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临床试验/NCT07560696
NCT07560696招募中不适用

A Feasibility Study to Explore Rehabilitation Outcomes, Usability and User Experience of a Web-Based Platform for Delivering Treatment for Cognitive and Language Impairment Amongst Adults With Acquired Neurological Disorders

Liverpool University Hospitals NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年7月3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
To assess the feasibility of using the Cognishine web-based platform in a large NHS Trust in acute care setting.

研究概览

简要总结

The goal of this feasibility study is to explore rehabilitation outcomes, usability and user experience of a web-based platform for delivering treatment for cognitive and language impairment amongst adults with acquired neurological disorders in critical illness and stroke disorders.

The main question it aims to answer is:

" Is it feasible to use a web-based platform for delivering rehabilitation treatment in a large acute National Health Care Organisation"

Participants will undergo therapy sessions prescribed by therapists on a web-based platform instead of the conventional paper-based therapy sessions for their cognitive and speech rehabilitation needs.

详细描述

The population group will be adult patients admitted to critical care unit and stroke unit and diagnosed to have speech and cognitive impairment.

The intervention is to provide therapy prescribed by therapist through Cognishine, a web-based platform instead of paper-based therapy session.

The primary objective is to assess feasibility of using the Cognishine web-based platform in a large NHS Trust in acute care setting measured by number of completed therapy sessions, per patient days.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • Patients with cognitive impairment and/or speech impairment being treated at the LUHFT Intensive Care Units and the Stroke wards
  • Need for Cognitive and/or speech and Language rehabilitation

排除标准

  • Inability to obtain consent
  • Refusal to take part in the study
  • Failure to engage with the Cognishine platform
  • Inability to operate a mobile device/ tablet with support
  • Unavailability of study therapist to provide training of patients
  • Unstable medical condition

研究组 & 干预措施

Web-based patient-led therapy sessions

Experimental

All patients will receive standard of care rehabilitation. In addition, patients recruited into the study will use the Cognishine platform for cognitive and/or language rehabilitation

干预措施: a Web-Based Platform for delivering treatment for cognitive and language impairment amongst adults with acquired neurological disorders (Behavioral)

结局指标

主要结局

To assess the feasibility of using the Cognishine web-based platform in a large NHS Trust in acute care setting.

时间窗: From recruitment until discharge from rehabilitation therapy or discharge from hospital, which ever comes first. Time frames will vary dependent on patient recovery .The anticipated time frame is 1 to 6 months. Maximum follow up is 12 months.

Total number of completed sessions per patient on the cognishine platform

次要结局

  • To assess staff and patient experience of using the Cognishine platform during therapy sessions.(Patients will be asked to complete this on discharge from hospital. Therapists will be asked to complete the questionnaire one month after starting the study (in the middle of recruitment))
  • To generate qualitative data about how to improve the end user experience for therapist to target barriers to implementation(12 month into the study.)
  • To generate preliminary data on the rehabilitation progress associated with the use of the Cognishine platform.(As recovery is highly individualised time frames will vary amongst participants .It is anticipated that the time frame will range from 1 to 6 months.)
  • To generate preliminary data on the rehabilitation progress associated with the use of the Cognishine platform.(As recovery is highly individualised time frames will vary amongst participants .It is anticipated that the time frame will range from 1 to 6 months)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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