Norwegian Adult Mental Health Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Depression, Schizophrenia, Bipolar Disorder, Eating Disorders. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
"The Norwegian Adult Mental Health Registry" (NAMHR) is a medical quality register collecting and systematizing data on patients and their treatment in specialist mental health care for adults in Norway. The main purpose is to create a documentation basis for quality assurance, evaluation, and improvement of assessment and treatment for patients who are offered treatment for mental disorders in the specialist health service. The register uses automatic data capture from various existing data sources. New patients are automatically included, but given the opportunity for reservations from the register without affecting their services and treatment.
Primary outcome measures
- Patient Reported Outcome Measures (PROMs) [Time frame: Baseline defined as: From start of treatment date (inclusion in the register) until the date of first documented assessment or date of discharge from any cause, whichever came first, assessed up to 24 months]
- Patient Reported Outcome Measures (PROMs) [Time frame: Discharge defined as: date of discharge from any cause, assessed up to 60 months]
- Patient Reported Outcome Measures (PROMs) [Time frame: Six months after discharge]
- Drug name and dosage from electronic medication management solutions [Time frame: Baseline defined as: From start of treatment date (inclusion in the register) until the date of first documented assessment or date of discharge from any cause, whichever came first, assessed up to 24 months]
- Drug name and dosage from electronic medication management solutions [Time frame: Discharge defined as: date of discharge from any cause, assessed up to 60 months]
- Drug name and dosage from electronic medication management solutions [Time frame: Six months after discharge from any cause, assessed up to 12 months]
- Rate of overweight defined as BMI > 25 (body mass index) [Time frame: Baseline defined as: From start of treatment date (inclusion in the register) until the date of first documented assessment or date of discharge from any cause, whichever came first, assessed up to 24 months]
- Rate of overweight defined as BMI > 25 (body mass index) [Time frame: Discharge defined as: date of discharge from any cause, assessed up to 60 months]
- Level of glycated haemoglobin (HbA1c) [Time frame: Baseline defined as: From start of treatment date (inclusion in the register) until the date of first documented assessment or date of discharge from any cause, whichever came first, assessed up to 24 months]
- Level of glycated haemoglobin (HbA1c) [Time frame: Discharge defined as: date of discharge from any cause, assessed up to 60 months]
Eligibility criteria
Inclusion criteria
- Residents in Norway aged 18 years or older assessed and granted right to treatment in specialized mental in- and out-patient settings
Exclusion criteria
- Persons who have reserved themselves against participation
- Persons already included in more specialized register for mental disorder and/or treatment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06115200 · NAMHR001