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Patients' Illness Perception of Peri-implant Diseases. A Cross-sectional Study

NCT06383351 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 148

Last updated 2025-09-04

No results posted yet for this study

Summary

Despite extensive research on periodontitis, little attention has been given to the symptoms and perception of peri-implant diseases and their impact on oral health-related quality of life. The study aims to assess patient perception of these diseases and their impact on quality of life through a cross-sectional observational study. Patients will be recruited from the Unit of Periodontics at "Le Scotte" University Hospital and will undergo diagnosis followed by questionnaire assessments. No follow-up visits are planned, and validated questionnaires will be administered to evaluate perception and impact on quality of life. Study procedures will include recording biometric peri-implant parameters and administering questionnaires such as the Brief Illness Perception Questionnaire (BIPQ) and Oral Health Impact Profile-14 (OHIP-14).

Conditions

  • Peri-implant Mucositis
  • Perception
  • Survey
  • Questionnaires
  • Peri-Implantitis

Interventions

OTHER

Questionnaire

Two sets of questionnaires will be administered to patients: * Questionnaire about their perception of peri-implant disease (Brief Illness Perception Questionnaire; 9 questions, answers will be registered on a scale of 0 to 10); * Oral Health Impact Profile 14 (OHIP-14) questionnaire.

Sponsors & Collaborators

  • University of Siena

    lead OTHER

Principal Investigators

  • Nicola Discepoli, DDS, MsC, PhD · Department of Medical Biotechnologies, University of Siena

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-16
Primary Completion
2024-06-27
Completion
2024-06-27

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06383351 on ClinicalTrials.gov