Can Psychotherapy Reduce Sickness Absence?

This study is currently recruiting participants.
Verified January 2012 by Lovisenberg Diakonale Hospital
Sponsor:
Information provided by (Responsible Party):
Lovisenberg Diakonale Hospital
ClinicalTrials.gov Identifier:
NCT01181635
First received: August 12, 2010
Last updated: January 20, 2012
Last verified: January 2012

August 12, 2010
January 20, 2012
August 2010
July 2012   (final data collection date for primary outcome measure)
Sickness absence [ Time Frame: Before, after and 6 months after treatment. ] [ Designated as safety issue: No ]
Present status (working or sick).
Same as current
Complete list of historical versions of study NCT01181635 on ClinicalTrials.gov Archive Site
  • Psychiatric symptoms [ Time Frame: Before, after and 6 months after treatment. ] [ Designated as safety issue: No ]
    CORE-OM.
  • Quality of life (QALY) [ Time Frame: Before, after and 6 months after treatment. ] [ Designated as safety issue: No ]
    15 D
Same as current
Not Provided
Not Provided
 
Can Psychotherapy Reduce Sickness Absence?
Can Psychotherapy Reduce Sickness Absence?

The purpose of this study is to examine if psychotherapy can reduce sickness absence.

Sickness absence due to psychiatric problems is considered a growing problem in Norway. Little research is done to examine if psychotherapy can reduce sickness absence. Since 2007 there is a government sponsored program in Norway (Raskere tilbake) aimed at reducing sickness absence. This study examines if psychotherapy within this program, delivered at an out-patient clinic, actually reduces sickness absence. Levels of absenteeism is measured before, after and 6 months after treatment. This is a quasi-experimental study, where the treatment-group will be compared with a statistical group in the general population, that is socio-demographical similar and has similar history of sickness absence but haven't been to treatment. Changes in levels of symptoms and quality of life will also be measured. The participants will be asked to describe their working environment, and this will be related to outcome-measures.

Interventional
Not Provided
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Mental Disorders
Behavioral: Psychotherapy
Standard psychotherapy for psychiatric disorders.
Experimental: Psychotherapy
Intervention: Behavioral: Psychotherapy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
400
July 2012
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients receiving psychotherapy at Lovisenberg DPS/Raskere Tilbake

Exclusion Criteria:

-

Both
18 Years and older
No
Contact: Mattias Victor 22028900 ext +47 vicm@lds.no
Norway
 
NCT01181635
2010/494 (REK)
No
Lovisenberg Diakonale Hospital
Lovisenberg Diakonale Hospital
Not Provided
Study Director: Torleif Ruud, dr.med Akershus universitetssykehus
Lovisenberg Diakonale Hospital
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP