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NCT06431009Recruiting

The Danish Region Midt Schizophrenia Cohort

The Danish Region Midt Schizophrenia (RMS) Cohort: Representative Cohort of Patients With a First-episode Schizophrenia Spectrum Disorder With Long-term Follow-up

Source: ClinicalTrials.gov · Last updated 29 May 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The objective of this study is to recruit patients at the first diagnosis with a schizophrenia spectrum disorder (SSD) and ultra-high risk patients (UHR), defined as patients with drug abuse and psychotic symptoms indicating a risk for developing schizophrenia. Thereby, the investigators aim to establish a large representative cohort of patients with a first-episode SSD or patients at UHR, enabling investigations of the etiology and long-term prognosis of SSDs. The primary aim is to learn more about the importance of adverse childhood experiences (ACEs) and the immune system in the etiology and course of schizophrenia. Patients will be followed with planned visits after 1, 2, 3, 12 and 24 months including online questionnaires after 2, 6, 10 and 26 weeks. There will be the possibility to contact patients again for subsequent follow-up visits.

Status (registry)
Recruiting
Study type
Observational
Enrollment
350 (estimated)
First submitted
23 Feb 2024
Start date
20 Feb 2024
Primary completion date
31 Dec 2026
Lead sponsor
University of Aarhus
NCT number
NCT06431009

What you commit to

  • Study type: Observational
  • Planned participants: 350
  • From 20 Feb 2024 to the primary completion date, 31 Dec 2026
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • In a clinical condition where the treating clinician evaluates that the patient is not able to attend the research study.

Other

  • Any coercive measure including patients in forensic psychiatry

Who the study is looking for

  • Age ≥15 years
  • Diagnosed within the previous 3 months with first-episode SSD (ICD-10: F20-29) or UHR (ICD-10: F1X.5)
  • Able to give informed oral and written consent.

Age in the registry: 15 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Aarhus University Hospital Psychiatry
Coordinator of this site? Confirm its status
AarhusDenmarkRecruiting
Psychiatric Hospital Gødstrup
Coordinator of this site? Confirm its status
HerningDenmarkRecruiting
Psychiatric Hospital Horsens
Coordinator of this site? Confirm its status
HorsensDenmarkRecruiting
Psychiatric Hospital Randers
Coordinator of this site? Confirm its status
RandersDenmarkRecruiting
Psychiatric Hospital Midt
Coordinator of this site? Confirm its status
SilkeborgDenmarkRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.