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Идёт набор NCT05023785

The HIMALAYAS Trial and Lifestyle Changes in Pediatric, Adolescent and Young Adult Cancer Survivors Study: A Multicentre Randomized Controlled Trial

Без фазы С лечением Heart Failure Cardiotoxicity Cancer

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: Cardio-oncology Rehabilitation (CORE).
Кому может быть актуально
Состояния в реестре: Heart Failure, Cardiotoxicity, Cancer. Базовые параметры: 18 лет — 45 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
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Harmonized Interventions to Maintain Health Via Appropriate Risk Factor Modification and Lifestyle Changes in Pediatric, Adolescent and Young Adult Cancer Survivors Study: A Multicentre Randomized Controlled Trial

Обзор

Pediatric, adolescent and young adult cancer survivors (PAYA-CS) are at higher risk of cardiovascular (CV) morbidity and mortality. This is a consequence of prior cancer-related therapies that have the potential of producing cardiac dysfunction, reducing cardiorespiratory fitness (reduced VO2peak) and psychosocial morbidities (i.e., anxiety and depression). A reduction of physical activity levels can evoke functional limitations resulting in a vicious cycle of reduced exercise tolerance and physical deterioration. To date, there is limited evidence on the use of non-pharmacological strategies such as Cardio-Oncology Rehabilitation (CORE) including structured exercise, behavioural support and risk factor management to improve the outcomes of this underserved population. The HIMALAYAS study is a randomized controlled trial designed to evaluate the impact of a CORE intervention (consisting of six-months home and onsite-based structured moderate to high-intensity aerobic exercise training and CVD risk factor management) on CV and psychosocial health, and the cardiovascular disease risk in PAYA-CS with mild heart dysfunction (stage B heart failure) compared to standard of care (i.e. providing guidance on the current exercise recommendations for cancer survivors). The primary objective of the HIMALAYAS study is to determine whether a six-month supervised CORE intervention, consisting of individualized moderate to high-intensity aerobic exercise training, CVD risk factor modification and enhanced online behavioral support, improves cardiorespiratory fitness (VO2peak; primary outcome), cardiac function, CVD risk factors and biomarkers, and patient-reported outcomes (PROs) at six- months follow-up compared to standard of care (CON) in PAYA-CS with stage B heart failure. The secondary objective is to assess the same outcomes at 12- and 24-months follow-up. We will recruit 336 patients across 5 sites in Canada and upto 134 patients at UHN in 3 years and conclude in 6 years.

Подробное описание

Over 90,000 North Americans are diagnosed with cancer before the age of 40. Improved cancer therapies have led to an exponential growth in the number of pediatric, adolescent, and young adult cancer survivors (AYA-CS) who are expected to live 50-60 years beyond diagnosis. However, AYA-CS are at increased risk of developing multiple cancer- and treatment-related morbidities including poor fitness (e.g., low VO2peak), hypertension (HTN), diabetes, and poor mental health, which all contribute to premature cardiovascular disease (CVD). The prevalence of CVD events (e.g. heart failure, heart attack, stroke) is up to 23.8% in adult survivors of pediatric cancers with long term follow-up after treatment. The incidence of subclinical CVD, which is a precursor to CVD events, is even higher in AYA-CS; up to 40%, 11%, and 5% experience subclinical cardiomyopathy measured by abnormal global longitudinal strain (GLS), diastolic dysfunction (DD) or mild reduction in left ventricular ejection fraction (LVEF), respectively, and 18% experience reduced aerobic fitness. The treatment of modifiable CVD risk factors must be considered a fundamental target for improving CVD health-related outcomes in AYA-CS. To this end, exercise and best-practices for CVD risk factor modification are integral to a cardiac rehabilitation model. Traditional cardiac rehabilitation models for patients with CVD (consisting of exercise, CVD risk factor treatment, and patient education) are safe and effective in improving HRQoL, morbidity, and mortality risk. However, by virtue of their age and low short-term CVD risk, AYA-CS do not meet traditional criteria for initiating cardiac rehabilitation (CR) and are less likely to receive treatments to reduce CVD risk. AYA-CS with stage B heart failure (SBHF): (1) are at high risk for subsequent HF/CVD death; (2) have lower cardiopulmonary fitness; and (3) are more likely to benefit from CVD risk factor management. Considering that AYA-CS have an estimated 33% prevalence of SBHF, this vulnerable cohort of cancer survivors represent an opportunity for intervention that is highly feasible and potentially impactful. Exercise is a preferred method for optimizing health and survival in PAYA-CS. However, we need models that safely and effectively deliver exercise interventions that meet the unique needs of this population. The cardio-oncology rehabilitation (CORE) model is an intervention that would provide AYA-CS with SBHF a supervised and home-based high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) exercise therapy, CVD risk factor modification, and behavioural support to reduce the risk of CVD. The primary objective of the HIMALAYAS study is to determine whether supervised CORE (Group 1A) improves cardiorespiratory fitness (VO2peak; primary outcome), cardiac function, CVD risk factors and biomarkers, and PROs at 6 months (primary timepoint) as well as 12 and 24 months compared to standard of care group control group (CON) in AYA-CS with SBHF.

