跳至主要内容
临床试验/NCT06698653
NCT06698653招募中不适用

Assessment of the Benefit of the Mobility Assistance System (SAM) on Transfer Independence for a Reimbursement Request

WINNCARE6 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2025年2月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
54
试验地点
6
主要终点
The impact on transfer independence will be measured by comparing the "bed transfer" item of the Functional Independence Measure (FIM), carried out at D7 and D14 by direct observation of the participant by the therapist.

研究概览

简要总结

This is a randomized, cross-over, multi-center, intention-to-treat, open-label study to assess the impact of the SAM Ergonom light (SAM) device on independence when transferring from the supine to the sitting position at the edge of the bed in a population of individuals with an inability to transfer independently from the supine to the sitting position in bed, compared with the use of a raising arm.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
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

入选标准

  • Aged 18 and over
  • Unable to transfer from lying to sitting independently
  • Requiring technical assistance or the help or supervision of a third party
  • Using a medical bed
  • In-patient care for a minimum of 3 weeks in a medical or rehabilitation facility
  • Having freely consented to participate
  • Affiliated with a social security scheme or entitled to benefits

排除标准

  • Non-consolidated spinal or pelvic fracture
  • Degenerative shoulder
  • Cardiovascular disorders caused by physical exertion
  • Joint pain localized to dorsolumbar spine
  • Behavioural disorders (opposition, agitation, dementia)
  • Invalid patient (disability, low tonicity), agitated, not lucid (confused, disoriented) at risk of falling, requiring physical restraint with bed rails on medical prescription
  • Functional inability to move independently
  • Cognitive impairment affecting reliability of response to questionnaires
  • Motor or algic incapacity of the 2 upper limbs not allowing the use of a technical aid (lifting frame or SAM) to ensure transfer from lying to sitting position in bed
  • Patient less than 146 cm tall
  • Patient weighing less than 30 kg or more than 200 kg
  • Patient with a mattress incompatible with the OS'CARE device
  • Mattress length less than 190 cm or greater than 200 cm, and width less than 85 cm or greater than 120 cm
  • In addition, vulnerable persons covered by articles L. 1121-5 to 8 and L. 1122-1-2 of the French Public Health Code are excluded from the study:
  • Pregnant, parturient or breast-feeding women
  • Persons deprived of their liberty by judicial decision (including guardianship, curatorship and safeguard of justice) or administrative decision
  • Persons under psychiatric care or admitted to a health or social institution for purposes other than research.
  • Person in an emergency situation unable to give prior consent

结局指标

主要结局

The impact on transfer independence will be measured by comparing the "bed transfer" item of the Functional Independence Measure (FIM), carried out at D7 and D14 by direct observation of the participant by the therapist.

时间窗: At day 7 and day 14 of the experiment

次要结局

  • Satisfaction with the use of the SAM device will be measured by comparing the satisfaction scale with the technical aid (ESAT) at D7 or D14.(At day 7 and day 14 of the experiment)
  • The psychosocial impact, including quality of life, will be measured by comparing the scale for measuring the psychosocial impact of a technical aid (F-PIADS) at D7 and D14.(At day 7 and day 14 of the experiment)
  • Device acceptability will be measured by a questionnaire based on the Unified Theory of Acceptance and Use of Technology (UTAUT) model at D7 and D14.(At day 7 and day 14 of the experiment)
  • Overall independence will be measured by comparing global FIM at D7 and D14.(At day 7 and day 14 of the experiment)
  • Effort during supine-to-sitting transfers will be measured by comparing the duration of a supine-to-sitting transfer at the edge of the bed at D7 and D14, and by the average duration of the transfer during the period of use of the devices.(At day 7 and day 14 of the experiment)
  • The quantity and quality of the transfer will be evaluated indirectly by the total number of lifts and attempted lifts from the bed over 7 days for each device, measured by OS'CARE bed presence sensors.(At day 7 and day 14 of the experiment)

研究者

发起方
WINNCARE
申办方类型
Industry
责任方
Sponsor

研究点 (6)

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