Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05723133
Other study ID # BC-11037
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 24, 2022
Est. completion date July 30, 2024

Study information

Verified date January 2024
Source University Ghent
Contact Véronique Christiaens, Prof. Dr.
Phone 093324017
Email vchristi.christiaens@ugent.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to learn about the influence of providing visual feedback on brushing technique and habits on oral health of patients undergoing periodontal treatment. The main question[s] it aims to answer are: - Is patients' oral health improved by providing visual feedback on their brushing technique using the smartphone brushing app? - Is there behavioural change of patients based on this daily visual feedback? Participants will receive oral hygiene instructions after initial periodontal treatment and will be randomized in group 1, 2 or 3. Participants will be asked to - fulfill a brushing diary with the time of brushing every day. - come back for a check-up appointment every 3 weeks during the study to evaluate oral hygiene. Researchers will compare manual toothbrush, electric toothbrush without daily personal feedback and electric toothbrush with daily personal feedback to see if visual feedback provide improved oral health


Description:

Periodontitis is gum disease with jawbone deterioration. Diagnosis is based on clinical examination: plaque score, pocket measurement (measuring the pockets or gum pockets around the teeth with a probe), gingival bleeding index (= bleeding after probing) and radiographic examination. Smoking, genetic factors, and systemic diseases such as diabetes, for example, are known risk factors for this condition. Treatment consists of a deep cleaning, where the tooth roots are freed of plaque and tartar under local anaesthesia, complemented by the necessary oral hygiene instructions. It is important that patients follow these oral hygiene instructions carefully at home and perform them daily, as the aim is to achieve optimal oral hygiene. Good oral hygiene is fundamental in the treatment of periodontitis (Arweiler et al, 2018). Despite many patients undergoing the proposed professional treatment (deep cleaning), they are often insufficiently able to remove the dental plaque present on a daily basis. To optimise brushing efficiency, both behavioural change and improved brushing technique should be obtained at the patient level. The primary aim of this randomised clinical trial is to improve patients' oral health by providing visual feedback on their brushing technique using the smartphone brushing app. The secondary aim of the study is to investigate possible behavioural changes of patients based on this daily visual feedback. Patients requiring periodontal treatment will be recruited at the Department of Periodontology & Oral Implantology at Ghent University Hospital. Patients will be assigned to three groups by randomisation. In group 1, patients will receive oral hygiene instructions and a new manual toothbrush. In group 2, patients receive the same oral hygiene instructions and a basic electric toothbrush without daily personal feedback using the brushing application. In group 3, patients receive the same oral hygiene instructions and an electric toothbrush with daily personal feedback using the brushing app (Oral-B app). No raw study data will be transferred to Oral B. The only data that will be available to Oral-B is the data that will be included in the publication of this study (A1 article). The use of the app does not require registration of personal data. Brushing time, tooth surface cleaning and brushing pressure will be recorded. Patients will only complete the brushing time in the brushing diary. Oral hygiene will be evaluated at the start and every 3 weeks during the study through a check-up appointment. Only the first (after 3 weeks) and the last check-up appointment (after 12 weeks) are standard protocol, the remaining appointments (after 6 and 9 weeks) are study-specific. Oral hygiene will be assessed by: plaque score, gingival bleeding index, brushing frequency and brushing duration. The full study will take 12 weeks. Pocket depth will be measured according to usual protocols, namely at intake and at the last check-up (after 12 weeks). The patient's brushing technique and frequency will be recorded through a brushing diary completed by the patient. Where necessary, oral hygiene can be adjusted during each sitting. The check-up after 3 weeks and 12 weeks with measurement of plaque scores, gingival bleeding index and pocket depth are part of the standard protocol for treating periodontitis and are therefore not study-specific. Monitoring after 6 and 9 weeks are study-specific. The primary goal will be evaluated by comparing plaque scores and gingival bleeding index at intake with those at the final check. The secondary goal will be evaluated by brushing frequency and brushing duration throughout the study course. All data collected will be pseudonymised. Overview: - Consultation 1 - at start: o Standard treatment: Evaluation of oral hygiene Determination of clinical score: plaque score, gingival bleeding index Determination of pocket depth o Study-specific treatment (duration: 10 minutes): Clinical photographs - Consultation 2 - after 3 weeks: o Standard treatment: Evaluation of oral hygiene and brushing frequency. Determination of clinical score: plaque score, gingival bleeding index o Study-specific treatment (duration: 10 minutes): Clinical photographs - Consultation 3 - after 6 weeks: o Study-specific treatment (duration: 30 minutes ): Evaluation of oral hygiene + clinical photographs Determination of clinical score: plaque score, gingival bleeding index - Consultation 4 - after 9 weeks: o Study-specific treatment (duration: 30 minutes ): Evaluation of oral hygiene + clinical photographs Determination of clinical score: plaque score, gingival bleeding index - Consultation 5 - after 12 weeks: o Standard treatment: Evaluation of oral hygiene and brushing frequency. Determination of clinical score: plaque score, gingival bleeding index Determination of pocket depth o Study-specific treatment (duration: 10 minutes): Clinical photographs - Completion of the brushing diary by the patient: - Brushing time, cleaning of tooth surfaces, brushing pressure, brushing technique, frequency and motivation - 2x a day, 2 min per brushing


