ClinicalTrials.gg
RecruitingNCT07627113Updated Oct 9, 2026

Prenatal Androgen and Skills

An observational study in Health Adults, sponsored by Nigde Omer Halisdemir University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Nigde Omer Halisdemir University · Observational

From the registry’s dates

  • Started Oct 2026; still recruiting 1 month later.
Updated Oct 9, 2026Now RecruitingSite recruiting status changed+2 moreGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
94
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Due to the difficulties and risks of directly measuring prenatal hormone levels, biomarkers that indirectly reflect this exposure are used in research. In this context, the ratio of second to fourth finger length (2D:4D) is widely preferred because it is an easily applicable and non-invasive measurement. Evidence shows that 2D:4D stabilizes from the second trimester of pregnancy onward and exhibits strong sex differences across populations. The 2D:4D ratio is generally lower in men than in women. 2D is more strongly influenced by prenatal estrogen, while 4D is more strongly influenced by prenatal testosterone; this occurs during the first trimester of intrauterine fetal development. To our knowledge, studies examining the relationship between the 2D:4D ratio, an indirect indicator of prenatal androgen exposure, and dexterity and tactile discrimination are limited. Accordingly, the planned study aims to evaluate the relationship between the 2D:4D ratio and fine motor skills and tactile discrimination in healthy young adults.

Read the detailed description

Sex hormones experienced during prenatal exposure play a significant role in shaping certain lifelong characteristics by influencing both the physical and neurological development of individuals. The effects of these hormones, particularly on the developing nervous system, contribute to the emergence of behavioral and functional differences. Hand preference and certain behavioral traits in humans have been shown to be related to prenatal hormonal exposure. However, the development of these traits is not limited to hormonal influences alone, but is shaped by the interaction of genetic, environmental, and sociocultural factors. Due to the difficulties and risks of directly measuring prenatal hormone levels, biomarkers that indirectly reflect this exposure are used in research. In this context, the ratio of second to fourth finger length (2D:4D) is widely preferred because it is an easily applicable and non-invasive measurement. The 2D:4D ratio is generally lower in men than in women. 2D is more strongly influenced by prenatal estrogen, while 4D is more strongly influenced by prenatal testosterone; this occurs during the first trimester of intrauterine fetal development. However, whether the 2D:4D ratio is a reliable indicator of prenatal hormonal exposure is still a controversial issue in the literature. Therefore, examining the relationship between the 2D:4D ratio and various biological and functional characteristics remains important. To our knowledge, studies examining the relationship between the 2D:4D ratio, an indirect indicator of prenatal androgen exposure, and dexterity and tactile discrimination are limited. Accordingly, the planned study aims to evaluate the relationship between the 2D:4D ratio and fine motor skills and tactile discrimination in healthy young adults. It is hypothesized that prenatal hormonal exposure may indirectly shape finger morphology and receptor distribution by affecting skin and nervous system development, which may be a determining factor in tactile sensitivity and dexterity.

02

Conditions studied

  • Health Adults

Keywords

  • Digit Ratios
  • Prenatal Androgens
  • Motor Skills
  • Two-Point Discrimination
  • Tactile Acuity
03

In context

Lead sponsor

Nigde Omer Halisdemir University is the lead sponsor of 93 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

- Healthy individuals aged 18-40

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy individuals aged 18-40
  • Having sufficient visual and auditory function to understand and administer the test,
  • Voluntary agreement to participate in the study and providing .

Exclusion criteria

Exclusion Criteria:

  • Individuals with any musculoskeletal pathology,
  • History of upper extremity trauma,
  • Individuals diagnosed with metabolic, neurological, or genetic diseases,
  • Individuals with a history of hand surgery within the last 6 months,
  • Pregnancy or breastfeeding.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
94 participants (estimated)
Patient registry
No

Groups and cohorts

  • Healthy adults

    Young and healthy adults aged 18-40

    Other: Digit Ratio · Behavioral: Fine motor skills · Behavioral: Tactile Discrimination

Interventions

  • OtherDigit Ratio

    The second (2D) and fourth (4D) finger lengths of the participants will be measured separately in both hands by a physiotherapist with over thirteen years of clinical experience.

  • BehavioralFine motor skills

    Hand dexterity will be assessed using the Purdue Pegboard Test. The test will be administered according to standard procedure with participants seated at a table. Participants will be asked to place the pegs into the corresponding holes as quickly and accurately as possible within a specified time (30 seconds).

