Collaborative treatment of late-life depression in primary care: Implementation of the IMPACT program in Germany
- Conditions
- F32F33F34.1Depressive episodeRecurrent depressive disorderDysthymia
- Registration Number
- DRKS00003589
- Lead Sponsor
- niversitätsklinikum Freiburg Klinik für Psychiatrie und Psychotherapie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 248
• age: = 60
• major depression of moderate severety (PHQ-9 score 10-14)
• willingness and possibility to partake in telephone calls and personal meetings with the care manager on a regular basis
• willingness to take part in three written surveys (questionnaires) and to be contacted by members of the data management team via telephone
• signing of the patient consent form after having been sufficiently informed about the trial (informed consent)
• alcohol, drug or pharmaceutical abuse
• significant cognitive impairment (e.g., dementia)
• treatment of depression by a clinical specialist (e.g., psychiatrist, psychotherapist) at time of inclusion
• bipolar disorder
• psychotic symptoms/ severe behavioral symptoms
• risk of suicide at time of inclusion
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome variable is the PHQ-9 score (Kroenke et al. 2001) as a measure of change in the depressive symptoms over the course of the trial. The PHQ-9 questionnaire is the 9-item depression module of the Patient Health Questionnaire which has proven to be a valid instrument for the population of older people with depression in international trials.<br> <br>Along the lines of similar trials (Unützer et al. 2002; IJiff et al. 2007; Gensichen et al. 2009), the change of symptoms in terms of a response to treatment is defined as a decrease of symptoms (PHQ-9 score) by 50% or more. Remission is defined as a reduction of the PHQ-9 score to a score of 4 or less.<br><br>The PHQ-9 will be assessed at the involvement of the patient, after 6 months and after 12 months.
- Secondary Outcome Measures
Name Time Method