- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07469930
Psychometric Evaluation of a Dutch Attribution Questionnaire for Trauma-Related Attributions (PEDAQTRA)
Study Overview
Status
Conditions
Detailed Description
This study investigates the psychometric properties of a newly developed Dutch attribution questionnaire specifically designed to assess trauma-related attributional styles. The instrument includes 32 dichotomously scored items divided across general and personal attributional perspectives, each covering four attribution dimensions: locus of causality, controllability, stability, and globality.
Two samples were included: (1) a non-clinical sample of first-year psychology students from Radboud University (N = 418 in Part I; N = 382 in Part II), and (2) a clinical sample of individuals receiving inpatient or outpatient mental healthcare for trauma-related conditions at the Psychotraumacentrum Zuid-Nederland (PTC ZN; N = 112). All participants provided informed consent, and the study was approved by the relevant institutional ethics committee.
Participants completed the new questionnaire along with established measures of PTSD symptoms (PCL-5), trauma-related cognitions (PTCI), and general locus of control (IE-18; non-clinical sample only). Data were collected via secure online platforms. Analyses will include descriptive statistics, internal consistency (Cronbach's alpha), exploratory and confirmatory factor analyses, item response theory modelling, and correlation analyses to assess construct, convergent, and divergent validity. Group comparisons (clinical vs. non-clinical) and within-subject contrasts between general and personal attribution perspectives will be conducted using t-tests, MANOVAs, repeated measures ANOVAs, and regression models. Moderation and mediation analyses will examine the role of perspective contrast in predicting PTSD severity.
The study is guided by the following a priori hypotheses:
- The questionnaire will demonstrate a clear and theoretically consistent factor structure reflecting the attribution dimensions of locus of causality, controllability, stability, and globality.
- The total scale and subscales will show adequate internal consistency, with Cronbach's α values of at least .70.
- Higher levels of maladaptive attributional patterns will be positively associated with PTSD symptom severity (PCL-5) and negative trauma-related cognitions (PTCI).
- Personal attribution items will show stronger associations with psychopathology than general attribution items, reflecting the heightened impact of self-referential cognitive biases.
- Clinical participants with trauma-related disorders will score higher on maladaptive attribution patterns than non-clinical students, indicating the instrument's sensitivity to trauma-related cognitive profiles.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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North Brabant
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's-Hertogenbosch, North Brabant, Netherlands, 5211LJ
- Reinier van Arkel, Psychotraumacentrum Zuid-Nederland
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
- Non-clinical sample: first-year psychology students
- Clinical sample: individuals receiving outpatient trauma treatment at PTC ZN
Description
Inclusion Criteria
- Age ≥ 18
- Sufficient proficiency in Dutch
- For clinical sample: history of traumatic exposure and current trauma-related symptoms
- For non-clinical sample: enrollment as first-year psychology student at Radboud University
Exclusion Criteria
- Incomplete questionnaire data
- Cognitive impairment preventing informed consent or questionnaire completion
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Non-clinical sample
First-year psychology students - Clinical sample: individuals receiving outpa
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Clinical sample
Individuals receiving outpatient trauma treatment at PTC ZN
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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1. Change in Maladaptive Attributional Style (Dutch Attribution Questionnaire for Trauma-Related Attributions)
Time Frame: Baseline
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The Dutch Attribution Questionnaire for Trauma-Related Attributions is a 32-item self-report instrument assessing attributional patterns across four dimensions (locus of causality, controllability, stability, globality) from both general and personal perspectives.
Items are scored dichotomously (0 = disagreement; 1 = agreement), yielding a total score ranging from 0 to 32.
Higher scores indicate stronger maladaptive attributional patterns.
Change from baseline to the specified follow-up point will be calculated.
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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2. Change in PTSD Symptom Severity (PCL-5)
Time Frame: Baseline
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The PTSD Checklist for DSM-5 (PCL-5) is a 20-item self-report measure assessing PTSD symptom severity over the past month.
Total scores range from 0 to 80, with higher scores indicating more severe symptoms.
Change from baseline to follow-up will be calculated.
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Baseline
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3. Change in Trauma-Related Cognitions (PTCI)
Time Frame: Baseline
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The Posttraumatic Cognitions Inventory (PTCI) assesses negative trauma-related cognitions about the self, the world, and self-blame.
Total scores range from 33 to 231, with higher scores indicating more negative cognitions.
Change from baseline to follow-up will be calculated.
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Baseline
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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4. Change in General Locus of Control (IE-18)
Time Frame: Baseline
|
The IE-18 is a shortened version of the Internal-External Control Scale, measuring general locus of control.
Scores range from 0 to 18, with higher scores indicating a more external locus of control.
This measure is administered only in the non-clinical sample.
Change from baseline to follow-up will be assessed.
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Baseline
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ESCW-2023-062R1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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