Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04012853 · ClinicalTrials.gov registry record · NA

Remotely Supervised tDCS for Persistent Post-traumatic Headache

A NA study, sponsored by VA Office of Research and Development.

Completed
Registry status
NA
Development phase
26
Enrollment target

NCT04012853: Completed NA study, sponsored by VA Office of Research and Development.

NCT04012853 is a NA study that has completed, run by VA Office of Research and Development. The registered enrollment target is 26 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT04012853, a NA study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
NA
Development phase
26 participants
Enrollment target

Study Summary

This pilot study is designed to provide preliminary data for a large scale, randomized clinical trial to evaluate the efficacy of remotely administrated at home transcranial Direct Current Stimulation (tDCS) with real-time monitoring via VA Tele-health for persistent post traumatic headache associated with mild traumatic brain injury (mTBI). Participants will receive total of 20 sessions of tDCS over four weeks. The investigators anticipate that the results generated from the study will directly translate into immediate meaningful clinical application: not only in management of chronic post traumatic headache, but also in reduction of acute pain medication use, and improving quality of life for our veterans with this debilitating neurological disorder.

Primary Outcome

To evaluate the improvement in numbers of moderate to severe headache days per month from baseline period to end of treatment phase, and to the end of follow-up phase

Interventions

  • DEVICE transcranial direct current stimulation

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2019-11-04
Est. Completion 2022-03-31
Phase NA
VA Office of Research and Development

1,668 total trials

What the finished NCT04012853 record still lists

NCT04012853 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which transcranial direct current stimulation is the first listed.

NCT04012853 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04012853 about?

NCT04012853 is a clinical study titled "Remotely Supervised tDCS for Persistent Post-traumatic Headache". This pilot study is designed to provide preliminary data for a large scale, randomized clinical trial to evaluate the efficacy of remotely administrated at home transcranial Direct Current Stimulation (tDCS) with real-time monitoring via VA Tele-health for persistent post traumatic headache associat...

What is the current status of trial NCT04012853?

This trial is currently completed. It is a NA study. The enrollment target is 26 participants. The study started on 2019-11-04. Estimated completion is 2022-03-31.

What interventions are being tested in trial NCT04012853?

The interventions under investigation include: transcranial direct current stimulation (DEVICE).

Who is sponsoring clinical trial NCT04012853?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04012853's enrollment target sits among peer trials

26 1710th of 2000 higher than 289 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02646475 · 26 participants · Phase 1

    Metabolic Effects of Angiotensin-(1-7)

  • NCT03603223 · 26 participants · Phase 2

    Pembrolizumab in Treating Participants With Leukoplakia

  • NCT04063592 · 26 participants · NA

    AMI Construction in Lower Extremity Residual Limbs

  • NCT04906460 · 26 participants · Phase 1

    Open-label Study of WVE-N531 in Patients With Duchenne Muscular Dystrophy (FORWARD-53)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04012853, the US trial registry maintained by the National Library of Medicine. NCT04012853 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.