跳至主要内容
临床试验/NCT07026890
NCT07026890招募中不适用

The Value of Virtual Reality in the Care of Elderly People With Psychomotor Disadaptation Syndrome: a Randomised Controlled Trial of Mixed Efficacy and Implementation vs. Conventional Rehabilitative Care

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月16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
50
试验地点
1
主要终点
Change in 'Timed Up and Go' time between initial and final assessment

研究概览

简要总结

Psychomotor Disadaptation Syndrome (PMDS) is characterised by a deterioration in postural function, gait and psychomotor automatisms in the elderly. It is often associated with falls and can manifest itself as retropulsion, gait abnormalities, neurological disorders and psycho-behavioural problems. For the majority of these patients, a stay in a geriatric medical and rehabilitation centre is necessary, enabling an objective assessment of these disorders and multi-professional care, including physiotherapists, occupational therapists and adapted physical activity teachers, aimed at restoring safe movement and motor independence. However, rehabilitation relies on traditional exercises that are limited, repetitive and sometimes far removed from everyday activities. Technological innovations such as virtual reality (VR) offer opportunities to improve care by creating immersive environments that reproduce real-life situations. VR could thus help to rehabilitate the motor problems associated with MS.

The aim of the VIR-AGE project is to study the clinical benefits of VR in the rehabilitation of hospitalised elderly people suffering from PMDS in terms of functional deficits, particularly motor deficits.

The study will take place at the Centre gériatrique Champmaillot of the CHU Dijon Bourgogne. A total of 50 patients with SPDM will take part.

The total duration of your participation is 5 weeks.

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
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Person who has given written consent
  • •Person aged ≥ 65 years;
  • •With a proven diagnosis of motor maladjustment syndrome;
  • •Hospitalised in a geriatric care unit;
  • •Able to understand a simple instruction and answer a closed question;
  • •Ability to perform the TUG within 7 days of arriving on site

排除标准

  • •Person not affiliated to or not benefiting from a social security scheme
  • •Person subject to a legal protection measure (curatorship, guardianship)
  • •Person subject to a judicial protection measure
  • •An adult who is incapable or unable to give consent
  • •Persons with epilepsy, kinetosis or known claustrophobia Persons unable to understand simple instructions for carrying out tests
  • •Anyone with a severe visual and/or hearing impairment
  • •Any person with a behavioural disorder (agitation, aggressiveness)
  • •Any person with a severe walking or balance problem that makes motor exercises unsuitable
  • •Anyone with a pathology, injury, wound or severe deformity to the head or cervical spine
  • •Any person suffering from severe vertigo, diagnosed at the discretion of the investigating doctor
  • •Inability to use arm for pointing
  • •Persons susceptible to migraines
  • •Non-French speakers
  • •Anyone with an inter-pupillary distance outside the range of possible helmet adjustments

研究组 & 干预措施

Control: conventional rehabilitation + 3 additional rehabilitation sessions

Active Comparator

干预措施: Evaluation visits (Other)

Control: conventional rehabilitation + 3 additional rehabilitation sessions

Active Comparator

干预措施: Rehabilitation sessions (Other)

Experimental: conventional rehabilitation + 3 virtual reality sessions

Experimental

干预措施: Rehabilitation sessions (Other)

Experimental: conventional rehabilitation + 3 virtual reality sessions

Experimental

干预措施: Evaluation visits (Other)

Experimental: conventional rehabilitation + 3 virtual reality sessions

Experimental

干预措施: Virtual reality sessions (Other)

Control: conventional rehabilitation + 3 additional rehabilitation sessions

Active Comparator

干预措施: Additional rehabilitation sessions (Other)

结局指标

主要结局

Change in 'Timed Up and Go' time between initial and final assessment

时间窗: 5 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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