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Impact of a Personalized Video in Oral Hygiene Motivation

Impact of a Personalized Video in Oral Hygiene Motivation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03109808
Acronym
GOPERIO
Enrollment
86
Registered
2017-04-12
Start date
2017-02-15
Completion date
2018-10-15
Last updated
2017-04-12

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

Conditions

Dental Hygiene

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.

Interventions

OTHERe-health strategy

* 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.

OTHERTraditional Oral Hygiene Education

traditional oral hygiene education

Sponsors

University of Liege
CollaboratorOTHER
Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Intervention model description

* Allocation : Randomized (with stratification on center and gender) * Endpoint Classification : Safety/Efficacy Study * Intervention Model : Parallel Assignment * Masking : Double blind (Operator, Outcomes Assessor) * Primary Purpose : Prevention

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
O'Leary Plaque Control Record8 weeksMeasures the presence (1) or absence (0) of dental plaque on 6 sites per tooth for all teeth in mouth

Secondary

MeasureTime frameDescription
Bleeding on Probing Index8 weeksMeasures 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 satisfaction8 weeksMeasured by a dedicated questionnaire
Patient motivation8 weeksMeasured by a dedicated questionnaire

Countries

Belgium, France

Contacts

Primary ContactBrigitte GROSGOGEAT
brigitte.grosgogeat@univ-lyon1.fr+33 6 62 16 25 25
Backup ContactFrançois GUEYFFIER
francois.gueyffier@univ-lyon1.fr+33 4 78 78 57 55

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026