No patients recruited due to decreased levels of patients requiring non-invasive ventilation during the study.
How the Introduction of an Oral Intake Screening Tool Can Benefit Patients Receiving Non-Invasive Ventilation
Sponsor study identifier
observational
0
1 country
2
Study Start
April 2013
Actual (reported)Primary Completion
August 2013
Actual (reported)Study Completion
August 2013
Actual (reported)This study aims to explore how the introduction of an oral intake screening tool can benefit patients requiring noninvasive ventilation. The Quality Care Commission has identified nutritional problems in hospital and there is much literature on the importance of nutrition when critically ill. Literature is short however concerning the specialized population of those requiring noninvasive ventilation and they are a high risk group of suffering from malnutrition. This study will potentially benefit patients by improving their nutritional care through guided assessment and nurse training. The study will use mixed methodology, a prospective cohort study and qualitative interviews. The prospective cohort study will collect data from patients prior to the tool introduction, the control group, and post the tool introduction, the exposure group. This will enable comparisons to be made between the exposure and the control groups. Nurses will be interviewed in semi structured focus groups prior to tool introduction and post to identify themes and sub themes to give a deeper understanding of nutrition in hospital and to examine the use of the tool in practice. Patients will be eligible if they are over 18 and requiring noninvasive ventilation and nurses will be eligible if they work on the high dependency unit. Patients will be visited daily and have four mid arm circumference measurements at day 1, day 3, day 7 and day 14. The other daily visits will involve collecting data, which is recorded as part of routine care. Nurses will undergo 2 focus group interviews and a teaching session. The study will take place at St Mary's hospital funded by Imperial College London. The study will be split into two periods with a two week gap in between. Each period will last until 22 patient participants have been recruited.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
August 2013
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
April 2013
Actual (reported)May 2, 2013
Actual (reported)August 2013
Actual (reported)August 2013
Actual (reported)March 18, 2014
Actual (reported)Mid Arm Circumference Change
Day 1, 3, 7, 14
Fluid Intake Change
Daily over 14 days
fluid balance change
daily for 14 days
New formation of or worsening of existing pressure sores
daily for 14 days
new diagnosis of aspiration pneumonia
daily for 14 days
number of days requiring non-invasive ventilation
14 days
Pre tool introduction cohort 22 patient participants who will receive standard care (no patients were recruited)
12 nurse participants who will take part in 2 focus group interviews and a teaching session (6 nurse participants were recruited)
Pre tool introduction cohort 22 patient participants who's ability to eat and drink orally will be assessed using the Oral Intake Screening Tool (no patient participants were recruited)
A screening tool developed from a literature review and expert opinion. It will be used by nurses to assess patients receiving non-invasive ventilation ability to eat and drink orally and suggest what actions should be taken if they are unable to do so
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Patients; Medical High Dependency Unit Patients Staff; Full time employees on the Douglas Acute Admission Unit
St Marys Hospital
London, W2 1NY, United Kingdom
Imperial College Healthcare NHS Trust
London, United Kingdom
Gary Frost
Imperial College London
0 participants (actual enrollment reported by the registry).
First Submitted
May 2, 2013
First Posted
March 18, 2014
Study Start
April 2013
Actual (reported)Primary Completion
Contact the study team to confirm eligibility.
August 2013
Actual (reported)Study Completion
August 2013
Actual (reported)Last Updated
August 27, 2020
Record last verified: 2020-08
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Source: ClinicalTrials.gov.
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