Trial · NCT07902869
Online Written Imagery Rescripting for Shame and Negative Self-Cognitions in Malaysian Adults With Childhood Emotional Neglect
NCT07902869, Not applicable, Completed, Taylor's University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Online Written Imagery Rescripting for Shame and Negative Self-Cognitions in Malaysian Adults With Childhood Emotional Neglect. Trials, record NCT07902869. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902869
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Online Written Imagery Rescripting for Shame and Negative Self-Cognitions in Malaysian Adults With Childhood Emotional Neglect
- NCT number
- NCT07902869
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 34 participants, actual
- Lead sponsor
- Taylor's University
- Conditions
- Shame, Childhood Emotional Neglect, Adult Survivors of Child Adverse Events
- Interventions
- Internet-Based Written Imagery Rescripting (W-ImRs), Psychoeducation
- First posted
- 2026-10-29
- Last updated
- 2026-11-05
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change From Baseline in Shame on the External and Internal Shame Scale (EISS) at Post-Intervention | Baseline (Day 0) and Post-Intervention (Collected 3 days after each participant's final session) | The EISS is an 8-item self-report questionnaire measuring external and internal shame. Items are rated from 0 to 4, giving a total score from 0 to 32. Higher scores indicate greater shame. |
| Secondary | Change From Baseline in Negative Self-Cognitions on the Posttraumatic Cognitions Inventory-9 (PTCI-9) at Post-Intervention | Baseline (Day 0) and Post-Intervention (Collected 3 days after each participant's final session) | The PTCI-9 is a 9-item self-report questionnaire measuring negative cognitions about the self, negative cognitions about the world, and self-blame. Items are rated from 1 to 7, giving a total score from 9 to 63. Higher scores indicate more negative cognitions. |
| Secondary | Number of Participants Showing Reliable Improvement in Shame on the EISS | Baseline (Day 0) and Post-Intervention (Collected 3 days after each participant's final session) | Reliable improvement is defined as a decrease in EISS total score from baseline to post-intervention with a Reliable Change Index (RCI) greater than 1.96 (Jacobson \& Truax, 1991). An RCI above 1.96 means there is 95% confidence that the decrease is a real change, and not due to chance or small day-to-day differences in how a person answers the questionnaire. |
| Secondary | Number of Participants Showing Reliable Improvement in Negative Self-Cognitions on the PTCI-9 | Baseline (Day 0) and Post-Intervention (Collected 3 days after each participant's final session) | Reliable improvement is defined as a decrease in PTCI-9 total score from baseline to post-intervention with a Reliable Change Index (RCI) greater than 1.96 (Jacobson \& Truax, 1991). An RCI above 1.96 means there is 95% confidence that the decrease is a real change, and not due to chance or small day-to-day differences in how a person answers the questionnaire. |
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.
Papers4
The papers the trial lists on ClinicalTrials.gov.
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/NCT07902869
GET https://conductscience.org/api/trials/v1/NCT07902869/registered