跳至主要内容
临床试验/NCT06799806
NCT06799806招募中不适用

The Impact of the Therapeutic Virtual Reality Headset on Patient Anxiety in the Waiting Room Before Flexible Bronchoscopy in Vigil

Centre Hospitalier le Mans1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年2月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
80
试验地点
1
主要终点
Anxiety assessment

研究概览

简要总结

Bronchial fibroscopy is a frequently used procedure in the management of pneumology patients, and can be a source of anxiety, particularly while waiting for the examination.

Investigator's professional experience has shown us that many patients are anxious in the waiting room before a flexible bronchoscopy in vigile.

A great deal of research has been carried out into the use of virtual reality to reduce anxiety and pain during care but shortly before bronchoscopy. The innovative aspect is to target the patient's waiting time for the examination. Waiting is a highly anxiety-provoking time, and nurses play a vital role in supporting patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adult patients with no age or gender restrictions, seen on an outpatient basis at Le Mans Hospital.
  • •In whom bronchial fibroscopy is indicated.
  • •Person affiliated with or benefiting from a social security .
  • •Free, informed and written consent signed by the participant and the investigator (no later than the day of inclusion and before any examination required by the research).
  • •Patient able and willing to answer questionnaires

排除标准

  • •Patient refusing to participate in research
  • •Patient who has already undergone bronchoscopy in vigil
  • •Patient premedicated for bronchial fibroscopy (anxiolytic, etc.)
  • •Patients with a history of epilepsy or psychiatric pathology
  • •Patient with vertigo
  • •Patient uncooperative, demented or unable to tolerate headgear.
  • •patient under guardianship or curatorship
  • •Patients suffering from blindness or deafness
  • •Patient with known significant intolerance to screens and/or virtual reality devices
  • •Pregnant, nursing or parturient women
  • •Unscheduled patients: emergencies, etc.
  • •Hospitalized patients

研究组 & 干预措施

virtual reality

Experimental

virtual reality headset

干预措施: virtual reality device (Device)

结局指标

主要结局

Anxiety assessment

时间窗: Immediately after intervention

Anxiety assessment is measured using a Numerical Rating Scale (NRS) from 0 to 10, supplemented by a self-assessment questionnaire before and after using the Therapeutic Virtual Reality Headset.

次要结局

  • Assessment of bronchoscopy realisation and sample collection(Immediately after intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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