- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07424612
Comparison of Mobile Application and Traditional Methods in Classification (CMATMCPP:ACS)
Comparison of Mobile Application and Traditional Methods in Classification of Periodontitis Patients: A Cross-Sectional Study
In this study, periodontal disease classifications of patients with periodontitis were performed using a mobile application and conventional methods. A total of 122 patients with periodontitis who presented to the Periodontology Clinic of the Faculty of Dentistry at Bolu Abant İzzet Baysal University were included in the study. The classification of periodontitis was carried out according to the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions and the EFP S3-level clinical practice guideline.
In the study, periodontal classification of 122 patients with periodontitis was performed using a mobile application (Peribrain) by a student, a clinical student (manual), and a clinician (manual). In the mobile application, the following parameters were assessed: age, presence of diabetes, smoking status, deepest periodontal pocket depth, interproximal attachment loss, tooth loss, furcation defects, bite collapse, tooth migration, radiographic interproximal bone loss (%), and vertical bone loss.
For classification, plaque index, gingival index, bleeding on probing, gingival recession, and clinical attachment level were measured in the patients. The results of the three groups were compared with each other.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Bolu, Turkey (Türkiye), 14030
- Bolu Abant İzzet Baysal Üniversity
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants aged between 18 and 65 years who were diagnosed with periodontitis
- Participants did not have any intellectual disabilities
Exclusion Criteria:
- Individuals with intellectual disability
- Individuals with severe suicidal tendency
- Individuals with dementia
- Individuals with psychosis
- Individuals receiving long-term corticosteroid therapy
- Pregnant or lactating individuals
Individuals who had received periodontal treatment within the past six months
Individuals currently using antibiotics
Individuals with uncontrolled systemic diseases
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
İntern group: Fifth-year dental studentswho performed for classification.
Periobrain: Fifth-year dental students using Periobrain for classification.
|
Periodontal classifications performed manually and using a mobile application were compared.
|
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Faculty member: Assistant professor who performed the classification.
|
Periodontal classifications performed manually and using a mobile application were compared.
|
|
Periobrain: Fifth-year dental students using Periobrain for classification.
Faculty member: Assistant professor who performed the classification.
|
Periodontal classifications performed manually and using a mobile application were compared.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Periodontal classification
Time Frame: Baseline
|
Determination of the stage and grade of periodontitis according to the latest classification.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
periodontal pocket depth (PPD)
Time Frame: Baseline
|
Periodontal pocket depth measured in millimeters using a Williams periodontal probe.
The distance from the gingival margin to the bottom of the periodontal pocket was recorded at each site.
|
Baseline
|
|
Bleeding on probing (BOP)
Time Frame: Baseline
|
Bleeding on probing assessed using a periodontal probe.
After gently inserting the probe into the gingival sulcus and moving it laterally along the pocket wall, bleeding was recorded as present (+) or absent (-).pocket and gently moved laterally along the pocket wall.
+ is maximum and - is minimum.
+ indicates a worse outcome.
|
Baseline
|
|
Plaque index (PI)
Time Frame: Baseline
|
Oral hygiene status assessed using the Plaque Index, which measures dental plaque accumulation adjacent to the gingival margin.
Scores range from 0 (no plaque) to 3 (abundant plaque), with higher scores indicating poorer oral hygiene.
|
Baseline
|
|
Gingival index (GI)
Time Frame: Baseline
|
Gingival inflammation assessed using the Löe and Silness Gingival Index.
Each site was scored on a 0-3 scale, where 0 = normal gingiva and 3 = severe inflammation with edema, redness, and spontaneous bleeding.
Higher scores indicate worsening gingival inflammation.
|
Baseline
|
|
Clinical attachment level (CAL)
Time Frame: Baseline
|
Clinical attachment level measured in millimeters using a periodontal probe.
CAL was calculated as the distance from the cementoenamel junction to the bottom of the periodontal pocket and used to assess periodontal tissue support loss.
|
Baseline
|
|
Gingival recession (GR)
Time Frame: Baseline
|
Gingival recession is the apical migration of the gingival margin away from the cemento-enamel junction (CEJ), resulting in the exposure of the root surface of a tooth.
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BAIBU-DH-TS-06
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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