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N/A N=151 Randomized Single-blind Treatment

Clinical Management of Anxiety and Access to Health Care

Dental Anxiety

Enrolled (actual)
151
Serious AEs
0.0%
Results posted
Jan 2017
Primary outcome: Primary: Change in Modified Dental Anxiety Scale — 19.5; 19.6; 15.4; 17.6 units on a scale — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Computerized Dental Anxiety Treatment (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Temple University
Primary completion
Dec 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Modified Dental Anxiety Scale
19.5; 19.6; 15.4; 17.6 <0.05 sig
SECONDARY
Change in Clinical Severity Rating for Specific Phobia Module of Anxiety Disorders Interview Schedule for DSM-IV
5.3; 4.8; 3.4; 4.0 <0.05 sig
SECONDARY
Change in Fear Rating for Specific Phobia Module of Anxiety Disorders Interview Schedule for DSM-IV
5.6; 5.2; 3.8; 4.8 <0.05 sig
SECONDARY
Change in Avoidance Rating for Specific Phobia Module of Anxiety Disorders Interview Schedule for DSM-IV
4.6; 3.9; 1.3; 1.0 <0.05 sig

Summary

Dental and health anxiety are common and potentially distressing problems, for both patients and health care providers. Anxiety has been identified as a barrier to regular dental visits and as an important target for enhancement of oral health-related quality of life. possible groups, (1) high dental anxiety and (2) low dental anxiety. The study aimed to develop and evaluate a computerized cognitive-behavioral therapy dental anxiety intervention (C-CBT) that could be easily implemented in dental healthcare settings. A cognitive-behavioral protocol based on psychoeducation, exposure to feared dental procedures, and cognitive restructuring was developed. A randomized controlled trial was conducted (N=151) to test its efficacy. Consenting adult dental patients who met inclusion (e.g., high dental anxiety) and exclusion criteria were randomized to one of two groups, (1) immediate treatment (IT) (n=74) or (2) a waitlist control (WL) (n=77).

Eligibility Criteria

Inclusion Criteria

  • high dental anxiety
  • fluent in spoken and written English

Exclusion Criteria

  • unable to provide written, informed consent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02081365). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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