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The WhiteTeeth app to promote oral hygiene

A Randomized Control Trail to Evaluate the Effectiveness a Smartphone Intervention - WhiteTeeth App - in improving Oral Health Behavior and Oral Hygiene in Adolescents with Fixed Orthodontic Appliances

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON27130
Enrollment
144
Registered
2017-02-20
Start date
2016-12-02
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral hygiene, prevention of dental caries, WhiteTeeth app, smartphone intervention, psychosocial factors, oral health behavior

Interventions

This study is a parallel randomized controlled trial with two conditions: the experimental group, which receives the WhiteTeeth app in addition to care as usual, and the control group receiving only c

Sponsors

no sponsors.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients are eligible for the study if they meet the following criteria: - Boys and girls aged 12 to 16 - For at least 1,5 month maxillary and mandibular fixed orthodontic appliance therapy, which consists of bonding of at least premolar-to-premolar with edgewise appliances and their modifications. - Not scheduled to remove fixed orthodontic treatment before the end of the study. - Able to perform their own oral hygiene activities, without physical and/or mental disabilities. - Not engaged in other oral health education or research program. - No enamel and dentine dysplasia and/or craniofacial malformation (e.g. cleft). - Sufficient command of the Dutch language. - In the possession of smart-phone with the software IOS >7 or Android > 4.1. - Patients and their parents are able or willing to give informed consent. - Patients that have not use medication that may affect plaque accumulation, for example antibiotics and antibacterial mouth rinses. - All patients in the study receive upper and lower fixed orthodontic treatment.

Exclusion criteria

Exclusion criteria: See the inclusion/eligibility criteria.

Design outcomes

Primary

MeasureTime frame
The primary outcomes of the study are the presence of dental plaque (measured with a modified Silness and Loë Plaque Index), gingival bleeding (measured with the Bleeding on Marginal Probing Index), and self-reported oral health behaviors. The plaque index will be used to describe the amount of plaque on the buccal surfaces of the first premolars, canines and incisors using a mouth mirror and a probe. The buccal surface of each tooth is divided into four zones according the position of the orthodontic bracket: mesial, distal, gingival and incisal to the bracket. Each of the four sites of the buccal tooth surface is given a score from 0 (absence) to 3. For the bleeding score, three sections (mesio-vestibular, vestibular, disto-vestibular) of the vestibular surfaces of the first premolar, canines and incisors will be assessed to determine whether probing elicited marginal bleeding (score 1) or not (score 0). Data are collected at baseline, and 6 and 12 weeks follow-up.

Secondary

MeasureTime frame
Secondary outcomes include changes in psychosocial factors of the HAPA model, such as outcome-expectancies, intention, action-self-efficacy, coping planning and action control. A self-administered digital questionnaire contains questions with both single and multiple response items concerning oral health behaviors and their psychosocial factors. Data are collected at baseline, and 6 and 12 weeks follow-up.

Contacts

Public ContactJanneke F.M. Scheerman

Hogeschool Inholland Amsterdam

janneke.scheerman@inholland.nlMob: +31 630 9887 01

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)