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Набор скоро начнётся NCT07155681

Evaluating Healthcare Professionals' Satisfaction and Stress Mitigation Using Virtual Reality Intervention in Surgical Ward

Без фазы С лечением Stress Stress (Psychology)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Virtual Reality intervention.
Кому может быть актуально
Состояния в реестре: Stress, Stress (Psychology). Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Дания, Германия
Следующий шаг
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Официальное название

Evaluating Healthcare Professionals' Satisfaction and Stress Mitigation Using Virtual Reality Intervention in Surgical Ward: a Multination Feasibility Study

Обзор

The goal of this feasibility study is to learn whether a VR intervention is feasible, acceptable, and satisfactory for healthcare workers in surgical wards to help mitigate stress. Secondary objectives include assessing its potential contribution to stress reduction, user comfort, and practical integration into daily workflows. Participants will take part in a single 10-minute VR intervention session.

Подробное описание

This study investigates the use of the HealthyMind Virtual Reality (VR) application as an innovative intervention to reduce stress among healthcare workers in surgical departments. Although workplace stress is common, there is currently a lack of structured interventions to address it.

The VR application provides healthcare professionals with the opportunity to relax through immersive, calming three-dimensional environments, such as a sunset by the sea or a mountain landscape. The VR headset is paired with an armband that non-invasively measures physiological parameters, including heart rate and heart rate variability. Based on these data, the VR environment automatically adapts to the user's stress level, for example by introducing a guided breathing exercise.

The intervention can be used at any self-selected moment during a shift, with the aim of offering a short and effective recovery break. The primary aim of this study is to evaluate the feasibility, acceptability, and user satisfaction of the VR intervention among healthcare workers. Secondary objectives include assessing its potential contribution to stress reduction, user comfort, and practical integration into daily workflows.

Вмешательства

  • Устройство Virtual Reality intervention
    Virtual Realtiy intervention with biofeedback for 10 minutes during a shift on the ward for healthcare professionals

Первичные конечные точки

  • AIM-IAM-FIM • Acceptability of Intervention Measure (AIM), • Intervention Appropriateness Measure (IAM), • Feasibility of Intervention Measure (FIM) [Срок оценки: Immediately after the VR intervention the scale will be filled in by the participant]
  • User satisfaction [Срок оценки: Immediately after the VR intervention]
Вторичные конечные точки (3)
  • Stress level [Срок оценки: immediately before the intervention (pre-intervention) and immediately after the intervention (post-intervention)]
  • CSQ-VR [Срок оценки: immediately after the VR intervention]
  • Best organizational fit [Срок оценки: At a scheduled moment within 1 month after the intervention]

Критерии участия

Критерии включения

  • Volunteering healthcare professionals (≥18 years old) working in direct patient care, such as nurses, residents, physician assistants, and surgeons, on the surgical ward.

Критерии исключения

  • Diagnosed with epilepsy
  • Experienced VR as a trigger for their migraines
  • Severe dizziness, nausea or physical disabilities will be excluded.
  • Diagnosed with arrythmias, bradycardia or tachycardia
  • Not able to wear the VR headset due to physical or psychological conditions

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Поддерживающая терапия

Центры проведения

Дания · 1 центр
  • Rhigshospitalet — Copenhagen
Германия · 1 центр
  • University Medical Center Hamburg-Eppendorf — Hamburg

Идентификаторы

NCT: NCT07155681 · 2025.0425

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