PSYCHEQUALI: Qualitative Study About Psychedelics Using in Psychiatric Disorders

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06014164
Collaborator
(none)
25
18

Study Details

Study Description

Brief Summary

This study is set up to better understand the current use of psychedelics in France in the general population. We focus on individuals who have used any type of psychedelic drug in order to suppress or alleviate a psychiatric symptom in the context of a diagnosed pathology. The data are collected during a semi-structured interview and then studied in a thematic analysis.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Interview

Study Design

Study Type:
Observational
Anticipated Enrollment :
25 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Qualitative Study of the Self-administered Therapeutic Use of Psychedelics in People With Psychiatric Disorders
Anticipated Study Start Date :
Sep 10, 2023
Anticipated Primary Completion Date :
Mar 10, 2025
Anticipated Study Completion Date :
Mar 10, 2025

Arms and Interventions

Arm Intervention/Treatment
Patients using psychedelic substances

Adult patients self-administering psychedelic substances in psychiatric disorders

Diagnostic Test: Interview
An interview will be conducted to describe the experiences of people with psychiatric disorders who use psychedelic substances for therapeutic purposes

Outcome Measures

Primary Outcome Measures

  1. Experiences of people using psychedelic substances [Baseline]

    The experiences of people with psychiatric disorders who use psychedelic substances for therapeutic purposes will be assessed by interview

Secondary Outcome Measures

  1. Profile of people using psychedelic substances [Baseline]

    The profile of people with psychiatric disorders who use psychedelic substances for therapeutic purposes will be assessed by interview

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients diagnosed with a psychiatric disorder by a psychiatrist or general practitioner

  • Patients used psychedelic or related substances in order to treat psychiatric symptoms

  • Adults patients (>18 years old)

  • Patients have given their oral non-opposition

  • Patients affiliated to a social security scheme

Exclusion Criteria:
  • Patients who don't speak or understand French

  • Patients under protection, guardianship or curators

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Toulouse

Investigators

  • Principal Investigator: Antoine YRONDI, PH, University Hospital, Toulouse

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT06014164
Other Study ID Numbers:
  • RC31/23/0396
  • 2023-A01575-40
First Posted:
Aug 28, 2023
Last Update Posted:
Aug 28, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 28, 2023