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

U

University of Siena

Status

Completed

Conditions

Questionnaires
Perception
Peri-implant Mucositis
Peri-Implantitis
Survey

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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).

Full description

Peri-implant diseases are inflammatory processes, influenced by biofilm, affecting the soft and hard tissues surrounding dental implants. They encompass two main conditions: peri-implant mucositis and peri-implantitis. While professional biofilm removal, coupled with plaque control, is considered the gold standard treatment, its efficacy is limited. Therefore, enhancing prevention and early diagnosis strategies for peri-implant complications is crucial. Despite extensive research on patient perception of periodontitis symptoms, little attention has been given to the symptoms and perception of peri-implant diseases and their impact on oral health-related quality of life. This observational study aims to assess patient perception of peri-implant diseases and their impact on oral health-related quality of life (OHRQoL). The study is a cross-sectional observational study. Patients will be recruited from the Unit of Periodontics, Department of Medical Biotechnologies, at "Le Scotte" University Hospital. Following diagnosis of peri-implant disease, patients meeting inclusion and exclusion criteria specified in the protocol will be included. Given the study's cross-sectional nature, no follow-up visits are planned. Validated questionnaires regarding the perception and impact on the quality of life of peri-implant diseases will be administered. Study procedures will include recording biometric parameters extracted from a complete periodontal examination and administering questionnaires on the perception and impact on the quality of life of peri-implant diseases: Brief Illness Perception Questionnaire (BIPQ) and Oral Health Impact Profile-14 (OHIP-14).

Enrollment

148 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 70 years old;
  • Presence of at least one dental implant;
  • Presence of bleeding and/or suppuration upon probing of the peri-implant mucosa;
  • Ability and willingness to provide written consent for participation in the study.

Exclusion criteria

  • Pregnancy or breastfeeding status;
  • Patients unable to communicate in Italian or English;
  • Inability to perform proper oral hygiene maneuvers;
  • Inability or unwillingness to provide written consent for participation in the study.

Trial design

148 participants in 1 patient group

Peri-implant disease patients
Description:
Patients with a diagnosis of peri-implant mucositis or peri-implantitis
Treatment:
Other: Questionnaire

Trial contacts and locations

1

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Central trial contact

Nicola Discepoli, DDS, MsC, PhD

Data sourced from clinicaltrials.gov

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