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Evaluation of the Efficacy of a Messaging Application to Improve Oral Hygiene in Orthodontic Patients.ECA

Not Applicable
Not yet recruiting
Conditions
Oral Hygiene
Mobiles Applications
Interventions
Other: whatsapp application with oral hygiene reminder for orthodontic patients
Registration Number
NCT05527613
Lead Sponsor
Fundación Universitaria CIEO
Brief Summary

The aim of this article was to compare the efficacy of a messaging application compared to verbal instructions for improving oral hygiene in patients undergoing fixed orthodontic treatment with conventional ligature brackets (MBT technique) over a 3-month period. Randomized clinical trial of two parallel groups with 1:1 allocation ratio. Conducted in the orthodontic postgraduate clinic of the conventional ligation technique (MBT) at the Fundación Universitaria CIEO- UniCIEO, Bogotá, Colombia.

Sixty patients aged 18 to 30 years with periodontal health and active WhatsApp application on smartphone, who started fixed orthodontic treatment with conventional ligation brackets (MBT technique) were included.

Randomization Intervention: all participants received verbal oral hygiene instructions, were randomly assigned by software to the mobile app group (GAM) (n=30) (mean-----DE---- years) that used WhatsApp to reinforce oral hygiene, or to the control group (CG) (n=30) (mean-----DE---- years).

The primary outcome was bacterial plaque level determined with the orthodontic plaque index (OPI) and bleeding on probing (BOP) index measured at three points, after appliance cementation (T0), 1 month later (T1), 2 months later (T2) and 3 months later (T3). Blinding: By two trained operators and blinded to the assignment. The secondary outcome was the identification of microorganisms in the bacterial plaque of the bracket ligation. The data were analyzed by

Detailed Description

In this study the researchers are going to recruit patients from the orthodontic clinics with conventional ligation brackets of the MBT technique, from the CIEO - UniCIEO University Foundation; who receive a sequence of archwires, according to the phases of the treatment such as the initial alignment and leveling phase: Nickel - titanium archwires of caliber 0.014, 0.016. Patients entering the study will be randomly assigned to each of the groups; participants in group 1 will receive the WhatsApp application, and at the same time they will receive verbal instructions in oral hygiene; they will be sent reminders, through images and videos with necessary, accurate and instructive information; messages will be sent twice a week for three months. In group 2 the participants will receive verbal instructions given by the researcher on oral hygiene and a video with instructions on the important elements to perform oral hygiene in orthodontic patients. Two indices will also be evaluated: the orthodontic plaque index and the bleeding on probing index.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Voluntarily agree to participate in the study.
  • Age from 18 to 30 years
  • Patients undergoing orthodontic treatment with fixed appliances using the MBT technique.
  • Periodontal health on intact periodontium or diminished periodontium with no history of periodontitis, no presence of bacterial plaque score 0 No plaque deposits on tooth surfaces surrounding the bracket base; according to OPI index, no presence of periodontal pockets, calculus, gingival inflammation and bleeding verified by the periodontist.
  • Have cell phone with active WhatsApp application and possibility to connect twice a week, verified by patient interview previously.
  • No kinship between participants (affinity/consanguinity)
Exclusion Criteria
  • Systemic history (diabetes, hypertension, poor nutrition), verified by previous patient interview.
  • Smokers (smoke 10 cigarettes per day), verified by previous patient interview.
  • Pregnancy and lactation.
  • Participating in another research or oral health education program.
  • Difficulty in speaking or writing Spanish.
  • Physical or mental limitation.
  • Diagnosis of SARS COV-2.
  • Use of mouthwash during the three months of the study.
  • Use of additional appliances (lingual arch, transpalatal bar, among others)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Conventional bracket bonding with instructions by WhatsAppwhatsapp application with oral hygiene reminder for orthodontic patientswill receive the WhatsApp application, through which oral hygiene reminders will be sent through images and videos with the necessary information, and at the same time they will receive verbal oral hygiene instructions
Conventional bracket bonding without instructions by whatsappwhatsapp application with oral hygiene reminder for orthodontic patientsreceive verbal instructions on oral hygiene
Primary Outcome Measures
NameTimeMethod
Changes in oral hygiene (plaque index (OPI)the OPI index will be measured over a three-month period

It will be assessed by the orthodontic plaque index (OPI). The dentition is divided into sextants and the degree of plaque accumulation on each bracket surface (mesial, distal, gingival, incisal/occlusal) and the condition of the adjacent marginal gingivae is assessed. The OPI index is evaluated by four scores or grades; score 0 indicates absence of plaque and inflammation; scores 1 to 3 refer to the severity of plaque accumulations on adjacent brackets and score 4 includes the state of gingival inflammation.

Changes in oral hygiene (bleeding on probing index)the bleeding on probing index will be measured over a three-month period

It will be measured by means of the bleeding index according to Loe and Silness. The teeth chosen to apply the gingival index are: 1.6, 2.1, 2.4, 3.6, 4.1, and 4.4, and they are applied in four sites per tooth: distal, vestibular, mesial, and palatal. This means that 24 measurements should be recorded for each patient. The average of the 24 measurements constitutes the Bleeding Index for the whole mouth. At grade 0, there is no bleeding, no bleeding on probing (wait 10 to 30 seconds); at grade 1, there is bleeding, bleeding on probing immediately

Secondary Outcome Measures
NameTimeMethod
microbiological changes (microbiological composition of biofilm)biofilm sample and microbiological study will be performed at the beginning and in the third month of the study

The collection of supragingival microbial samples will be collected at the beginning (T0) of the study and at day 90 (T3), after recording the clinical parameters, an explorer will be used as an instrument to remove the elastie or ligature from the bracket and collect the sample from the plaque, which will then be transferred to a transport medium.

Trial Locations

Locations (1)

Fundación Universitaria CIEO -UniCIEO

🇨🇴

Bogotá, Cundinamarca, Colombia

Fundación Universitaria CIEO -UniCIEO
🇨🇴Bogotá, Cundinamarca, Colombia
Maria Gutierrez
Contact
3223120616
mf.gutierrez@unicieo.edu.co
Rocio Duarte
Contact
3118248146
jr.duarte@unicieo.edu.co
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