Psychosis proneness
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Groningen
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: All participants: - Are aged between 18 and 35 years - Read and speak Dutch fluently - Should be capable of following the research procedures - Provide Informed Consent;Participants subsample 1: - Are currently (i.e. at moment of screening) not in clinical care for mental health (e.g. GGZ, POH-GGZ, Psychologist);Participants subsample 2: - Are currently in clinical care for mental health - Have mild, non-psychotic psychopathology, as evidenced by a score below 6 on the Prodromal Questionnaire (PQ) ;Participants subsample 3: - Are currently in clinical care for mental health - Have mild psychopathology including subclinical psychotic symptoms, as evidenced by a score of or above 6 on the PQ, but are not at UHR for psychosis, as indexed by the Comprehensive Assessment of At Risk Mental State (CAARMS) ;Participants subsample 4: - Are currently in clinical care for mental health - Are at clinical high risk for psychosis, as indexed by the CAARMS
Exclusion criteria
Exclusion criteria: - History of or current psychotic episode, according to the DSM-IV criteria - Pregnancy - Significant hearing or visual problems impairments - No internet connection at home or on mobile phone or tablet
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Network parameters of individuals in different clinical stages will be compared. These network parameters include the strength and directionality of symptom connections and centrality indices. Also, within-individual changes in these network parameters (from baseline to follow-up) will be linked to progression through clinical stages. | — |
Secondary
| Measure | Time frame |
|---|---|
| Please, see "primary study parameters" for the most important primary and secundary study parameters. | — |
Countries
Netherlands
Outcome results
None listed