NCT07357077

Brief Summary

Our study aimed to examine the relationship between upper extremity anthropometric measurements and reaction time in healthy individuals. Also, we aimed to investigate whether there are differences between dominant and non-dominant upper extremity anthropometric measurements and reaction time.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2025

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 15, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2025

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 6, 2026

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

January 7, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

January 21, 2026

Completed
Last Updated

January 21, 2026

Status Verified

May 1, 2025

Enrollment Period

8 months

First QC Date

January 7, 2026

Last Update Submit

January 15, 2026

Conditions

Healthy Persons

Keywords

reaction timeanthropometric measurementupper extremity

Outcome Measures

Primary Outcomes (1)

  • Upper Extremity Anthropometric Measurements

    Upper extremity length measurements were performed twice and the average score was recorded. Total upper extremity, arm and forearm length measurements were taken with a Harpenden anthropometer. Hand, palmar (palm), thumb, index finger, middle finger, ring finger, little finger, hand width and hand opening length measurements were taken with a digital caliper (Dasqua, Italy).

    Baseline

Secondary Outcomes (1)

  • Reaction time measurement

    Baseline

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Having undergone surgery on their upper and lower extremities, Using orthotics Having deformities and contractures Having neurological diseases

You may qualify if:

  • Being between 18-30 years old
  • Not having undergone any surgery on the upper or lower extremities

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kütahya Health Sciences University

Kütahya, Turkey (Türkiye)

Location

Study Officials

  • Hasan Hüseyin GÜNGÖR, Undergraduate Student

    Kütahya Health Sciences University

    PRINCIPAL INVESTIGATOR

  • Yusuf ÖZTÜRK, Undergraduate Student

    Kütahya Health Sciences University

    PRINCIPAL INVESTIGATOR

  • Lütfiye AKKURT, PhD

    Kütahya Health Sciences University

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 7, 2026

First Posted

January 21, 2026

Study Start

May 15, 2025

Primary Completion

December 30, 2025

Study Completion

January 6, 2026

Last Updated

January 21, 2026

Record last verified: 2025-05

Locations

TU(1)