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date July 30, 2024
Est. primary completion date July 30, 2024
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - Patients in need of periodontal treatment - Willing to keep a brushing diary - Possess a smartphone so that they are able to install and handle the application on their phone Exclusion Criteria: - Smoking - Systemic disease - Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Electric toothbrush
Patients will receive oral hygiene instructions and an electric toothbrush with or without daily personal feedback using the brushing app (Oral-B app).
Behavioral:
Oral hygiene instructions
The same oral hygiene instructions are given to all patients. It is important for the patient to scrupulously follow these oral hygiene instructions at home and carry them out daily.

Locations

Country Name City State
Belgium BV Paro Glibert Geraardsbergen Oost-Vlaanderen
Belgium Ghent University Ghent Oost-Vlaanderen
Belgium Praktijk voor Parodontologie Sint-Niklaas Oost-Vlaanderen
Belgium Centrum voor Parodontologie en Orale Implantologie Zottegem Oost-Vlaanderen

Sponsors (1)

Lead Sponsor Collaborator
University Ghent

Country where clinical trial is conducted

Belgium, 

References & Publications (3)

Adam R, Ram Goyal C, Qaqish J, Grender J. Evaluation of an oscillating-rotating toothbrush with micro-vibrations versus a sonic toothbrush for the reduction of plaque and gingivitis: results from a randomized controlled trial. Int Dent J. 2020 Apr;70 Supp — View Citation

Grender J, Ram Goyal C, Qaqish J, Adam R. An 8-week randomized controlled trial comparing the effect of a novel oscillating-rotating toothbrush versus a manual toothbrush on plaque and gingivitis. Int Dent J. 2020 Apr;70 Suppl 1(Suppl 1):S7-S15. doi: 10.1 — View Citation

Nathoo S, Mankodi S, Mateo LR, Chaknis P, Panagakos F. A clinical study comparing the supragingival plaque and gingivitis efficacy of a specially engineered sonic powered toothbrush with unique sensing and control technologies to a commercially available — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Oral hygiene with or without visual feedback Comparing the plaque scores at intake with those at final check-up 12 weeks
Primary Oral hygiene with or without visual feedback Comparing the gingival bleeding index at intake with those at final check-up 12 weeks
Secondary Behavioural changes Brushing frequency will be evaluated using the brushing diary (minutes) 12 weeks
Secondary Behavioural changes Brushing durations will be evaluated using the brushing diary (number of times) 12 weeks
See also
  Status Clinical Trial Phase
Completed NCT04881357 - Antiplaque/Antigingivitis Effect of Lacer Oros Integral N/A
Completed NCT04561960 - Efficacy of Miswak in Oral Hygiene Maintenance Phase 4
Completed NCT04025684 - Efficacy of Manual Toothbrushes in Removing Dental Plaque N/A
Completed NCT03394729 - Effect of a Propolis Tablet on the Saliva and the Amount of Adolescent Dental Plaque Microbes Phase 2/Phase 3
Completed NCT05187507 - Effectiveness of Theobromine Toothpaste N/A
Completed NCT04485520 - Efficacy of the Extract of Carica Papaya as an Inhibitor of Streptococcus Mutans N/A
Completed NCT02884817 - Essential Oil+ELA, Plaque and Gingivitis Phase 4
Completed NCT02552589 - Effect of Toothpaste on the Reduction of Plaque and Inflammation N/A
Completed NCT02194023 - Clinical Effects of Two New Chlorhexidine Digluconate Formulations: 0.12% and 0.03%. Phase 2
Completed NCT01237782 - Efficacy of a Propolis-based Denture Cleanser N/A
Completed NCT00758394 - Clinical Study to Compare Dental Plaque Control Phase 3
Completed NCT00254345 - Effect of Provisional-Crown Surface Coating on Biofilm Formation Phase 1
Completed NCT05579938 - Effect of Enzymes on Dental Biofilm Accumulation N/A
Completed NCT05038293 - Efficacy of Plaque Removal of a Novel Brushing Device N/A
Terminated NCT05082103 - Effect of Enzymes on Dental Biofilm Accumulation in Healthy Individuals N/A
Not yet recruiting NCT06081868 - RCT on Effectiveness of Oral Health Preventive Programmes in School Children in Uganda N/A
Completed NCT05853679 - Regular Antibacterial Photodynamic Therapy on Oral Hygiene in Elderly Residents N/A
Completed NCT05521230 - Short-Term Anti-plaque Effect of Cymenol Mouthwash Analysed Using Dentius Deep Plaque Software Phase 1
Completed NCT03311438 - Oral Health Intervention Program for Children With Congenital Heart Defects N/A
Enrolling by invitation NCT06122636 - Efficacy of a Probiotic and Microbiological Analysis on Oral Complications Induced by Antineoplastic Therapies in Patients With HNC N/A