Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Home-based brain stimulation for treating ADHD

Official title: Home-based Transcranial Direct Current Stimulation (tDCS) for Treatment of Attention-deficit/Hyperactivity Disorder (ADHD)

Run by Massachusetts General Hospital · NCT05354232 · Data updated 2026-11-12

This study tests whether a home-based brain stimulation treatment can help people with ADHD feel better and improve their focus over four weeks.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment60 (estimated)
SponsorMassachusetts General Hospital
Academic / other
Locations1 site (Charlestown, Massachusetts)
StatusRecruiting
StartedJuly 1, 2022
Main results expectedMay 2026
Study endsMay 2026
Registry record updatedDecember 12, 2025
Trial IDNCT05354232 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are outpatients aged 18-65 with a diagnosis of ADD/ADHD.

Probably not a fit

Patients with contraindications to tDCS, severe psychiatric disorders, or significant neurological conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of home-based transcranial direct current stimulation (tDCS) over four weeks to improve symptoms of ADHD and cognitive control. It aims to determine the relationship between tDCS dosage and therapeutic outcomes, while also assessing the feasibility and acceptability of this home-based approach. By eliminating the need for daily hospital visits, the study seeks to enhance access to advanced treatment options for a broader population of ADHD patients.

Why it matters

Potential benefit: If successful, this approach could provide a convenient and effective treatment option for individuals with ADHD, improving their daily functioning and quality of life.

How similar studies have gone: While this approach is novel in the context of home-based tDCS for ADHD, similar neuromodulation techniques have shown promise in other studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male and female outpatients 18-65 years of age
2. A diagnosis of ADD/ADHD or meeting the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria.

Exclusion Criteria:

1. Contraindication to tDCS: history or epilepsy, metallic implants in the head and neck, brain stimulators, vagus nerve stimulators, VP shunt, pacemakers, pregnancy.
2. Active substance dependence (except for tobacco).
3. Pregnant or nursing females.
4. Inability to participate in testing procedures.
5. Premorbid neurological conditions (including neurovascular and neurodegenerative diseases such as traumatic brain injury, stroke, Parkinson's, AD and other dementias) and severe psychiatric disorders (bipolar disorder, schizophrenia).

Where it's running

  • Massachusetts General Hospital
    Charlestown, Massachusetts, United States
    Recruiting

Study contacts

  • Principal investigator: Joan Camprodon, MD, PHD, MPH — MGB: Division of Neuropsychiatry and Neuromodulation
  • Study coordinator: DNN Inbox
  • Email: mghdnn@mgh.harvard.edu
  • Phone: 6177265348

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.