NCT06138405 · University of Florida
Dental-Child Interaction Training
(DCIT)
What this study is about
The goal of this behavioral, interventional clinical trial is to provide a specialized workshop training for dental providers (e.g., dentists, hygienists, assistants) to improve interactions with young children (2-10 years old) and parents/caregivers. The training is derived from a well-established behavior management program for preschoolers, Parent-Child Interaction Therapy (PCIT).
View original scientific description
The goal of this behavioral, interventional clinical trial is to provide a specialized workshop training for dental providers (e.g., dentists, hygienists, assistants) to improve interactions with young children (2-10 years old) and parents/caregivers. The training is derived from a well-established behavior management program for preschoolers, Parent-Child Interaction Therapy (PCIT). The main questions it aims to answer are: * Change in behavior of dental providers * Acceptability of training by dental providers All participants will receive the same behavior training; however, one group will receive the training on a delayed schedule. Researchers will compare the immediate intervention and control group to see if the training was effective in the dental providers usage of skills.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Dental Providers
- Licensed dentist, licensed or certified dental hygienist, or dental assistant
- Provides (or willing to consider providing) dental treatment for children between 2 years and 10 years old -\>= 18 years old
- Fluent in spoken and written English
- Willing to be videotaped Parent/Caregivers
- Understands spoken and written English
- Willing to be videotaped
- Provide signed and dated informed consent form
- Willing to comply with all study procedures and be available for the duration of the study Child Dental Patients
- Child between 2 years, 0 months, and 0 days, and 10 years, 11 months, 30 days old
- Receiving preventive, restorative, emergency or any other dental treatment
- Accompanied by a parent/caregiver
- Understands spoken and written English
- Willing to be videotaped
- Parent/guardian provides signed and dated informed consent form
- Provide assent (if 7+ years old and who do not have an obvious cognitive impairment or are "mentally immature")
- Willing to comply with all study procedures and be available for the duration of the study
- In good general health as evidenced by medical history
Exclusion criteria
- Cognitive impairment or developmental delay
- Major medical problem in child
- Autism or other developmental/neurodevelopmental disorders
- Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.
Where
- Fayetteville, Arkansas
- Gainesville, Florida
- Chapel Hill, North Carolina
- Morgantown, West Virginia
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Mar 16, 2026 · Source of record for eligibility and locations