Oral HygieneNCT07147998
Impact of 2D:4D Ratio on Oral Hygiene and Gingival Health
An observational study of Oral Hygiene and Gingivitis, run by Okan University at 1 site in Turkey (Türkiye).
Trial summary
The second-to-fourth digit ratio (2D:4D)-the ratio of the length of the index finger to that of the ring finger-has gained increasing attention as a non-invasive, stable biomarker of prenatal sex hormone exposure. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Oral Hygiene, Gingivitis
- What is being tested?
- Oral hygiene instruction
- Type of treatment
- Pill or oral medicine
- How many people
- 126 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Sep 2023to 1 Aug 2025
- How long will I take part?
- 1 Week
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Adults over 18 years of age, systemically healthy, without psychological or neurological disorders, able to cooperate during examinations and procedures, university students or graduates, with at least 28 natural teeth, non-smokers, with no fixed orthodontic appliances or crown prostheses, no prior oral hygiene education from a dental professional, and a clinical diagnosis of gingivitis.
Who may be able to join
- Systemically healthy University graduates or currently enrolled in a university program Presence of 28 natural teeth No orthodontic appliances or crown restorations in the oral cavity Non-smokers No previous oral hygiene instruction from a dental professional Clinical diagnosis of gingivitis
Who cannot join
- Presence of any systemic disease or condition that may affect periodontal health Not a university graduate and not currently enrolled in a university program Fewer than 28 natural teeth Orthodontic appliances or crown restorations present in the oral cavity Current smokers Previous oral hygiene instruction from a dental professional Clinical diagnosis of periodontitis
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
İstanbul Okan University, Faculty of Dentistry
Istanbul, 34947
About this study
Official title: Assessing the Impact of 2D:4D Ratio on Oral Hygiene Performance and Gingival Health
The second-to-fourth digit ratio (2D:4D)-the ratio of the length of the index finger to that of the ring finger-has gained increasing attention as a non-invasive, stable biomarker of prenatal sex hormone exposure. The 2D:4D ratio is believed to reflect the balance of prenatal androgens (especially testosterone) and estrogens. Lower ratios (more masculinized) indicate higher prenatal testosterone exposure, whereas higher ratios (more feminized) are associated with lower testosterone and higher estrogen levels. Research has linked variations in 2D:4D to a broad spectrum of behavioral traits, cognitive abilities, and health outcomes. 2D:4D has been shown to have strong associations with motor performance, especially skills that require fine motor coordination. However, while many studies have examined the role of 2D:4D in sports and cognition, its relationship to health-related behaviors involving motor skills remains underexplored. One such domain is oral hygiene, which requires sustained fine motor coordination-particularly in actions like tooth brushing and flossing. Despite the clear motor demands of such behaviors, the potential connection between 2D:4D and oral hygiene has not yet been systematically investigated. This study aims to fill this gap by exploring the association between the 2D:4D digit ratio and oral hygiene practices.
Read the detailed description
Background and Rationale The second-to-fourth digit ratio (2D:4D)-the ratio of the length of the index finger to that of the ring finger-is a morphological index thought to reflect prenatal sex-hormone exposure. The trait is determined during early fetal development and is generally stable from early childhood into adulthood. Prior research has examined associations between 2D:4D and behavioral, cognitive, and motor outcomes in various populations; however, the relationship between 2D:4D and everyday health behaviors that require fine motor coordination (e.g., tooth brushing and interdental cleaning) has not been comprehensively evaluated. This study is designed to test whether 2D:4D is associated with oral hygiene measures and practices.
Objectives and Hypotheses Primary objective: To evaluate the association between right-hand 2D:4D and dental plaque accumulation as measured by the Turesky Modification of the Quigley-Hein Plaque Index (QHPI) and the Löe-Silness Gingival Index (GI) at baseline and after standardized oral-hygiene instruction.
