Anxiety Assessment Intervention in Dental Patients (ANXDEN)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01190774
Recruitment Status : Completed
First Posted : August 30, 2010
Last Update Posted : August 30, 2010
University of Manchester
Information provided by:
University of St Andrews

Brief Summary:

Dental anxiety is a significant barrier to the acceptance of regular dental care, and has many negative consequences. A study by Dailey et al. (2002) found that providing the dentist with information of the high level of a patient's dental anxiety prior to treatment using the Modified Dental Anxiety Scale (MDAS, Humphris et al., 1995), lead to a significant reduction in state anxiety from pre- to post- dental consultation compared to a control group. The current study aimed to replicate the study by Dailey et al. (2002), and to further explore whether the reduction in state anxiety associated with the MDAS could be explained by a change in dentist behaviour on receiving it, or a change in patient expectancy about the treatment session, or both.

The design was a randomised control trial involving three groups, which aimed to manipulate possible changes in dentist behaviour and patient expectancy. In Group 1, the MDAS was left at reception, as expected by the patient. In Group 2, the dentist received the MDAS, although the patient did not expect this. In Group 3 the dentist received the MDAS and the patient did expect this. The sample (N=182) was taken from two dental access centres, and included participants obtaining a score of 19 or above, or 5 on any one item of the MDAS. Pre- and post-dental consultation measures of state anxiety were taken using the six-item short-form of the state scale of the Spielberger State-Trait Anxiety Inventory (STAI-S, Marteau & Bekker, 1992).

Condition or disease Intervention/treatment Phase
Anxiety State Behavioral: Information to health provider without patient knowledge Behavioral: dentist behaviour and patient expectancy Phase 2 Phase 3

Detailed Description:

The aim of the current study was to compare the degree of anxiety reduction in dentally anxious patients attending a Dental Access Center where the dentist did or did not receive the patients' assessment of dental anxiety.

METHODS Design of study A three group pre-and post-test design was adopted, a control group (Group1: patient completed the MDAS (Modified Dental Anxiety Scale) questionnaire and handed it to the receptionist) and the experimental group where the patient handed the MDAS to the dentist (Group 3). An additional group was included (Group 2). Patients completed the MDAS and handed it to the receptionist whereupon it was given to the dentist contrary to patient expectation. The dental staff were kept blind to the actual design of the study. The Local Research and Ethics Committee approved the study.

Test the hypothesis that patients sharing assessment information about their dental anxiety to members of the dental team has beneficial effects on their state anxiety.

Randomisation A block randomisation schedule was computer generated by University of Manchester statistician (BT). Pre-sealed opaque envelopes that contained questionnaires specific to the three groups were prepared by a colleague to minimise selection bias. All materials were pre-coded with the participant number.


Dental Access Centers provide: general dental services to those who are not registered with a NHS dentist, NHS patient charges and receipt of easily available treatment and advice (appointment not always necessary). The study was conducted at two Greater Manchester Dental Access Centers. These sites offered treatment to emergency dental patients who were more likely to become dentally anxious than regular attenders (Maggirias and Locker, 2002) . Participants were volunteers recruited, from October 2003 to April 2004.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 182 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Care Provider)
Primary Purpose: Health Services Research
Official Title: An Investigation Into Patients' State Anxiety Reduction Following the Administration of a Dental Anxiety Questionnaire in the Dental Treatment Setting
Study Start Date : September 2003
Actual Primary Completion Date : April 2004
Actual Study Completion Date : September 2004

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anxiety

Arm Intervention/treatment
Experimental: Dentist behaviour
Patient completes the MDAS which is handed to receptionist who then gives the information to the dentist with patient knowledge
Behavioral: Information to health provider without patient knowledge
The intervention consists of the assessment information from the MDAS questionnaire being given to the dentist via the receptionist without the knowledge of the patient

Experimental: Dentist behaviour and patient expectancy
Patient completes the MDAS and hands to the dentist
Behavioral: dentist behaviour and patient expectancy
patient give information about their dental anxiety to the dentist

Primary Outcome Measures :
  1. State Anxiety [ Time Frame: immediately after dental appointment ]
    Speilberger's State-Trait Anxiety Inventory, short form

Secondary Outcome Measures :
  1. Discussion of dental anxiety with dentist [ Time Frame: during appointment ]
    Simple 'yes' 'no' dichotomy

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • scores 19 and above on MDAS
  • read and write English
  • 18 years of age and above

Exclusion Criteria:

  • mental illness

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01190774

United Kingdom
University of Manchester
Manchester, United Kingdom, M13 9PL
Sponsors and Collaborators
University of St Andrews
University of Manchester
Study Director: Gerald M Humphris, PhD University of St Andrews

Responsible Party: Professor Nick Tarrier, University of Manchester Identifier: NCT01190774     History of Changes
Other Study ID Numbers: Denanx0103
First Posted: August 30, 2010    Key Record Dates
Last Update Posted: August 30, 2010
Last Verified: July 2003

Keywords provided by University of St Andrews:
dental anxiety
state anxiety
randomised control trial
psychological intervention

Additional relevant MeSH terms:
Anxiety Disorders
Mental Disorders