An Intervention Study on Transcranial Photobiomodulation in Children With Attention Deficit Hyperactivity Disorder
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: tPBM（active）, tPBM（sham）.
- Who it may be relevant to
- Registry conditions: ADHD - Attention Deficit Disorder With Hyperactivity. Basic parameters: 6 years — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
An Intervention Study on Transcranial Photobiomodulation for Children With Attention-Deficit/Hyperactivity Disorder
Overview
This study aims to intervene in children and adolescents with ADHD using transcranial photobiomodulation, comparing its effects on executive function at the levels of electroencephalography (EEG), eye tracking, and cognitive behavior. The goal is to identify the most effective clinical treatment strategy for ADHD patients.
Detailed description
This study is conducted as a randomized triple-blind trial to investigate the effects of photobiomodulation therapy on ADHD. Initially, standardized assessment tools (physician ratings and parent self-reports) are employed to evaluate baseline clinical symptoms in ADHD patients who meet the inclusion and exclusion criteria. The experiment utilizes a within-subject design (within-subject factors: active versus sham stimulation), with each participant randomly assigned to receive two interventions-one active and one sham stimulation-administered in a counterbalanced order, with at least a one-week interval between the two sessions. Immediately following the intervention, standardized assessment tools are used to evaluate multidimensional clinical symptoms, and data related to executive function, including cognitive behavioral data, electroencephalographic data, and eye-tracking data, are collected. The intervention is carried out by trained technicians in accordance with the randomization results, while maintaining blinding for both clinical evaluators and participants.
Interventions
- Device tPBM（active）
During the active stimulation condition, participants will receive a single session of tPBM intervention, lasting 12 minutes. - Device tPBM（sham）
During the sham stimulation condition, participants will receive the same intervention with identical target areas and wavelength, but only for the first and last 30 seconds of the session.
Primary outcome measures
- EEG(Electroencephalogram) [Time frame: From enrollment to the end of treatment at 3 weeks"]
- Executive Function Task [Time frame: From enrollment to the end of treatment at 3 weeks"]
Secondary outcome measures (3)
- Swanson, Nolan, and Pelham Version IV [Time frame: From enrollment to the end of treatment at 3 weeks"]
- Sleep Disturbances Scale for Children [Time frame: From enrollment to the end of treatment at 3 weeks"]
- Behavior Rating Inventory of Executive Function [Time frame: From enrollment to the end of treatment at 3 weeks"]
Eligibility criteria
Inclusion criteria
- Age between 6 and 18 years;
- Clinically diagnosed with ADHD by a psychiatrist;
- Confirmed by the researcher (child psychiatrist) to meet the diagnostic criteria for Attention-Deficit/Hyperactivity Disorder as outlined in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5);
- M.I.N.I. KID interview shows only ADHD, with no other comorbidities;
- Able to cooperate with transcranial photobiomodulation.
- The participant and their guardian fully understand the study procedures and content and agree to participate in the study, signing the informed consent form.
Exclusion criteria
- Diagnosis of other severe mental illnesses, such as schizophrenia or bipolar disorder;
- Presence of severe physical diseases or conditions, such as significant intracranial lesions, thyroid disorders, epilepsy, congenital heart disease, severe hematologic disorders, systemic lupus erythematosus, auditory or visual impairments, etc.;
- Presence of significant structural brain abnormalities on imaging studies;
- Presence of severe neurological diseases with a clear family history or potential risk;
- Presence of metal implants or a pacemaker, or holes or fractures in the skull;
- Currently undergoing other ADHD treatments (e.g., methylphenidate or other pharmacological treatments, behavioral therapy, etc.) or has discontinued such treatments for less than 2 weeks;
- Raven's Progressive Matrices IQ score < 85.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Quadruple blind
- Primary purpose
- Treatment
Study locations
China · 2 centers
- Qilu Hospital of Shandong University — Jinan
- Qilu Hospital of Shandong University — Jinan
Identifiers
NCT: NCT06685601 · QL000005