Trial · NCT07896148
Mindfulness Training to Promote Prosocial Tendencies in Nursing Students
NCT07896148, Not applicable, Completed, Qom University of Medical Sciences
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Mindfulness Training to Promote Prosocial Tendencies in Nursing Students. Trials, record NCT07896148. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896148
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Mindfulness Training to Promote Prosocial Tendencies in Nursing Students
- NCT number
- NCT07896148
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 168 participants, actual
- Lead sponsor
- Qom University of Medical Sciences
- Conditions
- Mindfulness Training in Nursing Students
- Interventions
- Mindfulness Training, Alternative Educational Workshop
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in prosocial tendencies scores from baseline to post-intervention and two-month follow-up | Baseline (before the intervention), immediately after the six-week intervention, and two months after the post-intervention assessment. | Prosocial tendencies were measured using the 25-item Revised Prosocial Tendencies Measure (PTM-R). Items are rated on a five-point Likert scale, with item 5 reverse-scored. Total scores range from 25 to 125, with higher scores indicating greater prosocial tendencies. Changes in scores were evaluated by comparing the intervention and control groups across the three assessment time points. |
| Primary | Change in mindfulness scores from baseline to post-intervention and two-month follow-up | Baseline (before the intervention), immediately after the six-week intervention, and two months after the post-intervention assessment. | Mindfulness was measured using the 15-item Mindful Attention Awareness Scale (MAAS). Total scores range from 15 to 90, with higher scores indicating greater mindfulness. Scores were compared between the intervention and control groups across the three assessment time points. |
| Primary | Change in moral identity scores from baseline to post-intervention and two-month follow-up | Baseline (before the intervention), immediately after the six-week intervention, and two months after the post-intervention assessment. | Among participants in the intervention group, associations between homework adherence scores and changes in mindfulness, prosocial tendencies, and moral identity scores were examined using regression analyses. Homework adherence was assessed using a researcher-developed six-item questionnaire, with higher scores indicating greater engagement with the assigned mindfulness practices. |
| Secondary | Association between homework adherence and changes in mindfulness, prosocial tendencies, and moral identity | Immediately after the six-week intervention and two months after the post-intervention assessment. | Homework adherence was assessed using a researcher-developed six-item questionnaire informed by previous literature on homework adherence. Higher scores indicated greater engagement with and completion of assigned mindfulness practices. Associations between homework adherence scores and changes in mindfulness, prosocial tendencies, and moral identity were examined among participants in the intervention group using regression analyses. |
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/NCT07896148
GET https://conductscience.org/api/trials/v1/NCT07896148/registered