VR and mozart take on high blood pressure in the ER
NCT ID NCT07272486
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether adding virtual reality (VR) and classical music to standard blood pressure medication can help people who come to the emergency room with very high blood pressure (hypertensive urgency). 130 adults with high blood pressure but no organ damage were randomly assigned to get either standard treatment alone or standard treatment plus VR and music. Researchers measured blood pressure and anxiety levels over two hours to see if the non-drug approach made a difference.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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130 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 years or older * Clinical diagnosis of primary hypertension * Presentation to the emergency department with hypertensive urgency * Absence of any signs of acute end-organ damage * Ability to understand the study and provide informed consent * Able to cooperate with serial blood pressure measurements Exclusion Criteria: * Age younger than 18 years * Diagnosis of secondary hypertension * Any medication intolerance or known hypersensitivity to captopril or nitrate therapy * Current severe psychiatric disorder or cognitive impairment interfering with participation * Contraindications to using virtual reality (history of severe vertigo, epilepsy, motion sickness, etc.) * Hemodynamic instability requiring immediate high-intensity medical intervention * Pregnancy or breastfeeding * Inability or unwillingness to provide informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ankara Bilkent City Hospital
Ankara, Çankaya, 06170, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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