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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:
Research design
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.
Enrollment
Sex
Ages
Volunteers
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.
Primary purpose
Allocation
Interventional model
Masking
60 participants in 2 patient groups
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Central trial contact
Abeer Hakam
Data sourced from clinicaltrials.gov
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