The secondary objective of the study is to assess the ongoing behavioural support strategy based on the exercise guidelines for cancer survivors (i.e. 90 to 150 minutes of moderate to vigorous PA per week) on VO2peak, cardiac function, CVD risk factors and biomarkers, and PROs at 24 months compared to standard of care \[CON\] in AYA-CS with SBHF. Due to the COVID-19 pandemic, CORE intervention will involve a facility-based HIIT session and home-based HIIT session (described as "HIIT at Home") per week.

Вмешательства

  • Поведенческое Cardio-oncology Rehabilitation (CORE)
    Exercise therapy, CVD risk factor management for the first 6 months (as per current standards in CR models) and behavioural support for the entire 2-year intervention period

Первичные конечные точки

  • Cardiorespiratory fitness [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
Вторичные конечные точки (12)
  • Cardiorespiratory fitness [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Ventilatory threshold [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
  • Ventilatory threshold [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Anaerobic threshold [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
  • Anaerobic threshold [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Post-exercise heart rate recovery [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
  • Post-exercise heart rate recovery [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Left ventricular ejection fraction (LVEF) [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
  • Left ventricular ejection fraction (LVEF) [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Global longitudinal strain (GLS) [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]
  • Global longitudinal strain (GLS) [Срок оценки: Baseline to 24-month follow-up (Primary and Secondary RCTs)]
  • Early (E) and late (A) diastolic mitral inflow velocities and deceleration time [Срок оценки: Baseline to 6-month follow-up (Primary RCT)]

Критерии участия

Критерии включения

  • Be a PAYA-CS, defined as ≤39 years of age at the time of cancer diagnosis;
  • Be 18-45 years of age at the time of enrolment;
  • Received cancer treatment(s) with known cardiovascular risks (e.g., anthracyclines, trastuzumab, radiotherapy, platinum-based agents, vascular endothelial growth factor inhibitors, tyrosine kinase inhibitors);
  • Be cancer-free at the time of enrollment;
  • Stage B Heart Failure (SBHF)
  • In patients with availability of pre-treatment imaging:
  • ≥10% decrease in LVEF at post-treatment compared to pre-treatment
  • ≥15% decrease in GLS at post-treatment compared to pre-treatment
  • No pre-treatment imaging:
  • LVEF ≤53% in women/51% in men
  • GLS >-18%
  • Left ventricular hypertrophy (LV mass/body surface area: >95 g/m2 for women or >115 g/m2 for men)
  • Concentric remodelling (>0.42 relative wall thickness)
  • Diastolic dysfunction (≥ grade 1)
  • BNP ≥35pg/ml or NT-proBNP ≥125pg/ml

Критерии исключения

  • Have an absolute or unresolved relative contraindication to exercise according to the American College of Sports Medicine guidelines;
  • Have an untreated physical or mental health concern that precludes safe and effective exercise participation;
  • Have established CVD (excluding mildly reduced LVEF as described above);
  • Be pregnant at time of recruitment;
  • Be currently engaging in frequent high-intensity exercise (>1 high-intensity exercise session per week);
  • Have substantial barriers to participating, including (1) living too far from study centre or (2) being unable or willing to comply with the study protocol.

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
Поддерживающая терапия

Центры проведения

Канада · 1 центр
  • University Health Network — Toronto

Идентификаторы

NCT: NCT05023785 · 23-5626

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