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Management of Depression in Primary Care

G

Göteborg University

Status

Completed

Conditions

Depression

Treatments

Behavioral: Structured patient-centered follow up of depression

Study type

Interventional

Funder types

Other

Identifiers

NCT01402206
Madrs 2010

Details and patient eligibility

About

Most people in Sweden with mild to moderate depression are treated in primary care, but follow-up is unstructured, and we know little about whether structured, follow-up would affect the prognosis for depression and working life. The purpose of this study is to determine the effectiveness of regular, structured, patient-centered visits on mild to moderate depression.

Enrollment

258 patients

Sex

All

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • Age 18 years and up
  • Attends a participating primary health care center in the region
  • Diagnosis of mild/moderate depressive disorder (new episode)
  • No change in possible antidepressant maintenance therapy during the preceding 1 month
  • Provided written informed consent

Exclusion criteria

  • Antidepressant medication initiated or changed during the preceding 1 month
  • Patient diagnosed with major depressive disorder (BDI-II >28)
  • Patients diagnosed of severe mental psychiatric disorder (i.e. bipolar disorder, antisocial personality disorder, psychosis, substance use disorder or other serious mental disorder)
  • Suicidal ideation or intentions
  • Inability to speak and understand Swedish language well enough to take part in the activities required in the study.
  • Cognitive impairment that makes it impossible to take part in the activities required in the study
  • Does not provide written informed consent to participation in the study

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

258 participants in 2 patient groups

Structured patient visits
Other group
Description:
Participants in the intervention group visit their general practitioner at baseline and 4, 8, and 12 weeks. At each visit, participants complete MADRS-s for the assessment of depression severity and discuss the results with their GP in a patient-centered consultation.
Treatment:
Behavioral: Structured patient-centered follow up of depression
Treatment as usual
Other group
Description:
The control group receives treatment as usual by general practitioner (no intervention).
Treatment:
Behavioral: Structured patient-centered follow up of depression

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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