Sensory Adapted Dental Environments to Enhance Oral Care for Children With and Without Dental Fear and Anxiety
University of Southern California · with Children's Hospital Los Angeles, National Institute of Dental and Craniofacial Research (NIDCR) · NCT06912854
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 6–12 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 312
- US sites recruiting
- 1
- Study start
- May 9, 2025
- Record last updated
- October 2, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study is a randomized clinical trial investigating the effectiveness of a Sensory Adapted Dental Environment (SADE) alone and together with a video-based modeling (VBM) component (VBM-SADE), compared to a regular dental environment (RDE) and/or VBM alone, to reduce anxiety, distress behavior, pain, and sensory discomfort during a dental cleaning in children with and without dental fear and anxiety.
Being studied: Sensory Adapted Dental Environment; Video-based Modeling
Conditions: Dental Fear and Anxiety
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Male or female, aged 6 through 12 years, of any race/ethnicity;
- English- or Spanish-speaking child and parent;
- Have experienced at least one prior dental cleaning;
- If recruited from the emergency department, Emergency Severity Index (ESI) must be level V or IV (to ensure that greater severity PED patients not be recruited).
Exclusion Criteria
- Dental cleaning within the previous 4 months (i.e., not in need of cleaning);
- Plan to move out of the area within 6 months;
- Intellectual or developmental disability (e.g. autism; highly co-morbid with sensory processing difficulties);
- Disability that would interfere with oral care (e.g. cleft lip/palate, cerebral palsy, genetic/endocrine/metabolic dysfunction) or medical condition that would place the child at increased risk during the study (e.g., uncontrollable seizures);
- Daily use of anti-cholinergic drugs (i.e., interferes with EDA recordings);
- Presence of orthodontia (braces) or with a plan to get braces in the upcoming 6 months
Recruiting US locations
Children's Hospital Los Angeles
Los Angeles, CA 90027
Site contact: Jose Polido, DDS, MS · 323-361-4116 · jpolido@chla.usc.edu
Study contacts (from the official record)
- Leah Stein Duker, PhD, OTR/L · 323-442-0371 · lstein@chan.usc.edu
- Riley McGuire, OTD, OTR/L, MA · 323-442-0672 · riley.mcguire@chan.usc.edu
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