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
- Diseases
- Schizophrenia
- 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
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Aarhus University Hospital Psychiatry Coordinator of this site? Confirm its status | Aarhus | Denmark | Recruiting |
| Psychiatric Hospital Gødstrup Coordinator of this site? Confirm its status | Herning | Denmark | Recruiting |
| Psychiatric Hospital Horsens Coordinator of this site? Confirm its status | Horsens | Denmark | Recruiting |
| Psychiatric Hospital Randers Coordinator of this site? Confirm its status | Randers | Denmark | Recruiting |
| Psychiatric Hospital Midt Coordinator of this site? Confirm its status | Silkeborg | Denmark | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.