Evaluation of Nutritional Habits, Oral Hygiene, Relationship Between Dental Caries and Periodontal Condition

November 8, 2023 updated by: Dilek Özkan Şen, Necmettin Erbakan University

Evaluation of Nutritional Habits, Oral Hygiene Status, Relationship Between Dental Caries and Periodontal Condition

The purpose of this observational study is to identify the dental and periodontal health issues, oral hygiene practices, and potential relationships between them by assessing the variables that may have an impact on them.The main questions its aims to answer are:

Is there a relationship between compliance with the Mediterranean diet and periodontal status? Is there a relationship between physical activity and periodontal status?

Study Overview

Detailed Description

Patients who will visit the Periodontology Clinic will be consecutively enrolled in the study by one of the researchers (D.O.S), if they meet the following criteria:

  • No smoking.
  • Not having undergone dental scaling and root surface correction treatment in the last 6 months.
  • Presence of at least 20 teeth in the mouth.
  • Not pregnant and/or breastfeeding.
  • Patients taking drugs known to alter bone metabolism or having established degenerative bone diseases (hyperparathyroidism, osteoporosis).
  • Patients who have not received antibiotics, nonsteroidal anti-inflammatory drugs, or corticosteroids for >2 weeks in the 3 months prior to the study.
  • Patients who agree to participate will undergo an oral examination and answer a questionnaire survey.

Periodontal Examination: Routine clinical periodontal parameters such as plaque index (PI), gingival index (GI), Probing pocket depth (PPD), bleeding on probing (BOP), clinical attachment levels, and gingival recession will be recorded in all patient groups before treatment [13]. Individuals will be classified according to the 2017 classification [14].

After 30 seconds, at six locations per tooth, a calibrated clinical researcher will measure the probing depth (PD), which is the distance between the free gingival margin and the pocket depth, the clinical attachment level (CAL), which is the distance between the cement-enamel attachment and the pocket depth, and the bleeding on probing (BOP) [15]. According to the World Workshop on Classification and Conditions of Periodontal and Peri-implant Diseases 2017, periodontitis will be identified [14]. The PD severity index will be calculated as the percentage of teeth with PD higher than or equal to 4 mm in two or more interproximal locations [16]. Mean PD, CAL, and BoP will also be obtained. Additionally, the quantity of teeth will be recorded.

To the individuals included in the research; A questionnaire consisting of 16 questions including demographic data of individuals, the number of daily snacks, daily carbohydrate-containing food and sugary drink consumption frequency, tooth brushing frequency, and duration, education level, and oral care habits will be filled [17].

Dietary habits: assessed by the Mediterranean Diet Score (MDS) questionnaire and classified as low adherence (score ≤5), medium adherence (score 6-9), or high adherence (score ≥10) [18, 19].

Dental Examination: Number of decayed, missing, and filled teeth (DMFT) assessed by visual inspection and radiographic assessment following the International Caries Detection and Assessment System (ICDAS). All tooth surfaces will be examined, but the observations will be recorded per tooth [20].

Physical activity assessment: PA will be assessed through the validated short version of the International Physical Activity Questionnaire (IPAQ)[21]. The IPAQ automatic report will categorize the total PA level as low, moderate, or high (https: //theipaq/home).

2.5 Statistical analysis Using IBM SPSS V23, the data will be examined. The Kolmogorov-Smirnov and Shapiro-Wilk tests will be used to gauge conformity to the normal distribution. Multiple comparisons will be examined using the Bonferroni Corrected Z Test, and categorical variables will be examined using the Pearson Chi-Square Test. To compare the parameters with the normal distribution according to the groups, a one-way analysis of variance will be utilized. The parameters that do not meet the normal distribution according to the groups will be compared using the Kruskal-Wallis test and multiple comparisons using the Dunn test. For categorical variables, the analysis findings will be shown as frequency (%), whereas for quantitative variables, the results will be shown as mean, standard deviation, and median (minimum to maximum). P 0.050 will be used as the significance level. The risk factors affecting the disease will be examined by Binary Logistic Regression Analysis, and the Enter method will be used to include the variables in the model. Analysis results will be presented as frequency (percentage) for categorical variables and as mean ± standard deviation for quantitative variables. The significance level will be taken as p<0.050.

