Investigating the effectiveness of the intervention of Narrative Experiences Online in people with Attenuated Psychosis Syndrome

Investigating the effectiveness of the intervention of Narrative Experiences Online using both qualitative and quantitative methods in people with Attenuated Psychosis Syndrome

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230405057823N2

Enrollment

Registered

2023-10-13

Start date

2023-12-22

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Attenuated Psychosis Syndrome. Brief psychotic disorder

Interventions

Intervention group: Narrative Experiences Online The NEON programme evaluates whether having online access to people’s real-life stories of recovery from me

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. No diagnose Schizotypal personality disorder 2. No history of Schizophrenia and mood disorders 3. No history of taking Antipsychotic drugs 4. No drug abuse 5. No diagnose severe learning and mental disabilities and medical or neurological diseases that cause psychotic symptoms

Exclusion criteria

Exclusion criteria: 1.Diagnosis of psychotic spectrum disorders 2. Age below 18 years 3. Diagnosis of mood disorders 4. Lack of informed consent

Design outcomes

Primary

Measure	Time frame
Lived experiences. Timepoint: Pre-test and Post-test. Method of measurement: Semi-structured interview, unstructured interview and picture cards.	—

Secondary

Measure	Time frame
Quality of Life. Timepoint: Week 1, 12 and 52 (quantitative part). Method of measurement: Quality of life questionnaire.;Hope. Timepoint: Week 1, 12 and 52 (quantitative part). Method of measurement: Hope questionnaire.;Prodromal symptoms. Timepoint: Pre-test and Post-test. Method of measurement: Prodromal symptoms questionnaire and semi-structured interview.;Psychotic attachment. Timepoint: Pre-test and Post-test. Method of measurement: Psychotic attachment questionnaire.	—

Measure

Time frame

Quality of Life. Timepoint: Week 1, 12 and 52 (quantitative part). Method of measurement: Quality of life questionnaire.;Hope. Timepoint: Week 1, 12 and 52 (quantitative part). Method of measurement: Hope questionnaire.;Prodromal symptoms. Timepoint: Pre-test and Post-test. Method of measurement: Prodromal symptoms questionnaire and semi-structured interview.;Psychotic attachment. Timepoint: Pre-test and Post-test. Method of measurement: Psychotic attachment questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Amini Faskhoudi

Shahid Beheshti University of Medical Sciences

amini.maryam329@gmail.com+98 21 4470 2905

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026