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出境医 / 临床实验 / Online Surveys to Assess the Perception and Performance of Imaging and Associated Aspects

Online Surveys to Assess the Perception and Performance of Imaging and Associated Aspects

Study Description
Brief Summary:
In this exploratory study, we 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.

Condition or disease Intervention/treatment Phase
Perception of Imaging Other: Online surveys Not Applicable

Detailed Description:
We 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 us guide our research development, prepare for design of clinical trials, guide special interest groups, and serve as role data for appropriate scientific publications.
Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 5000 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Online Surveys to Assess the Perception and Performance of Imaging Associated Aspects
Estimated Study Start Date : April 30, 2018
Estimated Primary Completion Date : April 30, 2020
Estimated Study Completion Date : April 30, 2021
Arms and Interventions
Arm Intervention/treatment
Experimental: Volunteer participants
Volunteer participants will participate in surveys assessing their perception of various imaging aspects.
 Other: Online surveys
We are targeting health care providers for these surveys that are involved in or use imaging.
Outcome Measures
Primary Outcome Measures :
  1. Perception of PET/CT imaging agent Y-90 [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of Y-90 will be analyzed

  2. Perception of PET/CT imaging agent NaF [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of NaF will be analyzed

  3. Perception of MRI contrast agents [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of MR contrast agents will be analyzed


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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
Contacts and Locations

Contacts
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Contact: Melanie Hughes 614-293-9998 office@wcibmi.org
Contact: Michael V Knopp, MD, PhD 614-293-9998 knopp.16@osu.edu

Locations
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United States, Ohio
Martha Morehouse Medical Plaza Recruiting
Columbus, Ohio, United States, 43221
Contact: Michael V Knopp, MD, PhD    614-293-9998    knopp.16@osu.edu   
Sub-Investigator: Chadwick L Wright, MD, PhD         
Sub-Investigator: Katherine M Binzel, PhD         
Sub-Investigator: Michelle I Knopp, PhD         
Sponsors and Collaborators
Ohio State University
Investigators
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Principal Investigator: Michael V Knopp, MD, PhD Ohio State University
Tracking Information
First Submitted Date  ICMJE March 30, 2018
First Posted Date  ICMJE April 11, 2018
Last Update Posted Date April 11, 2018
Estimated Study Start Date  ICMJE April 30, 2018
Estimated Primary Completion Date April 30, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: March 30, 2018)
  • Perception of PET/CT imaging agent Y-90 [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of Y-90 will be analyzed
  • Perception of PET/CT imaging agent NaF [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of NaF will be analyzed
  • Perception of MRI contrast agents [ Time Frame: through study completion, on average 2-5 years ]
    Responses to online surveys assessing participants' perceptions of MR contrast agents will be analyzed
Original Primary Outcome Measures  ICMJE Same as current
Change History No Changes Posted
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Online Surveys to Assess the Perception and Performance of Imaging and Associated Aspects
Official Title  ICMJE Online Surveys to Assess the Perception and Performance of Imaging Associated Aspects
Brief Summary In this exploratory study, we 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.
Detailed Description We 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 us guide our research development, prepare for design of clinical trials, guide special interest groups, and serve as role data for appropriate scientific publications.
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Condition  ICMJE Perception of Imaging
Intervention  ICMJE Other: Online surveys
We are targeting health care providers for these surveys that are involved in or use imaging.
Study Arms  ICMJE Experimental: Volunteer participants
Volunteer participants will participate in surveys assessing their perception of various imaging aspects.
Intervention: Other: Online surveys
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Unknown status
Estimated Enrollment  ICMJE
 (submitted: March 30, 2018) 		5000
Original Estimated Enrollment  ICMJE Same as current
Estimated Study Completion Date  ICMJE April 30, 2021
Estimated Primary Completion Date April 30, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

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
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03494335
Other Study ID Numbers  ICMJE RP0320_S02/2018E0141
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Michael V. Knopp MD, PhD, Ohio State University
Study Sponsor  ICMJE Ohio State University
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Michael V Knopp, MD, PhD Ohio State University
PRS Account Ohio State University
Verification Date March 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP