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Идёт набор NCT07504276

Tele-Rehabilitation vs Conventional Rehabilitation for Cognitive Improvement in Stroke Survivors.

Без фазы С лечением Stroke Cognitive Impairment Post-Stroke Cognitive Impairment

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Tele-rehabilitation, Conventional Rehabilitation.
Кому может быть актуально
Состояния в реестре: Stroke, Cognitive Impairment, Post-Stroke Cognitive Impairment. Базовые параметры: 50 лет — 80 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Пакистан
Следующий шаг
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Официальное название

Comparison Of Tele-Rehabilitation Versus Conventional Rehabilitation To Improve Cognition Among Stroke Survivor.

Обзор

This study aims to: * Compare tele-rehabilitation and conventional rehabilitation for cognitive improvement after stroke. * Evaluate changes in cognitive function using standardized assessment tools. * Determine whether tele-rehabilitation is as effective as conventional therapy. * Improve evidence-based rehabilitation strategies for stroke survivors.

Подробное описание

Stroke is a leading cause of long-term disability and is frequently associated with cognitive impairments affecting attention, memory, executive function, and processing speed, which significantly reduce independence and quality of life among survivors. Cognitive rehabilitation plays a vital role in promoting neuroplasticity and functional recovery after stroke. Conventional rehabilitation, delivered through face-to-face clinical sessions, remains the standard approach; however, tele-rehabilitation has emerged as an accessible and innovative alternative that allows structured cognitive interventions to be delivered remotely using digital platforms. Despite increasing use of tele-rehabilitation, limited comparative evidence exists regarding its effectiveness versus conventional rehabilitation for cognitive improvement in stroke survivors. This randomized controlled trial aims to compare the effectiveness of tele-rehabilitation and conventional rehabilitation over a 8-weeks intervention period. Participants will be randomly allocated into two groups receiving comparable intensity and frequency of cognitive rehabilitation. Cognitive outcomes will be assessed at baseline and post-intervention using standardized tools such as the Montreal Cognitive Assessment (MoCA) and other validated measures such as Stroop Test. The findings of this study will contribute to evidence-based rehabilitation practices and help determine whether tele-rehabilitation can provide an effective alternative to conventional cognitive rehabilitation following stroke.

Вмешательства

  • Поведенческое Tele-rehabilitation
    Cognitive rehabilitation exercises delivered remotely using video-based sessions, targeting attention, memory, executive function, and processing speed. Sessions will be conducted over 8 weeks.
  • Поведенческое Conventional Rehabilitation
    In-person cognitive rehabilitation exercises targeting attention, memory, executive function, and processing speed delivered in a clinical setting for 8 weeks.

Первичные конечные точки

  • Change in Cognitive Function Measured by Montreal Cognitive Assessment (MoCA) [Срок оценки: Baseline]
  • Change in Cognitive Function Measured by Montreal Cognitive Assessment (MoCA) [Срок оценки: After 8 weeks]
Вторичные конечные точки (2)
  • Change in Executive Function Measured by stroop Test [Срок оценки: Baseline]
  • Change in Executive Function Measured by stroop Test [Срок оценки: After 8 weeks]

Критерии участия

Критерии включения

  • Adults with age 50-80
  • Diagnosed with ischemic or hemorrhagic stroke within subacute to chronic phase.
  • Moca Score 10-25 score atleast
  • For tele-rehab must accessible to a digital device.

Критерии исключения

  • History of neurodegenerative disorder e.g Alzheimer's Disease and Parkinson's Disease
  • Severe Cognitive Impairment
  • Lack of access to or inability to use a digital device

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Пакистан · 1 центр
  • Riphah International University — Islamabad

Идентификаторы

NCT: NCT07504276 · REC/02263 Imran Amjad

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