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A randomized controlled parallel trial of computer-assisted software based on different cognitive flexibility task paradigms for the treatment of ADHD in children

A randomized controlled parallel trial of computer-assisted software based on different cognitive flexibility task paradigms for the treatment of ADHD in children

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055511
Enrollment
Unknown
Registered
2022-01-11
Start date
2022-01-11
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Attention-deficit hyperactivity disorder

Interventions

Computer software intervention group1:Cognitive flexibility training of computer software
Computer software intervention group2:Cognitive flexibility training of computer software

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for ADHD in DSM-IV confirmed by a psychiatrist above the attending physician; 2. No gender restriction; 3. Aged 6 to 12 years; 4. Right-handedness; 5. Chinese children - Wechsler Intelligence quotient (IQ) >= 70; 6. Subjests whose parents are willing to participate in the treatment as required.

Exclusion criteria

Exclusion criteria: 1. Conduct disorder, various anxiety, mood disorders, tic disorders, etc. in patients with ADHD comorbidities; 2. Children with schizophrenia, affective disorders, mental retardation, autism, epilepsy, etc. and other organic diseases of the nervous system; 3. Children with hearing or obvious visual impairment; 4. Children currently participating in other non-drug treatments. 5. Children has taken central stimulant such as Ritalin, etc. 6. History of severe, coma-inducing traumatic brain injury. 7. Children with neurological disease or other serious physical disease.

Design outcomes

Primary

MeasureTime frame
Treatment effect;Social Function;Cognitive function;

Secondary

MeasureTime frame
Cognitive flexibility;Alert level;Personality characteristics;Basic demographic data Questionaire;Response inhibition;Adverse event;

Countries

China

Contacts

Public ContactFang Jianqun

Ningxia Medical University

fjq-7887@163.com+86 951 6743759

Outcome results

None listed

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