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临床试验/NCT03859271
NCT03859271已完成不适用

Using Information Communication Technology to Deliver Brief Motivational Interviewing to Promote Regular Physical Activity Among Chinese Childhood Cancer Survivors: A Randomized Controlled Trial

The University of Hong Kong2 个研究点 分布在 2 个国家目标入组 161 人开始时间: 2019年3月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
161
试验地点
2
主要终点
Change in levels of physical activity from baseline to 12-month follow-up between intervention and control group

研究概览

简要总结

This study aims to examine the efficacy of using Information Communication Technology (ICT) to deliver brief Motivational Interviewing (BMI) to promote regular physical activity among Hong Kong Chinese childhood cancer survivors.

详细描述

A substantial body of evidence has indicated that improved childhood cancer survival has inevitably been accompanied by increased chronic physical problems and adverse psychological late-effects of cancer and its treatment. The frequently reported physiological and psychological sequelae included cancer-related fatigue, reduced muscle strength, decreases in functional capacity, activity intolerance, depression and distorted self-esteem, which in turn severely comprises their quality of life.

There is a growing body of evidence highlighting the beneficial effects of physical activity on the physiological and psychological health of childhood cancer survivors. Particularly, substantial evidence reveals that engaging in regular moderate-intensity physical activity can help ameliorate some of the treatment-related adverse effects experienced by childhood cancer survivors, such as reduce cancer-related fatigue, enhance muscle strength, improve cardiovascular fitness and eventually lead to a better quality of life.

Evidence demonstrates that education alone is insufficient or unlikely to change behavior. Motivational interviewing (MI) is a directive, client-centered counseling strategy which differs from prevailing patient education to support clients to explore and resolve their ambivalence about changing their behaviors. Meanwhile, there is an increase in the use of Information Communication Technology (ICT) for health care delivery and health promotion. Using instant messaging (i.e. WhatsApp or WeChat) allows quick, direct and continuing professional advice and support for the parents to promote their child's level of physical activity. Therefore, the aim of this study is to examine the efficacy of using ICT to deliver BMI to promote regular physical activity among Hong Kong Chinese childhood cancer survivors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
9 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • The investigators will exclude childhood cancer survivors with evidence of recurrence or second malignancies, and those with physical impairment or cognitive and learning problems identified from their medical records.
  • Additionally, parents (either father or mother; the primary caregiver of childhood cancer survivors) must be able to:
  • Speak Cantonese and read Chinese,
  • Use a smartphone and can use an instant messaging tool (e.g., WhatsApp/WeChat); and
  • Are willing to receive health promotion advice and interact with our interventionist via WhatsApp/WeChat on a smartphone throughout the study period.

结局指标

主要结局

Change in levels of physical activity from baseline to 12-month follow-up between intervention and control group

时间窗: 12-month follow-up

The primary outcome measure is the physical activity levels of subjects at 12-month follow-up when compare to baseline. The Chinese University of Hong Kong: Physical Activity Rating for Children and Youth (CUHK-PARCY) will be used to assess participants' physical activity levels. It is a one-item scale, scores ranging from 0-2, 3-6 and 7-10 indicate low, moderate and high levels of physical activity respectively.

次要结局

  • Change in levels of physical activity from baseline at 6-month follow-up between intervention and control group(6-month follow-up)
  • Change in muscular strength from baseline at 1-month follow-up between intervention and control group(1-month follow-up)
  • Change in muscular strength from baseline at 6-month follow-up between intervention and control group(6-month follow-up)
  • Change in muscular strength from baseline at 3-month follow-up between intervention and control group(3-month follow-up)
  • Change in levels of physical activity from baseline at 3-month follow-up between intervention and control group(3-month follow-up)
  • Levels of cancer-related fatigue at baseline(Baseline)
  • Change in levels of cancer-related fatigue from baseline at 3-month follow-up between intervention and control group(3-month follow-up)
  • Change in lung functionality from baseline at 12-month follow-up between intervention and control group(12-month follow-up)
  • Quality of life at baseline(Baseline)
  • Levels of physical activity at baseline(baseline)
  • Change in levels of cancer-related fatigue from baseline at 12-month follow-up between intervention and control group(12-month follow-up)
  • Change in lung functionality from baseline at 3-month follow-up between intervention and control group(3-month follow-up)
  • Change in quality of life from baseline at 12-month follow-up between intervention and control group(12-month follow-up)
  • Change in levels of physical activity from baseline at 1-month follow-up between intervention and control group(1-month follow-up)
  • Change in levels of cancer-related fatigue from baseline at 1-month follow-up between intervention and control group(1-month follow-up)
  • Change in levels of cancer-related fatigue from baseline at 6-month follow-up between intervention and control group(6-month follow-up)
  • Muscle strength at baseline(Baseline)
  • Change in muscular strength from baseline at 12-month follow-up between intervention and control group(12-month follow-up)
  • Lung functionality at baseline(Baseline)
  • Change in lung functionality from baseline at 1-month follow-up between intervention and control group(1-month follow-up)
  • Change in lung functionality from baseline at 6-month follow-up between intervention and control group(6-month follow-up)
  • Change in quality of life from baseline at 1-month follow-up between intervention and control group(1-month follow-up)
  • Change in quality of life from baseline at 3-month follow-up between intervention and control group(3-month follow-up)
  • Change in quality of life from baseline at 6-month follow-up between intervention and control group(6-month follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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