Imaging in Clinical Trials - a Questionnaire Study to Assess Impact of Imaging Regimes on Patient Participation (ASK)
27. januar 2020 opdateret af: Nandita deSouza, Institute of Cancer Research, United Kingdom
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.
Studieoversigt
Detaljeret beskrivelse
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.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
207
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Surrey
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Sutton, Surrey, Det Forenede Kongerige, SM2 5PT
- The Royal Marsden NHS Foundation Trust
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
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
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Group 1
Patients currently recruited to studies with imaging at The Marsden
|
A short questionnaire (9 questions) will be given to the participants to complete.
|
|
Group 2
Patients who have previously participated in studies with imaging at The Marsden
|
A short questionnaire (9 questions) will be given to the participants to complete.
|
|
Group 3
Patients attending for scans as part of their clinical pathway
|
A short questionnaire (9 questions) will be given to the participants to complete.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Factors that affect patient participation in imaging research
Tidsramme: Duration of Study - 1 year
|
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
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Factors affecting participation in the different patient categories
Tidsramme: Duration of Study - 1 year
|
Duration of Study - 1 year
|
|
Effect of current participation in a study on the perceived acceptability of imaging burden
Tidsramme: Duration of Study - 1 year
|
Duration of Study - 1 year
|
|
Do opinions change after undergoing imaging procedures
Tidsramme: Duration of Study - 1 year
|
Duration of Study - 1 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2015
Primær færdiggørelse (Faktiske)
1. august 2018
Studieafslutning (Faktiske)
1. august 2018
Datoer for studieregistrering
Først indsendt
22. juli 2015
Først indsendt, der opfyldte QC-kriterier
3. september 2015
Først opslået (Skøn)
4. september 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
28. januar 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. januar 2020
Sidst verificeret
1. januar 2020
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 15 LO 1189
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .