ACTRN12620000877987已完成未知
Post-operative physiotherapy provided by Allied Health Assistants for Patients with Acute Hip Fracture: a feasibility randomised controlled trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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
- All
入选标准
- •Patient participants
- •Eligible participants will be patients who have undergone surgery for management of hip fracture at the participating acute hospital site. Participants must meet the following eligibility criteria:
- •Inpatient at acute hospital participating site
- •Admission diagnosis of hip fracture (S72.0–S72.2 according to the International Classification of Diseases 10th revision (ICD-10)
- •Walked independently pre-hip fracture with or without the use of a walking aid
- •Willingness and ability (i.e. medically stable), as determined by initial physiotherapy assessment, to participate in post-operative physiotherapy
- •Aged 18 years or older
- •Able to provide written, informed consent
- •Able to communicate in conversational English
- •Staff participants:
- •Staff participants for this project include any allied health assistant, physiotherapist or manager involved in the implementation of the allied health assistant model of care. They will include the following staff who either i) work on the orthopaedic ward at the acute hospital participating site or ii) have managerial oversight of physiotherapists working on the orthopaedic ward.
排除标准
- •Patient Participants:
- •Exclusion criteria are:
- •Patients unable to participate in physiotherapy rehabilitation (e.g. patients with a post-operative lower extremity touch or non-weight bearing status)
- •Patients who were non-ambulant OR required assistance of another person to walk pre-hip fracture
- •Patient not suitable for mobilisation or physiotherapy
- •Impaired cognition (Short Portable Mental Status Questionnaire Score <8)
- •If the patient is not appropriate for mobilisation they will not be eligible for participation in the study. However, participants are eligible for inclusion in the study if their medical stability improves on any day during their admission. Mobilisation will be contraindicated if the patient experiences any of the following complications:
- •Severe post-operative pain that restricts weight bearing
- •Nausea or vomiting with or without antimetic
- •Vitally unstable: postural blood pressure drop, febrile, bradycardia <40bpm or abnormal heart rhythm
- •Disorientated, heavily sedated or difficult to rouse.
- •Staff Participants:
- •Staff who are not involved in the implementation of the allied health assistant model of care will not be eligible for inclusion.
研究者
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