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Not yet recruitingNCT07740876Updated Aug 3, 2026

Effect of Dental Education Duration on Halitosis and Associated Factors

An observational study in Halitosis and Dentistry, sponsored by Recep Tayyip Erdogan University Training and Research Hospital. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-03.

Sponsored by Recep Tayyip Erdogan University Training and Research Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 25 Years
Sex
All
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Study summary

The study population will consist of undergraduate dental students enrolled at Recep Tayyip Erdoğan University Faculty of Dentistry. A total of 100 students, including 50 first-year and 50 fifth-year dental students, will be included. Eligible participants will be healthy students who meet the study criteria and provide written informed consent. Participants will undergo subjective and objective halitosis assessments, including questionnaires, organoleptic evaluation, volatile sulfur compound measurements, tongue coating assessment, and DMFT index recording.

Read the detailed description

Halitosis, also known as oral malodor, is a multifactorial condition primarily associated with volatile sulfur compounds produced by bacterial metabolism in the oral cavity. Although previous studies have investigated factors related to halitosis, limited information is available regarding the influence of dental education duration on objective halitosis measurements and associated behavioral and psychological factors.

This study will compare first-year and fifth-year dental students to evaluate whether the duration of dental education is associated with differences in halitosis levels. Objective measurements, including organoleptic assessment and portable digital halitometer measurements of volatile sulfur compounds, will be combined with subjective assessments of halitosis perception, oral hygiene habits, perceived stress levels, tongue coating index, and DMFT index.

The findings of this study may contribute to understanding the relationship between dental education, oral health awareness, lifestyle behaviors, psychological factors, and halitosis among future dental professionals.

02

Conditions studied

  • Halitosis
  • Dentistry

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03

In context

Halitosis

93 studies on the registry are indexed under Halitosis; 17 are open to participants now.

This study's planned enrollment of 100 is above the median of 60 across 13 observational studies indexed under Halitosis.

Browse Halitosis studies →

Lead sponsor

Recep Tayyip Erdogan University Training and Research Hospital is the lead sponsor of 88 studies on the registry; 19 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of undergraduate dental students enrolled at Recep Tayyip Erdoğan University Faculty of Dentistry. A total of 100 students, including 50 first-year and 50 fifth-year dental students, will be included in this cross-sectional observational study. Eligible participants will be healthy students who meet the inclusion criteria and provide written informed consent. The study aims to evaluate the relationship between duration of dental education and halitosis by comparing objective and subjective halitosis measurements, including organoleptic assessment, volatile sulfur compound (VSC) measurements using a portable digital halitometer, halitosis perception questionnaires, tongue coating index, DMFT index, and perceived stress levels.

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

  • Undergraduate students enrolled in the Faculty of Dentistry at Recep Tayyip Erdoğan University.
  • First-year and fifth-year dental students who agree to participate in the study and provide written .
  • Healthy students with no systemic diseases affecting oral health or halitosis assessment.
  • Students with normal nasal breathing ability.
  • Participants who comply with the pre-assessment instructions required for accurate halitosis measurements.
  • Participants who are able to complete the questionnaires and clinical evaluation procedures.

Exclusion criteria

Exclusion Criteria:

  • Students with systemic diseases that may affect halitosis, including diabetes mellitus, respiratory disorders, liver cirrhosis, chronic renal failure, or gastrointestinal disorders.
  • Participants with active upper respiratory tract infection, sinusitis, tonsilloliths, or other conditions affecting oral odor.
  • Participants with a history of antibiotic use within the previous 3 weeks.
  • Pregnant or breastfeeding students.
  • Students unwilling to provide written .
  • Students receiving active orthodontic treatment or requiring orthognathic treatment.
  • Participants unable to comply with the pre-assessment restrictions (dietary restrictions, oral hygiene restrictions, smoking and product-use restrictions) before halitosis evaluation.
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.

