Impact of a Personalized Video in Oral Hygiene Motivation
- Conditions
- Dental Hygiene
- Interventions
- Other: Traditional Oral Hygiene EducationOther: e-health strategy
- Registration Number
- NCT03109808
- Lead Sponsor
- Hospices Civils de Lyon
- Brief Summary
Impact of a personalized video in oral hygiene motivation: The study hypothesis is that the use of a personalized oral hygiene video, made available to the patient via a cloud-based system, in conjunction with a text-based two-way recall system will increase patient compliance, hence leading to improvement or oral hygiene.
- Detailed Description
The strategy studied is composite:
* First, a personalized video of the patient's oral hygiene routine (toothbrushing and interdental hygiene) is recorded and made available to him-her via a cloud-based system. The patient is instructed to view it with his-her smartphone and/or tablet when brushing his-her teeth.
* Second, the patient is registered in a text-based recall system. This recall system will remind him-her the oral hygiene regimen suited to his-her personal situation and contains a link to his cloud-hosted video. 12 text messages for each patient will be sent over the course of the study (8 weeks). This is a two-way system as patients will be inquired about their compliance to oral hygiene. If the patient declare compliance, he-she will be congratulated (positive reinforcement). If the patient declares non-compliance, he-she will be informed he-she will be offered additional counselling at the next appointment.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 86
- 18 years old and older, having a good understanding of French language (read, write, speak, listen)
- With at least 20 teeth, including 4 first molars and 4 first or second premolars (4 interdental sites between premolars and molars)
- Patient attending an appointment in a centre participating to the trial
- Patient able to support treatment
- Patient affiliated to a health insurance scheme
- Patient giving his informed consent and accepting the modalities of the study
- Patient agreeing to attend up to 4 appointments dedicated to the study, during 8 weeks after the initial appointment (motivational interview)
- Patient in possession of an internet-enabled smartphone or tablet
- Patient has a personal e-mail address
- Patient agreeing to be registered within the system of text-based recalls for the duration of the study
- Patient having previously benefited from a periodontal therapy (less than 1 year ago) or currently enrolled in a periodontal therapy program
- Patient having previously benefited from an oral hygiene motivation session less than 1 year ago
- Patient has had a calculus removal procedure less than 1 month ago
- Patient bears orthodontic appliances (any kind, for 1 or both arches)
- Patient bears removable dental prosthesis (any kind, for 1 or both arches)
- Patient allergic to benzoic acid preservatives (or thought to be)
- Patient has a high risk of infective endocarditis
- Patient benefiting from antiaggregant or anticoagulation therapy
- Patient is haemophilic
- Patient is unable to answer questions
- Patient is unable (from a cognitive or physical standpoint) to perform toothbrushing twice a day
- Patient is unable (from a cognitive or physical standpoint) to use interdental brushes and/or dental floss (at least once a day)
- Patient uses on a regular basis (more than once a week) interdental brushes and/or dental floss in addition to toothbrushing
- Patient under tutelage or guardianship
- Patient deaf or blind
- Non cooperative patient
- Patient will be changing geographical location (ie. moving away) during the duration of the study, hence compromising follow-up visits
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Traditional Oral Hygiene Education Traditional Oral Hygiene Education Assigned intervention: traditional oral hygiene education e-health strategy e-health strategy Assigned intervention: e-health strategy
- Primary Outcome Measures
Name Time Method O'Leary Plaque Control Record 8 weeks Measures the presence (1) or absence (0) of dental plaque on 6 sites per tooth for all teeth in mouth
- Secondary Outcome Measures
Name Time Method Bleeding on Probing Index 8 weeks Measures the presence (1) or absence (0) of bleeding at the gingival margin up to 30 seconds after the insertion of the periodontal probe in the sulcus
Patient satisfaction 8 weeks Measured by a dedicated questionnaire
Patient motivation 8 weeks Measured by a dedicated questionnaire
Trial Locations
- Locations (2)
Hospices Civils de Lyon - Service de Consultations et de Traitements Dentaires
🇫🇷Lyon, France
University Hospital Liege
🇧🇪Liege, Belgium