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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00794196
Other study ID # FIS PI070546
Secondary ID
Status Active, not recruiting
Phase N/A
First received November 17, 2008
Last updated July 22, 2011
Start date October 2008
Est. completion date October 2011

Study information

Verified date July 2011
Source Fundació Sant Joan de Déu
Contact n/a
Is FDA regulated No
Health authority Spain: Ministry of Health and Consumption
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the impact of pharmaceutical services among patients starting a treatment with antidepressants for a diagnosis of depression. The hypothesis of the study is that pharmacist intervention can improve compliance to antidepressants and patient wellbeing.


Description:

The aim of this study is to evaluate the efficacy of a support program in community pharmacy on the improvement of the compliance to antidepressants and the clinic of typical primary care patients under normal practice circumstances. That implies that the intervention is made by pharmacists without any specific requirement that work in the community pharmacies set up in the area of study and on patients following the usual medical circuit. As well, the cost of the support program is calculated in order to set the effectiveness of the program.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis for depression from a general practitioner

- Beginning a pharmacological antidepressant treatment

- Going to one of the participant community pharmacies

Exclusion Criteria:

- Used antidepressant medication in the past 2 months

- Had an appointment with an specialist in mental disorders in the past 2 months

- History of psychotic or bipolar episodes

- History of drug abuse or dependency

- Cognitive impairment that not allows assessment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Behavioral:
Pharmaceutical care program for antidepressant treatment
The pharmaceutical care program is a support program for patients starting and maintaining antidepressant treatment.

Locations

Country Name City State
Spain Primary Care Center Gavà 1 Gava Barcelona
Spain Primary Care Center Doctor Bartomeu Fabres Anglada Gavà Barcelona

Sponsors (4)

Lead Sponsor Collaborator
Fundació Sant Joan de Déu Carlos III Health Institute, Catalan Institute of Health, University of Barcelona

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adherence to antidepressant medication At 3 and 6 months No
Secondary Patient wellbeing 0, 3 and 6 months No
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