Secondary objectives: (1) To examine whether sex and hand dominance modify the association between 2D:4D and oral-hygiene outcomes; (3) To explore whether baseline 2D:4D is related to self-reported brushing frequency.
Hypotheses (a priori): Lower 2D:4D (putatively reflecting higher prenatal androgen exposure) will be associated with differences in oral-hygiene performance compared with higher 2D:4D. Direction and magnitude will be tested empirically.
Study Design and Setting This is a single-center, observational study with a baseline assessment and a planned follow-up visit approximately 7 days after standardized instruction. The study will be conducted in the Periodontology Clinic of the Faculty of Dentistry at Istanbul Okan University.
Participants Adults aged 18-56 years who attend the clinic for routine examination and provide written informed consent will be eligible. Key exclusion criteria will include conditions that could interfere with hand measurements or oral-hygiene procedures (e.g., hand injuries affecting the right index or ring finger, severe periodontal disease requiring urgent treatment, or systemic conditions judged by investigators to preclude participation). The planned sample size is approximately 126 participants, based on an a priori power calculation (two-tailed; α = 0.05; power [1 - β] = 0.80).
Procedures At the initial visit (Day 0), socio-demographic data will be recorded. Oral hygiene and gingival status will be assessed using the QHPI and GI, respectively. Brushing frequency will be recorded by self-report. All teeth except third molars will be scored on buccal and lingual surfaces. Dental plaque will be disclosed with Mira-2-Ton Disclosing Solution (Hager \& Werken, Germany) prior to QHPI scoring.
The lengths of the second (index) and fourth (ring) digits on the right hand will be measured on the ventral surface using a digital caliper, from the fingertip to the midpoint of the basal crease. Three measurements will be taken for each finger and averaged; the 2D:4D ratio will be computed as (2D length)/(4D length). For exploratory analyses, a prespecified cut-off of 1.0 will be used to define subgroups (2D:4D < 1.0 vs ≥ 1.0) within each sex.
Following baseline assessments, all participants will receive standardized oral-hygiene instruction from the same instructor, including the Modified Bass brushing technique and the use of dental floss or interdental brushes. A follow-up visit will occur approximately 7 days later (Day 7 ± 2), at which QHPI and GI will be reassessed by the same examiner.
Quality Control To minimize inter-examiner variability, all digit and oral-hygiene measurements will be performed by a single examiner who will undergo standardized training and calibration before data collection. Calibration will continue until predefined reproducibility thresholds for both measurement types are met.
Outcome Measures Primary outcome: QHPI score (0-5) per tooth surface, aggregated per participant at Day 0 and Day 7.
Secondary outcomes: GI score (0-3) per site, aggregated per participant at Day 0 and Day 7; self-reported brushing frequency (times/day).
Statistical Analysis Plan Descriptive statistics will be presented as Mean ± Standard Error (SE) or appropriate alternatives. Assumptions for parametric testing will be evaluated using the Shapiro-Wilk test (normality) and Levene's test (homogeneity of variance). Between-group comparisons of 2D:4D by sex and hand dominance will use Student's t-tests when assumptions are met.
To assess changes over time and the effects of prespecified factors (sex, hand dominance, and 2D:4D subgroup), two-way mixed-design ANOVA models (time: Day 0 vs Day 7; between-subject factors as specified) will be applied to QHPI and GI. When significant main effects or interactions are observed, pairwise comparisons will use a Bonferroni adjustment. Pearson correlation will be used to examine associations between continuous 2D:4D and oral-hygiene measures. All tests will be two-sided with α = 0.05. Analyses will be performed using SPSS version 30 or later.
Ethics The protocol will be conducted in accordance with the Declaration of Helsinki and has received approval from the relevant institutional ethics committee. Written informed consent will be obtained from all participants before enrollment.