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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • First-Year Dental Students

    Participants in this cohort are undergraduate dental students in their first year of dental education at Recep Tayyip Erdoğan University Faculty of Dentistry. This cohort represents students at the beginning of their dental education. Participants will undergo halitosis assessment using subjective and objective evaluation methods, including halitosis questionnaire, organoleptic assessment, portable digital halitometer measurement of volatile sulfur compounds (VSCs), tongue coating index evaluation, and DMFT index recording. Perceived stress levels will also be evaluated using the Perceived Stress Scale. No intervention will be applied.

  • Fifth-Year Dental Students

    Participants in this cohort are undergraduate dental students in their fifth year of dental education at Recep Tayyip Erdoğan University Faculty of Dentistry. This cohort represents students with advanced dental education and clinical training experience. Participants will undergo halitosis assessment using subjective and objective evaluation methods, including halitosis questionnaire, organoleptic assessment, portable digital halitometer measurement of volatile sulfur compounds (VSCs), tongue coating index evaluation, and DMFT index recording. Perceived stress levels will also be evaluated using the Perceived Stress Scale. No intervention will be applied.

06

What researchers measure

Primary outcomes

  1. Halitosis Level Assessed by Organoleptic Evaluation

    Halitosis level will be assessed using the organoleptic evaluation method performed by two trained evaluators. The perceived odor intensity will be scored according to a standardized 0-5 scale: 0 = no odor, 1 = barely noticeable odor, 2 = slight but noticeable odor, 3 = moderate odor, 4 = strong odor, and 5 = extremely strong odor. The mean score of the two evaluators will be recorded as the organoleptic halitosis score. A score of ≥2 will be considered indicative of halitosis.

    Time frame: Baseline

  2. Volatile Sulfur Compound (VSC) Levels Measured by Portable Digital Halitometer

    Exhaled breath volatile sulfur compound (VSC) levels will be measured using a portable digital halitometer. Three measurements will be obtained from each participant, and the mean value will be recorded in parts per billion (ppb). Values ≥125 ppb will be considered indicative of halitosis.

    Time frame: Baseline

  3. Self-Perceived Halitosis Level Assessed by Visual Analog Scale (VAS)

    Participants' self-perception of oral malodor will be evaluated using a Visual Analog Scale (VAS) ranging from 0 to 10, where 0 indicates no perceived halitosis and 10 indicates severe perceived halitosis.

    Time frame: Baseline

Secondary outcomes

  1. Perceived Stress Level Assessed by the Perceived Stress Scale (PSS)

    Participants' perceived stress levels will be evaluated using the Turkish validated version of the Perceived Stress Scale. The scale consists of 8 items scored on a 5-point Likert scale, with total scores ranging from 0 to 32. Higher scores indicate higher perceived stress levels.

    Time frame: Baseline

  2. Tongue Coating Index (TCI)

    Tongue coating will be evaluated visually on the dorsal surface of the tongue using the Tongue Coating Index. Scores range from 0 to 3: 0 = no coating, 1 = coating covering less than one-third of the tongue surface, 2 = coating covering less than two-thirds, and 3 = coating covering more than two-thirds of the tongue surface.

    Time frame: Baseline

  3. Dental Caries Experience Assessed by DMFT Index

    Dental caries experience will be assessed using the DMFT index, which records the number of decayed (D), missing due to caries (M), and filled (F) teeth. The total DMFT score will be calculated as D + M + F.

    Time frame: Baseline

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Study locations

1 site
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07740876
Lead sponsor
Recep Tayyip Erdogan University Training and Research Hospital
Responsible party
DİLARA NİL GÜNAÇAR (Assoc. Prof., Recep Tayyip Erdogan University Training and Research Hospital) — Principal investigator
First posted
Aug 3, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Oct 30, 2026 (estimated)
Completion
Nov 15, 2026 (estimated)
Last update
Aug 3, 2026

Study contacts

Dilara Nil GÜNAÇAR
Contact
dilaranil.tomrukcu@erdogan.edu.tr
+905412940104

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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