Recognition of personality disorder and anxiety disorder comorbidity in patients treated for depression in secondary psychiatric care.
Marie Asp, Daniel Lindqvist, Johan Fernström...
https://pubmed.ncbi.nlm.nih.gov/31895938Actively Recruiting
Led by Region Skane · Updated on 2026-04-30
415
Participants Needed
2
Research Sites
N/A
Total Duration
R
Region Skane
Lead Sponsor
L
Lund University
Collaborating Sponsor
Researchers are investigating the long-term outlook and factors predicting treatment results for people with difficult-to-treat depression under secondary psychiatric care. This study follows a group of 415 patients originally studied between 2012 and 2021, who were carefully assessed for their diagnosis and previous treatments. All participants were genotyped for enzymes CYP2D6 and CYP2C19, and blood samples were stored for further analysis related to prognosis. The current study involves a five-year follow-up of these patients through review of medical records and national register data. No new treatments or interventions are provided during this period. Data collected will include information on suicide attempts, hospital visits, treatments received, personality assessments, and clinical improvements. The study aims to examine symptom patterns, the clinical course of depression, suicidality, and the impact of earlier pharmacological counseling offered to some participants. Participants' involvement consists of allowing access to their medical and registry data for a period of five years after the original study. Researchers will track clinical outcomes such as suicide attempts, depression progression, personality disorder diagnoses, bipolar disorder characteristics, and biomarker effects. The study uses approved opt-out consent, where participants can decline but are otherwise included. The total follow-up period is five years from each participant's baseline enrollment in the original study.
CONDITIONS
Long-term Follow-up of Depressive Disorders in Psychiatric Care
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or digital)
Duration - 5 years
Participants are observed for long-term prognosis of depression through medical records review and registry data extraction without active intervention.
Data collection based on medical records and registers; no in-person visits required
Total: 2 locations
1
Psychiatry Reserach Unit
Lund, Sweden, 221 85
Active, Not Recruiting
2
Research Unit, Office of Psychiatricy, habilitation and technical aid
Lund, Sweden, 221 85
Actively Recruiting
M
Marie Asp, MD, PhD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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