Home-based Transcranial Direct Current Stimulation (tDCS) for Treatment of Attention-deficit/Hyperactivity Disorder (ADHD)
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- STATUS
- Recruiting
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- End date
- May 1, 2025
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- participants needed
- 60
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- sponsor
- Massachusetts General Hospital
Summary
The investigators are investigating whether home-based tDCS over the course of four weeks can improve ADHD symptom severity and improve dysexecutive functioning (cognitive control). Further, the investigators are investigating whether there is a dose-dependent response to tDCS.
Description
This mechanistic clinical trial will be the first of its kind to assess the clinical and cognitive efficacy of tDCS, and its relationship to physiological target engagement. It will also provide critical knowledge about tDCS dosing in a therapeutic context (i.e. 30 days of daily tDCS). Last, it will assess the feasibility and acceptability of home-based neuromodulation therapies for ADHD, reducing the most significant obstacle for the implementation of devices therapies (i.e. daily visits to the hospital for several weeks) and facilitating access to advanced therapeutics to a large population of patients with ADHD. An additional goal of the proposed study is to assess the feasibility and acceptability of home-based neuromodulation therapies for ADHD, reducing the most significant obstacle for the implementation of devices therapies (i.e. daily visits to the hospital for several weeks) and facilitating access to advanced therapeutics to a large population of patients with ADHD.
Details
| Condition | Attention Deficit Disorder, Attention Deficit Disorder With Hyperactivity |
|---|---|
| Treatment | sham transcranial direct current stimulation (tDCS), 2 mA transcranial direct current stimulation (tDCS), 1 mA transcranial direct current stimulation (tDCS) |
| Clinical Study Identifier | NCT05354232 |
| Sponsor | Massachusetts General Hospital |
| Last Modified on | 6 April 2023 |
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