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Идёт набор NCT06222762

Effect of Personalized Follow-up in Adapted Physical Activities in Subjects With Chronic Heart Failure.

Без фазы С лечением Heart Failure

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: Experimental arm.
Кому может быть актуально
Состояния в реестре: Heart Failure. Базовые параметры: 18 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Effect of a Personalized Follow-up in Adapted Physical Activities on the Long-term Benefits of Rehabilitation in Subjects With Chronic Heart Failure.

Обзор

France has one million people with heart failure (HF). Exercise intolerance, characterised by dyspnoea, is the main clinical symptom in HF patients and a key determinant of reduced quality of life. In addition to drug and surgical treatments, cardiac rehabilitation programmes have shown benefits in heart failure patients. Lasting at least 3 weeks, these programmes improve physical abilities, quality of life and reduce the risk of hospitalisation for heart failure patients. To date, the real challenge is no longer to prove the benefits of cardiac rehabilitation, but to find solutions to maintain its long-term effects. The transition between the end of the supervised programmes in the centre and the return home is a difficult phase for the majority of patients who do not continue regular physical activity and thus quickly lose the benefits of the programme. To help maintain the benefits of cardiac rehabilitation, some centres offer patients programmes to continue physical activity during phase III. Although these options are often beneficial in the first few months after the end of rehabilitation compared to control groups, the long-term results are mixed. These results imply that one of these maintenance options may not be suitable for all patients. It is therefore important to propose a personalised post-rehabilitation follow-up involving the patient in the choice of physical activities to optimise the maintenance of long-term benefits. We hypothesise that patients who receive personalised support from a sport and health professional following rehabilitation maintain long-term benefits compared to a control group who do not receive this support.

Вмешательства

  • Другое Experimental arm
    Personalized follow-up in adapted physical activities

Первичные конечные точки

  • To compare the evolution of the level of physical activity 12 months after a cardiac rehabilitation programme between patients benefiting from personalised support at the end of the rehabilitation and a control group benefiting from the usual management. [Срок оценки: 12 months]
Вторичные конечные точки (12)
  • To compare between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme of time spent in each level of activity : [Срок оценки: 12 months]
  • To compare physical capacities measured using the 6-minute walk test between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare physical capacities measured using the endurance test between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare physical capacities measured using the chair getting-up test between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare physical capacities measured using the hand-grip test between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare physical capacities measured using the incremental ergocycle test between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare the evolution of dyspnea scores 12 months after a cardiac rehabilitation programme between the experimental group and the control group [Срок оценки: 12 months]
  • To compare the psychological dimensions (motivation) between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare the psychological dimensions (anxiety/depression) between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare the psychological dimensions (quality of life) between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare the psychological dimensions (quality of life) between the experimental group and the control group, the evolution 12 months after a cardiac rehabilitation programme [Срок оценки: 12 months]
  • To compare, between groups, the evolution 12 months after a cardiac rehabilitation programme of the physiological adaptations during endurance test [Срок оценки: 12 months]

Критерии участия

Критерии включения

  • Diagnosis of stable heart failure with NYHA stage I, II or III
  • Participation in a cardiac rehabilitation programme
  • Patient agreement
  • Patient of legal age
  • Patient affiliated to the Social Security

Критерии исключения

  • Patient refusal
  • Minor patients
  • Subjects under guardianship or curatorship
  • Subjects over 80 years of age at the time of inclusion

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
Другое

Центры проведения

Франция · 2 центра
  • Fondation ILDYS — Brest
  • CHU de Brest — Brest

Идентификаторы

NCT: NCT06222762 · 29BRC23.0022 - BOUGE TON COEUR

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