NCT01972581

Brief Summary

Incorporating neurocognitive visual reaction training has been shown to increase bating performance in collegiate baseball players. However, poor methodology, such as lack of a control group and use of an unreliable outcome measure, limit the strength of the previous study. Therefore the purpose of this study is to determine the effects of neurocognitive visual reaction training on reaction time and coordination in an athletic population. The purpose of this study is to determine the effects of neurocognitive visual reaction training on reaction time and coordination.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2013

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2013

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

October 21, 2013

Completed
9 days until next milestone

First Posted

Study publicly available on registry

October 30, 2013

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
Last Updated

February 19, 2016

Status Verified

February 1, 2016

Enrollment Period

2.3 years

First QC Date

October 21, 2013

Last Update Submit

February 17, 2016

Conditions

Keywords

neurocognitive visual reaction trainingbaseball

Outcome Measures

Primary Outcomes (1)

  • Number of colored balls correctly identified

    5 weeks

Secondary Outcomes (2)

  • Number of ball catches on alternate ball toss

    5 weeks

  • Reaction time on dynavision reaction board

    5 Weeks

Study Arms (2)

Reaction Time Training

EXPERIMENTAL
Other: Reaction Time Training

Control

NO INTERVENTION

Interventions

Reaction Time Training

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • subjects that participate in a structured sport team
  • between the ages of 18-65
  • with or without a history of mild traumatic brain injury.

You may not qualify if:

  • subjects currently under medical supervision and not fully cleared to participate in structured sport team.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Human Biomechanics and Physiology Laboratory

High Point, North Carolina, 27262, United States

Location

Study Officials

  • Kevin Ford, PhD

    High Point University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director, Biomechanics Laboratory

Study Record Dates

First Submitted

October 21, 2013

First Posted

October 30, 2013

Study Start

October 1, 2013

Primary Completion

February 1, 2016

Study Completion

February 1, 2016

Last Updated

February 19, 2016

Record last verified: 2016-02

Locations