Prevalence of Tooth Wear and Its Association with Oral Health-related Quality of Life

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age31-45
SponsorCairo University

About this trial

The aim of this study is to detect the prevalence of tooth wear (All forms of cumulative surface loss of mineralized tooth substance loss due to physical and chemico-mechanical process according to the definition of the European Organization for Caries Research (ORCA) and the International Cariology Research Group for Dental Research (IADR) i.e.: attrition, erosion and abrasion) among middle aged adult patients attending educational hospital at the Faculty of Dentistry, Cairo University and to analyze the distribution of lesions by gender and age, frequency of acidic foods and drinks consumption, medicine usage, chewing habits, systemic diseases, tooth brushing habits, and family socio economic status. Moreover, to evaluate the quality of life among middle aged elderly patients in relation to existence of tooth wear.

The study focuses on middle-aged adult patients (31-45 years) attending the Faculty of Dentistry at Cairo University during 2025-2026. It is an analytical cross-sectional study aimed at assessing the prevalence and risk level of tooth wear using the Basic Erosive Wear Examination Index (BEWE). The BEWE categorizes tooth wear into four levels (0 = no wear, 3 = severe wear), and risk levels are determined by the cumulative score.

Primary outcome: the prevalence of tooth wear and associated risk levels. Secondary outcomes: identifying predictive risk factors and assessing the Oral Health Impact Profile (OHIP) for patients diagnosed with tooth wear. All participants will be examined, and those with a BEWE score above 0 will be considered affected. Risk levels will be stratified as no risk, low, medium, or high.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

1- Patients whose age between 31 to 45 years old. 2- Egyptian 3- Males & Females 4- Provide informed consent 5- Ability to comprehend asked questions

Disqualifiers

1- Patients under or over the selected age group 2- Patients using fixed orthodontic appliances, 3- Patients with special needs

Trial population

Middle aged adult patient attending educational hospital for dental treatments free of charfge

Trial design

Design model

Ecologic or community

Time perspective

Cross-sectional

Treatments tested in this trial

  • No Intervention: Observational study for prevalence of dental wear and its association with quality of life

    Other intervention

    not applicable as it is an observational study testing the prevalence of dental wear in patients attending Cairo University

Treatment groups

1,011 Participants
are divided into 2 treatment groups
Group A: Middle aged Adults NOT suffering from dental wear0 interventions
Group B: Middle aged adults Suffering from dental wear1 intervention

Trial outcomes

Primary outcomes

1

Prevalence and risk level of tooth wear

Prevalence of wear will be tested using Basic erosive wear examination index (BEWE) 0 =no tooth wear 1. =minimal loss of surface texture 2. = distinct defect, hard tissue loss \<50% of the surface area 3. = hard tissue loss ≥ 50% of the surface area The examination is repeated for all teeth in a sextant but only the surface with the highest score is recorded for each sextant. To calculate prevalence Examined participants with score 0 will represent unaffected population % Examined participants with scores above 0 will represent the affected population % Stratification of risk levels will be done for affected population according to BEWE risk levels. The sum of the scores is calculated to provide the BEWE risk level (0-14) 0-2 = no risk 3-8= low risk 9-13= medium risk 14= high risk

Time frame
1 year

Secondary outcomes

1

• Predictive risk factors for all participants using a questionnaire

Sociodemographic data: age, gender, occupation and education Predictive risk factors: 1. Frequency of consuming acidic food and fruits, carbonated beverages and alcohol. 2. Medicine usage ( vitamin c, aspirin) 3. Chewing habits 4. Systemic diseases 5. Tooth brushing habits 6. Family socio economic status.

Time frame
1year
2

Oral Health-Related Quality of Life (OHRQoL) using a questionnaire

OHRQoL will be measured using Oral Health Index Profile (OHIP-14) questionnaire OHIP-14 is a 14-item questionnaire that measures : Functional limitation Physical pain Phycological discomfort Physical disability Social disability Phycological disability Handicap It measures responses on a Likert scale (0-4) with the following values: Never (0) Hardly ever (1) Occasionally (2) Frequently (3) Very frequently (4) Points for each response are summed so that each patient can score a minimum of 0 points and a maximum of 56 points. Low scores indicate better self-perceived quality of life, and high scores indicate worse self-perception of oral quality of life Participants diagnosed with tooth wear

Time frame
1 year

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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