ACTRN12618001448235进行中(未招募)未知
The PATHway Trial: Participatory health through behavioural engagement and disruptive digital technology for post-operative rehabilitation of lumbar decompression and total knee replacement.
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中(未招募)
- 入组人数
- 167
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
- All
入选标准
- •1. Ability and willingness to participate in the study
- •2. Familiarity with the use of the Internet and smart devices
- •3. Ownership of a smartphone
- •4. Participants must have at least functional English to be able to understand the study procedures, complete the questionnaires, communicate during the health coaching sessions and consent to participate in the study
- •5. aged 18 years or older, male or female
- •6. Admission to one of the study sites for rehabilitation following total knee replacement or lumbar decompression with or without fusion
排除标准
- •1. Known or suspected serious spinal pathology (fracture, metastatic, inflammatory or infective diseases, widespread neurological disorder).
- •2. Any clinically significant acute or ongoing chronic medical conditions (e.g., uncontrolled diabetes) that could compromise patient safety, limit the patient’s ability to complete the study, and/or compromise the objectives of the study.
- •3. Patients undergoing bilateral knee replacement.
- •4. Patients undergoing revision for a previous total knee replacement or spinal surgery.
- •5. Participation in another clinical trial and/or treatment received with any investigational agent within 30 days before enrolment.
- •6. Current use of any intervention component (activity tracker, exercises app or health coaching) and unwillingness to stop using it for the duration of the study.
- •7. Spinal surgery beyond two spine levels.
- •8. Participants beyond 45 days post-op.
研究者
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