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

Status

Completed

Conditions

Intervention / Treatment

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

      • Cork, Ireland
        • Bon Secours Hospital
      • Cork, Ireland
        • Cork University Hospital
      • Dublin, Ireland
        • Mater Misericordiae University Hospital
      • Dublin, Ireland
        • Beacon Hospital
      • Dublin, Ireland
        • St James Hospital
      • Dublin, Ireland, 6
        • Saint Luke's Hospital Rathgar
      • Galway, Ireland
        • University Hospital Galway
      • Letterkenny, Ireland
        • Letterkenny General Hospital
      • Limerick, Ireland
        • University Hospital Limerick
      • Sligo, Ireland
        • Sligo University Hospital
    • Co Waterford
      • Waterford, Co Waterford, Ireland
        • University Hospital Waterford
    • Dublin
      • Beaumont Road, Dublin, Ireland, 9
        • Beaumont Hospital
    • Dublin 24
      • Tallaght, Dublin 24, Ireland
        • AMNCH
    • Dublin 4
      • Elm Park, Dublin 4, Ireland
        • St Vincent's University Hospital

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.

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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