Impact of a Personalized Video in Oral Hygiene Motivation (GOPERIO)
2017年4月11日 更新者：Hospices Civils de Lyon
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.
研究概览
详细说明
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.
研究类型
介入性
注册 (预期的)
86
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
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Liege、比利时、B-4000
- 招聘中
- University Hospital Liege
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接触：
- France Lambert
- 邮箱：France.lambert@chu.ulg.ac.be
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接触：
- Marine Robert
- 邮箱：mrobert@chu.ulg.ac.be
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Lyon、法国、69007
- 招聘中
- Hospices Civils de Lyon - Service de Consultations et de Traitements Dentaires
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接触：
- Brigitte Grosgogeat
- 电话号码：33(0)4 27 85 40 00
- 邮箱：brigitte.grosgogeat@univ-lyon1.fr
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
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
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：预防
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：e-health strategy
Assigned intervention: e-health strategy
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有源比较器：Traditional Oral Hygiene Education
Assigned intervention: traditional oral hygiene education
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traditional oral hygiene education
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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O'Leary Plaque Control Record
大体时间：8 weeks
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Measures the presence (1) or absence (0) of dental plaque on 6 sites per tooth for all teeth in mouth
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8 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Bleeding on Probing Index
大体时间：8 weeks
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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
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8 weeks
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Patient satisfaction
大体时间：8 weeks
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Measured by a dedicated questionnaire
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8 weeks
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Patient motivation
大体时间：8 weeks
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Measured by a dedicated questionnaire
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8 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2017年2月15日
初级完成 (预期的)
2018年2月15日
研究完成 (预期的)
2018年10月15日
研究注册日期
首次提交
2017年4月6日
首先提交符合 QC 标准的
2017年4月11日
首次发布 (实际的)
2017年4月12日
研究记录更新
最后更新发布 (实际的)
2017年4月12日
上次提交的符合 QC 标准的更新
2017年4月11日
最后验证
2017年2月1日
更多信息
与本研究相关的术语
其他研究编号
- 16/065
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.
e-health strategy的临床试验
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University of California, San FranciscoPatient-Centered Outcomes Research Institute完全的