ACTRN12622000898752尚未招募未知
Enhancing treatment outcomes after gynaecological cancer (ACUMEN For ALL): Investigating the effect of telehealth exercise on health-related quality of life after cancer therapy
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •1. Women aged 18 years or older diagnosed with cancer of the ovary, cervix, Fallopian tubes, placenta, endometrium, vagina or vulva in the previous 60 months, including early, recurrent, advanced or metastatic cancer.
- •2. > 1 month since end of intensive cancer treatment (including surgery, radiotherapy, chemotherapy). Supportive therapies such as bisphosphonate, pain medication and hormone replacement allowable.
- •3. Resident in Australia.
- •4. Have access to the internet.
- •5. Own, or have access to, a computer or mobile device.
- •6. Willing and able to comply with all study requirements, including intervention, timing and nature of required assessments.
- •7. Able to speak and read in English to ensure consent is informed and documentation of participant-reported outcome measures can be adhered to.
- •8. Can provide voluntary written informed consent.
- •9. Unable or unwilling to attend face-to-face exercise training and objective outcome assessment.
排除标准
- •1. Any clinical contraindication that precludes safe completion of the program in the judgement of the project team.
- •2. No intensive cancer treatments while enrolled.
- •3. In the care of an exercise professional at the time of enrolment.
研究者
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