Trial · NCT07907679
Virtual Reality for Pain and Anxiety During Surgical Uterine Evacuation After Early Pregnancy Loss
NCT07907679, Not applicable, Not yet recruiting, Tarsus University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Virtual Reality for Pain and Anxiety During Surgical Uterine Evacuation After Early Pregnancy Loss. Trials, record NCT07907679. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07907679
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Virtual Reality for Pain and Anxiety During Surgical Uterine Evacuation After Early Pregnancy Loss
- NCT number
- NCT07907679
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 90 participants, estimated
- Lead sponsor
- Tarsus University
- Conditions
- Early Pregnancy Loss, Procedural Pain, Anxiety
- Interventions
- Virtual reality distraction
- First posted
- 2026-10-30
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Peak procedural pain assessed by the Visual Analog Scale (VAS) | Once within 10-15 minutes after completion of surgical uterine evacuation, when the participant's clinical condition permits. | Peak procedural pain will be assessed retrospectively once, within 10-15 minutes after surgical uterine evacuation, when the participant's clinical condition permits. Before the procedure, participants in both groups will receive identical instructions explaining that they will be asked afterward to recall their highest pain during the procedure and mark it on a 10-cm Visual Analog Scale (VAS), scored from 0 (no pain) to 10 (unbearable pain). Higher scores indicate greater pain. No pain questions or scales will be administered during the procedure. Both groups will be assessed using the same method and time window. Existing pre-procedure pain will be measured separately at baseline using the same scale and distinguished from procedural pain. The timing and method of pain assessment are explained in the informed consent forms. |
| Secondary | State anxiety assessed by the State-Trait Anxiety Inventory-State Scale (STAI-I) | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | State anxiety will be assessed using the Turkish version of the 20-item State-Trait Anxiety Inventory-State Scale (STAI-I). Total scores range from 20 to 80, with higher scores indicating greater state anxiety. Scores will be compared between groups and between pre-procedure and post-procedure assessments. |
| Secondary | Systolic blood pressure | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | Systolic blood pressure will be measured in mmHg before and after the procedure and compared between groups and assessment times. |
| Secondary | Diastolic blood pressure | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | Diastolic blood pressure will be measured in mmHg before and after the procedure and compared between groups and assessment times. |
| Secondary | Pulse rate | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | Pulse rate will be measured in beats per minute before and after the procedure and compared between groups and assessment times. |
| Secondary | Respiratory rate | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | Respiratory rate will be measured in breaths per minute before and after the procedure and compared between groups and assessment times. |
| Secondary | Peripheral oxygen saturation (SpO2) | Before the intervention and procedure, and within the first 10-15 minutes after completion of surgical uterine evacuation. | Peripheral oxygen saturation will be measured as a percentage before and after the procedure and compared between groups and assessment times. |
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/NCT07907679
GET https://conductscience.org/api/trials/v1/NCT07907679/registered