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Monitoring Changes in Self Experience

Reflection on Experiences of Alteration of Lived Self and Reality (REAL): Monitoring Changes in Basic Self-Disturbances and Interaction With Context Over Time Through the Experience Sampling Method - 2REAL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON61377
Enrollment
30
Registered
2025-05-19
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

psychotic disorders, schizophrenia spectrum disorders, psychosis psychosis, schizophrenia

Interventions

None listed

Sponsors

Espria
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Either: Ultra-high-risk for psychosis, as assessed with the Comprehensive Assessment of At-Risk Mental States (CAARMS) no longer than 12 months before inclusion.  Or: First episode psychosis (maximally five years in the past), as assessed by a clinician. Participants must report the presence of basic self-disturbances during the initial screening and the Examination of Anomalous Self Experience (EASE) interview (see protocol for details). The individual is currently not acutely psychotic to such a degree that participation is not possible. Participants will be excluded if their psychotic experiences were solely during substance intoxication. Participants will be excluded if their psychotic experiences were solely during substance intoxication.Ability to speak and read the Dutch language. Participants must own a smartphone capable of running m-path. 

Exclusion criteria

Exclusion criteria: FEP participants must not have received diagnosis of an affective disorder. Participants must not have received a diagnosis of an intellectual disability or severe developmental disorder. Participants who do not answer yes to one of three main questions or affirm four items from sub-questions during the screening or EASE interview will be excluded from the study. We will also exclude participants who we judge to not fulfil clinical relevance for inclusion (e.g., participants with four items but who give the impression that their experience is non-specific for BSD).

Design outcomes

Primary

MeasureTime frame
The study’s main parameters are the within-person variability in intensity of basic self-disturbances over time as assessed with the self-report items in the REAL instrument. This will be operationalized by calculating the mean intensity of BSD experiences and measures of intra-individual variability (e.g., within-person standard deviations, mean squared successive differences) across the EMA measurements.

Secondary

MeasureTime frame
Secondary parameters are dynamic associations (correlations), between-person variability measures, and change over time: (a) contemporaneous correlations among BSD items and between BSD, contextual variables and psychotic symptoms (assessed with contextual ESM items and ESM items from the ESM Repository); (b) lagged (temporal) correlations and directed autoregressive coefficients (e.g., lag-1 effects) among BSD items and between BSD, and context; (c) time trends in mean BSD intensity and within-person means of individual BSD items (group- and individual-level slopes); and (d) the association of baseline BSD (EASE-score) and baseline psychotic symptoms (PANSS-6) with within-person-mean BSD, within-person variability (SD or MSSD) and change over time.

Countries

Netherlands

Contacts

Public ContactG. H. M. Pijnenborg-Nieuwland

Espria

marieke.pijnenborg@ggzdrenthe.nl0031626797086

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 10, 2026