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临床试验/NCT06296199
NCT06296199已完成不适用

Music, Virtual Reality and Mental Health of Inpatients in the Intensive Functional Rehabilitation Unit and Patients in the IUGM Geriatric Outpatient Clinic: Pilot Clinical Trial

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
Feasability

研究概览

简要总结

Promoting good care, well-being and quality of life for geriatric patients is a long-standing initiative in Quebec, and one in which the Institut Universitaire de Gériatrie de Montréal (IUGM) has always been a leader. For example, the IUGM played a major role in drafting the reference framework for the AAPA (approach adapted to the needs of the elderly), which was introduced by the Ministère de la Santé et des Services Sociaux in 2011. The investigator propose to continue this work by focusing in this project on the development of a new intervention aimed at the well-being and quality of life of geriatric patients and based on music and VR.

Thee investigator hypothesize (1) that a VR headset-based intervention based on listening to and observing a concert of musicians playing classical music is feasible for patients hospitalized at the IUGM's URFI and in patients attending the geriatric outpatient clinic, and (2) that this intervention can improve their mental health - i.e. their positive emotions, well-being and quality of life - and reduce their anxiety.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

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

入选标准

  • be hospitalized at the URFI of the IUGM, or being a patients attending the geriatric outpatient clinic
  • be 60 years of age or older,
  • not have an acute intercurrent pathology in the week preceding the procedure and during the two days of the procedure,
  • have no psycho-behavioural disorders,
  • no major neurocognitive disorder at a severe stage,
  • no severe visual or hearing impairment,
  • no vestibular balance disorders,
  • give written consent to participate in the study.

排除标准

  • Participate in another concurrent experimental clinical study, to avoid interference with our study.
  • Do not understand written or spoken French or English. The participants are French and/or English speakers, and the questionnaires are only available in these 2 languages.

结局指标

主要结局

Feasability

时间窗: 6 months

To determine if investigator is able to recruit 80 patients in 6 months, with a consent rate of 80% or more and less than 20% of withdrawal

次要结局

  • Affect variation(1 day)
  • Well-Being Variation(1 day)
  • Quality of life variation(1 day)
  • Anxiety variation(1 day)
  • Emotions variation(1 day)

研究者

发起方
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Olivier Beauchet

MD, PhD, director of AgeTeQ Lab at CRIUGM

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal

研究点 (2)

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