- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02836392
CRQ Survey Study: Clinical Research Questionnaire of Oncology Patients - A Nationwide Survey
August 9, 2017 updated by: Cancer Trials Ireland
This is a translational, multicentre questionnaire study.
The study design follows that of a cross sectional, quantitative research approach.
Data collection will involve self-administered, paper-based questionnaires.
The method of data collection allows for a large sample size without major expense.
The questionnaires are comprised of several questions examining areas such as demographic details, cancer diagnosis, understanding of the term 'clinical trials', attitudes to personal participation in cancer clinical research and the experience of patients who previously participated in a cancer clinical trial.
The study will be opened in all interested hospitals in Ireland following initiation of the study at each site.
Questionnaire completion will be seen as implied informed consent and no formal consent will need to be signed by the patient.
The paper-based questionnaire responses will be electronically and anonymously recorded in a computer database to facilitate analysis.
Study Overview
Study Type
Observational
Enrollment (Actual)
1000
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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-
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Cork, Ireland
- Bon Secours Hospital
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Cork, Ireland
- Cork University Hospital
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Dublin, Ireland
- Mater Misericordiae University Hospital
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Dublin, Ireland
- Beacon Hospital
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Dublin, Ireland
- St James Hospital
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Dublin, Ireland, 6
- Saint Luke's Hospital Rathgar
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Galway, Ireland
- University Hospital Galway
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Letterkenny, Ireland
- Letterkenny General Hospital
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Limerick, Ireland
- University Hospital Limerick
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Sligo, Ireland
- Sligo University Hospital
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Co Waterford
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Waterford, Co Waterford, Ireland
- University Hospital Waterford
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Dublin
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Beaumont Road, Dublin, Ireland, 9
- Beaumont Hospital
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Dublin 24
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Tallaght, Dublin 24, Ireland
- AMNCH
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Dublin 4
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Elm Park, Dublin 4, Ireland
- St Vincent's University Hospital
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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
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
This is a translational, multicentre questionnaire study.
Description
Inclusion Criteria:
- Clinical diagnosis of malignancy
- Aged 18 years or older
- Ability to complete the questionnaire or independently or with the help of a friend, relative, or staff member of the oncology department
Exclusion Criteria:
- N/A
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Oncology patients' understanding of the term 'clinical trials' and their attitudes towards personal participation in cancer clinical research will be evaluated by questionnaire.
Time Frame: 1 year
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The patient related factors, including level of education and socioeconomic status that influence their decision regarding participation in a cancer clinical trial (CCT) will be explored by questionnaire.
Time Frame: 1 year
|
1 year
|
|
The patients' experience surrounding the discussion regarding CCT participation and their actual experience when enrolled in a CCT will be investigated by questionnaire.
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
May 1, 2016
Primary Completion (ACTUAL)
December 1, 2016
Study Completion (ACTUAL)
January 1, 2017
Study Registration Dates
First Submitted
June 27, 2016
First Submitted That Met QC Criteria
July 18, 2016
First Posted (ESTIMATE)
July 19, 2016
Study Record Updates
Last Update Posted (ACTUAL)
August 10, 2017
Last Update Submitted That Met QC Criteria
August 9, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- ICORG 15-43
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
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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