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临床试验/NCT06382441
NCT06382441已完成不适用

A Pilot Study of "a Home-based and Group-based Tele-exercise Program for Breast Cancer Survivors: a Randomized Controlled Trial"

Hong Kong Baptist University2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年11月1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
24
试验地点
2
主要终点
Acceptability (qualitative)

研究概览

简要总结

The research protocol outlines a pilot study for a home-based and group-based tele-exercise program designed for breast cancer survivors. The study is a randomized controlled trial (RCT) led by Dr. Yang Gao from Hong Kong Baptist University, with multiple other investigators from Kwong Wah Hospital and the university itself.

Breast cancer is identified as the most prevalent cancer among women globally and in Hong Kong. The document states that adjuvant therapies post-surgery, such as radiation and chemotherapy, can have both short-term and long-term side effects, which may affect the survivors' physical and mental health.

The study is based on evidence that physical activity levels often decrease after a breast cancer diagnosis and that exercise can mitigate the side effects of treatment, improving health and quality of life. The pilot aims to test the acceptability and feasibility of a 12-week tele-exercise program that combines psychological theories and behaviour change techniques, transitioning from supervised to unsupervised exercise to build sustainable exercise habits.

The study will enrol 24 patients, randomly assigning them to an intervention group or an active control group. The intervention group will receive 12 online training sessions plus 4 psychological counselling sessions, whereas the control group will receive educational essays on exercise and health.

The training sessions for the intervention group will include various exercises with increasing intensity and duration over the 4 weeks, monitored by a pulse oximeter to ensure exercises are done at the appropriate heart rate. The sessions will be led by qualified coaches, with Dr. Gao overseeing quality control.

详细描述

It is a prospective and pilot study of RCT. It will be a pilot to test the acceptability and feasibility of a two-armed tele-exercise RCT to mitigate symptoms and improve health for breast cancer survivors. In this study, outcome assessors and data analysts will be masked from the allocation results. The pilot will recruit 24 patients and randomly assign them to an intervention group (Group A) and an active control group (Group B). All participants in both groups will continue receiving usual care from the study hospital during the study period. Additionally, those in Group A (intervention) will receive the tele-exercise (12 home-based online training sessions + 4 psychological counselling sessions), while those in Group B (active control) will receive 4 essays on exercise and health. Outcome measurements will be repeatedly performed before and after the intervention.

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
Double (Care Provider, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 64 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Females aged 40-64 years old;
  • Within 6 weeks after completion of chemotherapy;
  • Without severe anemia;
  • Without cancer metastasis;
  • Able to read and communicate in Cantonese or Mandarin;
  • Smartphone users.

排除标准

  • With any medical, physical and psychological conditions that may limit participation (e.g., uncontrolled severe cardiovascular disease, schizophrenia, severe neurological dysfunction, etc.).

结局指标

主要结局

Acceptability (qualitative)

时间窗: baseline, 13 weeks

Participants rated intervention regarding the aspects of satisfaction, enjoyment, perceptions of safety, difficulty, tolerability of treatment, adverse events by interviews.

Recruitment rate

时间窗: baseline, 13 weeks

The proportion of eligible participants who are enrolled at baseline of the study.

Attendance rate

时间窗: baseline, 13 weeks

The proportion of total sessions offered to participants to the actual number of sessions participants attended.

Compliance rate

时间窗: baseline, 13 weeks

Participants' level of adherence to the content, frequency, duration, and coverage of the treatment as delivered by the research team. Assessed by percentage of participants who complied with intervention procedures.

Acceptability (quantitative)

时间窗: baseline, 13 weeks

Participants rated intervention regarding the aspects of satisfaction, enjoyment, perceptions of safety, difficulty, tolerability of treatment, adverse events using a 5-Liker questionnaire, mean score was used to assess, and higher score indicates greater acceptability.

Retention rate

时间窗: baseline, 13 weeks

The proportion of enrolled participants who are present throughout the full length of the treatment.

次要结局

  • Cardiorespiratory fitness(baseline, 13 weeks)
  • Health-related quality of life(baseline, 13 weeks)
  • Limb circumference and lymphedema(baseline, 13 weeks)
  • muscle strength(baseline, 13 weeks)
  • % body fat(baseline, 13 weeks)
  • height(baseline, 13 weeks)
  • balance(baseline, 13 weeks)
  • skeletal muscle mass(baseline, 13 weeks)
  • Shoulder joint range of motion (ROM) of affected side(baseline, 13 weeks)
  • Physical activity level (min/week)(baseline, 13 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gao Yang

Associate Professor

Hong Kong Baptist University

研究点 (2)

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