Occupational Stress and Bipolar Disorder

October 10, 2018 updated by: University Hospital, Montpellier

Assessment of Occupational Stress and Well-being in French Patients Suffering From Bipolar Disorder

Bipolar disorder is a mental disorder characterized by alternance of depressive and manic phases, separated by intercritical phases (euthymia). The majority of patients report occupation and professional difficulties. Sixty percent of bipolar patients are inactive . Indeed, according to the World Health Organisation, bipolar disorder is the second cause of days not worked.

Several factors are related to the lower professional functioning observed in bipolar patients: early age of onset, delay of diagnosis and treatment, recurrence of thymic episodes, residual symptoms and cognitive disorders during euthymia, side effects of mood stabilizers.

To our knowledge, no study has ever focused on well-being at work in French patients. However, suffering from a psychiatric disorder and the lack of support from colleagues and the hierarchy are risk factors for burnout, a growing health issue.

Patients with mental illness are often victims of stigmatization, which may involve the professional field. In addition, thymic recurrences may alter professional functioning of active patients: multiplication of work disruptions, conflicts with peers. Conversely work can be stressful, promoting thyic relapses. It is therefore essential to better understand the occupational stresses of active patients suffering from bipolar disorder in order to promote functional remission beyond clinical remission.

The aim of this study is to assess the level of stress and well-being at work in active French bipolar patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Socio-demographic, psychiatric and occupational data of 200 bipolar patients will be collected over a period of 6 months.

Study Type

Observational

Enrollment (Actual)

200

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

      • Montpellier, France, 34295
        • Uhmontpellier

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

Probability Sample

Study Population

Patients with Bipolar disorder

Description

Inclusion Criteria:

  • out patients and inpatients in the Department of Emergency Psychiatry and Post Acute Care, CHU Montpellier, France
  • to have completed the self-administered questionnaire on professional activity.

Exclusion Criteria:

  • Deprived of liberty subject (by judicial or administrative decision)
  • Protected by law (guardianship)

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Level of occupational stress using a Likert scale
Time Frame: 1 day
level of occupational stress assessed at the patient visit will be collected, from 0 (none) to 10 (maximum possible occupational stress).
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Presenteism during the last month using the Stanford Presenteeism Scale
Time Frame: 1 day
Presenteism during the last month assessed at the patient visit will be collected
1 day
Support of colleagues and superiors using the Karasek questionnaire.
Time Frame: 1 day
Support of colleagues and superiors assessed at the patient visit will be collected
1 day
Impact of work on the private sphere using the SWING scale (survey work-home interaction-Nijmegen)
Time Frame: 1 day
Impact of work on the private sphere assessed at the patient visit will be collected
1 day
Balance effort - reward in using the Siegrist questionaire
Time Frame: 1 day
Balance effort - reward assessed at the patient visit will be collected
1 day

Collaborators and Investigators

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

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 (Actual)

May 22, 2017

Primary Completion (Actual)

May 31, 2018

Study Completion (Actual)

June 30, 2018

Study Registration Dates

First Submitted

May 19, 2017

First Submitted That Met QC Criteria

May 19, 2017

First Posted (Actual)

May 22, 2017

Study Record Updates

Last Update Posted (Actual)

October 11, 2018

Last Update Submitted That Met QC Criteria

October 10, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

NC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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