跳至主要内容
临床试验/ACTRN12626000973314
ACTRN12626000973314进行中(未招募)不适用

Phase III hybrid effectiveness implementation step wedge cluster randomized controlled trial of implementation of a geriatric model of care to optimize outcomes for older people with cancer

University of Technology Sydney0 个研究点目标入组 1,080 人开始时间: 2026年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,080

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
Randomized
干预模型
Other
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 No limit(—)
性别
All

入选标准

  • The population (CANCER SERVICE LEVEL AND PATIENT LEVEL) inclusion criteria are provided below:
  • Key inclusion criteria for cluster (cancer service level)
  • Ambulatory cancer service provided by a defined multidisciplinary team (defined as either a shared clinic or by specific tumour type)
  • Written informed consent of the cluster
  • Key inclusion criteria for patients participants
  • adults aged 65 years and older (non-Indigenous) and Aboriginal and Torres Strait Islander people 50 years and older
  • new diagnosis of cancer
  • who have been referred to a cancer specialist and are being considered for chemotherapy, targeted therapy, or immunotherapy (including in a clinical trial).
  • There are three participant groups for the qualitative sub-study.
  • Inclusion criteria for CLINICIAN PARTICIPANTS:
  • Written informed consent
  • Member of the multidisciplinary team who is involved in clinical care in the ‘cluster’ (as defined above)
  • Inclusion criteria for INFORMAL CARERS:
  • Informal carer as identified of the ‘index patient’ who received the intervention (partial or complete) in the geriatric model of care or comparator groups as identified by the ‘index patient’.
  • Written informed consent
  • able to participate in a brief semi-structured interview in person or virtually.
  • English speaking or able to undertake interview with support of a health care interpreter.
  • Inclusion criteria for PATIENT PARTICIPANTS:
  • Received the intervention (partial or complete) in the geriatric model of care or comparator groups
  • Written informed consent
  • able to participate in a brief semi-structured interview in person or virtually.
  • English speaking or able to undertake interview with support of a health care interpreter.

排除标准

  • Clinicians, patients and carers will be excluded if they don't meet the overall inclusion criteria for their participant category.

研究者

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