Trial · NCT07880093
Effects of Online and App-Based Prenatal Yoga on Birth Outcomes
NCT07880093, Not applicable, Completed, Vasviye Eroğlu
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Online and App-Based Prenatal Yoga on Birth Outcomes. Trials, record NCT07880093. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07880093
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Online and App-Based Prenatal Yoga on Birth Outcomes
- NCT number
- NCT07880093
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 85 participants, actual
- Lead sponsor
- Vasviye Eroğlu
- Conditions
- Pregnancy, Birth, Yoga
- Interventions
- Online and App-Based Prenatal Yoga
- First posted
- 2026-10-19
- Last updated
- 2026-10-19
Source ClinicalTrials.gov
Registered outcomes16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Birth Satisfaction Scale-Revised Total Score | A few hours after birth, before hospital discharge. | Birth satisfaction was assessed using the Turkish version of the 10-item Birth Satisfaction Scale-Revised (BSS-R). Total scores range from 0 to 40, with higher scores indicating greater birth satisfaction. The researcher administered the questionnaire face to face and recorded the mother's responses. |
| Primary | LATCH Breastfeeding Assessment Score | During the first breastfeeding session after birth. | Breastfeeding was assessed by the researcher through direct observation using the LATCH tool. Its five items assess latch, audible swallowing, nipple type, maternal comfort, and assistance with positioning. Total scores range from 0 to 10, with higher scores indicating better breastfeeding performance. |
| Primary | Active-Phase Labor Pain | During labor, after cervical dilatation exceeded 4 cm and before full dilatation. | Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). Assessment occurred at cervical dilatation greater than 4 cm. Cervical dilatation at assessment varied among participants. |
| Primary | Second-Stage Labor Pain | During the second stage of labor, before the birth of the baby. | Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). The rating was obtained during pushing, before the birth of the baby. |
| Primary | Third-Stage Labor Pain | After the birth of the baby and before delivery of the placenta. | Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). The rating was obtained after the birth of the baby and before delivery of the placenta. |
| Primary | Fourth-Stage Pain | Thirty minutes after delivery of the placenta. | Pain was assessed once using a 10-cm visual analog scale, ranging from 0 (no pain) to 10 (the most severe pain). |
| Primary | Duration of the Second Stage of Labor | From full cervical dilatation to the birth of the baby. | Duration in minutes from full cervical dilatation (10 cm) to the birth of the baby. |
| Primary | Cervical Dilatation at Hospital Admission | At the first vaginal examination on admission for labor. | Cervical dilatation, measured in centimeters, was recorded from the first vaginal examination at hospital admission for labor. |
| Primary | Number of Vaginal Examinations During Labor | From admission for labor to the birth of the baby. | The total number of vaginal examinations performed during labor was recorded for each participant. |
| Primary | Use of Labor Induction | During the labor and birth admission, before the birth of the baby. | Whether labor induction was administered was recorded as a binary outcome (yes/no). Decisions were made by the clinical team providing routine care. |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 registered outcomesOutcomes0
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 27152528 | RESULT |
Source PubMed
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/NCT07880093
GET https://conductscience.org/api/trials/v1/NCT07880093/registered