Cognitive Behavioural Therapy and Dental Fear

November 2, 2020 updated by: Tiril Willumsen, University of Oslo

The Effect of a Dentist Administered Cognitive Behavioural Therapy (D-CBT) in Adult Patients With Dental Fear

The study is an RCT study comparing a 3-5 intervention treatment with dentist administered Cognitive Behavioural Therapy ( D-CBT) with a control treatment. The control treatment is a "treatment as usual" concept using premedication with benzodiazepines and a common sense approach.

The treatment will be performed in a regular dental office. The dentist is working as a regular dentist and is trained in the CBT Method.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

Brief Summary:

The study is an randomized clinical trial (RCT) comparing a 3-5 intervention treatment with dentist administered Cognitive Behavioural Therapy ( D-CBT) with a control treatment. The control treatment is a "treatment as usual" concept using premedication with benzodiazepines and a common sense approach.

The treatment will be performed in a regular dental office. The dentist is working as a regular dentist and is trained in the CBT Method.

Detailed Description:

Background Dental fear is common in adults and has a prevalence of about 10-25%. Approximately 2/3 of fearful patients manage to get through treatment, but with great discomfort. The remaining 1/3 avoid dental visits and some of them qualify for the diagnosis odontophobia (prevalence 1,4-7,1%).

Several studies demonstrate reduced oral health in people with dental fear and odontophobia compared to the general population.

Dental phobia often develops gradually and patients' dental health would often benefit from treatment of dental anxiety before the manifestations of phobia; before dental health deteriorate and avoidance of dental treatment has lasted too long.

Consequently, it would be beneficial if dental anxiety were effectively treated in a dentist general practice and thereby easily accessible. Thus there is a need for evidence based treatment methods for this context.

Psychological treatment of dental phobia is well documented in multidisciplinary treatment programmes were psychologists and dentists work together. However, there is a lack of psychologist resources and high cost of a treatment approach that requires 2 specialists. This emphasises the need for treatment programs of dental anxiety within dentist's competence. Dentists can, provided the right training, be successful in the utilisation of psychological techniques for the treatment of anxiety. Willumsen et al developed and tested dental anxiety treatment methods including the use of CBT interventions for use by dentists. This RCT study showed good results at post treatment, also in a 5 year follow up. Two CBT methods (applied relaxation and cognitive therapy) with contrasting principles (relaxation vs activation) were tested against nitrous oxide sedation. All three treatment approaches showed adequate effect but CBT interventions were superior in a longer time perspective. However, the treatment methods were resource demanding; requiring 10 sessions of treatment. It would therefore be beneficial to develop a shorter method of treatment that could be used by a dentist in a general practice and also to test its use within the context of a regular dental practice.

Premedication with benzodiazepines and a common sense approach including tell-show-do is the recommended and most frequent used alternative in Norway when treating this group of patients in general dental practice; Therefore the study is designed to compare the psychological intervention with these treatment modalities to explore differences in effect.

The hypothesis is that a treatment programme with D-CBT have more reduction of dental fear than traditional treatment with common sense/ premedication

The aims:

  1. Test D-CBT against a combined pharmacological common sense approach in a RCT study performed in a general dental practice.
  2. To explore whether demographical data, levels of dental fear, comorbidity, coping strategies or dentist-patient relation can predict treatment outcome of D-CBT.

  3. To do a 1-year- and 3 year follow-up on the RCT-patients with assessment of levels of dental fear in the patient, quality of life, oral quality of life and ability to receive dental treatment.

    Methods Design The study is a randomized controlled trial. Population Patients will be recruited through written and oral information to local dentists and physicians, advertising in local newspapers or referred from a waiting list at a local dental fear clinic .

