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Набор скоро начнётся NCT07308301

Examination of the Relationship Between Quality of Life and Caregiving Burden Among Caregivers of Pediatric Oncology Patients

— Наблюдательное Childhood Cancer Childhood Cancers Caregiver Subjective Burden Primary Caregivers of Children Newly Diagnosed With 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: Assessment of caregiver quality of life and burden.
Кому может быть актуально
Состояния в реестре: Childhood Cancer, Childhood Cancers, Caregiver Subjective Burden, Primary Caregivers of Children Newly Diagnosed With Cancer. 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Официальное название

EXAMİNATİON OF THE RELATİONSHİP BETWEEN QUALİTY OF LİFE AND CAREGİVİNG BURDEN AMONG CAREGİVERS OF PEDİATRİC OCOLOGY PATİENTS

Обзор

Primary Aim The primary aim of this study is to determine the quality of life and caregiving burden levels of caregivers of pediatric oncology patients and to examine the relationship between these two variables. Secondary Aims To evaluate the differences between caregivers' sociodemographic characteristics (age, gender, education level, marital status, income level, etc.) and their quality of life. To examine the differences between caregivers' sociodemographic characteristics and their caregiving burden levels. To determine whether caregivers' quality of life and caregiving burden differ according to the diagnosis and treatment characteristics of pediatric oncology patients (duration of diagnosis, type of treatment, frequency of hospitalization, etc.). Significance of the Study Childhood cancer is a process that deeply affects not only the patient but also the family, particularly the caregivers. Family members who provide care for children often face intense physical, psychological, social, and economic burdens. These challenges reduce caregivers' quality of life and increase their caregiving burden. Identifying the relationship between the quality of life and caregiving burden among caregivers of pediatric oncology patients is highly important in planning support services for families during the care process and in strengthening family-centered care practices by healthcare professionals. The findings of this study will contribute to the development of family-centered approaches in nursing care, the design of psychosocial support programs, and a better understanding of caregivers' needs.

Вмешательства

  • Поведенческое Assessment of caregiver quality of life and burden
    This intervention consists of assessing the quality of life and caregiving burden of primary caregivers of children diagnosed with cancer using standardized questionnaires and scales. It does not involve any medical procedures, treatments, or experimental applications. The intervention includes only the administration of data collection tools to caregivers and is therefore distinct from treatment-based interventions used in other clinical studies.

Первичные конечные точки

  • Caregiver Quality of Life Index-Cancer (CQOLC) [Срок оценки: From the enrollment phase until the end of the 12-week data collection period.]
Вторичные конечные точки (1)
  • Caregiver Burden Scale [Срок оценки: From the enrollment phase until the end of the 12-week data collection period.]

Критерии участия

Критерии включения

  • Being a family member who provides care for a child aged 0-18 years diagnosed with cancer
  • The child being in the active treatment phase (chemotherapy, radiotherapy, post-surgical follow-up, etc.)
  • Being able to read and write in Turkish and having sufficient literacy to complete the research questionnaire
  • Willingness to participate in the study

Критерии исключения

  • Not being the primary caregiver of the child (serving only as a short-term companion)
  • Being unable to complete the questionnaire due to a psychiatric diagnosis or communication difficulties
  • The child having a disability

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

Здоровые добровольцы: Да

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07308301 · 2024-KAEK-11

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