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NCT Number: NCT06622863

EFFECTIVENESS OF ORAL HYGIENE INSTRUCTIONS GIVEN BY AI-GENERATED VIDEOS VS. TRADITIONAL APPROACH IN PERIODONTAL PATIENTS

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

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.

Treatment and study plan

Standard oral hygiene instructions will be given verbally by the periodontics resident

Behavioral

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

Behavioral

Avatar-based group will receive oral hygiene instructions from a digital avatar of their choice

Primary outcomes

  1. Plaque and bleeding score

    Time frame: At baseline and after 3 months

Study contacts

Contact information is provided by the study sponsor or research team.

Abeer Hakam

CONTACT

[email protected]

3053353797

Sponsors and collaborators

Lead sponsor

Mohammed Bin Rashid University of Medicine and Health Sciences

Other

Registry information

Acronym: OHI

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 2, 2024
Registry last updated
Oct 2, 2024

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.

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