跳至主要内容
临床试验/ISRCTN78764132
ISRCTN78764132暂停未知

Early Supported discharge with Pulmonary REhabilitation following Severe acute exacerbations of COPD – Safety and Outcomes (ESPRESSO)

Royal Brompton & Harefield NHS Foundation Trust0 个研究点目标入组 80 人开始时间: 2019年10月10日最近更新:

试验速览

阶段
未知
状态
暂停
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Randomised controlled trial inclusion criteria:
  • 1.1 > 40 years of age
  • 1.2 Diagnosis of chronic obstructive pulmonary disease (COPD)
  • 1.3 Hospitalisation (inpatient on a medical assessment unit or hospital ward) with a primary diagnosis of an acute exacerbation of COPD
  • 1.4 Accepted for Hospital at Home care by Hillingdon Integrated Respiratory Service according to local Standard Operating Procedures (no impaired consciousness – Glasgow Coma Scale < 15; no acute confusion state; pH greater than 7.35kPa; no acute changes on radiograph; no concomitant medical problem requiring in-patient stay such as suspected pulmonary embolus or acute coronary syndrome; and adequate social support)
  • 1.5 Able to give valid informed consent
  • 2. Patient participant interview purposive sampling criteria:
  • 2.1 Protocol completion:
  • 2.1.1 Completed course of care per protocol
  • 2.1.2 Did not complete course of care per protocol
  • 2.2 Readmission in three months of hospital discharge:
  • 2.2.1 Readmitted
  • 2.2.2 Not readmitted
  • 2.3 Social history:
  • 2.3.1 Lives alone
  • 2.3.2 Does not live alone
  • 2.4 Improvement in COPD Assessment Test (CAT) in three months from hospital discharge:
  • 2.4.1 Change in CAT score of > = -2 points
  • 2.4.2 Change in CAT score of < -2 points
  • 3. Family member and carer interview purposive sampling criteria:
  • This is the person nominated by the participant as giving them the most help and support due to their COPD and who is not a health care professional who must be:
  • 3.1 Aged > 18 years of age
  • 3.2 Able to understand and speak English
  • 3.3 Able to give valid informed consent
  • 4. Staff focus groups purposive sampling criteria:
  • 4.1 Provider of usual care
  • 4.2 Provider of outpatient-based PR
  • 4.3 Provider of study intervention procedures
  • 4.4 Provider of study assessments

排除标准

  • Randomised controlled trial exclusion criteria:
  • 1. Receiving specialist palliative care with expectation of death within three months as judged by the specialist palliative care service;
  • 2. No fixed abode or contact number;
  • 3. Evidence of an environment that would make delivery of study intervention and/or usual care unsafe;
  • 4. Evidence of acute coronary syndrome, unstable ischaemic heart disease or any condition that would make exercise unsafe.

研究者

相似试验