Tokyo, July 8 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062160) titled 'Evaluation of the usefulness of dental health guidance using an intraoral scanner: comparison with an intraoral camera' on July 7.
Study Type:
Interventional
Study Design:
Basic Design - Parallel
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Active
Primary Sponsor:
Institute - Institute of Science Tokyo
Condition:
Condition - Not applicable / Healthy volunteers
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - The purpose of this study is to compare the effects of dental health guidance using an intraoral scanner with those using an intraoral camera in individuals aged 18 to under 30 years who have not received professional education in dentistry or oral health science.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Dental health guidance using an intraoral scanner (TRIOS 3, 3Shape) will be provided. After plaque disclosure, intraoral scanner images will be used to show the oral condition and plaque accumulation sites to the participants, and toothbrushing points and the basic technique of the Bass method will be explained. The intervention will be provided twice: at baseline and at the second visit, which will be conducted between 21 and 35 days after the initial guidance.
Interventions/Control_2 - Dental health guidance using an intraoral camera (WAVE PICT SD, Yoshida) will be provided. After plaque disclosure, intraoral camera images will be used to show the oral condition and plaque accumulation sites to the participants, and toothbrushing points and the basic technique of the Bass method will be explained. The intervention will be provided twice: at baseline and at the second visit, which will be conducted after 21 days or later after the initial guidance.
Eligibility:
Age-lower limit - 18
years-old
Gender - Male and Female
Key inclusion criteria - Participants who meet all of the following criteria will be included:
1. Individuals aged 18 to under 30 years at the time of consent
2. Individuals who have not received professional education in dentistry or oral health science; however, first-year dental students may be included
3. Individuals who provide written informed consent to participate in the study
Key exclusion criteria - Participants who meet any of the following criteria will be excluded:
1. Individuals with a history of allergy to plaque disclosing agents
2. Individuals with a severe gag reflex
3. Individuals who are judged by the principal investigator to be unsuitable for participation in this study
Target Size - 30
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2026 Year 07 Month 01 Day
Anticipated trial start date - 2026 Year 07 Month 07 Day
Last follow-up date - 2026 Year 10 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071136
Disclaimer: Curated by HT Syndication.