(Short) stay and, if possible, treatment at the PMU, will give an improvement in regular psychometrics or at least in some of them.
ID
Bron
Aandoening
somatoform disorder (somatoforme stoornis, SOLK)
anxiety disorder (angststoornis)
depressive disorder (depressieve stoornis)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Change in somatic as well as psychiatric symptomatology.
Achtergrond van het onderzoek
The psychiatric Medical unit of the Atrium MC in Heerlen is one of three in Limburg and Noord Brabant (others are located in Eindhoven en Maastricht). Suitable patients for stay at the PMU are patients with a psyciatric disorder as well as a somatic disorder. Very common is the somatoform disorder, fibromyalgia and IBS etc. Frequently seen psychiatric comorbidity are anxiety disorder and depressive disorder. Patients are referred by medical specialist, GP, clinical psychologist or mental health institution. At the PMU furter analysis will be performed, next to observation and (if possible) start of treatment.
The study is an observational study, no specific intervention will be studied, all of the interventions that are used on the PMU will be included, as needed in the individual treatment. There will be no placebo/non-interventiongroup.
In this study we want to observe systematically if there's any change on regular standard psychometrics before and after stay at the PMU. And if there's a change; describe the trend that can be seen. Patient will be recruited only in the Netherlands.
Doel van het onderzoek
(Short) stay and, if possible, treatment at the PMU, will give an improvement in regular psychometrics or at least in some of them.
Onderzoeksopzet
t0 (day 1 at PMU):
1. MINI (Mini-International Neuropsychiatric Interview);
2. JTV-SV (Jeugd Trauma Vragenlijst 1997);
3. HADS (Hospital Anxiety and Depression Scales);
4. HAM-D (Hamilton Rating Scale for Depression);
5. SCL-90 (Symptom Checklist);
6. ORS (Outcome Rating Scale);
7. WHO Quality of life questionnaire.
T=1 week: ORS;
T=2 weeks: HADS, HAM-D, ORS;
T=8 weeks: WHO Quality of life questionnaire, SCL-90, HADS, HAM-D, ORS.
Onderzoeksproduct en/of interventie
The study is an observational study, no specific intervention will be studied, all of the interventions that are used on the PMU will be included, as needed in the individual treatment.
Most common interventions are:
1. (Re)activation (therapy);
2. Medication: Most common are; antidepressants, anxiolytic med., antipsychotic med., benzodiazepines;
3. Psychoeducation;
4. Combination.
The study is an observational study, so there will be no placebo/non-interventiongroup.
In this study we only want to observe systematically if there's any change on regular standard psychometrics before and after stay at the PMU. And if there's a change; describe the trend that can be seen.
Publiek
Atrium Medisch Centrum Parkstad
Henri Dunantstraat 5
H.J.H. Bremer
Heerlen 6419 PC
The Netherlands
045-5766490
h.bremer@atriummc.nl
Wetenschappelijk
Atrium Medisch Centrum Parkstad
Henri Dunantstraat 5
H.J.H. Bremer
Heerlen 6419 PC
The Netherlands
045-5766490
h.bremer@atriummc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. > 18 yr;
2. Reffered by GP, medical specialist or psychologist to the "Soma en Psyche" centre of the Atrium MC;
3. Axis I disorder according to DSM IV;
4. "SOLK" / Somatoform disorder according to DSM IV;
5. Informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. < 18 yr;
2. Cognitive disorder / dementia according to DSM IV.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL2530 |
NTR-old | NTR2648 |
Ander register | METC Atrium Orbis Zuyd : 10-N-98 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |