Skip to content

Imaging in Clinical Trials - a Questionnaire Study to Assess Impact of Imaging Regimes on Patient Participation

Imaging in Clinical Trials - a Questionnaire Study to Assess Impact of Imaging Regimes on Patient Participation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02541266
Acronym
ASK
Enrollment
207
Registered
2015-09-04
Start date
2015-04-01
Completion date
2018-08-01
Last updated
2020-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Imaging, Questionnaire

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.

Detailed description

This is a questionnaire study aimed at gaining a greater understanding of the patient perspective on undertaking imaging procedures, MRI and PET/CT, for research purposes. The study is to evaluate the patient opinion and perceptions of the burden of imaging associated with research. We will look at different scanning procedures of varying duration, intensity, frequency and scheduling; this will enable us to have a better understand of the factors that influence participation in research and thus help us develop protocols that are more patient focused and acceptable.

Interventions

OTHERQuestionnaire

A short questionnaire (9 questions) will be given to the participants to complete.

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
Royal Marsden NHS Foundation Trust
CollaboratorOTHER
Institute of Cancer Research, United Kingdom
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

- * Inability to complete the questionnaire. * Previously completed questionnaire.

Design outcomes

Primary

MeasureTime frameDescription
Factors that affect patient participation in imaging researchDuration of Study - 1 yearFactors 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.

Secondary

MeasureTime frame
Factors affecting participation in the different patient categoriesDuration of Study - 1 year
Effect of current participation in a study on the perceived acceptability of imaging burdenDuration of Study - 1 year
Do opinions change after undergoing imaging proceduresDuration of Study - 1 year

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026