NCT06072144

Brief Summary

The Smart Speed device developed at Zafer Teknopark in Turkey was developed to objectively assess reaction time. The aim of this study was to evaluate the validity and reliability of the Smart Speed device in comparison with BlazePod and Nelson Reaction Test.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
37

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2024

Shorter than P25 for all trials

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

September 22, 2023

Completed
18 days until next milestone

First Posted

Study publicly available on registry

October 10, 2023

Completed
7 months until next milestone

Study Start

First participant enrolled

May 6, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 7, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 24, 2024

Completed
Last Updated

July 31, 2024

Status Verified

July 1, 2024

Enrollment Period

1 month

First QC Date

September 22, 2023

Last Update Submit

July 30, 2024

Conditions

Healthy Volunteers

Outcome Measures

Primary Outcomes (1)

  • Assessment of reaction time

    To determine the validity and reliability of the Smart Speed device in assessing reaction time

    15 minutes

Interventions

Validity and reliability studyOTHER

Test-retest method will be used to assess reliability. For this purpose, participants will be re-evaluated one week later with the Smart Speed device. For validity assessment, concurrent validity and agreement between measurements will be evaluated. Concurrent validity will be assessed by correlation analysis and agreement between measurements will be assessed by Bland Altman.

Eligibility Criteria

Age18 Years - 24 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Participants will be healthy young people between the ages of 18-24. All participants will be recruited from Afyonkarahisar Health Sciences University Physiotherapy and Rehabilitation Department.

You may qualify if:

  • Without having systemic disease
  • To be able to speak Turkish language

You may not qualify if:

  • Having a problem that affects physical performance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fatma EKEN

Afyonkarahisar, Center, 03030, Turkey (Türkiye)

Location

Study Officials

  • Emel TAŞVURAN HORATA, PhD

    Afyonkarahisar Health Sciences University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

September 22, 2023

First Posted

October 10, 2023

Study Start

May 6, 2024

Primary Completion

June 7, 2024

Study Completion

July 24, 2024

Last Updated

July 31, 2024

Record last verified: 2024-07

Locations

TU(1)