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

NCT03635775 · ClinicalTrials.gov registry record · NA

Single-session tDCS in Cerebral Palsy

A NA study, sponsored by University of Minnesota.

Completed
Registry status
NA
Development phase
20
Enrollment target

NCT03635775: Completed NA study, sponsored by University of Minnesota.

NCT03635775 is a NA study that has completed, run by University of Minnesota. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03635775, a NA study, has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
NA
Development phase
20 participants
Enrollment target

Study Summary

The goal of this study is to characterize individual responses to a single application of transcranial direct current stimulation (tDCS) in children with unilateral cerebral palsy (UCP), and to test which electrode configuration produces changes in brain excitability and motor function. Participants with UCP, ages 7-21 years, will be assigned to one of four tDCS groups. Using single-pulse transcranial magnetic stimulation, the investigators will assess cortical excitability before and at regular intervals up to 1 hour following tDCS. The knowledge gained from this study will advance the field through more targeted approaches of neuromodulatory techniques in this population and others, using individual characteristics to guide optimal treatment

Primary Outcome

Motor evoked potential is a measure of cortical excitability using transcranial magnetic stimulation. MEP is measured as the amplitude of electrical activity from finger muscles. Outcome is reported as the percent change in MEP amplitude from pre-intervention to immediately post-intervention.

Interventions

  • DEVICE Sham tDCS
  • DEVICE Active tDCS

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-05-01
Est. Completion 2020-02-21
Phase NA
University of Minnesota

966 total trials

What the finished NCT03635775 record still lists

NCT03635775 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Sham tDCS is the first listed.

NCT03635775 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03635775 about?

NCT03635775 is a clinical study titled "Single-session tDCS in Cerebral Palsy". The goal of this study is to characterize individual responses to a single application of transcranial direct current stimulation (tDCS) in children with unilateral cerebral palsy (UCP), and to test which electrode configuration produces changes in brain excitability and motor function. Participants...

What is the current status of trial NCT03635775?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2018-05-01. Estimated completion is 2020-02-21.

What interventions are being tested in trial NCT03635775?

The interventions under investigation include: Sham tDCS (DEVICE), Active tDCS (DEVICE).

Who is sponsoring clinical trial NCT03635775?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03635775's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 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

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

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 NCT03635775, the US trial registry maintained by the National Library of Medicine. NCT03635775 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.