- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02051010
ABC Survey - do we Meet the Needs of Patients With Advanced Breast Cancer?
March 27, 2015 updated by: Cancer Trials Ireland
ABC Survey: Are we Meeting the Needs of Patients With Advanced Breast Cancer (ABC) in Ireland? A Nationwide Survey
The study will follow a descriptive design involving a survey.
Data collection will involve paper based questionnaires.
The questionnaires have been developed in conjunction with breast cancer support groups associated with the Irish Cancer Society and patients.
Study Overview
Status
Completed
Conditions
Detailed Description
The purpose of the study is to identify and categorise the need of Metastatic Breast Cancer (MBC) patients in Ireland with particular focus on; quality of life, symptom burden and access to and value of support available.
The study also aims to evaluate future service developments that will provide support to these patients.
Study Type
Observational
Enrollment (Actual)
500
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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Cork, Ireland
- Bon Secours Hospital
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Cork, Ireland
- Cork University Hospital
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Cork, Ireland
- South Infirmary - Victoria University Hospital
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Donegal, Ireland
- Letterkenny General Hospital
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Dublin, Ireland
- Beaumont Hospital
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Dublin, Ireland, 8
- Saint James's Hospital
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Dublin, Ireland, 4
- Saint Vincent Universtiy Hospital
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Dublin, Ireland, 7
- Mater Misericordiae University Hospital and Mater Private Hospital
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Galway, Ireland
- Galway University Hospital
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Kerry, Ireland
- Kerry General Hospital
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Limerick, Ireland
- Midwestern Regional Hospital
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Sligo, Ireland
- Sligo General Hospital
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Waterford, Ireland
- Waterford Regional 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
Female
Sampling Method
Non-Probability Sample
Study Population
All patients must have metastatic breast cancer
Description
Inclusion Criteria:
- Signed written informed consent
- Clinical diagnosis of MBC
- Female aged 18 years or older
- Able to complete the questionnaires independently
Exclusion Criteria:
- Any patient who does not meet the above mentioned inclusion criteria.
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
Cohorts and Interventions
Group / Cohort |
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Metastatic Breast Cancer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Needs of MBC patients in Ireland
Time Frame: Following analysis of the questionnaires completed by the patients, estimated 24 months
|
The needs of MBC patients to be identified and categorised with particular focus on; quality of life, symptom burden and access to and value of available support
|
Following analysis of the questionnaires completed by the patients, estimated 24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Future service developments
Time Frame: Following analysis of the questionnaires completed by patients, estimated 24 months
|
Evaluation of future service developments that will provide support to these patients
|
Following analysis of the questionnaires completed by patients, estimated 24 months
|
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, 2013
Primary Completion (Actual)
March 1, 2015
Study Registration Dates
First Submitted
January 24, 2014
First Submitted That Met QC Criteria
January 29, 2014
First Posted (Estimate)
January 31, 2014
Study Record Updates
Last Update Posted (Estimate)
March 30, 2015
Last Update Submitted That Met QC Criteria
March 27, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ICORG 13-01
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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