacts

Public ContactDengna Zhu

The Third Affiliated Hospital of Zhengzhou University

zhudengna@126.com+86 138 3814 1626

Outcome results

None listed

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