An interventional study of AI Chatbot and Standard Oral Hygiene Education in Peri-Implant Mucositis, Peri-implantitis and Peri-Implant Health, sponsored by University of Catania. Completed at 1 site in Italy. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-12-24.
Sponsored by University of Catania · Not applicable, Interventional, and Supportive care
Background: Dental implant therapy is a well-established and predictable procedure for replacing missing teeth, with high long-term survival rates. However, poor oral hygiene remains one of the main modifiable risk factors for peri-implant diseases such as mucositis and peri-implantitis.
Objective: The aim of this randomized controlled clinical trial is to evaluate the effectiveness of an artificial intelligence (AI)-based chatbot, developed and validated by dental experts, in improving oral hygiene and clinical outcomes in patients with implant-supported restorations, compared to traditional educational methods such as printed leaflets and dental hygienist sessions.
Methods: A total of 110 adult patients rehabilitated with dental implants were randomly assigned to either an AI chatbot intervention group or a control group receiving standard oral hygiene education. The chatbot provides continuous, personalized education and motivation through natural language interaction. Clinical and radiographic parameters, including plaque index (PI), bleeding on probing (BOP), probing pocket depth (PPD), and marginal bone loss (MBL), were recorded at baseline and at follow-up visits.
Expected outcomes: It is hypothesized that the use of an AI-based chatbot will significantly improve oral hygiene compliance and clinical outcomes compared to conventional methods.
Significance: The study aims to demonstrate the potential of AI-assisted patient education in promoting long-term peri-implant health and preventing peri-implant diseases.
Rationale and Background:
Dental implant therapy is highly successful, but peri-implant diseases, primarily caused by inadequate plaque control, remain a major cause of implant failure. Conventional oral hygiene education methods, such as verbal instructions and printed materials, often fail to ensure long-term patient compliance. Artificial intelligence (AI)-based chatbots, powered by large language models, offer a new way to provide continuous, personalized education and motivation to patients. Although their potential has been explored in orthodontics, little is known about their role in peri-implant maintenance.
Study Objective:
This randomized controlled clinical trial investigates whether an AI-based chatbot developed by dental experts can improve oral hygiene compliance and peri-implant health compared to traditional educational methods.
Study Design:
A total of 110 participants were enrolled between June 2024 and June 2025 in private dental practices in Catania, Italy. The study was approved by the local ethics committee (Protocol ID: 60/2024/CL-PAR) and conducted in accordance with the Declaration of Helsinki (2016 revision). Eligible participants were adults (≥18 years), systemically healthy or with controlled conditions, attending regular supportive periodontal therapy, and having at least one osseointegrated implant. Exclusion criteria included active periodontal disease, heavy smoking, systemic immunosuppression, and pregnancy.
Interventions:
Participants were randomly assigned to two groups:
Chatbot group: Received oral hygiene education and motivational support through an AI-based chatbot specifically developed for implant maintenance.
Control group: Received standard oral hygiene instructions through printed materials and sessions with a dental hygienist.
After the study, the chatbot was made available to the control group.
Outcome Measures:
The primary outcome was the Plaque Index (PI) at implant sites. Secondary outcomes included bleeding on probing (BOP), suppuration (SUP), probing pocket depth (PPD), and radiographic marginal bone loss (MBL).
Expected Impact:
This study aims to validate the use of AI-based educational tools as a complementary strategy for improving patient compliance, plaque control, and peri-implant health. The findings could support the safe and effective integration of AI chatbots into clinical dental practice and patient education programs.
303 studies on the registry are indexed under Peri-Implantitis; 83 are open to participants now.
This study's enrollment of 110 is above the median of 40 across 182 interventional studies indexed under Peri-Implantitis.
Browse Peri-Implantitis studies →University of Catania is the lead sponsor of 68 studies on the registry; 14 are open to participants now.
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Exclusion Criteria:
Participants receive oral hygiene education and motivational support through an AI-based chatbot developed and validated by dental professionals.
Behavioral: AI Chatbot
Participants receive standard oral hygiene education through printed informational leaflets and scheduled sessions with a dental hygienist.
Behavioral: Standard Oral Hygiene Education
An artificial intelligence-based chatbot specifically designed and validated by dental experts to provide personalized oral hygiene education and motivational support.
Participants in the Control Group receive traditional oral hygiene education, including printed informational leaflets and scheduled sessions with a dental hygienist.
Plaque Index (PI) Score at Implant Sites
The PI is considered a direct indicator of the quality of oral hygiene at home and reflects the level of plaque control achieved by each participant. Measurements will be recorded using a standard four-grade scale (0-3) at six sites per implant by a blinded examiner.
Time frame: Baseline (prosthetic loading of implant) and 6 months after intervention start.
Presence of Bleeding on Probing (BOP) at Implant Sites
Bleeding on probing (BOP) is used to assess peri-implant tissue inflammation and is defined as the occurrence of bleeding immediately upon probe withdrawal. This parameter will be recorded at six sites per implant.
Time frame: Baseline (prosthetic loading of implant) and 6 months after intervention start.
Presence of Suppuration on Probing (SUP) at Implant Sites
Suppuration (SUP) is used to assess peri-implant bacterial infection and is defined as the presence of pus upon probe withdrawal. SUP will be recorded at six sites per implant.
Time frame: Baseline (prosthetic loading of implant) and 6 months after intervention start.
Marginal Bone Loss (MBL) in Millimeters at Implant Sites
Marginal bone loss (MBL) will be assessed radiographically at the mesial and distal aspects of each implant and measured in millimeters (mm) to evaluate peri-implant bone level changes over time using standardized periapical radiographs.
Time frame: Baseline (prosthetic loading of implant) and 6 months after intervention start.
Plan to share: Yes — De-identified individual participant data (IPD) from this study, including clinical outcomes (Plaque Index, Bleeding on Probing, Probing Pocket Depth) and radiographic outcomes (Marginal Bone Loss), will be shared. Data will be provided in a format suitable for secondary analysis and will exclude any information that could directly identify participants.
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This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.
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University of Catania