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Recruiting Not applicable Interventional

Study of Anxiety Free Experiences at the Dentist

ClinicalTrials.gov ID: NCT07931131

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT07931131. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 2:12 PM EST

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Official title

One Session Treatment for Dental Phobia in an Underserved Population

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this clinical trial is to compare two treatments for dental phobia in children and adolescents: One-Session Treatment for Dental Phobia (OSTD) and psychoeducation plus relaxation training (RELAX). The main questions this study aims to answer are: * Is one intervention more effective in reducing the severity of dental phobia 6 months after treatment? * Are improvements in dental fear and anxiety maintained 12 months after treatment? * How do changes in fear-related learning and beliefs contribute to treatment outcomes? * How acceptable and practical are these treatments for youth, their parents, and the professionals delivering the treatments? Researchers will enroll approximately 160 youth with dental phobia and randomly assign them to one of two treatment groups. Participants will receive either OSTD or RELAX. Participants will: * Complete an initial assessment of their dental fear and anxiety. * Participate in their assigned treatment. * Complete assessments 1 week, 6 months, and 12 months after treatment to evaluate changes in dental fear, anxiety, and related beliefs and behaviors. Researchers will compare the two groups to determine which treatment is more effective in reducing dental phobia, whether improvements last over time, and how changes in fear-related learning may contribute to treatment outcomes.

Study identification

NCT ID
NCT07931131
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
7 Years to 16 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2026 (Estimated)
Primary completion
Mar 2030 (Estimated)
Completion
Mar 2030 (Estimated)
Last update posted
Nov 12, 2026

2026 – 2030

United States locations

U.S. sites
2
U.S. states
1
U.S. cities
2
Facility City State ZIP Site status
University of Texas Rio Grande Valley Brownsville Texas 78520 Not yet recruiting
University of Texas Rio Grande Valley Edinburg Texas 78539 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07931131, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 12, 2026 · Synced Nov 13, 2026

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