Feasibility of Web-based Therapy Sessions

Официальное название

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

Обзор

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.

Подробное описание

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.

Вмешательства

• Поведенческое a Web-Based Platform for delivering treatment for cognitive and language impairment amongst adults with acquired neurological disorders
  The Cognishine platform is a digital (web-based) general health and wellness monitoring platform. It is designed to support health care professionals specialised in rehabilitation of patients with neurological disorders, through a wide range of multi-media based generalised activities across speech, language, social-emotional, and cognition.

Первичные конечные точки

• To assess the feasibility of using the Cognishine web-based platform in a large NHS Trust in acute care setting. [Срок оценки: 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.]

Вторичные конечные точки (5)

• To assess staff and patient experience of using the Cognishine platform during therapy sessions. [Срок оценки: 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 [Срок оценки: 12 month into the study.]
• To generate preliminary data on the rehabilitation progress associated with the use of the Cognishine platform. [Срок оценки: 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. [Срок оценки: 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. [Срок оценки: 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.]

Критерии участия

Критерии включения

• 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

Критерии исключения

• 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

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Другое

Центры проведения

Великобритания · 1 центр

• Liverpool University Hospitals NHS Foundation Trust — Liverpool

Идентификаторы

NCT: NCT07560696 · LHS0204

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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