Trial · NCT07896447
Mobile-Based Resilience Intervention for Moral Injury, Compassion Fatigue, and Distress in ICU Nurses
NCT07896447, Not applicable, Not yet recruiting, Alexandria University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Mobile-Based Resilience Intervention for Moral Injury, Compassion Fatigue, and Distress in ICU Nurses. Trials, record NCT07896447. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896447
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Mobile-Based Resilience Intervention for Moral Injury, Compassion Fatigue, and Distress in ICU Nurses
- NCT number
- NCT07896447
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 160 participants, estimated
- Lead sponsor
- Alexandria University
- Conditions
- Moral Injury
- Interventions
- Behavioral
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Moral injury: Moral Injury Symptom Scale-Healthcare Professionals (MISS-HP) total score | Baseline (T0), immediately after the 8-week intervention (T1, week 8), and one-month follow-up (T2, week 12) | Moral injury symptoms measured with the Moral Injury Symptom Scale-Healthcare Professionals (MISS-HP; Mantri et al., 2020), a 10-item self-report questionnaire. Items are rated from 1 (strongly disagree) to 10 (strongly agree); items 5, 6, 7, and 10 are reverse-coded. Minimum total score 10, maximum 100. Higher scores indicate greater moral injury (worse outcome). Unit of measure: score on a scale. |
| Primary | urnout: Professional Quality of Life Scale version 5 (ProQOL-5), Burnout subscale score | Baseline (T0), immediately after the 8-week intervention (T1, week 8), and one-month follow-up (T2, week 12) | Burnout measured with the 10-item Burnout subscale of the Professional Quality of Life Scale version 5 (ProQOL-5; Stamm, 2009), one of two subscales used to operationalize compassion fatigue. Items are rated from 1 (never) to 5 (very often) for the past 30 days; items 1, 4, 15, 17, and 29 are reverse-scored. Minimum subscale score 10, maximum 50. Higher scores indicate greater burnout (worse outcome). Unit of measure: score on a scale. |
| Primary | Secondary traumatic stress: Professional Quality of Life Scale version 5 (ProQOL-5), Secondary Traumatic Stress subscale score | Baseline (T0), immediately after the 8-week intervention (T1, week 8), and one-month follow-up (T2, week 12) | Secondary traumatic stress measured with the 10-item Secondary Traumatic Stress subscale of the Professional Quality of Life Scale version 5 (ProQOL-5; Stamm, 2009), one of two subscales used to operationalize compassion fatigue. Items are rated from 1 (never) to 5 (very often) for the past 30 days. Minimum subscale score 10, maximum 50. Higher scores indicate greater secondary traumatic stress (worse outcome). Unit of measure: score on a scale. |
| Primary | Psychological distress: Kessler Psychological Distress Scale (K10) total score | Baseline (T0), immediately after the 8-week intervention (T1, week 8), and one-month follow-up (T2, week 12) | Non-specific psychological distress (anxiety and depressive symptoms) measured with the Kessler Psychological Distress Scale (K10; Kessler et al., 2002), a 10-item self-report questionnaire covering the preceding four weeks. Items are rated from 1 (none of the time) to 5 (all of the time). Minimum total score 10, maximum 50. Higher scores indicate greater psychological distress (worse outcome). Unit of measure: score on a scale. |
| Secondary | Resilience: 10-item Connor-Davidson Resilience Scale (CD-RISC-10) total score | Baseline (T0), immediately after the 8-week intervention (T1, week 8), and one-month follow-up (T2, week 12) | Resilience measured with the 10-item Connor-Davidson Resilience Scale (CD-RISC-10; Campbell-Sills and Stein, 2007), a self-report questionnaire covering the past month. Items are rated from 0 (not true at all) to 4 (true nearly all the time). Minimum total score 0, maximum 40. Higher scores indicate greater resilience (better outcome). Unit of measure: score on a scale. |
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/NCT07896447
GET https://conductscience.org/api/trials/v1/NCT07896447/registered