The collaborative care approach is expected to be more effective and more cost-effective compared to care as usual.
ID
Bron
Verkorte titel
Aandoening
The intervention group receives treatment based on a collaborative care approach. This intervention is compared with a control group who receive care as usual.
Ondersteuning
(Netherlands institute of Mental Health and Addiction)
Onze Lieve Vrouwe Gasthuis (OLVG).
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Severity of depressive symptoms.
Achtergrond van het onderzoek
Introduction
Depressive disorder is one of the two most common disorders and is even more prevalent in chronic medically ill patients. The presence of comorbid depression has a negative influence on quality of life, costs, morbidity, and mortality. Early diagnosis and well-organized treatment of depression has a positive influence on these aspects. However, recognition and treatment of depression remains unsatisfactory since the knowledge needed to perform the treatment is still unavailable in various settings. Prior research in the US has shown good results regarding the treatment of depression using a collaborative care approach and an antidepressant algorithm. In the UK ‘Problem Solving Treatment’ has proved to be feasible. In the general hospital setting, this approach has not yet been evaluated.
Methods/design
CC: DIM (Collaborative Care: Depression Initiative in the Medical setting) is a two armed randomized clinical trial with randomization between patients. Aim of the trial is to evaluate the treatment of depressive disorder in the general hospital in the Netherlands by means of a collaborative care framework including contracting, problem solving treatment, antidepressant algorithm, and manual guided self-help. 150 outpatients with diabetes, COPD, cardiovascular diseases, and HIV are randomised between intervention and control group. Patients are included who are diagnosed with moderate to severe depression based on DSM-IV criteria by a two-step screening method. The intervention group receives treatment based on the collaborative care approach; the control group receives ‘Care As Usual’. Baseline and follow-up measures (3, 6, 9, and 12 months) are done by means of questionnaires. Primary outcome measure is severity of depressive symptoms as measured with the PHQ-9. Secondary outcome measure is the cost-effectiveness of these treatments as measured by the TiC-P, EuroQol and the SF-36.
Discussion
Prior research has pointed out that depressive disorder is a chronic, mostly recurrent illness, which tends to cluster with physical comorbidity. Furthermore, even though the treatment of depressive disorder as described in the guidelines on depression are proven effective, they are often used insufficiently. Collaborative care and problem solving treatment will be specifically tailored to the medically ill with depressive disorders and evaluated in the Dutch general hospital setting.
Doel van het onderzoek
The collaborative care approach is expected to be more effective and more cost-effective compared to care as usual.
Onderzoeksproduct en/of interventie
A treatment of depression fit in the collaborative care model with problem solving treatment, an antidepressant algorithm, contracting, care management, and a manual guided self-help depression for chronically ill patients.
Algemeen / deelnemers
Da Costakade 45,
P.O. Box 725
Eva Horn
Utrecht 3500 AS
The Netherlands
+31 (0)30 2959303
ehorn@trimbos.nl
Wetenschappers
Da Costakade 45,
P.O. Box 725
Eva Horn
Utrecht 3500 AS
The Netherlands
+31 (0)30 2959303
ehorn@trimbos.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
All patients of the Onze Lieve Vrouwe Gasthuis visiting the participating outpatient clinics (diabetes, cardiology, HIV, and part of lung medicine [patients with COPD]) and who already have a diagnosis specified in their file. Patients are included in the study if a cut off score of 15 (moderate to severe depressive disorder) is reached on a the PHQ-9, which measures depression severity. The symptoms have to be present for at least six weeks or have to cause marked dysfunctioning (e.g. problems at work, housekeeping).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Suicidality (in case of a high risk for suicide, patients will be referred.)
(Concerning the following criteria a suggestion is given to the patients concerning a different kind of help:)
-Psychotic
-Suffering from dementia or delirium
-Insufficient knowledge of the Dutch language to fill in questionnaires
-Serious mental impairment
-Alcohol or drug addiction
-Already receiving psychiatric treatment
-Pregnancy
-Bipolar disorder
Concerning HIV patients:
-Organic psychosyndrome
-Personality change
-In terminal phase
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 | NL805 |
NTR-old | NTR818 |
Ander register | : N/A |
ISRCTN | ISRCTN95575369 |