Imaging in Clinical Trials - a Questionnaire Study to Assess Impact of Imaging Regimes on Patient Participation
ASK
1 other identifier
observational
207
1 country
1
Brief Summary
This research is aimed at finding out what may influence the decision of patients to participate in trials involving imaging so that the investigators may improve our future studies so they are more patient focused and acceptable in regards to scan schedules.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2015
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2015
CompletedFirst Submitted
Initial submission to the registry
July 22, 2015
CompletedFirst Posted
Study publicly available on registry
September 4, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2018
CompletedJanuary 28, 2020
January 1, 2020
3.3 years
July 22, 2015
January 27, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Factors that affect patient participation in imaging research
Factors about an imaging scan - type, length, frequency or scheduling (timing in relation to treatment) - that are perceived as a significant burden when considering participation in a research study involving imaging.
Duration of Study - 1 year
Secondary Outcomes (3)
Factors affecting participation in the different patient categories
Duration of Study - 1 year
Effect of current participation in a study on the perceived acceptability of imaging burden
Duration of Study - 1 year
Do opinions change after undergoing imaging procedures
Duration of Study - 1 year
Study Arms (3)
Group 1
Patients currently recruited to studies with imaging at The Marsden
Group 2
Patients who have previously participated in studies with imaging at The Marsden
Group 3
Patients attending for scans as part of their clinical pathway
Interventions
A short questionnaire (9 questions) will be given to the participants to complete.
Eligibility Criteria
Group 1: Patients recruited to studies with imaging Group 2: Patients who have previously participated in studies with imaging Group 3: Patients attending for scans as part of their clinical pathway
You may qualify if:
- Being treated at The Royal Marsden Hospital
- Over the age of 18
- Having imaging (MRI or PET/CT) as part of research or clinical care.
- Group 1
- Currently enrolled in a research project that involves imaging (either MRI or PET/CT)
- Group 2
- Previously enrolled in a research project that involved imaging (either MRI or PET/CT), where the patients involvement in the research project has now ended.
- Group 3
- Patients attending the MRI or PET/CT departments for imaging as part of their standard clinical care.
You may not qualify if:
- Inability to complete the questionnaire.
- Previously completed questionnaire.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Royal Marsden NHS Foundation Trust
Sutton, Surrey, SM2 5PT, United Kingdom
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Translational Imaging
Study Record Dates
First Submitted
July 22, 2015
First Posted
September 4, 2015
Study Start
April 1, 2015
Primary Completion
August 1, 2018
Study Completion
August 1, 2018
Last Updated
January 28, 2020
Record last verified: 2020-01