NCT07237529

Brief Summary

The goal of this interventional study is to evaluate the feasibility of Narrative Exposure Therapy (NET) for people experiencing psychosis. The secondary goal of this study is to evaluate the potential impact of NET in reducing symptoms of psychosis and post-traumatic stress. Participants will be patients accessing local NHS mental health services who are between the age of 18 to 65 years-old who have been diagnosed with a psychotic disorder and have a history of trauma. The main questions the study aims to answer are: Is NET feasible to deliver to people experiencing psychosis Can NET impact symptoms of psychosis in people experiencing psychosis? Can NET impact symptoms posttraumatic stress in people experiencing psychosis? Can NET impact symptoms of depression, anxiety and stress in people experiencing psychosis? Participants will be asked to: Undertake the NET intervention with a trained NET therapist (the number of sessions will be decided based on the need of the participant) Complete a questionnaire to assess the traumas they have experienced over the course of their life (called the 'Trauma and Life Events' Scale) Complete a weekly interview to assess their symptoms of psychosis (called the 'Simplified Negative and Positive Symptoms Interview') Complete weekly measures to assess symptoms of post-traumatic stress (called the 'International Trauma Questionnaire') Complete weekly measures to assess symptoms of depression, anxiety and stress (using the Depression, Anxiety and Stress 21 item Scale \[DASS-21\]) Complete a follow-up interview to discuss their personal experience of the NET intervention)

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1

participants targeted

Target at below P25 for not_applicable

Timeline
6mo left

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress32%
Feb 2026Nov 2026

First Submitted

Initial submission to the registry

September 19, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

November 19, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

February 5, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 2, 2026

Expected
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 16, 2026

Last Updated

February 2, 2026

Status Verified

September 1, 2025

Enrollment Period

9 months

First QC Date

September 19, 2025

Last Update Submit

January 30, 2026

Conditions

Keywords

Narrative Exposure TherapyPsychosisTraumaIntervention Study

Outcome Measures

Primary Outcomes (1)

  • Change Interview

    A change interview is a semi-structured interview designed to explore participants' experiences of therapy, its feasibility, acceptability, and perceived effects. It covers general wellbeing, views on specific NET components (psychoeducation, lifeline, questionnaires, session length), and reflections on discussing traumatic memories. Participants are asked about any changes they noticed, the importance of these changes, whether they attribute them to therapy or other factors, and what aspects were helpful or unhelpful. The interview also explores challenges, unexpected experiences, and the significance of specific traumas or positive memories (flowers) discussed in therapy, as well as differences observed between initial and later lifeline sessions.

    The Change Interview will be conducted at the follow-up phase of study which will occur 4 weeks within the final NET session.

Secondary Outcomes (3)

  • PANSS-6

    From baseline to the end of follow up which occurs within 4 weeks of the final NET session.

  • International Trauma Questionnaire (ITQ)

    From baseline to the end of follow up which occurs within 4 weeks of the final NET session.

  • DASS-21 (Depression, Anxiety, and Stress Scale)

    From baseline to the end of follow up which occurs within 4 weeks of the final NET session.

Study Arms (1)

Narrative Exposure Therapy (NET) Arm

EXPERIMENTAL

In Narrative Exposure Therapy (NET), patients construct a detailed narration of their life story with the therapist, focusing on integrating traumatic memories into a coherent whole, including sensory, cognitive, emotional, and physiological aspects. The therapist documents the testimony. After an initial evaluation, including a questionnaire (TALE in this study), patients receive psychoeducation about trauma symptoms, followed by a preparatory introduction. Therapy begins with creating a "lifeline," an autobiographic overview of positive and traumatic events. Patients then undergo "Narrative Exposure," chronologically recounting their life story with in-depth exploration of emotionally charged experiences, particularly trauma, to contextualize and integrate them into reorganized memory. Patients will also be complete assessments pre, during and post the intervention to assess and monitor changes to their symptoms.

Other: Narrative Exposure Therapy (NET)

Interventions

NET always begins with a face-to-face personal interview between the patient and the therapist to carefully assess life events using checklists, followed by an interview about trauma reactions and a thorough psychoeducation about the findings and suggested procedure of NET. In another session, he arousing and meaningful specific events from birth to present are symbolized in their valence in an autobiographical timeline (or 'lifeline'). The patient is then encouraged to share their life story, focusing on adverse and emotionally charged experiences, which are explored in depth using 'Narrative Exposure', and those are reviewed in the subsequent session.

Narrative Exposure Therapy (NET) Arm

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Schizophrenia Spectrum and Other Psychotic Disorders
  • Schizophrenia
  • Schizoaffective Disorder
  • Brief Psychotic Disorder
  • Delusional Disorder
  • Substance/Medication-Induced Psychotic Disorder
  • Postpartum (Postnatal) Psychosis
  • Individuals will be eligible to take part in the study if they meet all of the following:
  • Age - between 18 and 65 years old.
  • Language - able to speak and understand English well enough to take part in the research activities.
  • Diagnosis - have a psychosis-related diagnosis as defined above.
  • Trauma history - have experienced more than one traumatic event in their lifetime. A traumatic event means something that was deeply distressing, frightening, or life-threatening, such as abuse, assault, serious accident, disaster, or war.
  • Current care - are under the care of a Local Mental Health Team (LMHT) within Nottinghamshire Healthcare NHS Foundation Trust and on the Care Programme Approach (CPA) pathway. CPA is an NHS care plan for people with complex mental health needs, setting out the support they will receive and who will provide it.
  • Mobility - can travel independently to an NHS clinic or can be supported to attend.
  • Consent - able to understand the study information and give informed consent to take part (in line with the Mental Capacity Act, 2005).

You may not qualify if:

  • Recent change in antipsychotic medication - If the person has recently started, stopped, or changed their antipsychotic medication. This is because there are no specific medical tests ("biomarkers") to predict how someone will respond to a new medication, and the effects can vary greatly between individuals. The first few weeks after a medication change can be a time of increased risk for worsening symptoms or relapse. Research also shows that stopping and starting medication can temporarily affect thinking skills such as memory and attention.
  • Recent serious mental health crisis -
  • If the person has experienced a significant adverse event within the last three months, such as:
  • A suicide attempt
  • A hospital admission for mental health reasons This is because there is currently little research on how trauma-focused therapy affects people with severe mental illness who have recently been suicidal, and starting therapy too soon after a crisis may not be safe.
  • Currently receiving another structured psychological therapy - For example, Cognitive Behavioural Therapy (CBT) or another regular talking therapy programme. This is to ensure that the results of the study reflect the effects of Narrative Exposure Therapy (NET) alone, without being influenced by another therapy.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Psychotic DisordersSchizophreniaWounds and Injuries

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

Study Officials

  • Thomas Schroder, PhD

    University of Nottingham

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lewis Albie MacDonald-Winship, BSc Psychology

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: This is a single group assignment. All participants will get the same intervention, Narrative Exposure Therapy.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 19, 2025

First Posted

November 19, 2025

Study Start

February 5, 2026

Primary Completion (Estimated)

November 2, 2026

Study Completion (Estimated)

November 16, 2026

Last Updated

February 2, 2026

Record last verified: 2025-09