Effect of Dental Education Duration on Halitosis and Associated Factors
Assessment of the Relationship Between Duration of Dental Education and Halitosis, Oral Hygiene Behaviors, and Associated Factors Among Dental Students
1 other identifier
observational
100
1 country
1
Brief 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.
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 Sep 2026
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
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 28, 2026
CompletedFirst Posted
Study publicly available on registry
August 3, 2026
CompletedStudy Start
First participant enrolled
September 15, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2026
Study Completion
Last participant's last visit for all outcomes
November 15, 2026
August 3, 2026
July 1, 2026
2 months
July 28, 2026
July 31, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
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.
Baseline
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.
Baseline
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.
Baseline
Secondary Outcomes (3)
Perceived Stress Level Assessed by the Perceived Stress Scale (PSS)
Baseline
Tongue Coating Index (TCI)
Baseline
Dental Caries Experience Assessed by DMFT Index
Baseline
Study Arms (2)
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.
Eligibility Criteria
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.
You may qualify if:
- 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 informed consent.
- 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.
You may not qualify if:
- 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 informed consent.
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Recep Tayyip Erdoğan University
Rize, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc. Prof.
Study Record Dates
First Submitted
July 28, 2026
First Posted
August 3, 2026
Study Start (Estimated)
September 15, 2026
Primary Completion (Estimated)
October 30, 2026
Study Completion (Estimated)
November 15, 2026
Last Updated
August 3, 2026
Record last verified: 2026-07