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Evaluation of Changes in Consumption of Drugs and Substances After Incarceration (COSMOS)

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ClinicalTrials.gov Identifier: NCT02849574
Recruitment Status : Completed
First Posted : July 29, 2016
Last Update Posted : July 29, 2016
Sponsor:
Information provided by (Responsible Party):
Nantes University Hospital

Brief Summary:
To improve the management and risk reduction, it is essential to understand the evolution of the consumption of psychoactive substances, medicated or not in detention; it does not have at present no data on this subject. This work has as main objective to evaluate the development of substance use terms (goods and consumption practices) by the inmates between the period preceding their incarceration and their fifth month in detention.

Condition or disease
Addictions

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Study Type : Observational
Actual Enrollment : 629 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Evaluation of Changes in Consumption of Drugs and Substances After Incarceration
Study Start Date : January 2015
Actual Primary Completion Date : January 2015
Actual Study Completion Date : July 2016



Primary Outcome Measures :
  1. change in practices of consumption of psychoactive substances between the period prior to incarceration and detention period [ Time Frame: Until 5 months ]
    composite endpoint representing the existence of a change in practices of consumption of psychoactive substances between the period prior to incarceration and detention period



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
The eligible study population is incarcerated major subjects. The topics will be selected subjects incarcerated in remand centers participating in the study. All subjects were medical examination, Home Maintenance arriving at their entrance into custody. On this occasion, the medical staff will verify the absence of non inclusion criterion and the subject will be informed orally and via an information sheet that will retain an invitation to respond to an anonymous questionnaire will be sent after him 4 or 5 months of detention (as prisons). He may accept or reject this invitation.
Criteria

Inclusion Criteria:

  • Major subject
  • Subject in the fourth or fifth month of incarceration
  • Held about agreeing to participate in the study

Exclusion Criteria:

  • Patient refusing to participate
  • Patient unable to respond to the questionnaire (major difficulties understanding of the French language)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02849574


Locations
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France
Angers University Hospital
Angers, France, 49000
Fontenay Le Comte Hospital
Fontenay Le Comte, France, 85200
La Roche sur Yon Hospital
La Roche sur Yon, France, 85000
Laval Hospital
Laval, France, 53000
Le Mans Hospital
Le Mans, France, 72000
Nantes University Hospital
Nantes, France, 44093
Sponsors and Collaborators
Nantes University Hospital
Investigators
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Principal Investigator: Caroline VICTORRI-VIGNEAU, Dr Nantes University Hospital

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Responsible Party: Nantes University Hospital
ClinicalTrials.gov Identifier: NCT02849574     History of Changes
Other Study ID Numbers: RC14_0259
First Posted: July 29, 2016    Key Record Dates
Last Update Posted: July 29, 2016
Last Verified: July 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Additional relevant MeSH terms:
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Behavior, Addictive
Compulsive Behavior
Impulsive Behavior