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Work Participation of Workers with Common Mental Complaints.

A clinical trial evaluating a minimal psychological intervention, administered by trained nurses, aimed at reducing levels of fatigue and/or depression and increasing work participation in employees.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25736
Enrollment
130
Registered
2011-11-25
Start date
2007-04-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fatigue, minor depression, sick leave, work participation.

Interventions

Minimal Psychological Intervention (MPI) vs care as usual The MPI is based = on priciples of cognitive behavioural therapy and self management by occupa= tional health nurses. The number of consutatio

Sponsors

Maastricht University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Score PHQ-9; at least 2 depressive symptoms at least at “more than half the days” and at least one of these symptoms was depressed mood or anhedonia; 2. Score CIS-20 >76; 3. VAS score >3; 4. Completed informed consent.

Exclusion criteria

Exclusion criteria: 1. Recent medical events as an explanation for fatigue or recent medical events as an explanation for fatigue and/or depression; 2. Serious physical impairment; 3. Serious psycho social problems; 4. Former episodes of depression or bipolar disorder or psychiatric co morbidity; 5. Passive death wish or suicidal thoughts; 6. Alcohol or drug dependency; 7. Non Dutch speaking.

Design outcomes

Primary

MeasureTime frame
Fatigue measured with CIS 20, and Depression measured with BDI, assessed at baseline and at 4, 6 and 12 months after inclusion.

Secondary

MeasureTime frame
Sick-leave, mastery, self efficacy, and perceived impairment (VAS).

Contacts

Public ContactE.W.M. Aelfers

ARBOdienst DSM PO Box 27

ed.aelfers@dsm.com+30 (0)464764311

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)