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Effects of mild brain stimulation in children with attention deficit hyperactivity disorder (ADHD)

The effect of transcranial direct current stimulation in combination with occupational therapy on attention span, impulsivity and symptom severity in children with attention deficit hyperactivity disorder

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614001331628
Enrollment
20
Registered
2014-12-18
Start date
2015-01-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Applying a mild electrical current to the head is known to improve brain functions related to attention and learning without causing significant adverse side effects other than a mild local skin irritation at the stimulation site. The current study investigates stimulation effects whilst children - diagnosed with mild to moderate attention deficit hyperactivity disorder - undergo their regular occupational therapy.

Interventions

The study will investigate the effect of 20 min of 2mA anodal transcranial direct current stimulation (tDCS) in combination with 45 min of standard occupational therapy in 20 children diagnosed with mild to moderate attention deficit hyperactivity disorder. Children will undergo 10 weekly consecutive sessions of their standard occupational therapy of which 5 consecutive sessions of active and 5 consecutive sessions of sham tDCS will be randomly assigned by employing a double-blind cross-over des

The study will investigate the effect of 20 min of 2mA anodal transcranial direct current stimulation (tDCS) in combination with 45 min of standard occupational therapy in 20 children diagnosed with mild to moderate attention deficit hyperactivity disorder. Children will undergo 10 weekly consecutive sessions of their standard occupational therapy of which 5 consecutive sessions of active and 5 consecutive sessions of sham tDCS will be randomly assigned by employing a double-blind cross-over design. The standard occupational therapy will be administered by an occupation therapist while the tDCS will be performed by qualified research staff.

Sponsors

University of Newcastle
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

First contact patients meeting the DSM-V criteria for mild to moderate Attention Deficit Hyperactivity Disorder

Exclusion criteria

Taking psychotropic medication, history of seizures

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026