Comparison of the Effectiveness of Three Teaching Methods in Oral Hygiene in Adolescent Orthodontic Patients

Not Applicable

Recruiting

• Conditions: Orthodontic Appliance
• Interventions: Behavioral: Control group; Behavioral: Group with active participation; Behavioral: Group with video and quizz

• Registration Number: NCT04444154
• Lead Sponsor: Rennes University Hospital

Brief Summary

Orthodontic appliances have been shown to interfere with oral hygiene maneuvers by providing many additional sites for formation and retention of biofilm.

Its accumulation is responsible for undesirable effects such as decays and periodontal pathologies. These lower the benefit / risk ratio of orthodontic treatments. In addition, their management is not negligible at the macroeconomic level.

As such, it is more than necessary for the orthodontist to teach oral hygiene methods adapted to each of his patients fitted to limit the risk of appearance of biofilm.

Detailed Description

Patients applying for orthodontic treatment with braces in the orthodontic unit of the Rennes dental center will be offered to participate in the study. For each patient, the inclusion and non-inclusion criteria will be checked, and consent and a document explaining the course of the study will be delivered to them personally. The duration of the study will be 6 months for each of them. Each will be randomized to one of three study groups. Throughout the study, patients in groups 1 and 2 will have to make 5 appointments. Group 3 patients must honor 6 appointments.

Patients in group 1 (control group) will receive oral hygiene advice given orally in the chair during the bonding appointment and at each check-up appointment. Patients in group 2 will receive these same oral advice, associated with a demonstration of brushing methods in the sink with active participation (use of plate developer and then the Oral B electric toothbrush with special orthodontic head) during the bonding appointment as well than at each check-up appointment. Patients in group 3 will receive the same treatment as those in group 1 but will have an additional appointment between the device bonding appointment and the first check-up. This is a 15-minute session dedicated to teaching oral hygiene. This session will include watching of an educational video followed by a quiz, as well as the application of the methods taught in the sink (using plate developer and the Oral B electric toothbrush with special orthodontic head).

At the end of the appliance bonding appointment (first appointment) each patient (from each group) will leave with a hygiene kit including an electric toothbrush with two orthodontic heads, an Oral B toothpaste, from orthodontic wax and the analgesic prescription conventionally performed when installing a device.

The plaque index readings, i.e. the taking of 3 macrophotographic shots (with reflex camera, allowing the MOP plaque index to be assessed in a second step), and the clinical index of gingival inflammation will be performed at each appointment (except during the dedicated session of group 3) by an examiner who will be blind from the group belonging to each patient.

Exception made for the day of bonding, during which the plate index reading will be made just before the placement of the multi fasteners via the Loë and Silness plate index (which is an index adapted to patients not fitted).

Study Timeline

• Study First Submitted: 2020-05-12
• Study First Submitted QC: 2020-06-22
• Study First Posted: 2020-06-23
• Study Start: 2022-01-29
• Status Verified: 2023-01
• Last Update Submitted: 2023-01-17
• Last Update Posted: 2023-01-18
• Primary Completion: 2025-01-29
• Study Completion: 2025-01-29

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

• Patient aged 11 to 17 * years;

• Patient with stable adolescent teeth, young adult or adult teeth;

• Requiring a fixed orthodontic treatment without extraction (other than wisdom teeth) at least to the maxillary arch;

• Affiliated, himself or through his parents to a social security scheme;

• Having received information on the protocol and having given free, informed and written consent.

• Whose holders of parental authority have received information on the protocol and have given free, informed and written consent.

  • Aged under 18 at the end of the 6 months of participation

Exclusion Criteria

• Patient with periodontal disease or progressive carious lesions;
• Patient with a prosthetic crown or composite restoration on the central and / or lateral maxillary incisor;
• Patient with systemic disease, major syndrome or cleft palate;
• Patient with an abnormal dental structure (eg fluorosis, MIH, imperfect amelogenesis, etc.);
• Patients taking long-term medication influencing periodontal health (corticosteroids, anti-epileptics, etc.);
• Patient with a physical or mental handicap preventing him from carrying out oral hygiene maneuvers independently;
• Patient refusing to use the products and instruments prescribed for the study;
• Patients with dental agenesis;
• Patients with poor command of the French language
• Patient deprived of liberty by judicial or administrative decision or subject to a legal protection measure;
• Pregnant patient;
• Smoking patient.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control group	Control group	oral hygiene advice given orally
Group with active participation	Group with active participation	oral hygiene advice given orally and demonstration of brushing methods in the sink with active participation
Group with video and quizz	Group with video and quizz	oral hygiene advice given orally and an additional appointment between the device bonding appointment and the first check-up. This is a 15-minute session dedicated to teaching oral hygiene. This session will include watching of an educational video followed by a quiz, as well as the application of the methods taught in the sink (using plate developer and the Oral B electric toothbrush with special orthodontic head).

Primary Outcome Measures

Name	Time	Method
Compare the effectiveness of 3 methods of teaching oral hygiene in terms of controlling biofilm formation: MOP (Modified Orthodnotic Plaque Index) classification	6 months of intervention	The average plaque index at six months after inclusion according to the MOP (Modified Orthodnotic Plaque Index) classification. It is evaluated on macro photography in a standardized manner by a blind examiner of the patient's randomization arm. The values range from 0 to 4 for each tooth, which makes an average score of 0 to 48 for the maxillary arch. 0 is the absence of plaque while 48 is an abundance of plaque on all teeth, the worst situation. The score is expressed in absolute value without unit.

Secondary Outcome Measures

Name	Time	Method
Compare the effectiveness of three teaching methods in oral hygiene for the control of gum inflammation: gingival index at six months after inclusion according to the Loë and Silness scale	6 months after bonding the device.	The mean gingival index at six months after inclusion according to the Loë and Silness scale. It will be evaluated in the mouth in a standardized manner by a blind examiner of the patient's randomization arm. The values range from 0 to 3 for each side of each tooth, which makes an average score of 0 to 144 for the maxillary arch. 0 corresponds to no bleeding on probing whereas 3 characterizes a situation of spontaneous bleeding of the gum, worst situation. The score is expressed in absolute value without unit.
Compare the effectiveness of three methods of teaching oral hygiene over time: MOP classification plate index	at 4½ months after installation of the device	The comparison of the three treatment groups as a function of time will be based on two judgment criteria. The first is the MOP classification plate index. It is evaluated on macrophotographs in a standardized manner by a blind examiner of the patient's randomization arm. The values range from 0 to 4 for each tooth, which makes an average score of 0 to 48 for the maxillary arch. 0 is the absence of plaque while 48 is an abundance of plaque on all teeth, the worst situation. The score is expressed in absolute value without unit.
Compare the effectiveness of three methods of teaching oral hygiene over time: gingival index according to the Loë and Silness scale	at 4½ months after installation of the device	The comparison of the three treatment groups as a function of time will be based on two judgment criteria. The second is the gingival index according to the Loë and Silness scale. It will be evaluated in the mouth in a standardized manner by a blind examiner of the patient's randomization arm. The values range from 0 to 3 for each side of each tooth, which makes an average score of 0 to 144 for the maxillary arch. 0 corresponds to no bleeding on probing whereas 3 characterizes a situation of spontaneous bleeding of the gum, worst situation. The score is expressed in absolute value without unit.

Trial Locations

Locations (1)

CHU de RENNES; 🇫🇷 Rennes, France