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Effect of Novel Oral Hygiene Regimen on Non-surgical Treatment of Stage II and III Periodontitis

Primary Purpose

Periodontitis

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
oral hygiene instruction
Sponsored by
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis focused on measuring mobile health, oral hygiene instruction, internet of things network, artificial intelligence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Aged 18 and above
  • Generalized Stage II and Stage III periodontitis
  • Subjects willing to receive NSPT necessary for the management of periodontitis and to comply with research appointments/schedule
  • Use of a compatible Android cell phone with Oral-B 8.5.1 Application

Exclusion Criteria:

  • Edentulism
  • Presence of any systemic disease that can alter the manifestation/outcome of periodontal treatment
  • Pregnancy or intention to become pregnant at any point during the study duration
  • Having received antibiotics within the previous 3 months
  • Need for antibiotic prophylaxis in the context of dental treatment
  • Having received professional periodontal treatment (other than supragingival cleaning) within the previous 12 months
  • Presence of xerostomia interfering with saliva sampling
  • Participation in another intervention trial
  • Inability or unwillingness of individual to give written informed consent.

Sites / Locations

  • Shanghai PerioImplant Innovation Center, Ninth People Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Test group

Control group

Arm Description

The test group will receive the novel regimen of oral hygiene instruction, including use of a commercially available intelligent toothbrush connected to the Chinese consumer version of an application and receiving targeted oral health message as well as use of interdental toothbrush

The test group will receive the standard regimen of oral hygiene instruction, including use of a commercially available manual toothbrush and receiving a brochure for oral hygiene instruction as well as use of interdental toothbrush

Outcomes

Primary Outcome Measures

changes in probing pocket depth (PPD)
changes in probing pocket depth (PPD) after non-surgical periodontal treatment (NSPT)
changes in proportion of periodontal pocket closure
changes in proportion of periodontal pocket closure defined by probing pocket depth (PPD) ≤4mm without bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)

Secondary Outcome Measures

changes in clinical attachment level (CAL)
changes of clinical attachment level (CAL) after non-surgical periodontal treatment (NSPT)
changes in bleeding on probing (BOP)
changes in bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)
changes in periodontal soft tissue volumes
changes in periodontal soft tissue volumes or reduction of tissue edema after non-surgical periodontal treatment (NSPT)
changes in oral biomarker concentration
the changes in biomarker concentration in saliva and oral rinse after non-surgical periodontal treatment (NSPT)
changes in proportion of periodontal pocket closure
changes in proportion of periodontal pocket closure is defined by probing pocket depth (PPD) ≤4mm without bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)
changes in probing pocket depth (PPD)
changes in probing pocket depth (PPD) after non-surgical periodontal treatment (NSPT)

Full Information

First Posted
November 3, 2021
Last Updated
October 24, 2023
Sponsor
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
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1. Study Identification