    Criteria for inclusion

    • Strong dental anxiety that affects the patients self-perceived ability to go through dental treatment
    • Age over 18
    • Agreement to all the practical arrangements of the study Criteria for exclusion
    • Substance abuse
    • Not being able to communicate fluently in Norwegian Sample size Sample size was estimated with power (1-Betta) 0,8 og type error (alfa) 5%. From these criteria sample size was calculated to 30 in each group. Drop out is expected to be about 15% giving 35 participants in each group and a total of 70 participants in the RCT-study.

    Location and operator The study will be performed in a general dental practice in Mandal, a small town in the south of Norway. All patients will be treated by the same dentist, an experienced private practitioner with an interest in treating dentally anxious patients; MSH.

    Research psychologists and dentists experienced in treating patients with dental fear have developed the dentist-based cognitive behaviour treatment method (D-CBT). D-CBT is based on existing literature.

    In addition an expert group consisting of clinical psychologists and dentists, all of which are experienced in treating dental anxiety, have assessed the practical aspects of implementing the method and manual.

    A manual describes the intervention in detail. The method will be tested in 5 patients in a pilot study.

    Randomisation procedure Patients are randomized in two groups by simple randomisation. Lists will be constructed by statistical software and treatments will then be allocated to patients in sequence using numbered opaque envelopes containing treatment allocations.

    The intervention group All patients in the D-CBT group will go through 3- 5 consultations with a duration of 60 minutes or 3 sessions of 90 minutes aimed at treating their dental anxiety. The appointments will be spaced with a maximum of 2 weeks to minimize the setback that will often occur between appointments (detailed description in appendix).

    All sessions will be videotaped throughout the study. The control group The non-intervention group will be offered premedication with midazolam during dental treatment per standard procedures. Common sense principles as communication skills, control and tell-show-do will be implemented.

    Similarities between the control and the intervention groups:

    • Building a good relation with the patient
    • Stop signal will be utilized
    • Explain and show what the dentist wants to do before doing treatment (tell-show-do)
    • The treatment should be as painless as possible

    Differences between the control and the intervention groups:

    Midazolam/tell-show-do

    • Sedation is an alternative
    • Minimalizing exposure to the patient (for example hiding instead of showing the syringe while putting the anaesthetics).

    Psycological intervention -characteristics

    • Psychoeducation about anxiety
    • Exploration of the individual anxiety
    • Exposure to the frightening stimuli (no hiding, but actively showing in detail all components of dental treatment, preferably utilizing a mirror while doing treatment).

    Data Each patient receives a project number. A codebook between project number and journal number is stored at the Specialist Center of Public Dental Health in South Norway All data will be registered online using Nettskjema to collect data directly into Services for sensitive data (TSD). The research data from each patient will only be identified by the project number.

    All data will be stored and analysed using the TSD platform. TSD complies with the directive of privacy and electronic communication in Norway. TSD is developed and operated by the University of Oslos' centre for IT (USIT).

    Only MSH and the supervisors will be given access to the data in TSD. All video recordings will be stored on encrypted memory sticks locked in a filing cabinet. The key to the filing cabinet is kept in a key cabinet locked by a code. The code is known only by the dentist (MSH) and the dental secretary (KL). The recordings will be stored up until publication of articles and TW is responsible for deleting them.

    Statistics The current project uses a traditional experimental research design to assess the research hypothesis. In order to compare differences between the 35 participants in the two research conditions the data will be analysed with regression analysis. A 2x2 repeated measures ANOVA will be used to test if the experimental condition of five sessions of D-CBT treatment is superior to the control condition of premedication and gradual habituation. A factor analytic approach will be used to assess the level of influence on the results by factors like: age; gender; social economic status and substance abuse. The statistical analysis will be completed using the IBM SPSS statistical software version 16.0.

    Measure of treatment quality and adherence All sessions will be videotaped throughout the study. At least 20% of the tapes will be viewed by the supervisors to ensure continued treatment quality and adherence to manuals.

    Measures

    Demographics data:

    The following demographics will be registered: Sex, age, Norwegian skills, civil status, children, education, work status, self-assessment of health, self-assessment of oral health and substance abuse. The patients register time since last regular appointment with a dentist.

