Standard oral hygiene instructions will be given verbally by the periodontics resident
BehavioralStandard oral hygiene instructions will be given verbally by the periodontics resident
NCT Number: NCT06622863
Patients attending Dubai Dental Hospital and requiring nonsurgical periodontal therapy will be invited to take part in the study. Potential participants will be screened and selected based on the inclusion and exclusion criteria
The aims of the randomized controlled trial are:
1. To compare the influence of AI-generated instructions versus traditional methods in improving the oral hygiene habits of patients diagnosed with periodontitis 2. To assess the time and cost effectiveness of applying AI-generated oral hygiene instructions in daily practice 3. To evaluate the level of patients' engagement, preference, and satisfaction with technology-based interactions vs. patient-doctor interaction
Research design
* Prospective, in which participants will be recruited and then followed up throughout a specified period of time. * Randomized, parallel designed, concurrent controlled trial with participants randomly allocated to either control or test groups.
The study will involve two stages, 1) Digital Avatar creation and 2) Clinical component.
The participants will be randomly allocated to two equal sized groups (30 per group) using computer-generated numbers:
Control group (C): Standard oral hygiene instructions will be given verbally by the periodontics resident.
Test group (T): Avatar-based group will receive oral hygiene instructions from a digital avatar of their choice.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Aged 18 or over.
Diagnosed with gingivitis or generalized periodontitis, Stage I-IV and Grade A-C.
Good compliance and commitment to attend follow-up review appointments.
Willing to provide informed consent.
Exclusion criteria
Received periodontal treatment in the last 12 months.
Received systemic anti-inflammatory or antibiotic treatment in the last 3 months.
History of malignancy, radiotherapy, or chemotherapy.
Pregnant or lactating women.
Use of medication known to cause gingival overgrowth.
Participants that require prophylactic antibiotic.
Standard oral hygiene instructions will be given verbally by the periodontics resident
Avatar-based group will receive oral hygiene instructions from a digital avatar of their choice
Time frame: At baseline and after 3 months
Contact information is provided by the study sponsor or research team.
Mohammed Bin Rashid University of Medicine and Health Sciences
Other
Acronym: OHI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07397104
Gingival Diseases, Gingivitis
View Trial DetailsNCT07164573
Disease, Gingival Diseases
Shanghai, Shanghai Municipality, China
View Trial DetailsNCT06510608
Gingival Diseases, Gingivitis
View Trial DetailsNCT07488403
Gingival Diseases, Gingivitis
Antalya, KONYAALTI, Turkey (Türkiye)
View Trial Details