- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03494335
Online Surveys to Assess the Perception and Performance of Imaging and Associated Aspects
January 16, 2024 updated by: Michael V Knopp MD PhD, University of Cincinnati
Online Surveys to Assess the Perception and Performance of Imaging Associated Aspects
In this exploratory study, the researchers would like to investigate the background, perception, current use practices, potential unmet needs and/or challenges in regard to imaging procedures, imaging technology, or any other aspect related to the broader field of imaging.
Study Overview
Detailed Description
The researchers plan to include volunteer participants to complete these surveys.
The goal of these exploratory efforts will be to increase the currently very limited information available in the topics of interest stated above, and the findings, even if only from limited group of respondents, will help guide research development, prepare for design of clinical trials, guide special interest groups, and serve as role data for appropriate scientific publications.
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Ohio
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Columbus, Ohio, United States, 43221
- Martha Morehouse Medical Plaza
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study population consists of volunteers agreeing to complete the survey tool.
It is anticipated that the surveys will be completed by participants that can be considered stakeholders, such as physicians, technologist's physicists, imaging scientists, administrative staff, or others with interest in the topic.
Description
Inclusion Criteria:
- Male and female participants who have access to the online survey tool and can read and write in English
Exclusion Criteria:
- None, as this is voluntary
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Volunteer participants
Volunteer participants will participate in surveys assessing their perception of various imaging aspects.
|
The investigators are recruiting health care providers for these surveys that are involved in or use imaging.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perception of PET/CT imaging agent Y-90
Time Frame: through study completion, on average 2-5 years
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To evaluate participants' perceptions of Y-90 using a likert scale on an online survey
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through study completion, on average 2-5 years
|
|
Perception of PET/CT imaging agent NaF
Time Frame: through study completion, on average 2-5 years
|
To evaluate participants' perceptions of NaF using a likert scale on an online survey
|
through study completion, on average 2-5 years
|
|
Perception of MRI contrast agents
Time Frame: through study completion, on average 2-5 years
|
To evaluate participants' perceptions of MR contrast agents using a likert scale
|
through study completion, on average 2-5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Michael V Knopp, MD, PhD, Ohio State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 30, 2022
Primary Completion (Estimated)
December 31, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
March 30, 2018
First Submitted That Met QC Criteria
March 30, 2018
First Posted (Actual)
April 11, 2018
Study Record Updates
Last Update Posted (Actual)
January 18, 2024
Last Update Submitted That Met QC Criteria
January 16, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- RP0320_S02/2018E0141
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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