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Идёт набор NCT07719517

Morning Activation to Improve Mood After Stroke

Без фазы С лечением Stroke Depressive Symptoms

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: Morning Activation Program, Health Education Program.
Кому может быть актуально
Состояния в реестре: Stroke, Depressive Symptoms. Базовые параметры: от 18 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
Гонконг
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

This pilot randomized controlled trial will evaluate the feasibility and preliminary effects of a six-week behavioral intervention designed to improve mood and daily functioning in adults who have experienced a stroke and report depressive symptoms and difficulty becoming engaged in activities after waking. Participants will be randomly assigned to either the behavioral intervention or a health education program. Assessments will be completed before and immediately after the six-week program and will include questionnaires and seven-day monitoring of sleep, activity, and mood. The study will also examine feasibility indices such as participant retention, intervention attendance, acceptability, and preliminary changes in mood.

Вмешательства

  • Поведенческое Morning Activation Program
    A six-week individualized behavioral program delivered in weekly sessions of approximately 60 minutes. The program is designed to support engagement in daily activities after waking, establish consistent daily routines, and improve mood and functioning after stroke. Sessions will be tailored to participants' needs and abilities.
  • Поведенческое Health Education Program
    A six-week health education program delivered in weekly sessions of approximately 60 minutes. The program will provide general information relevant to health and recovery after stroke and will be matched to the experimental program in session frequency and duration. It will not include the individualized behavioral strategies provided in the experimental arm.

Первичные конечные точки

  • Recruitment Rate [Срок оценки: From the start of recruitment until enrollment of the final participant.]
  • Retention Rate [Срок оценки: Immediately after completion of the 6-week intervention]
  • Intervention Attendance [Срок оценки: Throughout the 6-week intervention period]
  • Intervention Acceptability [Срок оценки: Immediately after completion of the 6-week intervention]
  • Participants Experiencing Adverse Events [Срок оценки: From enrollment through completion of the immediate post-intervention assessment.]
Вторичные конечные точки (1)
  • Change in Depressive Symptoms [Срок оценки: Baseline and immediately after completion of the 6-week intervention]

Критерии участия

Критерии включения

  • Age 18 years or older.
  • History of stroke at least 6 months before enrollment.
  • Patient Health Questionnaire-9 score of 10 or higher.
  • Difficulty getting started or engaging in activities in the morning.
  • Able to provide informed consent.

Критерии исключения

  • Conditions that would interfere with study participation.
  • Neurological condition other than stroke.
  • Currently receiving psychological therapy for depression.
  • Significant cognitive impairment or dementia.
  • Current or past diagnosis of psychosis, bipolar disorder, or mania.
  • Hospitalization that would interfere with study participation.
  • Acute or significant suicidal ideation
  • Alcohol or substance use problems within the past month.
  • Use of antidepressant or anti-anxiety medication unless the dosage has been stable for at least 4 weeks and no changes are planned during the study.

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
Простое слепое
Основная цель
Лечение

Центры проведения

Гонконг · 1 центр
  • The Hong Kong Polytechnic University — Гонконг

Идентификаторы

NCT: NCT07719517 · HSEARS20260321001

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