Trial · NCT07908186
Trauma-Related Attributions in Trauma Treatment: An Observational Study
NCT07908186, Completed, Reinier van Arkel
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Trauma-Related Attributions in Trauma Treatment: An Observational Study. Trials, record NCT07908186. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07908186
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Trauma-Related Attributions in Trauma Treatment: An Observational Study
- NCT number
- NCT07908186
- Status
- Completed
- Enrollment
- 112 participants, actual
- Lead sponsor
- Reinier van Arkel
- Conditions
- PTSD
- First posted
- 2026-10-30
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in PTSD Symptoms as Measured by the PCL-5 | Baseline (pre-treatment) and post-treatment (upon completion of trauma-focused treatment; approximately 3-6 months after baseline, depending on treatment duration). | Change in total score on the Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5). Scores range from 0 to 80, with higher scores indicating greater PTSD symptom severity. The primary outcome is the difference between baseline and post-treatment scores. |
| Secondary | Change in Trauma-Related Attributions | Baseline (pre-treatment) and post-treatment (upon completion of trauma-focused treatment; approximately 3-6 months after baseline, depending on treatment duration). | Change in maladaptive trauma-related attributions, including internal, stable, global, and uncontrollable attributions, as assessed using a validated attribution measure. |
| Secondary | Change in Posttraumatic Trauma-Related Cognitions (PTCI Total Score) | Baseline (pre-treatment) and post-treatment (upon completion of trauma-focused treatment; approximately 3-6 months after baseline, depending on treatment duration). | Posttraumatic trauma-related cognitions will be assessed using the Posttraumatic Cognitions Inventory (PTCI). The PTCI measures maladaptive trauma-related beliefs across domains including negative cognitions about the self, negative cognitions about the world, and self-blame. Higher scores indicate more negative and dysfunctional trauma-related cognitions. The secondary outcome is the change in total PTCI score from pre-treatment to post-treatment. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07908186
GET https://conductscience.org/api/trials/v1/NCT07908186/registered