Clinical Study of Percutaneous Acupoint Electrical Stimulation in Children with Intellectual Disability Based on Electro - optic Biofeedback Technique

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2200005828

Enrollment

Unknown

Registered

2022-04-08

Start date

2021-01-01

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Intellectual Disability

Interventions

The treatment group:Retain the original routine rehabilitation + Percutaneous Acupoint Electrical Stimulation

The control group:Retain the original routine rehabilitation

Eligibility

Sex/Gender

All

Age

3 Years to 9 Years

Inclusion criteria

Inclusion criteria: ?Meeting the above diagnostic criteria ;? Age l-6 years old, gender unlimited ;? Children and guardians were informed of the test methods and contents and signed informed consent.

Exclusion criteria

Exclusion criteria: ?Patients with mental illness and severe epilepsy.?Patients with large area lesions by CT scan. ?Patients with hereditary metabolic diseases such as endoketonuria and congenital hydrocephalus of congenital Keting disease can be cured by modern medicine through etiological treatment.? patients with eye diseases ; ?Individuals who were in line with disease diagnosis but without obvious cognitive impairment.

Design outcomes

Primary

Measure	Time frame
modified social adaptation scale for infants-junior middle school students;gesell developmental schedules;goal attainment scaling;	—

Countries

China

Contacts

Public ContactDong Lin

bluelike1@sina.com13860625772

Outcome results

None listed

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