跳至主要内容
临床试验/NCT03177161
NCT03177161已完成不适用

Assessment of Patient Reported Health Status Questions Via Four Different Methods of Administration, in Stroke Survivors. A Randomised Controlled Trial. A Non-inferiority Study of the Response Rate for Four Alternative Methods of Administration of 15 Patient Reported Health Status Questions in Stroke Survivors.

Dr Jonathan Hewitt8 个研究点 分布在 1 个国家目标入组 472 人开始时间: 2017年8月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
472
试验地点
8
主要终点
Total response rate for all 4 methods of delivery

研究概览

简要总结

A Patient Reported Outcome Measure (PROM) is a questionnaire that asks patients for their views on their own health or the impact of healthcare they have received on their health and quality of life (RCN, 2011). The benefit of PROMS is that they gather information from the patient's perspective, which offers great potential to improve the quality and outcomes of health services (Department of Health 2011).

There is a PROM (the PROMIS-10 Global Health) and a number of extra questions that are recommended for use in people who have had a stroke by the International Consortium for Health Outcomes Measurement, but the best way of delivering these questions for stroke survivors is unknown.

At present, the NHS in England, Scotland and Wales are required to offer every stroke survivors a 6 month post stroke follow-up appointment. Currently, the information collected at the 6 month review is not from the patient's perspective and the best method of collecting this information has not been established. The Sentinel Stroke National Audit Programme (SSNAP) which is led by the Royal College of Physicians in London promote the 6 month follow-up assessment. SSNAP recognise that currently 4 different methods of 6 month follow-up appointment occur. The current methods in use are face-to-face assessment, telephone interview, online questionnaire or postal questionnaire.

The aim of this research is to understand if there is a difference between these 4 methods of delivering these questions in people who have had a stroke.

As part of the 6 month review this research study will assess the response rate for 15 Patient Reported Health Status questions across the 4 recognised methods of delivery;

  • Face-to-Face
  • Telephone
  • Online
  • Post

To conduct this research study a sample of 808 stroke survivors will be asked to take part in the research. From these 808 people, 202 participants will be randomly assigned to each method of administration (Face-to-Face Interview, Telephone Interview, Postal Questionnaire and Online Questionnaire).

The questionnaires received by the research team will not record any personally identifiable information. The data will then be utilised by the researchers for statistical analysis in order to identify, which method of the 4 methods of administration, under investigation, is the most acceptable for stroke survivors. The conclusions of this research will inform the roll-out of the most appropriate method of delivering the 6 month stroke follow-up review for stroke survivors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

盲法说明

Participants will not be made aware of the other modes of delivery available and will be assigned a single method of delivery prior to consent.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinically confirmed diagnosis of stroke either Cerebral Infarct (ICD I63), Cerebrovascular Haemorrhage (ICD161) or Stroke, not specified as haemorrhage or infarction (ICD I64).
  • Patients over 18 years old (≥ 18 years old)
  • Had a diagnosis of stroke within the last 4-8 months (Stroke diagnosis ≥ 4months to ≤ 8 months)

排除标准

  • Diagnosis of a Transient Ischaemic Attack (ICD G45)
  • Diagnosis of a Subarachnoid Haemorrhage (ICD I60)

研究组 & 干预措施

Postal Questionnaire

Experimental

干预措施: 15 Patient Reported Health Status Questions (Other)

Online Questionnaire

Experimental

干预措施: 15 Patient Reported Health Status Questions (Other)

Face-to-face Questionnaire

Experimental

干预措施: 15 Patient Reported Health Status Questions (Other)

Telephone Questionnaire

Experimental

干预措施: 15 Patient Reported Health Status Questions (Other)

结局指标

主要结局

Total response rate for all 4 methods of delivery

时间窗: 120 to 240 days post index event

As defined by response rate. This will be measured by the number of individuals that return the questionnaire for each of the four allocation groups.

次要结局

  • Total response rate across the four different methods of administration for 15 Patient Reported Health Status questions with people with communication issues (e.g. aphasia)(120 to 240 days post index event)
  • Total response rate across the four different methods of administration for 15 Patient Reported Health Status questions by stroke severity (as defined by NIHSS on admission)(120 to 240 days post index event)
  • Total response rate across the four different methods of administration for 15 Patient Reported Health Status questions by stroke type (as defined by ICD classification)(120 to 240 days post index event)

研究者

发起方
Dr Jonathan Hewitt
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr Jonathan Hewitt

Clinical Senior Lecturer (Cardiff University) & Honorary Consultant Physician (ABUHB)

Aneurin Bevan University Health Board

研究点 (8)

Loading locations...

相似试验