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Dental Fear clinical trials

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NCT ID: NCT06228989 Active, not recruiting - Quality of Life Clinical Trials

Analysis of Treatment Outcomes in Patients Affected by Molar-Incisor Hypomineralization (MIH)

GuREx-MIH
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

The aim is to long-term evaluate extraction or restoration therapy, of first permanent molars with extensive treatment needs as a result of severe MIH in a national multicenter study concerning dental fear and anxiety, oral health-related quality of life, jaw development, and health economics.

NCT ID: NCT06142227 Not yet recruiting - Dental Fear Clinical Trials

The Effect of Reading a Pictorial Storybook on Children's Fear, Anxiety and Emotional Symptoms Before Dental Treatment

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of reading a picture storybook on children's fear, anxiety and emotional symptoms before dental treatment.

NCT ID: NCT06024395 Recruiting - Dental Fear Clinical Trials

A Stepped Care Approach to Treating Dental Fear

Start date: August 21, 2023
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT05082298 Completed - Dental Fear Clinical Trials

Dissemination of a Brief Dental Fear Intervention

Start date: August 31, 2021
Phase: N/A
Study type: Interventional

Despite the fact that several efficacious interventions for dental fear exist, it continues to be among the most common, and least addressed phobias among individuals. This reality is largely due to dissemination, or lack thereof. Research is needed on how to disseminate and implement such treatment in a way that recognizes the barriers to accessing and entering treatment for dental fear. Using a collaborative care approach, the investigators will pilot test, for feasibility and acceptability, a brief 2-step dental fear intervention. The first step will be an app intervention for moderate-to-severe dental that can be accessed by participants on a mobile device. The second step will consist of a one-hour face-to-face CBT intervention for participants delivered by a mental health professional at their dentist's office.

NCT ID: NCT05038540 Completed - Periodontitis Clinical Trials

The Effect of Virtual Reality Glasses on Dental Anxiety Control

Start date: October 8, 2021
Phase: N/A
Study type: Interventional

In this clinical study, it was aimed to evaluate whether there is a decrease in patient anxiety by applying virtual reality glasses, which are the product of new technology, during scaling and root planing treatment. Patients who required scaling and root planing treatment and also scored 9 or above according to the Dental Anxiety Scale were included in our study. Scaling and root planing was performed in a randomly selected intraoral quadrant of the patients, in the same way, with or without the use of virtual reality glasses. In the virtual reality glasses application, a video consisting of images of nature landscapes developed for patient rehabilitation was projected onto the screen in front of the patient's eyes. The Dental Anxiety Scale was reapplied after the completion of the treatment. In the intraoral quadrant where virtual reality glasses were used, it is expected that lower Corah Dental Anxiety Scale scores may be obtained after the treatment is completed, compared to the intraoral quadrant where the treatment is performed without glasses, thus reducing anxiety.

NCT ID: NCT04653974 Completed - Pain Clinical Trials

Pain Perception of Needle-free System

Start date: March 11, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate and compare the pain perception associated with a needle-free injection system( Comfort-In) and dental injection method in filling and pulpotomy treatments

NCT ID: NCT04582422 Completed - Nursing Clinical Trials

Interventional Touch Therapy in the Treatment of Children's Dental Clinics

Start date: May 20, 2020
Phase: N/A
Study type: Interventional

This study mainly wants to discuss the anxiety and fear of children's dental visits. For preschool children, separation anxiety can be obvious at this time. The main research is 1. To explore the degree of fear of dental visits in preschool children;2. Children who are touched therapy, there differences in fear of children 's dental treatment? If parents or important others can provide touching care to increase children 's sense of safety, reduce children 's fear of dental visits, and improve the quality of dental care The main purpose of the study.

NCT ID: NCT04580316 Completed - Clinical trials for Parent-Child Relations

Parental Presence and Preschoolers' Behavior

Start date: December 20, 2017
Phase: N/A
Study type: Interventional

Purpose: This study aimed to assess the effect of parental active/passive presence technique (PAP/PPP) on the overall behavior of preschool children with different intelligence and fear levels. Methods: This randomized controlled trial recruited 150 healthy children, 3-6 years old, with no history of previous dental pain/treatment, IQ level ≤70 to ≤110. After sample collection, in the first visit, children were stratified according to their Intelligence Quotient into 3 equal groups (high, average, low) in which each group was further equally and randomly divided into 2 sub-groups (test and control). In the second visit, before intervention with preventive measures, dental fear was assessed using facial image scale. During intervention, the control sub-groups were managed using PPP technique, while the test sub-groups were managed using PAP technique. Overall behavior was assessed using Frankl behavior rating scale at the end of the 2nd visit. Data was analyzed using chi-square test and logistic regression analysis. Results: The PAP technique had significantly higher odds of positive behavior than the PPP technique (P=0.002). Conclusions: Children with low intelligence showed higher dental fear and negative behavior in the dental setting. PAP technique had significant positive effect on the children's overall behavior with different fear and intelligence levels.

NCT ID: NCT04483336 Completed - Dental Anxiety Clinical Trials

Virtual Reality Distraction During Dental Local Anesthesia Among Children

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

To evaluate the effect of virtual reality (VR) distraction on anxiety and pain during buccal infiltration anesthesia (BIA) in pediatric patients.

NCT ID: NCT04207515 Completed - Dental Anxiety Clinical Trials

The Effect of Conscious Sedation on Acute Stress

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

The specific aims of the present study were to evaluate sAA responses to impacted third molar extractions at different time points in the patients under conscious sedation with local anesthesia and to examine the relationship between sAA, conscious sedation and dental anxiety. The null hypothesis was that conscious sedation could be considered to reduce salivary alpha amylase level during the wisdom tooth surgery.