    Level of dental anxiety: Modified Dental Anxiety Scale (MDAS) and Index of dental anxiety and fear (IDAF-4C+). .

    Measures to identify factors that may influence treatment outcome:

    Post-traumatic stress disorder: Post-traumatic stress disorder-checklist (PCL).

    Depression and anxiety: The hospital anxiety and depression scale (HADS)

    Satisfaction with life:

    The Satisfaction With Life Scale (SWLS) Oral quality of life: Oral impact on daily performance (OIDP). Patient-dentist relation: Working Alliance Inventory -12 (WAI-12).

    Coping strategies: The dental coping strategy questionnaire (DCSQ). Patient assessment of the treatment: An questionnaire containing a likert scale assessing how the patients evaluate different elements of the treatment they have received has been developed based on similar scales in comparable studies Personality traits: The Big Five Inventory

    Dental reports:

    Oral examination and assessment of x-rays. Three. dentists separately record oral health and treatment needs based on the radiographs (BWs and OPG). With access to the initial clinical recordings, the diagnostic registrations will then be discussed among the three dentists until a consensus is achieved.

    Oral Health: Decayed, missed or filled teeth (DMFT).Root-filled teeth. Remnants of roots Periradicular bone lesions. Number of third molars.

    Oral treatment needs: Number of teeth with need for restorations, periodontal treatment,root fillings, bridges , dentures and extractions.

    Ethics: The study is approved by the Regional Ethics. To make sure the quality of the intervention meets adequate standards, the dentist will go through training by qualified personnel before the study is initiated and there will be a continuous surveillance by watching videotapes of the treatment to ensure that the quality will be upheld throughout the study.

    The associate supervisor of the project, psychologist Bent Storå, will be available for guidance and help when needed.

    Researchers:

    Dentist, PhD candidate Mariann Saanum Hauge (MSH), Main supervisor professor dr. odont, Tiril Willumsen (TW), Associated supervisor clinical psychologist PhD, Bent Storå(BS), Research assistant, dental secretary Kari Laudal (KL) Financial matters The study receives financial support from the Norwegian Directorate of Health through the Specialist Center of Public Dental Health in South Norway.

Study Type

Interventional

Enrollment (Actual)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Norway
      • Oslo, Norway, 0317
        • University of Oslo

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 100 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Strong dental anxiety that affects the patients self-perceived ability to go through dental treatment
  • Age over 18
  • Agreement to all the practical arrangements of the study

Exclusion Criteria:

  • Substance abuse
  • Not being able to communicate fluently in Norwegian

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Control
Treatment as usual
Combination product: Control

Intervention:

Traditional treatment of dental fear common sense/ benzodiazepine
Experimental: D CBT
Dentist administered cognitive behaviioral treatment
Behavioral: D CBT

Intervention:

a 3-5 session treatment of dental fear.

  • Psychoeducation about anxiety
  • Exploration of the individual anxiety
  • Exposure to the frightening stimuli (no hiding, but actively showing in detail all components of dental treatment, preferably utilizing a mirror while doing treatment).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Level of Dental anxiety, Dental Anxiety Scale ( MDAS)
Time Frame: At baseline, after 3-5 weeks of treatment, after 1 year and after 5 years
MDAS is a 5 item scale measuring dental anxiety in a range from 5-25. Outcome measure: change in MDAS
At baseline, after 3-5 weeks of treatment, after 1 year and after 5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Oslo

Investigators

  • Principal Investigator: Professor Willumsen, PdD, University of Oslo

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 10, 2017

Primary Completion (Actual)

November 2, 2020

Study Completion (Anticipated)

December 20, 2022

Study Registration Dates

First Submitted

September 14, 2017

First Submitted That Met QC Criteria

September 24, 2017

First Posted (Actual)

September 26, 2017

Study Record Updates

Last Update Posted (Actual)

November 3, 2020

Last Update Submitted That Met QC Criteria

November 2, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • REC-2017/97

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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