Music Against Psychological Pain in Suicide

NCT ID: NCT04085848

Last Updated: 2025-07-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

264 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-25

Study Completion Date

2026-05-31

Brief Summary

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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

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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.

Conditions

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Suicide, Attempted Suicidal Ideation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Caregivers

Study Groups

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Groupe intervention

Usual care and music therapy

Group Type EXPERIMENTAL

music therapy

Intervention Type OTHER

4 music therapy sessions during a period of time of 48 hours. Each session lasts 30 minutes.

Groupe contrôle

Usual care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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music therapy

4 music therapy sessions during a period of time of 48 hours. Each session lasts 30 minutes.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de la Réunion

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Erick GOKALSING

Role: PRINCIPAL_INVESTIGATOR

EPSMR

Locations

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Etablissement Public de Santé Mentale de La Réunion

Saint-Paul, , Reunion

Site Status RECRUITING

Countries

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Reunion

Central Contacts

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Emilie TECHER

Role: CONTACT

+2 62 262 90 62 89

Facility Contacts

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Erick GOKALSING

Role: primary

Other Identifiers

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2017/CHU/19

Identifier Type: -

Identifier Source: org_study_id

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