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Psychometric Properties of the International Trauma Interview (ITI) for ICD-11 PTSD and CPTSD

Psychometric Properties of the International Trauma Interview (ITI) for ICD-11 PTSD and CPTSD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04086654
Enrollment
77
Registered
2019-09-11
Start date
2020-03-02
Completion date
2021-10-15
Last updated
2022-11-22

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

Conditions

Complex Post-Traumatic Stress Disorder (CPTSD), Post Traumatic Stress Disorder (PTSD)

Brief summary

The aim of the project is to evaluate the psychometric properties (e.g. validity, reliability) of the International Trauma Interview (ITI) - German version. The ITI is a structured clinical interview that corresponds to the ICD-11 criteria for diagnosing both posttraumatic stress disorder (PTSD) and complex posttraumatic stress disorder (CPTSD). Eligible participants from psychiatric inpatient and outpatient facilities in Switzerland who have provided informed will complete various self-report measures about trauma-related mental health complaints. In addition, the ITI will be conducted by a trained clinician. Lastly, information from the medical chart will be further used for scientific purpose. The overall assessment will take approximately 1-2 hours to complete.

Interventions

DIAGNOSTIC_TESTInternational Trauma Interview (ITI) for ICD-11 PTSD and Complex PTSD - German version

The ITI consists of 18 items and for each symptom, standardized questions as well as probes are presented. A trained professional rates both symptom frequency and intensity, which are converted into an overall index of symptom severity. A diagnosis of PTSD/CPTSD is established by applying the ICD-11 diagnostic rules. It takes approximately 30-60 minutes to administer.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

Study-specific Inclusion criteria * Structured diagnostic procedures upon hospital entry not yet started, except for orienting assessments * Able to give informed consent as documented by signature * Able to understand and communicate in German

Exclusion criteria

* Clinical signs for impaired cognitive abilities * Other contraindications to undergo the clinical interview

Design outcomes

Primary

MeasureTime frame
International Trauma Interview (ITI)Up to two weeks upon psychiatric ward entry
Life Event Checklist DSM-5Up to two weeks upon psychiatric ward entry

Secondary

MeasureTime frame
Impact of Event Scale Revised VersionUp to seven days upon psychiatric ward entry
Beck Depression Inventory IIUp to seven days upon psychiatric ward entry
Borderline Symptom ListUp to seven days upon psychiatric ward entry
PTSD Checklist for DSM-5Up to seven days upon psychiatric ward entry
Brief Symptom ChecklistUp to seven days upon psychiatric ward entry

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026