NCT04787601

Brief Summary

The aim of this study is to examine the changes in cognitive performance, coordination, anticipation time, proprioception and pass quality of cognitive-based neuromuscular exercises.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
24

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Mar 2021

Shorter than P25 for not_applicable healthy

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

First Submitted

Initial submission to the registry

March 3, 2021

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 8, 2021

Completed
7 days until next milestone

Study Start

First participant enrolled

March 15, 2021

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2021

Completed
Last Updated

August 10, 2021

Status Verified

August 1, 2021

Enrollment Period

3 months

First QC Date

March 3, 2021

Last Update Submit

August 9, 2021

Conditions

Keywords

cognıtıve-based neuromuscular exercısescognıtıve functıonssportıve performance

Outcome Measures

Primary Outcomes (1)

  • Cognitive performance

    Lumosity is a cognitive training platform developed by containing the results of more than 600 million cognitive training tests from more than 35 million people, which contains the largest data set of human cognitive performance available, either web-based or accessible from a mobile phone application. One test selected for each parameter will be applied and evaluated from the tests that include 6 parameters, namely speed, memory, attention, cognitive flexibility, problem solving and mathematics, in cognitive functions through this program on the computer. Each test will be applied to the participants for the first 2 times to practice, and for the next 3 times to be used as a test score. Higher scores mean a better outcome.

    Change from baseline score at the end of 8 week

Secondary Outcomes (6)

  • Reaction test

    change from baseline time at the end of 8 week

  • Coordination test

    change from baseline score at the end of 8 week

  • Anticipation time

    change from baseline time at the end of 8 week

  • Evaluation of Proprioceptive Force Sense

    change from baseline score at the end of 8 week

  • Loughborough Soccer Passing Test

    change from baseline score at the end of 8 week

  • +1 more secondary outcomes

Study Arms (2)

Cognitive training

EXPERIMENTAL

Cognitive-based neuromuscular exercises will be applied to the experimental group for a total of 8 weeks.

Other: ExerciseOther: Classic Training

Control

OTHER

The control group will only do the classic training.

Other: Classic Training

Interventions

Cognıtıve-based neuromuscular exercıses will be applied.

Cognitive training

Classic match preparation training

Cognitive trainingControl

Eligibility Criteria

Age16 Years - 19 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • being healthy
  • years old football players
  • footballers who train at least 3 days a week
  • agree to participate in the study

You may not qualify if:

  • who have had an injury in the last 6 months that could affect balance and performance
  • orthopedic, neurological or congenital problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kozaklİ Sport Center

Nevşehir, Kozakli, 50600, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Exercise

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Muhammet Ozalp, Msc

    Nevsehir Haci Bektas Veli University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Individuals who meet the inclusion criteria, who volunteered to participate in the study and signed the informed consent form will be divided into two groups, the control group and the study group, by simple random randomization. Experimental group cognitive based neuromuscular exercises + classical training; the control group will only do the classic training. A total of 8-week exercise program will be applied.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

March 3, 2021

First Posted

March 8, 2021

Study Start

March 15, 2021

Primary Completion

June 15, 2021

Study Completion

July 20, 2021

Last Updated

August 10, 2021

Record last verified: 2021-08

Data Sharing

IPD Sharing
Will not share

Locations