ACTRN12617000411347已完成未知
The ADAPT Program to support the management of anxiety and depression in adult cancer patients: a cluster randomised trial to evaluate different implementation strategies of the Clinical Pathway for Screening, Assessment and Management of Anxiety and Depression in Adult Cancer Patients.
Psycho-oncology Co-operative Research Group (PoCoG)0 个研究点目标入组 1,280 人开始时间: 2017年3月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,280
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
- •This study has 3 groups of research participants:
- •1. Group 1 is the site
- •2. Group 2 is the staff at the participating sites
- •3. Group 3 is the patients at the participating sites.
- •Group 1: Cancer services (sites)
- •Cancer services in New South Wales are eligible to participate providing they commit to the following:
- •1. Formally agree to participate at the site level
- •2. Sign an ADAPT Research Participation Agreement
- •3. Endorse and enable staff training
- •4. Allow a complete site profile audit
- •5. Allow release of their Organisational Chart
- •6. Authorise release of MBS/PBS provider information and statistics
- •Sites will be required to have the following IT infrastructure:
- •1. Wi-Fi/broadband/internet access
- •2. Internet browser version to comply with Portal requirements
- •Sites will be required to have the following characteristics:
- •1.. At least 50% of patient population have cancer
- •2. At least 100 active patients
- •3. At least 1 IT liaison contact person
- •4. At least 1 local champion
- •Group 2: Cancer service staff
- •1. Employed on an ongoing (6 months or more) or permanent basis, either full or part time or as a visiting medical officer at a participating centre
- •2. Work in a role that provides clinical care to patients with cancer or client focused administrative support or IT/managerial support.
- •3. Aged 18 years and over
- •4. Staff will be identified as part of the organisation chart mapping exercise at site engagement.
- •5. Participation in giving feedback is voluntary
- •Group 3: Patients
- •1. Recruitment for this study will be at the site level so any patients seen at participating sites will be exposed to the outcome of the intervention as part of their usual care.
- •2. Adult patients (aged 18 and over) who have cancer of any type will be offered screening as part of their routine care by cancer service staff.
- •3. Patients choose whether to take part in screening or not.
排除标准
- •Group 1: Sites
- •Cancer services who are unable to commit to the mandatory study components will be excluded.
- •Group 2: Staff
- •Casual staff, and any staff member under the age of 18 are unable to take part.. Staff who have no clinical or administrative contact with cancer patients, and IT staff who are not involved in the implementation of the ADAPT RCT are also excluded.
- •Group 3: Patients
- •Patients who do not consent to sharing their MBS and PBS data will not be included in secondary outcome analyses.
研究者
相似试验
已完成
不适用
Development of the ANSHIN support program for patients with unruputured intracranial aneurysms in a wait and see approach.unruputured intracranial aneurysmsJPRN-UMIN000033526Juntendo University, School of Medicine37
已完成
不适用
Development of an assistance evacuation program focusing on physical assistance in fire evacuation trainingHealthy adultJPRN-UMIN000034847Hokkaido University of Science20
已完成
不适用
Development of the intervention program about the mental health support for Japanese caseworkers employed at social welfare officesJPRN-UMIN000025910Yamagata University Department of Nursing,Yamagata University School of Medicine30
招募中
不适用
Establishing and developing support system for affection and emotions of severe stutterersStutteringJPRN-UMIN000032890Kawasaki University of Medical Walfare50
招募中
不适用
Evaluation of a screening program for older adults visiting the Emergency DepartmentEN: older patients, emergency department, geriatric emergency medicine, functional decline, mortality, cognitive impairment, screening, implementationNL: acuut presenterende oudere patiënt, spoedeisende hulp, functionele achteruitgang, mortaliteit, cognitieve beperkingen, screening, implementatieNL-OMON23854eiden University Medical Center2,000