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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01798355
Other study ID # KIPED20130218
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2013
Est. completion date September 2015

Study information

Verified date September 2018
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender All
Age group 7 Years to 19 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Behavioral Therapy
The treatment group is offered cognitive behavior therapy(CBT) by psychologists/psychotherapists. CBT is offered according to a treatment manual and consists of 10- sessions during 12-15 weeks.
Treatment As Usual
Treatment as usual consist of strategies such as habituation, tell-show-do, premedication with midazolam, nitrous oxide sedation and general anesthesia. All offered by dentists and dental hygienist and/or dental assistants.

Locations

Country Name City State
Sweden Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet Stockholm Huddinge

Sponsors (2)

Lead Sponsor Collaborator
Karolinska Institutet Public Dental Health Services, Eastmaninstitutet, Pediatric Dentistry, Sweden

Country where clinical trial is conducted

Sweden, 

References & Publications (3)

Shahnavaz S, Hedman E, Grindefjord M, Reuterskiöld L, Dahllöf G. Cognitive Behavioral Therapy for Children with Dental Anxiety: A Randomized Controlled Trial. JDR Clin Trans Res. 2016 Oct;1(3):234-243. doi: 10.1177/2380084416661473. Epub 2016 Aug 15. — View Citation

Shahnavaz S, Hedman-Lagerlöf E, Hasselblad T, Reuterskiöld L, Kaldo V, Dahllöf G. Internet-Based Cognitive Behavioral Therapy for Children and Adolescents With Dental Anxiety: Open Trial. J Med Internet Res. 2018 Jan 22;20(1):e12. doi: 10.2196/jmir.7803. — View Citation

Shahnavaz S, Rutley S, Larsson K, Dahllöf G. Children and parents' experiences of cognitive behavioral therapy for dental anxiety--a qualitative study. Int J Paediatr Dent. 2015 Sep;25(5):317-26. doi: 10.1111/ipd.12181. Epub 2015 Jul 4. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other General psychopathology Changes in general psychopathology is assessed by Developmental and Well-Being Assessment Questionnaire 3 months, 12 months from baseline
Other Changes in Self efficacy Self Efficacy is assessed by the Self Efficacy Questionnaire for Specific Phobias 3 months and 12 months from baseline
Primary Changes in dental anxiety Both child and parental versions of Children's Fear Survey Schedule - Dental Subscale will be administered. 3 months and 12 months from baseline
Secondary Changes in Behavioral Avoidance Behavioral Avoidance Test consists of 18 dental situations. The patient is exposed to a situation at a time. Patients receive 1 point for every step he / she manage. The test is stopped when the patient does not want to go further. 3 months and 12 months from baseline
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