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A Study on the Intervention Efficacy and Neural Mechanisms of Transcranial Magnetic Stimulation in Children with Developmental Coordination Disorder

A Study on the Intervention Efficacy and Neural Mechanisms of Transcranial Magnetic Stimulation in Children with Developmental Coordination Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600130203
Enrollment
Unknown
Registered
2026-08-17
Start date
2026-08-19
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Developmental Coordination Disorder

Interventions

Sponsors

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: Healthy Children: 1. Age 3-12 years old (inclusive), any gender; 2. Right-handed (confirmed by a simplified handedness questionnaire); 3. DCDQ score > 57 (or above the 15th percentile for age norms); 4. MABC-2 total score above the 15th percentile; 5. SDQ score =8 years old) gives verbal consent; 9. Able to cooperate and complete an MRI scan (lying still for about 25-30 minutes). Children with DCD: 1. Age 3-12 years old (inclusive), any gender; 2. Right-handed (confirmed by a simplified handedness questionnaire); 3. DCDQ score = 17; 6. CBCL T-score >= 70; 7. CSHQ-CH-R >= 44; 8. Guardian signs the informed consent form, child (>=8 years old) gives verbal consent; 9. Able to cooperate and complete an MRI scan (lying still for about 25-30 minutes).

Exclusion criteria

Exclusion criteria: 1. History of epilepsy, or a first-degree relative with idiopathic epilepsy; 2. Abnormal electroencephalography (EEG) findings; 3. Presence of intracranial or intraocular metal implants; 4. Intracranial structural abnormalities; 5. Wearing non-removable metal dental braces; 6. Currently taking medications that lower the seizure threshold; 7. History of head trauma with loss of consciousness > 5 minutes; 8. Prior history of intracranial surgery; 9. Presence of non-removable metal objects in the body; 10. History of claustrophobia; 11. Unable to remain still during MRI scanning; 12. Requiring sedation to complete MRI; 13. Diagnosed neurological disorders (e.g., cerebral palsy, epilepsy, muscular dystrophy, intellectual disability, etc.); 14. Severe uncorrected visual or auditory impairments; 15. Currently receiving other interventional treatments (e.g., physical/occupational therapy, transcranial electrical stimulation, etc.); 16. Participation in another clinical trial within 3 months prior to enrollment; 17. Judged by the investigator to be unable to comply with the study procedures.

Design outcomes

Primary

MeasureTime frame
Movement Assessment Battery for Children - Second Edition Score;

Secondary

MeasureTime frame
Resting-state fMRI functional connectivity;DCDQ score;Sleep efficiency;Motor Fluency;Child Behavior Checklist score;SDQ score;3D T1 structural brain region volume;Children's Sleep Habits Questionnaire – Chinese Revised Version score;The rate of glucose and oxygen consumption by the brain;Postural Stability;Distribution and concentration of neurotransmitters such as glutamate and GABA;

Countries

China

Contacts

Public ContactWang Guanghai

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine

wang-guanghai@163.com+86 21 3808 7422

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026