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Music Against Psychological Pain in Suicide

Not Applicable
Recruiting
Conditions
Suicide, Attempted
Suicidal Ideation
Interventions
Other: music therapy
Registration Number
NCT04085848
Lead Sponsor
Centre Hospitalier Universitaire de la Réunion
Brief Summary

This study compares the efficacy of music therapy associated with standard care versus the standard care alone on the psychological pain in suicidal patients.

Detailed Description

Music therapy consists of using the Music Care tool. Each patient randomized in the music therapy arm should perform 4 music therapy sessions of 30 minutes on 48h.

Before and after each music therapy sessions, the psychological pain will be measured by the analogical visual scale.

Standard care consists of a medical and paramedical interview lasting 20-30 minutes. At the end of the interview, a drug treatment (BZD anxiolytic and/or hypnotic) is prescribed and the patient is hospitalized. During hospitalization, patient is regularly interviewed in order to evaluate his psychological status.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
264
Inclusion Criteria
  • Patient with suicidal ideas, thoughts or surviving suicide attempt
  • Patient whose emergency somatic management lasted less than 48h
  • Patient who, according to the physician, is still in suicidal mood
  • Patient admitted in the psychiatric hospitalization unit of the Public Mental Health Establishment
  • Patient with voluntary admission and agrees to stay in hospital from 48h to 60h
  • Patient able to write and read in french
  • Patient affiliated to a social security scheme
  • Patient who gives his Informed consent before any procedure related to the study
Exclusion Criteria
  • Patient with attempt suicide requiring a somatic care (intensive, surgery, gastric lavage...)
  • Patient with medical history of audiogenic and/or musicogenic epilepsy
  • Patient with major impairment of hearing function
  • Patient unable to support the headhset earphone
  • Patient with contra indication to BZD, hypnotics (Zopiclone) or requiring more sedative and/or psychotic drugs
  • Patient under guardianship or under judicial protection
  • Patient hospitalized at the request of a third party or ex officio

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Groupe interventionmusic therapyUsual care and music therapy
Primary Outcome Measures
NameTimeMethod
Change from inclusion psychological pain at 48 hours after inclusion48 hours after inclusion

Pain analogical visual scale (scale ranges : from 0 to 10) min = 0 = no psychological pain and max = 10 = maximum psychological pain

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Etablissement Public de Santé Mentale de La Réunion

🇷🇪

Saint-Paul, Réunion

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