Unique Protocol Identification Number
NCT05137392
Brief Title
Effect of Novel Oral Hygiene Regimen on Non-surgical Treatment of Stage II and III Periodontitis
Official Title
Impact of Intensive Oral Hygiene Regimen Based on Individualized Messages and an Intelligent Power-driven Toothbrush on Non-surgical Treatment of Stage II and III Periodontitis: A Randomized, Standard of Care-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
July 1, 2023 (Actual)
Study Completion Date
October 15, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Achievement of adequate oral hygiene standards is critical to the successful treatment of gum disease. The improvement of the patient's adherence to good oral hygiene is of great importance to obtain the satisfactory treatment outcomes. However, patients' adherence to a proper daily oral hygiene regimen generally remains poor. New electric artificial intelligence powered toothbrushes are able to precisely sense the location of the brushing being performed by the patient and transmit information to the clinician who is able to analyze the data and provide targeted instructions, if needed. This study evaluates whether a novel oral hygiene instruction regimen can provide some additional benefit for periodontal treatment compared with routine oral hygiene instructions.
Detailed Description
Dental plaque is causally linked to gingival inflammation and essential for the onset of periodontitis. The main goal of periodontal treatment is the establishment of adequate infection control to reduce the bacterial load below individual threshold levels of inflammation. Achievement of adequate oral hygiene standards is critical to effective periodontal therapy. Classical studies have shown that professional tooth cleaning during healing of subgingival debridement provides superior outcomes. Regrettably, costs do not allow routine implementation of these regimens. By far, patient-centred homecare is the most cost-effective approach to maintaining good oral hygiene. Therefore, improving the adherence with self-performed oral hygiene is a priority in periodontal practice. Conventionally, clinicians provide oral hygiene instructions to the patients based on the results of their clinical examinations, sometimes supplemented with written information in brochure and disclosing agents to show the location of the biofilm. However, patients' adherence to a proper daily oral hygiene regimen generally remains poor. New technology based on an internet of things network of intelligent toothbrushes (i-Brush) has shown excellent adherence of use in a pilot study in a maintenance population. Other studies have shown that electronic messaging and mobile health (mHealth) supported by smartphones and applications improve oral hygiene performance, particularly in younger individuals undergoing orthodontic treatment. New electric artificial intelligence powered toothbrushes are able to precisely sense the location of the brushing being performed by the patient and transmit information to the clinician who is able to analyze the data and provide targeted instructions, if needed. Remote sensing of oral hygiene practices through the connected intelligent powered toothbrush allows more specific and targeted messages, thereby promoting personalized oral health care and eventually improving the healing outcomes of periodontal therapy through a two-way communication between patients and clinicians. This study aims to investigate the clinical efficacy of a novel regimen consisting of a new generation of power-driven internet connected i-Brush and targeted m-Health messages in improving periodontal treatment outcomes in comparison with routine oral hygiene instructions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis
Keywords
mobile health, oral hygiene instruction, internet of things network, artificial intelligence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Test group
Arm Type
Experimental
Arm Description
The test group will receive the novel regimen of oral hygiene instruction, including use of a commercially available intelligent toothbrush connected to the Chinese consumer version of an application and receiving targeted oral health message as well as use of interdental toothbrush
Arm Title
Control group
Arm Type
Other
Arm Description
The test group will receive the standard regimen of oral hygiene instruction, including use of a commercially available manual toothbrush and receiving a brochure for oral hygiene instruction as well as use of interdental toothbrush
Intervention Type
Other
Intervention Name(s)
oral hygiene instruction
Intervention Description
The treatment process is identical for both test and control groups except for the methods of oral hygiene instructions. In the control group, the participants will receive the following oral hygiene instructions at completion of debridement, at week-1 and week-3. In the test group, apart from the standard oral hygiene instructions at completion of debridement, at week-1 and week-3 , additional analysis of brushing data and provision of targeted brief interventions will be provided on a daily basis for the first week, 3 times/week until week 6 and once a week thereafter until 6 months after the debridement.
Primary Outcome Measure Information:
Title
changes in probing pocket depth (PPD)
Description
changes in probing pocket depth (PPD) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Title
changes in proportion of periodontal pocket closure
Description
changes in proportion of periodontal pocket closure defined by probing pocket depth (PPD) ≤4mm without bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Secondary Outcome Measure Information:
Title
changes in clinical attachment level (CAL)
Description
changes of clinical attachment level (CAL) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Title
changes in bleeding on probing (BOP)
Description
changes in bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Title
changes in periodontal soft tissue volumes
Description
changes in periodontal soft tissue volumes or reduction of tissue edema after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Title
changes in oral biomarker concentration
Description
the changes in biomarker concentration in saliva and oral rinse after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 6 months
Title
changes in proportion of periodontal pocket closure
Description
changes in proportion of periodontal pocket closure is defined by probing pocket depth (PPD) ≤4mm without bleeding on probing (BOP) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 3 months
Title
changes in probing pocket depth (PPD)
Description
changes in probing pocket depth (PPD) after non-surgical periodontal treatment (NSPT)
Time Frame
from baseline to 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged 18 and above Generalized Stage II and Stage III periodontitis Subjects willing to receive NSPT necessary for the management of periodontitis and to comply with research appointments/schedule Use of a compatible Android cell phone with Oral-B 8.5.1 Application Exclusion Criteria: Edentulism Presence of any systemic disease that can alter the manifestation/outcome of periodontal treatment Pregnancy or intention to become pregnant at any point during the study duration Having received antibiotics within the previous 3 months Need for antibiotic prophylaxis in the context of dental treatment Having received professional periodontal treatment (other than supragingival cleaning) within the previous 12 months Presence of xerostomia interfering with saliva sampling Participation in another intervention trial Inability or unwillingness of individual to give written informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maurizio Tonetti, DMD PhD
Organizational Affiliation
Shanghai Clinical Research Unit
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shanghai PerioImplant Innovation Center, Ninth People Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200125
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30761580
Citation
Toniazzo MP, Nodari D, Muniz FWMG, Weidlich P. Effect of mHealth in improving oral hygiene: A systematic review with meta-analysis. J Clin Periodontol. 2019 Mar;46(3):297-309. doi: 10.1111/jcpe.13083.
Results Reference
result
PubMed Identifier
6594355
Citation
Johansson LA, Oster B, Hamp SE. Evaluation of cause-related periodontal therapy and compliance with maintenance care recommendations. J Clin Periodontol. 1984 Nov;11(10):689-99. doi: 10.1111/j.1600-051x.1984.tb01317.x.
Results Reference
result
PubMed Identifier
31889320
Citation
Suvan J, Leira Y, Moreno Sancho FM, Graziani F, Derks J, Tomasi C. Subgingival instrumentation for treatment of periodontitis. A systematic review. J Clin Periodontol. 2020 Jul;47 Suppl 22:155-175. doi: 10.1111/jcpe.13245.
Results Reference
result
PubMed Identifier
32748486
Citation
Tonetti MS, Deng K, Christiansen A, Bogetti K, Nicora C, Thurnay S, Cortellini P. Self-reported bleeding on brushing as a predictor of bleeding on probing: Early observations from the deployment of an internet of things network of intelligent power-driven toothbrushes in a supportive periodontal care population. J Clin Periodontol. 2020 Oct;47(10):1219-1226. doi: 10.1111/jcpe.13351. Epub 2020 Aug 31.
Results Reference
result
PubMed Identifier
29926952
Citation
Tonetti MS, Greenwell H, Kornman KS. Staging and grading of periodontitis: Framework and proposal of a new classification and case definition. J Periodontol. 2018 Jun;89 Suppl 1:S159-S172. doi: 10.1002/JPER.18-0006. Erratum In: J Periodontol. 2018 Dec;89(12):1475.
Results Reference
result
PubMed Identifier
32383274
Citation
Sanz M, Herrera D, Kebschull M, Chapple I, Jepsen S, Beglundh T, Sculean A, Tonetti MS; EFP Workshop Participants and Methodological Consultants. Treatment of stage I-III periodontitis-The EFP S3 level clinical practice guideline. J Clin Periodontol. 2020 Jul;47 Suppl 22(Suppl 22):4-60. doi: 10.1111/jcpe.13290. Erratum In: J Clin Periodontol. 2021 Jan;48(1):163.
Results Reference
result

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Effect of Novel Oral Hygiene Regimen on Non-surgical Treatment of Stage II and III Periodontitis

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