- Conditions
- Oral Hygiene, Gingivitis
- Being tested
- Oral hygiene instruction
- Medical subject headings
- Gingivitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Oral hygiene instructionOther
Oral hygiene and gingival health of all patients were assessed using the Turesky Modification of the Quigley-Hein Plaque Index and the Gingival Index. Tooth brushing frequency was recorded. The 2D:4D ratio was calculated by dividing the second digit length by the fourth, with three measurements taken per finger to ensure reliability. A cut-off value of 1 was used to evaluate prenatal androgen influence, and participants were grouped by 2D:4D ratio (≥1 or <1). All participants received standardized oral hygiene instructions from the same instructor, including Modified Bass brushing and interdental cleaning. A second clinical exam was performed one week later by the same examiner, and both indices were re-scored.
What is being measured
The primary outcome is the main question the study is designed to answer.
Mean Quigley-Hein Plaque Index Score (Turesky Modification)
Dental plaque will be scored on buccal and lingual surfaces of all teeth except third molars using the Turesky Modification of the Quigley-Hein Plaque Index (scale 0-5; 0 = no plaque, 5 = plaque covering ≥ two-thirds of crown). Scores per tooth will be averaged per participant.
Measured: Baseline (Day 0) and 1 week after oral hygiene instruction.
Mean Löe-Silness Gingival Index Score
Gingival inflammation will be assessed on buccal and lingual surfaces at mesial, mid-buccal, and distal sites using the Löe-Silness Gingival Index (scale 0-3; 0 = healthy, 3 = severe inflammation with spontaneous bleeding). Scores will be averaged per participant.
Measured: Baseline (Day 0) and 1 week after oral hygiene instruction.
Secondary outcomes (2)
Right-hand 2D:4D Digit Ratio
Lengths of the index (2D) and ring (4D) fingers of the right hand will be measured three times using a digital caliper (ventral surface, fingertip to basal crease). The mean lengths will be used to calculate the 2D:4D ratio.
Measured: Baseline (Day 0)
Self-reported Tooth Brushing Frequency
Participants will report their average number of daily tooth brushing episodes.
Measured: Baseline (Day 0)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Aug 2025
- Study start1 Sep 2023
- Primary completion1 May 2024
- Study completion1 Aug 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Oral HygieneStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 126 participants (actual)
- Target duration
- 1 Week
Sponsor and investigators
- Lead sponsor
- Okan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ekin Besiroglu, Okan University
- Investigators
- Ekin Beşiroğlu Turgut, Study director, Okan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07147998
- Sponsor's protocol ID
- 2023/165-01
- Status last verified
- Aug 2025
- First submitted
- 8 Aug 2025
- Last updated
- 29 Aug 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 29 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Assessing the Impact of 2D:4D Ratio on Oral Hygiene Performance and Gingival Health
- ClinicalTrials.gov ID
- NCT07147998
- Acronym / sponsor ID
- 2023/165-01
- Conditions
- Oral Hygiene, Gingivitis
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 126 participants (actual)
- Lead sponsor
- Okan UniversityUniversity, hospital or other
- Study start
- 1 Sep 2023 (actual)
- Primary completion
- 1 May 2024 (actual)
- Study completion
- 1 Aug 2025 (actual)
- First posted
- 29 Aug 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The second-to-fourth digit ratio (2D:4D)-the ratio of the length of the index finger to that of the ring finger-has gained increasing attention as a non-invasive, stable biomarker of prenatal sex hormone exposure. The 2D:4D ratio is believed to reflect the balance of prenatal androgens (especially testosterone) and estrogens. Lower ratios (more masculinized) indicate higher prenatal testosterone exposure, whereas higher ratios (more feminized) are associated with lower testosterone and higher estrogen levels. Research has linked variations in 2D:4D to a broad spectrum of behavioral traits, cognitive abilities, and health outcomes. 2D:4D has been shown to have strong associations with motor performance, especially skills that require fine motor coordination. However, while many studies have examined the role of 2D:4D in sports and cognition, its relationship to health-related behaviors involving motor skills remains underexplored. One such domain is oral hygiene, which requires sustained fine motor coordination-particularly in actions like tooth brushing and flossing. Despite the clear motor demands of such behaviors, the potential connection between 2D:4D and oral hygiene has not yet been systematically investigated. This study aims to fill this gap by exploring the association between the 2D:4D digit ratio and oral hygiene practices.
