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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03098134
Other study ID # VR-DENT-1
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received March 14, 2017
Last updated March 27, 2017
Start date April 2017
Est. completion date May 1, 2018

Study information

Verified date March 2017
Source Ruhr University of Bochum
Contact Dirk Adolph, Dr.
Phone +492343223177
Email dirk.adolph@rub.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date May 1, 2018
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavior Therapy
Virtual Reality and Video based Exposure Therapy
Other:
Health Education
Video based health education covering common myths and false believes about dental surgeries

Locations

Country Name City State
n/a

Sponsors (4)

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

Outcome

Type Measure Description Time frame Safety issue
Other Change in dental avoidance behavior Each 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 within three month after the therapy took place
Primary Change in Subjective Dental Anxiety Assessed 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) 4 month
Primary Change in Dysfunctional Dental Cognitions Assessed 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) 4 months
Secondary Change in Psychophysiological defensive reactivity Participants 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) 4 weeks
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