Patient Understanding of LiverMultiScan

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

101 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-02-29

Study Completion Date

2017-12-31

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Liver Diseases

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Study Groups

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Experience of liver disease

This 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.

MRI

Intervention Type DEVICE

Transient Elastography

Intervention Type DEVICE

Interventions

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MRI

Intervention Type DEVICE

Transient Elastography

Intervention Type DEVICE

Other Intervention Names

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LiverMultiScan FibroScan

Eligibility Criteria

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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.