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临床试验/NCT05363137
NCT05363137已完成不适用

Herramienta De Procesamiento De Lenguaje Natural En Dispositivo Móvil Inteligente Para Fomentar La Adherencia a La Rehabilitación Domiciliaria

University of Valencia2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2022年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
65
试验地点
2
主要终点
Adherence

研究概览

简要总结

A Chatbot oriented to virtually assist patients in a physiotherapy treatment has been designed and developed to interact with patients with musculoskeletal disorders in need for domiciliary rehabilitation. The tool has been designed to promote adherence to rehabilitation, what in turn may have an impact on clinical outcome. A randomized clinical trial involving patients undergoing total knee replacement has bee designed to determine the applicability of the proposal. The participants will be assigned into exerimental group (intervention with the software tool) or control group (standard care).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
— 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals on the waiting list for total knee replacement surgery
  • Undergoing primary total knee replacement surgery
  • Who have a personal smartphone
  • Who have an instant messaging application installed
  • Familiar with the use of such application (more than 3 accesses per week),

排除标准

  • Evident cognitive state that prevents to understand care provider instructions
  • Vestibular or central nervous system affection (e.g. stroke)
  • Cannot read or write
  • Do not understand Spanish language
  • Not able to consent to participate

结局指标

主要结局

Adherence

时间窗: Change from baseline to 3 months after surgery date

Compliance with intervention measured as the percentage of sessions carried out with respect to the total planned

次要结局

  • Knee Pain(Change from baseline to 3 months and one year after surgery date)
  • Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(Change from baseline to 3 months and one year after surgery date)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jose María Blasco Igual

Principal investigator

University of Valencia

研究点 (2)

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