- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06083649
The Dental Care Revolution: Health Education Using AI or Humanized Counseling on Plague Control and Periodontal Treatment Outcome in Patients With Periodontal Disease
The aim of this study was to evaluate the long-term effectiveness of an AI dental monitoring intervention on patients' periodontal disease, preventive behaviors and motivation. This randomized controlled trial included experimental group: AI group (EG-A), AI-humanized group (EG-B) and control group(CG), respectively.
The EG-A and EG-B received AI dental monitoring intervention by taking mouth image at home once a week for six month. Baseline and follow-up surveys were used to collect the data in oral health related quality of life,periodontal parameters, periodontal preventive behaviors and motivation.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A randomized experimental design was used. Patients with periodontal disease whose aged 35-65 years were recruited through department of Periodontics in Kaohsiung Medical University Hospital.
Each group was expected for 100 per group, patients will be randomized into each group. G*Power (version 3.1.9.4) was used for power analysis.
All patients will underwent periodontal examination at baseline and at 1-month, 3-month, 6-month follow-ups.
Each patients will be diagnosed periodontal disease by dentist and have more than 16 functional teeth.
Each patients will completed the questionnaire at baseline and at 1-month, 3-month and 6-month follow-up.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hsiao-Ling Huang
- Phone Number: +886-7-312-1101#2159
- Email: hhuang@kmu.edu.tw
Study Locations
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Kaohsiung, Taiwan
- Recruiting
- Kaohsiung Medical University Chung-Ho Memorial Hospital
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Contact:
- FU-TZU YOU
- Phone Number: 2159 +886-7-3121101
- Email: alicedh110@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 35-65 years old
- Diagnosed periodontal disease by dentist (Comprehensive Periodontal Treatment Project)
- More than 16 functional teeth
Exclusion Criteria:
- Have received periodontal treatment within 3 months
- Patient has disease related to periodontal disease (ex. Drug-related excessive gum growth or blood clotting problems, pregnancy, mental illness)
- Disability patients
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Experimental group A (AI Group: EG-A)
The AI group scanned their own mouths at home once a week for 6 months, with each scan taking approximately 5 min.
After scanning, they uploaded the results to the AI system for evaluation.
The AI system then selected and sent a message to each patient depending on their intraoral conditions.
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DM is the first APP system used in orthopedics patients in the world,it has been widely used in Asian countries (Taiwan, Hong Kong, Singapore, Japan,etc.)
and has been used by 2140 patients so far.
DM allows patients to take in-mouth photos at home, and uses AI as a background analysis to evaluate the patient's current oral condition (including oral hygiene and gum status) based on the photo.
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Experimental: Experimental group B (AI and health counseling group: EG-B)
The AI and health counseling group scanned their own mouths at home once a week for 6 months, with each scan taking approximately 5 min.
After scanning, they uploaded the results to the AI system for evaluation.
The EG-B received both AI-assisted DM and real-person oral health counseling and advice from a counselor, who assessed their oral hygiene conditions on the basis of their scanning results and then provided individualized counseling, such as pointing out unclean teeth and offering suggestions on cleaning tools.
|
DM is the first APP system used in orthopedics patients in the world,it has been widely used in Asian countries (Taiwan, Hong Kong, Singapore, Japan,etc.)
and has been used by 2140 patients so far.
DM allows patients to take in-mouth photos at home, and uses AI as a background analysis to evaluate the patient's current oral condition (including oral hygiene and gum status) based on the photo.
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No Intervention: No Intervention: Control group (CG)
the control group(CG) only have standard oral hygiene education
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
plaque index (PI)
Time Frame: Change from Baseline PI at 1-month after intervention
|
The plaque status of 6 tooth was recorded using the plaque index, as followes: 0 = No plaque
For each patient, PI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline PI at 1-month after intervention
|
|
plaque index (PI)
Time Frame: Change from Baseline PI at 3-month after intervention
|
The plaque status of 6 tooth was recorded using the plaque index, as followes: 0 = No plaque
For each patient, PI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline PI at 3-month after intervention
|
|
plaque index (PI)
Time Frame: Change from Baseline PI at 6-month after intervention
|
The plaque status of 6 tooth was recorded using the plaque index, as followes: 0 = No plaque
For each patient, PI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline PI at 6-month after intervention
|
|
gingival index (GI)
Time Frame: Change from Baseline GI at 1-month after intervention
|
The gingival inflammation status of 6 tooth was recorded using the gingiva index, as follows: 0 = No inflammation.