Detailed description
Background and Rationale The second-to-fourth digit ratio (2D:4D)-the ratio of the length of the index finger to that of the ring finger-is a morphological index thought to reflect prenatal sex-hormone exposure. The trait is determined during early fetal development and is generally stable from early childhood into adulthood. Prior research has examined associations between 2D:4D and behavioral, cognitive, and motor outcomes in various populations; however, the relationship between 2D:4D and everyday health behaviors that require fine motor coordination (e.g., tooth brushing and interdental cleaning) has not been comprehensively evaluated. This study is designed to test whether 2D:4D is associated with oral hygiene measures and practices.
Objectives and Hypotheses Primary objective: To evaluate the association between right-hand 2D:4D and dental plaque accumulation as measured by the Turesky Modification of the Quigley-Hein Plaque Index (QHPI) and the Löe-Silness Gingival Index (GI) at baseline and after standardized oral-hygiene instruction.
Secondary objectives: (1) To examine whether sex and hand dominance modify the association between 2D:4D and oral-hygiene outcomes; (3) To explore whether baseline 2D:4D is related to self-reported brushing frequency.
Hypotheses (a priori): Lower 2D:4D (putatively reflecting higher prenatal androgen exposure) will be associated with differences in oral-hygiene performance compared with higher 2D:4D. Direction and magnitude will be tested empirically.
Study Design and Setting This is a single-center, observational study with a baseline assessment and a planned follow-up visit approximately 7 days after standardized instruction. The study will be conducted in the Periodontology Clinic of the Faculty of Dentistry at Istanbul Okan University.
Participants Adults aged 18-56 years who attend the clinic for routine examination and provide written informed consent will be eligible. Key exclusion criteria will include conditions that could interfere with hand measurements or oral-hygiene procedures (e.g., hand injuries affecting the right index or ring finger, severe periodontal disease requiring urgent treatment, or systemic conditions judged by investigators to preclude participation). The planned sample size is approximately 126 participants, based on an a priori power calculation (two-tailed; α = 0.05; power [1 - β] = 0.80).
Procedures At the initial visit (Day 0), socio-demographic data will be recorded. Oral hygiene and gingival status will be assessed using the QHPI and GI, respectively. Brushing frequency will be recorded by self-report. All teeth except third molars will be scored on buccal and lingual surfaces. Dental plaque will be disclosed with Mira-2-Ton Disclosing Solution (Hager \& Werken, Germany) prior to QHPI scoring.
The lengths of the second (index) and fourth (ring) digits on the right hand will be measured on the ventral surface using a digital caliper, from the fingertip to the midpoint of the basal crease. Three measurements will be taken for each finger and averaged; the 2D:4D ratio will be computed as (2D length)/(4D length). For exploratory analyses, a prespecified cut-off of 1.0 will be used to define subgroups (2D:4D < 1.0 vs ≥ 1.0) within each sex.
Following baseline assessments, all participants will receive standardized oral-hygiene instruction from the same instructor, including the Modified Bass brushing technique and the use of dental floss or interdental brushes. A follow-up visit will occur approximately 7 days later (Day 7 ± 2), at which QHPI and GI will be reassessed by the same examiner.
Quality Control To minimize inter-examiner variability, all digit and oral-hygiene measurements will be performed by a single examiner who will undergo standardized training and calibration before data collection. Calibration will continue until predefined reproducibility thresholds for both measurement types are met.
Outcome Measures Primary outcome: QHPI score (0-5) per tooth surface, aggregated per participant at Day 0 and Day 7.
Secondary outcomes: GI score (0-3) per site, aggregated per participant at Day 0 and Day 7; self-reported brushing frequency (times/day).
