Trial · NCT07901010
The Effect of a Virtual Reality Breastfeeding Experience on Breastfeeding Expectations and Avoidance
NCT07901010, Not applicable, Not yet recruiting, Ebru Ertas
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of a Virtual Reality Breastfeeding Experience on Breastfeeding Expectations and Avoidance. Trials, record NCT07901010. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07901010
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of a Virtual Reality Breastfeeding Experience on Breastfeeding Expectations and Avoidance
- NCT number
- NCT07901010
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 50 participants, estimated
- Lead sponsor
- Ebru Ertas
- Conditions
- Breastfeeding Expectations, Breastfeeding Avoidance
- Interventions
- Simulation of Virtual Reality
- First posted
- 2026-10-28
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Breastfeeding Expectations Score | From 36 weeks to 38 weeks of gestation | Breastfeeding expectations will be assessed using the Breastfeeding Expectations Scale at 36 weeks of gestation (baseline) and 38 weeks of gestation (follow-up). The change in scale scores from baseline to follow-up will be compared between the virtual reality intervention group and the control group. The scale consists of 12 items and follows a 5-point Likert format. The minimum score that can be obtained on the scale is 12, and the maximum score is 60. Lower scores on the scale indicate higher positive expectations regarding the breastfeeding experience. |
| Primary | Breastfeeding Avoidance Score at 1 Month Postpartum | 1 month after childbirth | Breastfeeding avoidance will be assessed using the Breastfeeding Avoidance Scale one month after childbirth. Scores will be compared between the virtual reality intervention group and the control group to evaluate the effect of the intervention on postpartum breastfeeding avoidance. The scale consists of 18 items and follows a 5-point Likert format. The minimum score that can be obtained on the scale is 18, and the maximum score is 90. As the score on the scale increases, the behavior of avoiding breastfeeding also increases. |
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/NCT07901010
GET https://conductscience.org/api/trials/v1/NCT07901010/registered