About this trial
The purpose of this study is to compare an intervention for dental fear to the usual approach (i.e., whatever participants' dentist typically does to help participants manage their fear). The dental fear intervention has 2 separate steps. Step 1 (the less intensive or 'light touch' intervention step) involves using a mobile application (app). Step 2 consists of a one-hour telehealth session with a mental health provider tailored to individualized dental fear.
This is a randomized study. The time spent participating in the study will depend on which study condition(s) participants are randomly assigned to. Because this study compares the dental fear intervention to the standard approach, 25% of participants will not get the intervention during the study period. These participants (called controls) will be offered the opportunity to provide feedback about their experiences with dentists. Participants will be offered the intervention free of charge at the conclusion of the study.
For each step of the intervention (Dental FearLess app or one-on-one session) relative to treatment as usual, the investigators hypothesize that participants will show greater declines in self-reported dental fear and improved oral health-related quality of life at post-treatment and follow-up period. De-identified attendance records will be collected from dental practices.
Eligibility criteria
Qualifiers
Provide signed and dated informed consent form
Access to a smartphone or tablet
Willing to comply with all study procedures and be available for the duration of the study
13 years or older, and if under 18 years, a parent or legal guardian can consent to their participation in the study
Disqualifiers
None
Trial design
Treatments tested in this trial
- A stepped-care approach to the treatment of dental fear; Dental Fearless
Treatment groups
Sponsors and collaborators
New York University
Lead sponsor
University of Pennsylvania
Collaborator