Evidence map›Paper›PMID 40440822›Full record

ArticleSchizophrenia research2025

The inventory of psychotic-like anomalous self-experiences (IPASE): Stability and relationships with attenuated psychotic symptoms and remission in individuals at-risk for psychosis.

Isabelle Scott, Alexandra Selloni, Zarina Bilgrami, Matthew Cotter, Cansu Sarac, Alessia McGowan, Marija Krcmar, Melanie Formica, Kate Gwyther, Cassandra Wannan and 6 more

Abstract read
In one paragraph

Article in Schizophrenia research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Anomalous self-experiences in biotypes of psychosis.European archives of psychiatry and clinical neuroscience · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Isabelle ScottCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia. Electronic address: isabelle.scott@orygen.org.au.
Alexandra SelloniIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Zarina BilgramiIcahn School of Medicine at Mount Sinai, New York, NY, USA; Emory University, Atlanta, Georgia.
Matthew CotterIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Cansu SaracIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Alessia McGowanIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Marija KrcmarCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.
Melanie FormicaCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.
Kate GwytherCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.
Cassandra WannanCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.
Agrima SrivastavaIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Guillermo A CecchiIBM TJ Watson Research Center, Yorktown Heights, NY, USA.
Romina MizrahiDouglas Research Centre, McGill University, Montreal, Quebec, Canada; Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Patrick McGorryCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.
Cheryl M CorcoranIcahn School of Medicine at Mount Sinai, New York, NY, USA.
Barnaby NelsonCentre for Youth Mental Health, The University of Melbourne, Parkville, Melbourne, Victoria, Australia; Orygen, The National Centre for Excellence in Youth Mental Health, 35 Poplar Rd, Parkville, VIC, Australia.

Funding

Computational phenotyping of face expression in early psychosisR01MH132239 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHERYL MARY CORCORAN · 2023 to 2026
$2.8M
Using the RDoC Approach to Understand Thought Disorder: A Linguistic Corpus-Based ApproachR01MH115332 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CORCORAN, CHERYL MARY · 2018 to 2020
$1.6M
NIMH NIH HHS R01 MH115332NIMH NIH HHS R01 MH132239
6 · The paper itself

Abstract

backgroundThe IPASE is a self-report measure of basic self-disturbance, a core feature of schizophrenia and ultra-high risk (UHR) states. However, the extent to which basic self-disturbance-as captured by the IPASE-is stable over time and related to the severity or progression of attenuated psychotic symptoms (APS) remains unclear. We examined the temporal stability of IPASE scores, their correlation with APS, and whether they predict changes in APS over time.

methodsThe baseline sample included 185 participants (healthy controls = 72, UHR = 66, first-episode psychosis = 47), with 29 UHR participants re-assessed at month-12. Correlations between IPASE scores and Comprehensive Assessment of At-Risk Mental States (CAARMS) positive symptom scores were evaluated at baseline and month-12. Stability between baseline and month-12 IPASE scores was examined in the longitudinal subsample. Regression was used to predict remission and change in CAARMS scores.

resultsAlthough mean IPASE scores were significantly higher in the UHR group compared to HCs, total IPASE scores were only weakly correlated with CAARMS total scores (ρ=0.27). IPASE subscales showed weak correlations (0.08<ρ<0.27) with CAARMS positive symptom domains. Changes in IPASE and CAARMS scores were not correlated. Moderate stability was found for IPASE total scores (ICC = 0.59) and four subscales (0.58 < ICC < 0.64), excluding the cognition subscale (ICC = 0.3). Baseline IPASE scores did not predict remission (partial R

conclusionThe IPASE is a moderately stable measure in UHR individuals, correlates with the presence of positive psychotic symptoms but only weakly with severity, and does not strongly predict positive symptom change.

Indexed as

Prodromal SymptomsPsychotic DisordersSchizophreniaAdolescentAdultFemaleHumansLongitudinal StudiesMalePsychiatric Status Rating ScalesRiskSelf ReportYoung Adult

Identifiers

PMID40440822
PMCPMC13283688

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.