Dental Pain and Sensation Disorders
Conditions
Brief summary
The main purpose of MUSANX study is to highlight analgesic effectiveness of musicotherapy in post-surgical periodontal and implant; and to measure its per-operative anxiolytic effectiveness
Detailed description
This study will be on music use as musicotherapy receptive or passive , using hearing aid for listening in order to relax and reduce the anxiety and pain state of the patient. This care will be focused on the acute stress and pain during the dental care. Another major secondary purpose will consist to explore the anxiolytic effect of the musicotherapy on diverse stress markers such as heart rate, respiratory rate, salivary cortisol ratio and electro-dermal intensity (RED).
Interventions
OTHERmusicotherapy
If the patient is randomized in the experimental group, he listens the Music-care® playlists and chose two closed to his musical tastes. The playlists are unique compositions create by Music-care® (french company), not known from the general public, categorized by theme (jazz, rock, world music…).
Sponsors
Fondation Apicil
Nantes University Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No
Inclusion criteria
* Majors aged between 18 and 55 years, with an appropriate hearing and able to use Music-Care© (selection of the playlist via internet access), * Needing treatment in odontology - periodontal surgery (coronary elongation or sanitation surgery or muco-gingival surgery) or implantary surgery (placement of an unit implant or two implant in the same localization), * Oral and dated consent, * Agreeing to be contacted via phone at J+1 and to fill follow-up study documents, * Profiting of social security or CMU.
Exclusion criteria
* Patients with a long-term taking of anxiolytic or analgesic, * Regular consumer of soft drug (cannabis) or hard drug (opioid), * Patient with medical history of psychiatry (mental harm), hearing problem, cognitive and behavioural impairment (claustrophobia), sensory disabilities, * Patient with problems of hemostasis, * Majors under trusteeship or guardianship, * Pregnant women or lactating, * Minors, * Protected person, deprived of freedom or under justice safeguard, * Profiting of a medical help from government (AME), * Not contactable after care, * Patient with hepatic impairment, * Patient with dry mouth, * Patient relevant a suboptimal hearing incompatible with musicotherapy or inability to use Music-care®.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain intensity | 24 hours after the dental surgery | the pain intensity will be measured with the Visual analogue scale (VAS). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Efficacy of musicotherapy | 24, 48 and 72 hours | Evaluate the anxiolytic effectiveness of passive musicotherapy on the reduction of peroperative anxiety during the dental surgery by STAY questionnaire |
Countries
France
Outcome results
None listed