Trial · NCT07887581
Coping and Adaptation for Recovery From Moral Injury: A Group Intervention for Clinical Psychology Residents
NCT07887581, Not applicable, Not yet recruiting, Universidad Complutense de Madrid
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Coping and Adaptation for Recovery From Moral Injury: A Group Intervention for Clinical Psychology Residents. Trials, record NCT07887581. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07887581
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Coping and Adaptation for Recovery From Moral Injury: A Group Intervention for Clinical Psychology Residents
- NCT number
- NCT07887581
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 10 participants, estimated
- Lead sponsor
- Universidad Complutense de Madrid
- Conditions
- Moral Distress, Moral Injury
- Interventions
- CARE-MI Group Intervention
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Moral Injury Assessed With the Health Care Moral Injury Scale | Baseline and Week 4 (immediately after completion of the four-session intervention). | Moral injury will be assessed using the 10-item Health Care Moral Injury Scale (HMIS). Each item is rated on a 5-point Likert scale from 1 (strongly disagree) to 5 (strongly agree). Item scores are summed to produce a total score ranging from 10 to 50, with higher scores indicating greater moral injury. The outcome will be the change in total HMIS score from baseline to post-intervention. |
| Secondary | Change in Mental Well-Being Assessed With the Warwick-Edinburgh Mental Well-Being Scale | Baseline and Week 4 (immediately after completion of the four-session intervention). | Mental well-being will be assessed using the 14-item Warwick-Edinburgh Mental Well-Being Scale (WEMWBS). Each item is rated from 1 to 5. Item scores are summed to produce a total score ranging from 14 to 70, with higher scores indicating greater mental well-being. The outcome will be the change in total WEMWBS score from baseline to post-intervention. |
| Secondary | Change in Depressive Symptoms Assessed With the Patient Health Questionnaire-9 | Baseline and Week 4 (immediately after completion of the four-session intervention). | Depressive symptoms will be assessed using the 9-item Patient Health Questionnaire (PHQ-9). Each item is rated from 0 to 3. Item scores are summed to produce a total score ranging from 0 to 27, with higher scores indicating greater severity of depressive symptoms. The outcome will be the change in total PHQ-9 score from baseline to post-intervention. |
| Secondary | Change in Anxiety Symptoms Assessed With the Generalized Anxiety Disorder-7 | Baseline and Week 4 (immediately after completion of the four-session intervention). | Anxiety symptoms will be assessed using the 7-item Generalized Anxiety Disorder scale (GAD-7). Each item is rated from 0 to 3. Item scores are summed to produce a total score ranging from 0 to 21, with higher scores indicating greater severity of anxiety symptoms. The outcome will be the change in total GAD-7 score from baseline to post-intervention. |
| Secondary | Intervention Completion Rate | From the first intervention session through Week 4. | The intervention completion rate will be calculated as the percentage of enrolled participants who attend at least three of the four CARE-MI group sessions. |
| Secondary | Participant Satisfaction With the CARE-MI Intervention | Week 4 (immediately after completion of the four-session intervention). | Acceptability will be assessed after the intervention using a participant satisfaction questionnaire. The questionnaire will evaluate participants' perceived usefulness, relevance, comprehensibility, and overall satisfaction with the CARE-MI intervention. Higher scores will indicate greater acceptability. |
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/NCT07887581
GET https://conductscience.org/api/trials/v1/NCT07887581/registered