NCT06953219

Brief Summary

Background: 2D:4D ratio (the ratio of the length of the second digit to the length of the fourth digit) has been reported to be associated with muscle strength and physical performance, numerical competencies, spatial skills and cognitive abilities. However, the relationship between 2D:4D ratio and proprioception is not well-known, which was therefore aimed at investigating in current study. Methods: 2D:4D ratio (electronic digital calliper) and proprioception (Join position error is measure with Cervical Range of Motion instrument) were assessed in all individuals (n=35.7 ± 11.2 years).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
88

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 29, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 24, 2025

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 9, 2025

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

April 22, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 1, 2025

Completed
Last Updated

May 1, 2025

Status Verified

April 1, 2025

Enrollment Period

2 months

First QC Date

April 22, 2025

Last Update Submit

April 29, 2025

Conditions

Keywords

digit ratioproprioception

Outcome Measures

Primary Outcomes (4)

  • Finger length measurement and 2D:4D ratio calculation

    The lengths of the second (2D) and fourth (4D) fingers on each hand were measured using an electronic digital caliper with a precision of 0.01 millimeters. Measurements were taken on the palmar surface of the hand, extending from the distal tip of the finger to the basal crease at the proximal end of the digit.The 2D:4D ratio was calculated separately for the right and left hands. To enhance the accuracy of the 2D:4D ratio measurements, each finger was measured three times during a single assessment session by the same investigator. The repeated measurements were not taken consecutively; instead, at least one other hand was measured between the first and second measurements of any given hand. This procedure was implemented to minimize the potential influence of recall bias on subsequent measurements.

    baseline

  • Cervical Range of Motion

    The cervical range of motion measurement was performed using a Cervical Range of Motion (CROM) device, which is a reliable and valid tool. The CROM unit is a mechanical instrument that measures cervical ranges by combining a magnetic reference with standard inclinometers. The individuals were told to sit comfortably with their hands on the armrest and their backs straight on the chair. The CROM unit was secured on the individuals' head by the physiotherapist. The CROM unit's magnetic yoke is positioned squarely around the neck with its arrow pointing directly north. Afterwards, physiotherapist asked individuals to perform cervical range of motion in all three directions: flexion- extension, lateral flexion and rotation.The maximum range of cervical flexion, extension, left and right rotation, and left and right lateral flexion was measured three times and averaged.

    baseline

  • Repositioning to neutral head position (NHP)

    For the NHP assessment, the individuals were asked to keep their head in the neutral head position, with their eyes closed. The deviations from the neutral (0) position in the sagittal (flexion-extension), frontal (lateral flexion), and transverse (rotation) planes were recorded using the CROM device.

    baseline

  • Repositioning the head to a predetermined reference point (Target Head Position, THP)

    For the assessment of THP, the target position will be defined as half of the maximum active range of motion measured during a standard cervical joint mobility assessment. While the patient's eyes are covered with an eye mask, the head will first be slowly positioned by the physiotherapist to the predetermined target angle and held in this position for five seconds for the patient to perceive. Subsequently, the head will be moved away from the target position, and the patient will be asked to actively reposition it to the original target. Each measurement will be repeated three times, and the mean deviation from the target angle will be recorded. Measurements will be conducted separately for flexion, extension, right rotation, left rotation, right lateral flexion, and left lateral flexion

    baseline

Study Arms (1)

assessment group

Finger length measurements(second digits and fourth digit) were made with acaliper. Range of motion (ROM) and joint position error measuremenst were made with a CROM device. Joint position error is assessed with neutral head positioning test and target head positioning test.

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Healthy adult individuals aged between 18 and 65 years, who volunteered to participate in the study. Participants had no sensory loss or severe neurological disorders affecting proprioception. Individuals with hand or cervical trauma history, congenital hand anomalies, or any condition preventing accurate 2D:4D measurement were excluded.

You may qualify if:

  • Age between 18 and 65 years
  • Agreeing to participate in the study.

You may not qualify if:

  • Individuals who have scars, finger deformities, and/or surgical interventions that would prevent accurate measurement of the 2D:4D ratio
  • Congenital hand anomalies
  • History of trauma involving the hand or cervical region were excluded from the study.
  • Having sensory loss or severe neurological disorder that would affect proprioception

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Izmir Democracy University

Izmir, Izmır, 35140, Turkey (Türkiye)

Location

Study Officials

  • Onur Engin, Assist Prof

    Izmir Democracy University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

April 22, 2025

First Posted

May 1, 2025

Study Start

January 29, 2025

Primary Completion

March 24, 2025

Study Completion

April 9, 2025

Last Updated

May 1, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

It was deemed appropriate to keep the data of the individuals participating in the study confidential

Locations