Study Type

Observational

Enrollment (Actual)

180

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Meram
      • Konya, Meram, Turkey, 42050
        • Necmettin Erbakan Üniversitesi Diş Hekimliği Fakültesi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

Patients who visited the Necmettin Erbakan University Faculty of Dentistry Periodontology Clinic ,if they met the following criteria:

Description

Inclusion Criteria:

  • Not having undergone dental scaling and root surface correction treatment in the last 6 months
  • Presence of at least 20 teeth in the mouth
  • Not pregnant and/or breastfeeding
  • Patients taking drugs known to alter bone metabolism or no established degenerative bone diseases (hyperparathyroidism, osteoporosis)
  • Patients who have not received antibiotics, nonsteroidal anti-inflammatory drugs, or corticosteroids for >2 weeks in the 3 months prior to the study.

Exclusion Criteria:

  • Individuals who did not meet the inclusion criteria and did not agree to participate in the study were excluded from the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Diagnosis of gingivitis
60
Diagnostic Test: Full periodontal chart A full periodontal chart will be carried out including all biometric periodontal variables: Probing Pocket Depth (PPD), Bleeding on Probing (BoP), presence of Plaque, recession (REC), Full Mouth Plaque Score (FMPS), Full Mouth Bleeding Score (FMBS), presence of furcation and mobility. Periodontal status, as assessed by the periodontal chart, will be evaluated following the New Classification of Periodontal and Peri implant diseases.
Diagnosed as periodontal healthys
60
Diagnostic Test: Full periodontal chart A full periodontal chart will be carried out including all biometric periodontal variables: Probing Pocket Depth (PPD), Bleeding on Probing (BoP), presence of Plaque, recession (REC), Full Mouth Plaque Score (FMPS), Full Mouth Bleeding Score (FMBS), presence of furcation and mobility. Periodontal status, as assessed by the periodontal chart, will be evaluated following the New Classification of Periodontal and Peri implant diseases.
Diagnosis of periodontitis
60
Diagnostic Test: Full periodontal chart A full periodontal chart will be carried out including all biometric periodontal variables: Probing Pocket Depth (PPD), Bleeding on Probing (BoP), presence of Plaque, recession (REC), Full Mouth Plaque Score (FMPS), Full Mouth Bleeding Score (FMBS), presence of furcation and mobility. Periodontal status, as assessed by the periodontal chart, will be evaluated following the New Classification of Periodontal and Peri implant diseases.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
INVESTIGATION OF THE RELATIONSHIP BETWEEN PERIODONTAL DISEASE AND ADAPTION TO THE MEDITERRANEAN DIET.
Time Frame: BASELİNE
Dietary habits: Assessed by the Mediterranean Diet Score (MDS) questionnaire and will be classified as low adherence (score ≤5), medium adherence (score 6-9) or high adherence (score ≥10). Its effect on periodontal status will be determined.
BASELİNE
INVESTIGATION OF THE RELATIONSHIP BETWEEN PERIODONTAL DISEASE AND ADAPTION TO THE PHYSİCAL ACTİVİTY
Time Frame: BASELİNE
Physical activity assessment: PA will be assessed through the validated short version of the International Physical Activity Questionnaire (IPAQ). The IPAQ automatic report will classify the total PA level into low, medium and high.A high score means high physical activity.
BASELİNE

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 2, 2023

Primary Completion (Actual)

May 15, 2023

Study Completion (Estimated)

November 20, 2023

Study Registration Dates

First Submitted

May 30, 2023

First Submitted That Met QC Criteria

November 8, 2023

First Posted (Actual)

November 13, 2023

Study Record Updates

Last Update Posted (Actual)

November 13, 2023

Last Update Submitted That Met QC Criteria

November 8, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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