Validity and Reliability of the Smart Speed Device

Sponsor
Afyonkarahisar Health Sciences University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06072144
Collaborator
(none)
46
36

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Validity and reliability study

Detailed Description

The capacity to perceive, analyze, and react to a signal is referred to as reaction time. Reaction time is influenced by many factors such as visual and auditory factors. It is also influenced by individual factors such as age, gender, body mass index, attention and fatigue. Having reaction time within normal limits is very important for maintaining activities of daily living. BlazePod is a valid and reliable device for the assessment of reaction time. The Nelson Reaction test is also a valid and reliable test frequently used in the clinic for the assessment of reaction time due to its simple and rapid application. 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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
46 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Investigating the Reliability and Validity of the Smart Speed Device
Anticipated Study Start Date :
Nov 15, 2023
Anticipated Primary Completion Date :
Nov 15, 2026
Anticipated Study Completion Date :
Nov 15, 2026

Outcome Measures

Primary Outcome Measures

  1. Assessment of reaction time [15 minutes]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 24 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Without having systemic disease

  • To be able to speak Turkish language

Exclusion Criteria:
  • Having a problem that affects physical performance

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Afyonkarahisar Health Sciences University

Investigators

  • Principal Investigator: Emel TAŞVURAN HORATA, PhD, Afyonkarahisar Health Sciences University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emel Taşvuran Horata, Associate Professor, Afyonkarahisar Health Sciences University
ClinicalTrials.gov Identifier:
NCT06072144
Other Study ID Numbers:
  • 2023/9
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 10, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Oct 10, 2023