Skip to main content
Clinical Trials/NCT01798355
NCT01798355CompletedNot Applicable

Children and Adolescents With Dental Anxiety - Randomized Controlled Study of Cognitive Behavioral Therapy

Karolinska Institutet2 sites in 1 country30 target enrollmentStarted: January 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
2
Primary Endpoint
Changes in dental anxiety

Study Overview

Brief Summary

The purpose of this study is to determine whether cognitive behaviour therapy is effective in the treatment of children and adolescents with dental anxiety. Our hypothesis is that children and adolescents who have been offered CBT shows significant better performance on outcome measures compared with patients in control group who have received treatment as usual.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
7 Years to 19 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • The patient and parents agree to participate in the research project
  • A primary diagnosis of specific phobia (dental anxiety or needle phobia) can be established according to the Diagnostic and Statistical Manual of Mental Disorders, 4th. Edition.

Exclusion Criteria

  • The diagnostic interview shows that other psychiatric or developmentally related diagnoses should be consider as the primary diagnosis
  • The patient undergoing psychiatric examination and/or psychotherapy
  • The patient has no dental treatment needs or the dental treatment needs are of an emergency nature.

Arms & Interventions

Treatment as usual

Active Comparator

Intervention: Treatment As Usual (Behavioral)

Cognitive Behavioral Therapy

Experimental

Intervention: Cognitive Behavioral Therapy (Behavioral)

Outcomes

Primary Outcomes

Changes in dental anxiety

Time Frame: 3 months and 12 months from baseline

Both child and parental versions of Children's Fear Survey Schedule - Dental Subscale will be administered.

Secondary Outcomes

  • Changes in Behavioral Avoidance(3 months and 12 months from baseline)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shervin Shahnavaz

PhD

Karolinska Institutet

Study Sites (2)

Loading locations...

Similar Trials