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CompletedNCT03259776VISIT_ICUUpdated Oct 9, 2018

Experiences of Visitors to a Regional Major Trauma Intensive Care Unit

An observational study in Major Trauma, sponsored by Kingston University. Completed at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-10-09.

Sponsored by Kingston University · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
57
Ages
18 Years and older
Sex
All
01

Study summary

Since 2011, people who have had a serious accident in England are no longer looked after at the hospital nearest to them. Instead, they are cared for at a specialist hospital called the regional major trauma centre. This is so that they can get the best possible care from specialist professionals.

St George's is the regional major trauma centre for the 2.6 million people living in South West London and Surrey County. This area stretches about 40 miles across.

About one fifth of major trauma patients who come to St George's live more than one hour's journey away. Their visitors often travel a similar distance or even further. Family members and friends play an important part during the patient's stay. It is important to support visitors.

The aim of this study is to describe the experiences of visitors whose family member or friend has been admitted to the major trauma intensive care unit at St George's. In particular, the aim is to describe the experiences of visitors who travel from far.

First, ten visitors will be interviewed to find out more about their experiences. From these data, a survey questionnaire will then be developed and approximately 150 visitors who have been to St George's in recent months will be surveyed. This will give in-depth insights to understanding peoples' experiences of visiting at St George's, and what people thought was going well and things that could be better. The study will end with a service improvement workshop with representatives from the team at St George's and visitors. Study findings will be discussed and decisions on what should be improved will be made.

This study is being funded by St George's Hospital Charity. The study runs from August 2017 to October 2018.

02

Conditions studied

  • Major Trauma

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Keywords

  • Intensive Care
  • Patient- and Family-Centred Care
  • Patient and Public Involvement
  • South West London Major Trauma Network
  • Service Improvement
  • Survey Questionnaire
  • Visitor Experiences
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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Visitors (i.e. designated next of kin and/or other family member or friend with a close relationship and significant involvement in the patient's circumstances and care) of a patient who has been admitted to ICUs at St George's University Hospitals NHS Foundation Trust under the major trauma care pathway

Inclusion criteria

  • Visitors (i.e. designated next of kin and/or other family member or friend with a close relationship and significant involvement in the patient's circumstances and care) of a patient who has been admitted to intensive care at St George's University Hospitals NHS Foundation Trust under the major trauma care pathway
  • Ordinary residence further away than one hour's drive from St George's Hospital (estimated driving time in mid-week mid-morning traffic according to Google Maps, equating to a distance of approximately 30 miles)
  • Adults (18 years and over)
  • Written informed consent (for semi-structured qualitative interviews)

Exclusion criteria

Exclusion Criteria:

  • Ordinary residence within one hour's drive from St George's Hospital (estimated driving time in mid-week mid-morning traffic according to Google Maps, equating to a distance of within approximately 30 miles)
  • Limited English (for semi-structured qualitative interviews)
04

Study design

Observational model
Other
Time perspective
Other
Enrollment
57 participants (actual)
Patient registry
No

Groups and cohorts

  • Visitors

    Qualitative interviews and questionnaire survey

    Other: Qualitative interviews and questionnaire survey

Interventions

  • OtherQualitative interviews and questionnaire survey

    Qualitative interviews and questionnaire survey

05

What researchers measure

Primary outcomes

  1. Visitors' experiences

    This study uses mixed-methods in a two-staged approach, to provide both depth and breadth in capturing data on visitors' experiences. In the first stage, a series of semi-structured qualitative interviews will capture in-depth data on visitors' experiences. Participants will be asked questions such as "Can you talk a bit about visiting your relative/friend here at St George's" and "How has your daily life been since you started visiting here at St George's". These in-depth qualitative data will inform the content and structure for a bespoke visitor experience questionnaire, which will be newly developed as part of the study and copyrighted. In the second stage, the newly developed, bespoke visitor experience questionnaire will be used to survey a larger number of visitors, gathering both quantitative and qualitative data to describe the experiences of visitors, areas of good practice and needs and opportunities for service improvement at the study site.

    Time frame: 15 months

06

Study locations

1 site
  • St George's University Hosptials NHS Foundation Trust
    London, SW17 0QT, United Kingdom
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03259776
Lead sponsor
Kingston University
Responsible party
Stefan Tino Kulnik (Postdoctoral Researcher, Kingston University) — Principal investigator
First posted
Aug 24, 2017
Start date
Nov 16, 2017
Primary completion
Aug 31, 2018
Completion
Aug 31, 2018
Last update
Oct 9, 2018

Study contacts

Stefan T Kulnik, PhD
principal investigator · Kingston University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2018. You cannot join it, but the record below documents what was studied.

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