Videomusic and Psychic Trauma

NCT ID: NCT04664907

Last Updated: 2022-10-13

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-31
• Study Completion Date: 2021-07-31

Brief Summary

This project is interested in the flow of consciousness and its modalizations during psychological trauma (post-traumatic stress disorder) and its resolution. It is based on the premise that in PTSD, consciousness becomes more rigid, less fluid, due to the memory always imposing itself on the consciousness. The resolution of the trauma and the subsequent reduction of anxiety might improve the fluidity of consciousness and thus lead to an overall improvement in the psychological state of PTSD patients. In cases of PTSD, music has been shown to reduce anxiety from the very first session and has a very positive effect on all PTSD symptoms.

In this project the following elements will be evaluated : on one hand, the changes in consciousness and its fluidity and, on the other hand, the evolution of anxiety following the listening of a new kind of work, videomusic (which associates a video scenario with music) exemplifying (metaphorizing) the trauma and its resolution.

Conditions

Post Traumatic Stress Disorder

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Patients suffering from post traumatic stress disorder

Group Type: EXPERIMENTAL

Videomusic listening

Intervention Type: OTHER

Patients will attend a 8 min videomusic session and questionnaires will be performed before and after this session.

Interventions

Videomusic listening

Patients will attend a 8 min videomusic session and questionnaires will be performed before and after this session.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Male or female at least 18 years of age
• Patients diagnosed with Simple Post Traumatic Stress according to DSM 5 criteria
• Patient able to express consent prior to participation in the study
• Patient affiliated to or beneficiary of a social security regimen

Exclusion Criteria

• Other serious psychiatric pathologies
• Serious chronic pathologies, especially neurological ones
• Epilepsy
• Blindness or deafness
• Psychiatric decompensation
• Pregnant Women
• Patient under judicial protection (guardianship, curatorship...) or justice safeguard
• Any other reason that, in the opinion of the investigator, could interfere with study objective evaluation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Manuel Dias Alves, MD

Role: STUDY_DIRECTOR

Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

Other Identifiers

2020-A02649-30

Identifier Type: OTHER

Identifier Source: secondary_id

2020-CHITS-07

Identifier Type: -

Identifier Source: org_study_id