Pain and Placebo Analgesia. Does Extended Information About Dental Procedures Reduce Pain Induced by Dental Treatment?
- Conditions
- AnxietyOdontophobia
- Interventions
- Other: anesthetics and extended information before dental treatmentOther: anesthetics and standard information before dental treatment
- Registration Number
- NCT02160028
- Lead Sponsor
- Norwegian University of Science and Technology
- Brief Summary
Information about the effectiveness of treatment has been found to reduce pain, termed placebo analgesia. In this study it will be investigated whether this finding translates to the dental clinic. It will be investigated whether information that suggested that minimal pain will be experienced during filling therapy, can reduce the pain associated with that procedure compared to a group that receives standard information. All patients will receive the same amount of anesthesia and similar procedures during filling therapy. It is predicted that extended information should reduce pain, and that the reduction in pain should be associated with a reduction in stress.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 52
- Patients to be treated for dental caries
- Patients should be able to read and communicate in Norwegian
- Patients with life threatening diseases
- Patients taking pain killers for other reasons on the day of treatment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Extended information anesthetics and extended information before dental treatment This group is given anesthetics and extended information before dental treatment about the anesthetics. Standard information anesthetics and standard information before dental treatment This group is given anesthetics and standard information before dental treatment about the anesthetics.
- Primary Outcome Measures
Name Time Method Reduction of pain 1 hour Pain intensity and pain discomfort will be measured by a VAS (Visual Analog Scale). The patients will report their experience of these factors verbally, four times during the treatment session.
- Secondary Outcome Measures
Name Time Method Reduction of stress One hour Stress is also measured using the VAS, i.e. using the same method as for pain. Stress or sympathetic activation is measured by using scin conductance on fingers (V-Amp (Brain Products, Munich, Germany).
Trial Locations
- Locations (1)
Tannlegesenteret Madlagården, TSMG
🇳🇴Hafrsfjord, Norway