Statistical Analysis Plan Descriptive statistics will be presented as Mean ± Standard Error (SE) or appropriate alternatives. Assumptions for parametric testing will be evaluated using the Shapiro-Wilk test (normality) and Levene's test (homogeneity of variance). Between-group comparisons of 2D:4D by sex and hand dominance will use Student's t-tests when assumptions are met.
To assess changes over time and the effects of prespecified factors (sex, hand dominance, and 2D:4D subgroup), two-way mixed-design ANOVA models (time: Day 0 vs Day 7; between-subject factors as specified) will be applied to QHPI and GI. When significant main effects or interactions are observed, pairwise comparisons will use a Bonferroni adjustment. Pearson correlation will be used to examine associations between continuous 2D:4D and oral-hygiene measures. All tests will be two-sided with α = 0.05. Analyses will be performed using SPSS version 30 or later.
Ethics The protocol will be conducted in accordance with the Declaration of Helsinki and has received approval from the relevant institutional ethics committee. Written informed consent will be obtained from all participants before enrollment.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Target follow-up
- 1 Week
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Adults over 18 years of age, systemically healthy, without psychological or neurological disorders, able to cooperate during examinations and procedures, university students or graduates, with at least 28 natural teeth, non-smokers, with no fixed orthodontic appliances or crown prostheses, no prior oral hygiene education from a dental professional, and a clinical diagnosis of gingivitis.
Key inclusion criteria (1 listed)
- Systemically healthy University graduates or currently enrolled in a university program Presence of 28 natural teeth No orthodontic appliances or crown restorations in the oral cavity Non-smokers No previous oral hygiene instruction from a dental professional Clinical diagnosis of gingivitis
Key exclusion criteria (1 listed)
- Presence of any systemic disease or condition that may affect periodontal health Not a university graduate and not currently enrolled in a university program Fewer than 28 natural teeth Orthodontic appliances or crown restorations present in the oral cavity Current smokers Previous oral hygiene instruction from a dental professional Clinical diagnosis of periodontitis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Oral hygiene instructionOral hygiene and gingival health of all patients were assessed using the Turesky Modification of the Quigley-Hein Plaque Index and the Gingival Index. Tooth brushing frequency was recorded. The 2D:4D ratio was calculated by dividing the second digit length by the fourth, with three measurements taken per finger to ensure reliability. A cut-off value of 1 was used to evaluate prenatal androgen influence, and participants were grouped by 2D:4D ratio (≥1 or <1). All participants received standardized oral hygiene instructions from the same instructor, including Modified Bass brushing and interdental cleaning. A second clinical exam was performed one week later by the same examiner, and both indices were re-scored. | Other | – |
Primary outcome
Mean Quigley-Hein Plaque Index Score (Turesky Modification)
Time frame: Baseline (Day 0) and 1 week after oral hygiene instruction.
Dental plaque will be scored on buccal and lingual surfaces of all teeth except third molars using the Turesky Modification of the Quigley-Hein Plaque Index (scale 0-5; 0 = no plaque, 5 = plaque covering ≥ two-thirds of crown). Scores per tooth will be averaged per participant.
Mean Löe-Silness Gingival Index Score
Time frame: Baseline (Day 0) and 1 week after oral hygiene instruction.
Gingival inflammation will be assessed on buccal and lingual surfaces at mesial, mid-buccal, and distal sites using the Löe-Silness Gingival Index (scale 0-3; 0 = healthy, 3 = severe inflammation with spontaneous bleeding). Scores will be averaged per participant.
2 secondary outcomes
Right-hand 2D:4D Digit Ratio
Time frame: Baseline (Day 0)
Self-reported Tooth Brushing Frequency
Time frame: Baseline (Day 0)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Aug 2025.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ekin Beşiroğlu Turgut study director
Okan University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Oral Hygiene and Gingivitis, run by Okan University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mean Quigley-Hein Plaque Index Score (Turesky Modification) (time frame: Baseline (Day 0) and 1 week after oral hygiene instruction.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2025.