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NCT07211919 · ClinicalTrials.gov registry record
Accelerated Transcranial Magnetic Stimulation Intervention for Post-Concussion Syndrome
A clinical trial of Post-Concussion Syndrome and Post-Concussion Symptoms, sponsored by Cognitive FX.
- Completed
- Registry status
- 11
- Enrollment target
- 1
- Study location
NCT07211919 is a study of Post-Concussion Syndrome and Post-Concussion Symptoms that has completed, run by Cognitive FX. The registered enrollment target is 11 participants, below the 59-participant average among 14 other Post-Concussion Syndrome trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07211919, a study of Post-Concussion Syndrome and Post-Concussion Symptoms, has completed, sponsored by Cognitive FX.
- COMPLETED
- Registry status
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
This study looks at the effects of accelerated intermittent theta burst stimulation (aiTBS) on patients with chronic and acute post-concussion syndrome. Each participant was treated in an outpatient setting for about 3 hours per day, over 3 days. The participants' symptom survey scores and brain scan data were then compared before and after treatment.
Conditions Studied
Study Locations (1)
Utah
- Cognitive FX TMS Clinic - Provo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2025-05-01 |
| Est. Completion | 2025-07-31 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07211919
The ClinicalTrials.gov registry entry for NCT07211919 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 59-participant average among 14 other Post-Concussion Syndrome trials with a reported enrollment target (81% lower). The listed sponsor is Cognitive FX, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Post-Concussion Syndrome appearing as the primary indexed condition, and to 0 interventions.
NCT07211919 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.
Frequently Asked Questions
What is clinical trial NCT07211919 about?
NCT07211919 is a clinical study titled "Accelerated Transcranial Magnetic Stimulation Intervention for Post-Concussion Syndrome". This study looks at the effects of accelerated intermittent theta burst stimulation (aiTBS) on patients with chronic and acute post-concussion syndrome. Each participant was treated in an outpatient setting for about 3 hours per day, over 3 days. The participants' symptom survey scores and brain sca...
What is the current status of trial NCT07211919?
This trial is currently completed. The enrollment target is 11 participants. The study started on 2025-05-01. Estimated completion is 2025-07-31.
What conditions does trial NCT07211919 study?
This clinical trial studies the following conditions: Post-Concussion Syndrome, Post-Concussion Symptoms, Post Concussive Syndrome, Post-Concussive Syndrome, Chronic, Anxiety Disorder Not Otherwise Specified.
Who is sponsoring clinical trial NCT07211919?
This trial is sponsored by Cognitive FX, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07211919 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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