MedPath

Patient Understanding of LiverMultiScan

Completed
Conditions
Liver Diseases
Interventions
Device: MRI
Device: Transient Elastography
Registration Number
NCT02877602
Lead Sponsor
Perspectum
Brief Summary

This is a qualitative study to determine which factors affect the patient experience of having a liver MRI, what information patients would like to receive after their MRI, and how patients would like this information communicated to them.

Detailed Description

This is a qualitative study to determine which factors affect the patient experience of having a liver MRI, what information patients would like to receive after their MRI, and how patients would like this information communicated to them. Each individual will receive at least an MRI scan (LiverMultiScan), with many also receiving a FibroScan (Transient Elastography). Patients will then undergo a focused qualitative interview, as well as filling out a questionnaire. The interviews will be thematically analysed and trends identified by significance.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
101
Inclusion Criteria
  • Individuals with experience of liver disease.
  • Individuals over the age of 16.
  • Individuals willing to give informed consent for participation in the study.
Exclusion Criteria
  • Individuals with any contraindication to magnetic resonance imaging.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Experience of liver diseaseMRIThis is defined as either those who have had direct experience of liver disease as sufferers, or the carers of those who have had liver disease. Each individual receives an MRI (LiverMultiScan), with many also receiving a FibroScan.
Experience of liver diseaseTransient ElastographyThis is defined as either those who have had direct experience of liver disease as sufferers, or the carers of those who have had liver disease. Each individual receives an MRI (LiverMultiScan), with many also receiving a FibroScan.
Primary Outcome Measures
NameTimeMethod
Factors effecting MRI experience and understanding.Immediately (within 1 hour) after undergoing the MRI scan, and receiving results feedback.

This will be analysed based on themes and trends emanating from answers within the focused interview and questionnaire following the scan, and results feedback.

Secondary Outcome Measures
NameTimeMethod
Comparison of MRI to ultrasound scan in terms of patient experience.Immediately (within 1 hour) after undergoing an MRI scan, and ultrasound (FibroScan) scan.

This will be analysed based on themes and trends emanating from answers within the focused interview and questionnaire following the scan, and results feedback.

Trial Locations

Locations (1)

University of Oxford Centre for Clinical Magnetic Resonance Research (OCMR)

🇬🇧

Oxford, Oxfordshire, United Kingdom

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