Music for Decreasing Dental Anxiety During Oral Surgery in Coronavirus Disease 2019 (COVID-19)

Sponsor
European University of Madrid (Other)
Overall Status
Completed
CT.gov ID
NCT05052034
Collaborator
(none)
100
1
6.4
15.5

Study Details

Study Description

Brief Summary

Approximately 100 patients undergoing oral surgery will be divided in 3 groups of musical audition to control anxiety: baroque (N=35), classicism (N=35) and control group (N=30). Systolic Blood Pressure, Diastolic Blood Pressure, Heart Rate and Oxygen Saturation will be recorded.

Condition or Disease Intervention/Treatment Phase
  • Other: Music

Detailed Description

The trend towards greater humanization in all fields of medicine encourages the implementation of non-pharmacological therapies in the management and control of pain and anxiety in patients during dental treatments. Some studies estimate this level of anxiety in up to 51% of patients, who would prefer to undergo some type of sedation during dental treatment. This fear or anxiety may have increased during the COVID-19 pandemic.

Scientific evidence recommends the use of music in daily practice to reduce anxiety and even pain. There are several studies comparing different musical styles. Some of them use a song from the so-called "classical music", but none have analyzed the possible benefits between the different stages of this type of music, which spans several centuries of history.

The purpose of this study is to verify the effect of the use of Baroque and Classical music as non-pharmacological therapy on the control of the level of intraoperative anxiety and pain experienced by patients during the COVID-19 pandemic, subjected to dental extractions. and implant placement.

This randomized controlled study would be carried out on approximately 100 patients who need tooth extractions and dental implant placement in private practice. The patients would be divided into 3 groups: baroque music, classicism music and control group. The patients would be correctly informed and would sign their consent to be part of the study. The music would be played through wireless headphones placed on the patient and connected to their respective music list according to the group to be studied. The parameters recorded during four different moments of surgery would be: systolic blood pressure, diastolic blood pressure, heart rate and oxygen saturation. After the treatment, the patient will complete a visual analog scale (VAS) on their level of pain and anxiety experienced before and after the treatment. For all of them, this surgery would be the first performed by the sole operator of the study, to reduce other subjective criteria associated with the level of pain or anxiety. Another operator would collect the data obtained.

Study Design

Study Type:
Observational
Actual Enrollment :
100 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Musical Flow for Decreasing Dental Anxiety During Oral and Implants Surgery in COVID-19: a Randomized Controlled Study
Actual Study Start Date :
Jun 1, 2020
Actual Primary Completion Date :
Nov 23, 2020
Actual Study Completion Date :
Dec 14, 2020

Arms and Interventions

Arm Intervention/Treatment
BAROQUE MUSIC

This group would listen to baroque music to control their anxiety level during their oral surgeries.

Other: Music
Through headphones, the patients would listen to different types of music during the intervention.

CLASSICISM MUSIC

this group would listen to classical music to control their anxiety level during their oral surgeries.

Other: Music
Through headphones, the patients would listen to different types of music during the intervention.

CONTROL GROUP

This group would not listen to music during their oral intervention, acting as a control group.

Outcome Measures

Primary Outcome Measures

  1. Systolic Blood Pressure (SPB) [SPB was recorded four times during intervention: "before starting the surgery once sitting in the chair", "immediately after anesthetizing", "immediately after introducing the first surgery drill", "immediately before getting up".]

    SPB was recorded in mmHg

  2. Diastolic Blood Pressure (DBP) [SPB was recorded four times during intervention: "before starting the surgery once sitting in the chair", "immediately after anesthetizing", "immediately after introducing the first surgery drill", "immediately before getting up".]

    DBP was recorded in mmHg

  3. Heart Rate (HR) [HR was recorded four times during intervention: "before starting the surgery once sitting in the chair", "immediately after anesthetizing", "immediately after introducing the first surgery drill", "immediately before getting up".]

    HR was recorded in bpm (beats per minute)

  4. Oxygen Saturation (Sp02) [Sp02 was recorded four times during intervention: "before starting the surgery once sitting in the chair", "immediately after anesthetizing", "immediately after introducing the first surgery drill", "immediately before getting up".]

    Sp02 was recorded in % (0-100)

Secondary Outcome Measures

  1. Change from Baseline in Anxiety on the 11-point Visual Analog Scale (VAS) [Baseline before starting surgery to the end of surgery approximately 40 minutes later.]

    The VAS is a validated instrument to identify anxiety. Possible scores range from 0 (no anxiety) to 10 (worst anxiety possible).

  2. Change from Baseline in Pain on the 11-point Visual Analog Scale (VAS) [Baseline before starting surgery to the end of surgery approximately 40 minutes later.]

    The VAS is a validated instrument to identify pain. Possible scores range from 0 (no pain) to 10 (worst pain possible).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Spanish-speaking patients over 18 years of age who require the placement of a single implant or the extraction of a single tooth.
Exclusion Criteria:
  1. Patients with mental illness (dementia)

  2. Patients with psychiatric disorders

  3. Patients under anxiolytic treatment

  4. Patients with visual or motor loss or with any disability that makes it impossible to fill in the forms provided and the visual analog scale (VAS).

  5. Patients under medical treatment that could interfere with the anesthesia used in oral surgery.

  6. All implant surgeries were ruled out in patients requiring any type of bone regeneration, due to their greater morbidity.

  7. All oral surgeries requiring a flap, due to their greater morbidity.

Contacts and Locations

Locations

Site City State Country Postal Code
1 European University of Madrid Madrid Spain

Sponsors and Collaborators

  • European University of Madrid

Investigators

  • Principal Investigator: Esteban Lorenzo, European University of Madrid

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lorenzo Ángel Esteban Pellicer, Esteban LA, European University of Madrid
ClinicalTrials.gov Identifier:
NCT05052034
Other Study ID Numbers:
  • EuropeanUM
First Posted:
Sep 22, 2021
Last Update Posted:
Sep 22, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lorenzo Ángel Esteban Pellicer, Esteban LA, European University of Madrid
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 22, 2021