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NCT04076657 · ClinicalTrials.gov registry record · NA

Efficacy of Brock String Therapy Post Concussion

A NA study of Concussion, Brain and Near Point Convergence, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT04076657 is a NA study of Concussion, Brain and Near Point Convergence that has completed, run by University of Pittsburgh. The registered enrollment target is 50 participants, below the 182-participant average among 20 other Concussion, Brain trials with a reported enrollment target (73% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04076657, a NA study of Concussion, Brain and Near Point Convergence, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

The purpose of the proposed study is to evaluate the efficacy of Brock String therapy prescribed in the acute stage of concussion recovery can improve clinical outcomes among patients with receded near point of convergence (NPC). Aim 1: Determine if participants receiving the Brock String have more significant improvements in NPC measurements at follow up 7-10 days post injury. Aim 2: Determine if participants receiving the Brock String 1) improve on computerized neurocognitive test scores from initial visit (\<48 hours post injury) to follow up visit (7-10 days post injury) compared to control participants, and 2) have reduced recovery time (i.e., days from injury until return to play) compared to control participants.

Interventions

  • BEHAVIORAL Standard of Care
  • BEHAVIORAL Brock String Therapy

Study Locations (1)

Pennsylvania

  • University of Pittsburgh Medical Center, Rooney Sports Complex - Pittsburgh

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2020-11-09
Est. Completion 2025-03-19
Phase NA

Sponsor

University of Pittsburgh

1,238 total trials

What the Registry Record Tells You About NCT04076657

The ClinicalTrials.gov registry entry for NCT04076657 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 182-participant average among 20 other Concussion, Brain trials with a reported enrollment target (73% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Concussion, Brain appearing as the primary indexed condition, and to 2 interventions - of which Standard of Care is the first listed.

NCT04076657 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT04076657 about?

NCT04076657 is a clinical study titled "Efficacy of Brock String Therapy Post Concussion". The purpose of the proposed study is to evaluate the efficacy of Brock String therapy prescribed in the acute stage of concussion recovery can improve clinical outcomes among patients with receded near point of convergence (NPC). Aim 1: Determine if participants receiving the Brock String have more...

What is the current status of trial NCT04076657?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2020-11-09. Estimated completion is 2025-03-19.

What conditions does trial NCT04076657 study?

This clinical trial studies the following conditions: Concussion, Brain, Near Point Convergence.

What interventions are being tested in trial NCT04076657?

The interventions under investigation include: Standard of Care (BEHAVIORAL), Brock String Therapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT04076657?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04076657 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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