F20 F25.SCHIZOAFFEKTIVESTOERUNGEN F31.BIPOLARESTOERUNGEN
Conditions
Interventions
Group 1: Intervention group:
All subjects received a baseline interview. It assess among others the medication adherence with MARS-D, but also the quality of life (WHOQOL).
Intervention: Every two wee
Sponsors
Universitätsmedizin Greifswald
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Medical diagnosis of schizophrenia, schizoaffective disorder or bipolar disorder. Signed consent to study participation.
Exclusion criteria
Exclusion criteria: Planned hospitalization in the next 6 months. No telephone access.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the evaluation medication adherence. The assesssment instrument is the MARS-D (German version of the Medication Adherence Report Scale). Times of measurement are baseline, 3- and 6-months-follow ups. The hypothesis is that after 6 months, the medication adherence in the intervention group is better than the control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints compare the frequency of anew and unplanned psychiatric (partly) inpatient stays, the periods until the unplanned (partly) inpatient treatment as well as quality of life, coping with everyday life and the development of symptoms within each of the 6 months. Data of unplannend readmissions are recorded with computer assistance. The quality of life is measured by the questionnaire WHOQOL-BREF (World Health Organsiation Quality Of Life), coping with everyday life with GAF (Global Assessment of Functioning) and symptoms with BPRS (Brief Psychiatric Rating Scale). Measurement times are baseline, 3- and 6-month follow-ups. | — |
Countries
Germany
Contacts
Public ContactNeeltje van den Berg
Universitätsmedizin GreifswaldInstitut für Community Medicine
Outcome results
None listed