Music Against Psychological Pain in Suicide
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: music therapy.
- Who it may be relevant to
- Registry conditions: Suicide, Attempted, Suicidal Ideation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Reunion
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Controlled, Randomized Study Evaluating the Effecacy of Receptive Music Therapy on Psychological Pain in Suicidal Patients
Overview
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.
Interventions
- Other music therapy
4 music therapy sessions during a period of time of 48 hours. Each session lasts 30 minutes.
Primary outcome measures
- Change from inclusion psychological pain at 48 hours after inclusion [Time frame: 48 hours after inclusion]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Other
Study locations
Reunion · 1 center
- Etablissement Public de Santé Mentale de La Réunion — Saint-Paul
Identifiers
NCT: NCT04085848 · 2017/CHU/19