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The Efficacy of a VR Enhanced Video Exposure Therapy for Dental Phobia

The Efficacy of a VR Enhanced Video Exposure Therapy for Dental Phobia - a Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03098134
Acronym
VR-DENT
Enrollment
100
Registered
2017-03-31
Start date
2017-04-30
Completion date
2018-05-01
Last updated
2017-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Phobia

Brief summary

Evaluation of a one session VR - enhanced Video exposure therapy for dental phobia. Diagnosed dental phobics will be randomly assigned to one of two conditions: (1) Psychoeducation + VR exposure (2) Psychoeducation + Video Control treatment. Prior to getting the therapy, participants will be evaluated with a questionnaire battery, diagnosed with a structured clinical interview and will participate in a psychophysiological symptom assessment. Then, after a 2-week waiting period, participants again fill in questionnaires, and the Intervention will take place. Within 2-weeks after the second questionnaire assessment participants will be screened with the structured interview again and will fill in questionnaires.

Interventions

BEHAVIORALBehavior Therapy

Virtual Reality and Video based Exposure Therapy

OTHERHealth Education

Video based health education covering common myths and false believes about dental surgeries

Sponsors

Ruhr University of Bochum (Dr. Andre Wannemüller)
CollaboratorUNKNOWN
Zahnklinik Bochum, Augusta Hospital (Prof. Dr. Peter Jöhren)
CollaboratorUNKNOWN
Ruhr University of Bochum (Prof. Dr. Jürgen Margraf)
CollaboratorUNKNOWN
Ruhr University of Bochum
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- diagnosed Specific Dental Phobia

Exclusion criteria

* Schizophrenia or other Psychotic Illnesses * Bipolar Disorder * Chronic Headache * other neurological disorders such as epilepsy * Hearing problems

Design outcomes

Primary

MeasureTime frameDescription
Change in Subjective Dental Anxiety4 monthAssessed at time 0 (at inclusion) 1 (pre therapy, two weeks after inclusion), 2(post therapy, 2 weeks after time 1) and at follow up (4 month after time 0) with Dental Anxiety Scale (DAS, 4-item scale, range 4-20)
Change in Dysfunctional Dental Cognitions4 monthsAssessed with Dental Cognition Questionnaire (DCQ, 38 dichotomous items, range 0-38) Assessed at time 0 (at inclusion), time 1 (pre therapy, two weeks after time 0), time 2 (post therapy, 2 weeks after time 1) and at follow up (4 month after time 0)

Secondary

MeasureTime frameDescription
Change in Psychophysiological defensive reactivity4 weeksParticipants will take part in a passive Picture viewing paradigm. They will be exposed to dental anxiety related Pictures, generally negative pictures, neutral, and positive pictures. Outcome measures will be withdrawal-related motor responding (assessed with the startle-reflex), as well as heart frequency change towards the pictures, The task will be applied at inclusion (time 0) and post therapy (4 weeks after inclusion)

Other

MeasureTime frameDescription
Change in dental avoidance behaviorwithin three month after the therapy took placeEach participant will be asked to arrange an appointment in a cooperating dental Hospital. It will be assessed (1) if participant makes a - (2) and attends to - first appointment (3) if participant tolerates oral inspection and dental treatment (4) how many further appointments will be made

Contacts

Primary ContactDirk Adolph, Dr.
dirk.adolph@rub.de+492343223177
Backup ContactAndre Wannemueller, Dr.
andre.wannemueller@rub.de+492343223106

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026