Trial · NCT07889986
Psychosocial Effects of Empathy-Based Midwifery Education on Midwifery Students and Pregnant Women
NCT07889986, Not applicable, Not yet recruiting, Kahramanmaras Sutcu Imam University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Psychosocial Effects of Empathy-Based Midwifery Education on Midwifery Students and Pregnant Women. Trials, record NCT07889986. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889986
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Psychosocial Effects of Empathy-Based Midwifery Education on Midwifery Students and Pregnant Women
- NCT number
- NCT07889986
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 224 participants, estimated
- Lead sponsor
- Kahramanmaras Sutcu Imam University
- Conditions
- Empathy, Anxiety, Childbirth
- Interventions
- Empathy-Based Midwifery Education, Empathy-Based Midwifery Support During Labor
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
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 Midwifery Students' Empathic Tendency Scores | Baseline (before the first training session) and immediately after the final training session, at the end of week 2. | Empathic tendencies will be assessed using the Empathic Tendency Scale, a 20-item instrument scored on a five-point Likert scale. Total scores range from 20 to 100, with higher scores indicating greater empathic tendency. Changes from baseline to the post-intervention assessment will be compared between students receiving empathy-based midwifery education and students receiving routine education. |
| Secondary | Change in Midwifery Students' State Anxiety Scores | Baseline (before the first training session) and immediately after the final training session, at the end of week 2. | State anxiety will be assessed using the 20-item state anxiety subscale of the State-Trait Anxiety Inventory. Items are rated on a four-point scale, and total scores range from 20 to 80. Higher scores indicate greater state anxiety. Changes from baseline to the post-intervention assessment will be compared between students receiving empathy-based midwifery education and students receiving routine education. |
| Secondary | Maternal Satisfaction with Childbirth | Within the first 24 hours after delivery. | Maternal satisfaction will be assessed using the Scale for Measuring Maternal Satisfaction in Normal Birth. The instrument consists of 43 items across 10 subscales, rated on a five-point Likert scale. Total scores range from 43 to 215, with higher scores indicating greater satisfaction. Scores will be compared between women receiving empathy-based midwifery support alongside routine care and women receiving routine delivery room care. |
| Secondary | Traumatic Birth Perception | Within the first 24 hours after delivery. | Traumatic birth perception will be assessed using the Traumatic Birth Perception Scale. The instrument consists of 13 items, each scored from 0 to 10. Total scores range from 0 to 130, with higher scores indicating greater perceived birth trauma. Scores will be compared between women receiving empathy-based midwifery support alongside routine care and women receiving routine delivery room care. |
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/NCT07889986
GET https://conductscience.org/api/trials/v1/NCT07889986/registered