For each patient, GI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline GI at 1-month after intervention
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gingival index (GI)
Time Frame: Change from Baseline GI at 3-month after intervention
|
The gingival inflammation status of 6 tooth was recorded using the gingiva index, as follows: 0 = No inflammation.
For each patient, GI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline GI at 3-month after intervention
|
|
gingival index (GI)
Time Frame: Change from Baseline GI at 6-month after intervention
|
The gingival inflammation status of 6 tooth was recorded using the gingiva index, as follows: 0 = No inflammation.
For each patient, GI will measured by the teeth 12,16,24,32,36,44 |
Change from Baseline GI at 6-month after intervention
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Probing Pocket Depth (PPD)
Time Frame: Change from Baseline PPD at 1-month after intervention
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Using periodontal probe to measure the depth from the bottom of the periodontal pocket to the gingival margin, recorded at six sites (mesial [buccal and lingual/palatal], distal [buccal and lingual/palatal], mid-buccal, and mid-lingual/palatal) around each tooth, except for the third molar.
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Change from Baseline PPD at 1-month after intervention
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Probing Pocket Depth (PPD)
Time Frame: Change from Baseline PPD at 3-month after intervention
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Using periodontal probe to measure the depth from the bottom of the periodontal pocket to the gingival margin, recorded at six sites (mesial [buccal and lingual/palatal], distal [buccal and lingual/palatal], mid-buccal, and mid-lingual/palatal) around each tooth, except for the third molar.
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Change from Baseline PPD at 3-month after intervention
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Probing Pocket Depth (PPD)
Time Frame: Change from Baseline PPD at 6-month after intervention
|
Using periodontal probe to measure the depth from the bottom of the periodontal pocket to the gingival margin, recorded at six sites (mesial [buccal and lingual/palatal], distal [buccal and lingual/palatal], mid-buccal, and mid-lingual/palatal) around each tooth, except for the third molar.
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Change from Baseline PPD at 6-month after intervention
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Clinical Attachment Loss(CAL)
Time Frame: Change from Baseline CAL at 1-month after intervention
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Using periodontal probe to measure the distance from the enamel-dentin junction to the bottom of the periodontal pocket. - Page 4 of 8 - For each patient, CAL will measured each teeth. |
Change from Baseline CAL at 1-month after intervention
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Clinical Attachment Loss(CAL)
Time Frame: Change from Baseline CAL at 3-month after intervention
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Using periodontal probe to measure the distance from the enamel-dentin junction to the bottom of the periodontal pocket. - Page 4 of 8 - For each patient, CAL will measured each teeth. |
Change from Baseline CAL at 3-month after intervention
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Clinical Attachment Loss(CAL)
Time Frame: Change from Baseline CAL at 6-month after intervention
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Using periodontal probe to measure the distance from the enamel-dentin junction to the bottom of the periodontal pocket. - Page 4 of 8 - For each patient, CAL will measured each teeth. |
Change from Baseline CAL at 6-month after intervention
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OHRQoL(OHIP-14T scales)
Time Frame: Change from Baseline at 1 month after intervention
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Item including that because of problems with your teeth or mouth, you:
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Change from Baseline at 1 month after intervention
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OHRQoL(OHIP-14T scales)
Time Frame: Change from Baseline at 3 month after intervention
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Item including that because of problems with your teeth or mouth, you:
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Change from Baseline at 3 month after intervention
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OHRQoL(OHIP-14T scales)
Time Frame: Change from Baseline at 6 month after intervention
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Item including that because of problems with your teeth or mouth, you:
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Change from Baseline at 6 month after intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Protection Motivation Theory (PMT) scores
Time Frame: Change from Baseline PMT at 1-month after intervention
|
Item including that "I think periodontal disease is a serious disease"
Cronbach's α was 0.70 for this scale. The scores ranged from one ("impossible") to ten ("very possible"), with the total possible score ranging from seven to seventy |
Change from Baseline PMT at 1-month after intervention
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Protection Motivation Theory (PMT) scores
Time Frame: Change from Baseline PMT at 3-month after intervention
|
Item including that "I think periodontal disease is a serious disease"
Cronbach's α was 0.70 for this scale. The scores ranged from one ("impossible") to ten ("very possible"), with the total possible score ranging from seven to seventy |
Change from Baseline PMT at 3-month after intervention
|
|
Protection Motivation Theory (PMT) scores
Time Frame: Change from Baseline PMT at 6-month after intervention
|
Item including that "I think periodontal disease is a serious disease"
Cronbach's α was 0.70 for this scale. The scores ranged from one ("impossible") to ten ("very possible"), with the total possible score ranging from seven to seventy |
Change from Baseline PMT at 6-month after intervention
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oral self-care behavior
Time Frame: Change from Baseline at 1 month after intervention
|
Item including that: "How many times do you brush your teeth a day?" The response was (once or twice day or three times or fours times or more/ day). "How long do you usually brush your teeth each time?" The response was lower than 1 min or 1-2 min or 2-3 min or more than 3 min/ day. "What is your main method of brushing your teeth?"The response was horizontally or vertically or Circle brush or Rotating brush or Horizontal+vertical+ and by the gum at a 45 degree angle. "How often do you replace your toothbrush?" The response was 3-6 month or more than 6 month or lower than 1 month or 1-2 month or 2-3 month. "Do you use a soft-bristled toothbrush?" The response was no or unknown or yes. "Do you have a habit of using interdental brushes?" The response was no or yes. "Do you have a habit of eating snack?" The response was no or yes. |
Change from Baseline at 1 month after intervention
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oral self-care behavior
Time Frame: Change from Baseline at 3 month after intervention
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Item including that: "How many times do you brush your teeth a day?" The response was (once or twice day or three times or fours times or more/ day). "How long do you usually brush your teeth each time?" The response was lower than 1 min or 1-2 min or 2-3 min or more than 3 min/ day. "What is your main method of brushing your teeth?"The response was horizontally or vertically or Circle brush or Rotating brush or Horizontal+vertical+ and by the gum at a 45 degree angle. "How often do you replace your toothbrush?" The response was 3-6 month or more than 6 month or lower than 1 month or 1-2 month or 2-3 month. "Do you use a soft-bristled toothbrush?" The response was no or unknown or yes. "Do you have a habit of using interdental brushes?" The response was no or yes. "Do you have a habit of eating snack?" The response was no or yes. |
Change from Baseline at 3 month after intervention
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oral self-care behavior
Time Frame: Change from Baseline at 6 month after intervention
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Item including that: "How many times do you brush your teeth a day?" The response was (once or twice day or three times or fours times or more/ day). "How long do you usually brush your teeth each time?" The response was lower than 1 min or 1-2 min or 2-3 min or more than 3 min/ day. "What is your main method of brushing your teeth?"The response was horizontally or vertically or Circle brush or Rotating brush or Horizontal+vertical+ and by the gum at a 45 degree angle. "How often do you replace your toothbrush?" The response was 3-6 month or more than 6 month or lower than 1 month or 1-2 month or 2-3 month. "Do you use a soft-bristled toothbrush?" The response was no or unknown or yes. "Do you have a habit of using interdental brushes?" The response was no or yes. "Do you have a habit of eating snack?" The response was no or yes. |
Change from Baseline at 6 month after intervention
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Collaborators and Investigators
Investigators
- Principal Investigator: Hsiao-Ling Huang, Dr.PH, Kaohsiung Medical University, College of Dental Medicine, Department of Oral Hygiene
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KMUHIRB-F(II)-20200059
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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