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Mental DisorderNCT04165733

Professional Quality of Life in German Psychiatrists

An observational study of Mental Disorder and Burnout, Caregiver, run by Charite University, Berlin, Germany at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The purpose of this study is to assess professional quality of life in German psychiatrists working with patients with mental disorders. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Online questionnaire
How many people
87 participants
Where
1 siteGermany
Study dates
16 Jan 2020to 20 Oct 2026
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Psychiatrists (already specialzied in psychiatry or currently in specialization for psychiatry) that currently work with patients with mental disorders in Germany.

Who may be able to join

  • Psychiatrits (Physician with specialization in psychiatry or currently in specialization for psychiatry)
  • Currently working with patients with mental disorders
  • At least 18 years old
  • Sufficient German skills for answering the questionnaire

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Charité Universitätsmedizin Berlin - Department for Psychiatry and Psychotherpy - Charité Campus Mitte

    Berlin, State of Berlin, 10117

Other trials in Germany

About this study

Official title: Professional Quality of Life in German Psychiatrists Working With Patients With Mental Disorders

The purpose of this study is to assess professional quality of life in German psychiatrists working with patients with mental disorders.

Read the detailed description

The purpose of this study is to assess professional quality of life, which includes compassion satisfaction, burnout and secondary traumatization in psychiatrists, working with patients with mental disorders, in Germany.

Being tested
Online questionnaire
Keywords
Professional quality of life, Compassion satisfaction, Burnout, Psychiatrists, Mental disorders, Mental health
Medical subject headings
Mental Disorders, Caregiver Burden, Burnout, Professional, Burnout, Psychological, Psychological Well-Being

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Online questionnaireDiagnostic test

    Clinical psychologists in Germany currently working with patients with mental disorders

Study groups in NCT04165733
Study groupRoleWhat they receive
Psychiatrists in GermanyPsychiatrists in Germany currently working with patients with mental disorders
Receives: Diagnostic Test: Online questionnaire

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Compassion Satisfaction

    Professional Quality of Life: Compassion Satisfaction and Fatigue Version 5 (ProQOL) - German Version - Subscale "Compassion Satisfaction" (Minimum: 10 - Maximum: 50 - Higher scores mean a higher compassion satisfaction.

    Measured: 1 day

  2. Burnout

    Professional Quality of Life: Compassion Satisfaction and Fatigue Version 5 (ProQOL) - German Version - Subscale "Burnout" (Minimum: 10 - Maximum: 50 - Higher scores mean a higher level of burnout.

    Measured: 1 day

  3. Traumatization

    Professional Quality of Life: Compassion Satisfaction and Fatigue Version 5 (ProQOL) - German Version - Subscale "Secondary Traumatization" (Minimum: 10 - Maximum: 50 - Higher scores mean a higher level of secondary traumatization.

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2019
  2. Study start16 Jan 2020
  3. Primary completion20 Oct 2026
  4. Study completion20 Oct 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
87 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04165733
Sponsor's protocol ID
ProQol_A
Status last verified
Oct 2026
First submitted
14 Nov 2019
Last updated
22 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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