Trial · NCT07908771
Virtual Reality for Anxiety and Birth Satisfaction During Elective Cesarean Section
NCT07908771, Not applicable, Not yet recruiting, Tarsus University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Virtual Reality for Anxiety and Birth Satisfaction During Elective Cesarean Section. Trials, record NCT07908771. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07908771
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Virtual Reality for Anxiety and Birth Satisfaction During Elective Cesarean Section
- NCT number
- NCT07908771
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 144 participants, estimated
- Lead sponsor
- Tarsus University
- Conditions
- Anxiety, Cesarean Section, Birth Satisfaction
- Interventions
- Virtual Reality Distraction
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | State Anxiety | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | State anxiety will be assessed using the State-Trait Anxiety Inventory - State Subscale (STAI-I), Turkish version. Scores range from 20 to 80; higher scores indicate higher anxiety levels. |
| Secondary | Face Anxiety Score | Preoperatively (before randomization), intraoperatively (immediately after birth, before first mother-infant contact), and 15-30 minutes after completion of surgery, once clinically stable | Momentary anxiety will be assessed using the single-item Face Anxiety Scale (Turkish version). Scores range from 1 to 5; higher scores indicate higher anxiety. |
| Secondary | Cesarean Birth Satisfaction | 6-8 hours postpartum | Cesarean birth satisfaction will be assessed using the 11-item Cesarean Birth Satisfaction Scale. Scores range from 11 to 55; higher scores indicate greater satisfaction. |
| Secondary | Systolic Blood Pressure | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | Systolic blood pressure (mmHg) will be measured and recorded on the Vital Signs Monitoring Form. |
| Secondary | Diastolic Blood Pressure | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | Diastolic blood pressure (mmHg) will be measured and recorded on the Vital Signs Monitoring Form. |
| Secondary | Heart Rate | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | Heart rate (beats per minute) will be measured and recorded on the Vital Signs Monitoring Form. |
| Secondary | Respiratory Rate | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | Respiratory rate (breaths per minute) will be measured and recorded on the Vital Signs Monitoring Form. |
| Secondary | Peripheral Oxygen Saturation (SpO₂) | Preoperatively (before randomization) and 15-30 minutes after completion of surgery, once clinically stable | Peripheral oxygen saturation (%) will be measured by pulse oximetry and recorded on the Vital Signs Monitoring Form. |
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/NCT07908771
GET https://conductscience.org/api/trials/v1/NCT07908771/registered