  • BehavioralTactile Discrimination

    To perform the 2-point discrimination tests, the Baseline® two-point discriminator will be used. Measurements will be applied to the distal phalangeal pulp of the index finger on both hands while participants are seated in a comfortable position with their eyes closed.

06

What researchers measure

Primary outcomes

  1. 2-point discrimination test

    To perform 2-point discrimination tests, the Baseline® two-point discriminator will be used. Measurements will be applied to the distal phalangeal pulp of the index finger on both hands while participants are seated in a comfortable position with their eyes closed. The test will begin at a distance of 8 mm, allowing participants to perceive the stimulus as two points, and then the distance will be gradually reduced. After 5 mm, measurements will continue at 1 mm intervals. In each application, both contact points will be applied to the skin simultaneously and with equal pressure, and participants will be asked to indicate whether the perceived stimulus is a single point or two points.

    Time frame: 12 months

  2. Digit Ratio

    Measurements will be taken after participants' hands are placed on a flat surface with palms facing upwards. Finger length is defined as the distance from the midpoint of the proximal crease line where the finger joins the palm to the distal point of the fingertip. Measurements will be performed using a digital caliper with 0.01 mm accuracy, two separate measurements will be taken for each finger, and the average value will be recorded. Based on the obtained measurements, the 2D:4D finger ratio will be calculated by dividing the 2D length by the 4D length in both hands .

    Time frame: 12 months

  3. Fine motor skills

    The test will be administered according to standard procedure while participants are seated at a table. Participants will be asked to place the pegs into the corresponding holes as quickly and accurately as possible within the specified time (30 seconds). In the dominant and non-dominant hand tests, participants will be asked to place pegs with one hand for 30 seconds, while in the both-hand test, the simultaneous use of both hands will be evaluated. The number of correctly placed pegs for each subtest will be recorded, and higher scores will be considered as better fine motor skill performance.

    Time frame: 12 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Butovskaya M, Adam Y, Batsevich V, Shackelford TK, Fink B. Associations between 2D:4D from direct and radiographic measurements with handgrip strength in young adult Tuvans. Early Hum Dev. 2024 Jun;193:106037. doi: 10.1016/j.earlhumdev.2024.106037. Epub 2024 May 8. PubMed 38743999 ↗
  • Fink B, Manning JT, Neave N, Tan U. Second to fourth digit ratio and hand skill in Austrian children. Biol Psychol. 2004 Nov;67(3):375-84. doi: 10.1016/j.biopsycho.2004.03.012. PubMed 15294393 ↗

Individual participant data

Plan to share: No

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2026 (actual). Primary completion is estimated for Jul 2027, 8 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
May 30, 2026
First posted
Jun 4, 2026
StartActual
Oct 6, 2026
Primary completionEst.
Jul 1, 2027
CompletionEst.
Jul 1, 2027
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Enrolling by invitation→Recruiting
changed Oct 9, 2026
Sites
Nigde Omer Halisdemir University is now Recruiting
Oct 9, 2026
Start date
Oct 1, 2026→Oct 6, 2026 (actual)
Oct 9, 2026
Contact
Study contact now listed: added r•••@gmail.com · •••2082; added r•••@gmail.com. See the current contact
Oct 9, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Nigde Omer Halisdemir University · Niğde, Turkey (Türkiye)Contact added r•••@gmail.com
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    Enrolling by invitation→Recruiting
    Nigde Omer Halisdemir University is now Recruiting
    Start date Oct 1, 2026→Oct 6, 2026 (now actual)
    Contact Study contact now listed: added r•••@gmail.com · •••2082; added r•••@gmail.com. See the current contact
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Nigde Omer Halisdemir University · Niğde, Turkey (Türkiye)Contact added r•••@gmail.com

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07627113
Lead sponsor
Nigde Omer Halisdemir University
Responsible party
Rabia ZORLULAR (Principal investigator, Nigde Omer Halisdemir University) — Principal investigator
First posted
Jun 4, 2026
Start date
Oct 6, 2026
Primary completion
Jul 1, 2027 (estimated)
Completion
Jul 1, 2027 (estimated)
Last update
Oct 9, 2026

Study contacts

Rabia ZORLULAR
Contact
rabiaeraslan118@gmail.com
+5424362082
Rabia Zorlular
Contact
rabiaeraslan118@gmail.com
Rabia ZORLULAR
principal investigator · Nigde Omer Halisdemir University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion