- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07392684
Optimisation of the Blood Culture Pathway Utilising Behaviour Change
Study Overview
Status
Conditions
Detailed Description
Retrospective data collection relating to the blood volume collected and time to incubation of adult blood culture sets (adult sets comprises of both aerobic and anaerobic blood culture bottle) received in the microbiology laboratory, between February 2023 and April 2024. These samples are routinely collected as standard of care and not for the purpose of this research.
Staff members that collect adult blood cultures within the Trust (nurses, Physician's associates and doctors) will be invited to volunteer for the study. Staff members will participate by completing the questionnaire and/or attending focus groups.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
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Gloucestershire
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Gloucester, Gloucestershire, United Kingdom, GL1 3NN
- Recruiting
- Gloucestershire Royal Hospital
-
Contact:
- Amy Read
- Phone Number: 0300 422 5077
- Email: amy.read3@nhs.net
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Principal Investigator:
- Amy Read
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Secondary data: adult blood culture sets received in the microbiology laboratory, between February 2023 and April 2024.
Staff member participants: Staff members that collect adult blood cultures within the Trust
Description
Inclusion Criteria:
Secondary data:
- adult blood culture sets received in the microbiology laboratory, between February 2023 and April 2024.
Staff member participants
- Staff members that collect adult blood cultures within the Trust
Exclusion Criteria:
Secondary data:
- paediatric blood culture samples
- samples where volume, collection and/or time to incubation data are not recorded on laboratory system and/or blood culture analyser
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Staff members that collect adult blood cultures within the Trust
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Compliance to optimal blood culture (BC) vol (8-10 mls per bottle).
Time Frame: Retrospective data collection from period February 2023 to April 2024.
|
Volume of blood cultures measured in ml.
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Retrospective data collection from period February 2023 to April 2024.
|
|
Compliance to 4- hour time target to incubation of blood culture from collection.
Time Frame: Retrospective data collection from period February 2023 to April 2024
|
Time taken from collection of blood culture to incubation in the laboratory, recorded in hours and minutes
|
Retrospective data collection from period February 2023 to April 2024
|
|
Time from collection of blood cultures to targeted antibiotics, hours and minutes
Time Frame: Retrospective data collection from period February 2023 to April 2024.
|
Measurement of time (hours, minutes) from time of blood culture collection to time of targeted antibiotic prescribing
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Retrospective data collection from period February 2023 to April 2024.
|
|
Staff experiences related to taking blood cultures
Time Frame: Approximately 10 minutes to complete electronic questionnaire. Attendance at single FOCUS group at agreed time.
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Staff experiences using questionnaires and focus group discussions exploring facilitators and barriers relating to blood culture collection .
Staff members will participate by completing the questionnaire and/or attending focus groups.
|
Approximately 10 minutes to complete electronic questionnaire. Attendance at single FOCUS group at agreed time.
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 24/043/GHT
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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