Alcohol Consumption and Stress at Patients Alcohol-dependants (CASPA)

September 24, 2018 updated by: Assistance Publique - Hôpitaux de Paris
This 3 weeks study examines the correlation between stress and alcohol using an ecological, prospective design.

Study Overview

Status

Completed

Conditions

Detailed Description

This 3 weeks study examines the correlation between stress and alcohol using an ecological, prospective design. Participants will be given phone calls 4 times a day for 3 weeks, assessing perceived stress and alcohol related craving.

Study Type

Observational

Enrollment (Actual)

42

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Colombes, France, 92701
        • Hopital Louis Mourier, Service de psychiatrie

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

This study includes alcohol dependent inpatients participating in a 3 weeks detoxification program.

Description

Inclusion criteria:

  • Males or Females aged 18-65 years
  • Alcohol use disorder defined by DSM 5 criteria
  • Fluent in French
  • Hospitalized for alcohol withdrawal for at least 7 days
  • Viable (working) telephone number

Exclusion criteria:

  • Participants without social care insurance
  • Any DSM Axis I disorder not defined in the inclusion criteria
  • Mandatory psychiatric treatment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Stress and craving
This 3 weeks study examines the correlation between stress and alcohol using an ecological, prospective design. Participants will be given phone calls 4 times a day for 3 weeks, assessing perceived stress and alcohol related craving.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stress level
Time Frame: 3 weeks follow-up
correlation between stress and alcohol related craving using a prospective ecological design
3 weeks follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Genetic association with stress level
Time Frame: 3 weeks follow-up
Correlation between stress and alcohol related craving using a prospective ecological design stratified for CRHR1 variant
3 weeks follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Assistance Publique - Hôpitaux de Paris

Investigators

  • Principal Investigator: Yann Le Strat, Pr MD, Psychiatrist Service

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2014

Primary Completion (Actual)

July 1, 2017

Study Completion (Actual)

December 1, 2017

Study Registration Dates

First Submitted

February 24, 2014

First Submitted That Met QC Criteria

March 12, 2014

First Posted (Estimate)

March 14, 2014

Study Record Updates

Last Update Posted (Actual)

September 25, 2018

Last Update Submitted That Met QC Criteria

September 24, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • P110908

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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