Relationship Between 2D:4D Finger Ratio and Proprioception
Investigation of the Relationship Between 2D:4D Ratio and Proprioception
1 other identifier
observational
88
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2025
Shorter than P25 for all trials
1 active site
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
January 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 9, 2025
CompletedFirst Submitted
Initial submission to the registry
April 22, 2025
CompletedFirst Posted
Study publicly available on registry
May 1, 2025
CompletedMay 1, 2025
April 1, 2025
2 months
April 22, 2025
April 29, 2025
Conditions
Keywords
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
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)
Study Officials
- PRINCIPAL INVESTIGATOR
Onur Engin, Assist Prof
Izmir Democracy University
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