Trial · NCT07892456
Breathing Meditation and VR Nature Videos in Angiography Patients: Effects on Anxiety, Comfort, and Physiology
NCT07892456, Not applicable, Recruiting, University of Yalova
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Breathing Meditation and VR Nature Videos in Angiography Patients: Effects on Anxiety, Comfort, and Physiology. Trials, record NCT07892456. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892456
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Breathing Meditation and VR Nature Videos in Angiography Patients: Effects on Anxiety, Comfort, and Physiology
- NCT number
- NCT07892456
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 123 participants, estimated
- Lead sponsor
- University of Yalova
- Conditions
- Coronary Angiography, Virtual Reality, Meditation
- Interventions
- Breathing Meditation Combined with Virtual Reality-Enhanced Nature Videos
- First posted
- 2026-10-23
- Last updated
- 2026-11-04
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Anxiety | 2 month | \*\*State Anxiety Inventory:\*\* The State Anxiety Inventory (STAI-I) will be used to assess patients' state anxiety before and after angiography. The inventory measures how individuals feel at a particular moment and consists of 20 items, each scored on a 4-point scale ranging from 1 to 4. Some items are reverse scored. Total scores range from 20 to 80, with higher scores indicating greater state anxiety. The inventory will be administered to patients before and after angiography to evaluate changes in anxiety levels following the intervention. |
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Pain | 2 month | \*\*Visual Analog Scale (VAS):\*\* The Visual Analog Scale (VAS) is a commonly used unidimensional tool for assessing pain intensity. It consists of a 10-cm (100-mm) line ranging from 0 (no pain) to 10 (worst imaginable pain). In this study, the VAS will be used to assess patients' pain levels before, during, and after angiography to evaluate the effect of breathing meditation combined with VR-enhanced nature videos on pain intensity. |
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Patient Comfort | 2 month | \*\*General Comfort Questionnaire (GCQ):\*\* The General Comfort Questionnaire will be used to assess patients' overall comfort levels before and after angiography. The questionnaire evaluates comfort across physical, psychospiritual, sociocultural, and environmental dimensions. The Turkish short form consists of 28 items and includes three subscales: relief (9 items), ease (9 items), and transcendence (10 items). Items are rated on a 6-point Likert scale, and negatively worded items are reverse-scored. The total score is divided by the number of items to obtain a mean score ranging from 1 to 6, with higher scores indicating greater comfort. The Turkish version demonstrated good internal consistency, with a Cronbach's alpha coefficient of 0.82. In this study, the questionnaire will be administered before and after angiography to evaluate the effect of breathing meditation combined with VR-enhanced nature videos on patients' comfort levels. |
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Blood Pressure | 2 month | Patients' blood pressure values will be recorded to evaluate the effect of breathing meditation combined with VR-enhanced nature videos on blood pressure during angiography. Blood pressure will be measured before, during, and after the angiography procedure in both the intervention and control groups. |
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Pulse Rate | 2 month | Patients' pulse rates will be recorded to evaluate the effect of breathing meditation combined with VR-enhanced nature videos on pulse rate during angiography. Pulse rate will be measured before, during, and after the angiography procedure in both the intervention and control groups. |
| Primary | The Effect of Breathing Meditation and VR-Enhanced Nature Videos on Oxygen Saturation | 2 month | Patients' peripheral oxygen saturation (SpO₂) levels will be recorded to evaluate the effect of breathing meditation combined with VR-enhanced nature videos on oxygen saturation during angiography. Oxygen saturation will be measured before, during, and after the angiography procedure in both the intervention and control groups. |
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.
Papers5
The papers the trial lists on ClinicalTrials.gov.
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/NCT07892456
GET https://conductscience.org/api/trials/v1/NCT07892456/registered