- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03849846
Using Focus Groups to Explore Perceptions of Adults With Low Socioeconomic Status Regarding the NutriQuébec Study
Recruiting Participants With Low Socioeconomic Status in the NutriQuébec Study: Using Focus Groups to Explore Their Beliefs, Preferences and Concerns
NutriQuébec is a web-based prospective cohort study aiming to monitor and analyse the evolution of Québec population eating habits through annual questionnaires. The recruitment and retention of participants with low socioeconomic status (SES), known to be more hard to reach and recruit into health studies, will be major challenges in obtaining a representative sample of the Québec population.
The purpose of this study is to identify the behavioural, normative and control beliefs of individuals from low SES regarding a hypothetical participation in the NutriQuébec study. Their preferences regarding recruitment methods as well as their concerns about the security, use and share of data will also be identified.
Four moderator facilitated focus groups will be conducted in community centres (n=28 participants). The focus groups will be recorded, transcribed and coded by two coders using NVivo.
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Québec, Canada, G1V 0A6
- Laval University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults (18 years of age and older)
- Living in the Québec City Metropolitan Area
- Attending one of the three community centers where the focus groups will be conducted
- Be able to answer questionnaires in French
Exclusion Criteria:
None
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Adults with low socio-economic status
Four focus groups will be conducted with adults with low socioeconomic status recruited through community centres in the Québec City area.
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Participants will also complete a sociodemographic questionnaire.
The moderator will conduct the discussion using a semi-structured interview guide, based on the construct of the Theory of Planned Behaviour.
The interview guide has been developed to identify the beliefs that determine the participants' attitudes (advantages/disadvantages), subjective norms (approval/disapproval of important others) and perceived behavioural control (facilitators/barriers) related to a hypothetical participation in the NutriQuébec study.
The participants will also be questioned about their preferences regarding the recruitment as well as their concerns about the security, use and share of data.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The perceived advantages related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (behavioural beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The perceived advantages related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (behavioural beliefs) and will be identified from focus groups.
The question asked to participants will be: In your opinion, what would be the advantages of participating in the NutriQuébec study?
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Baseline
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The perceived disadvantages related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (behavioural beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The perceived disadvantages related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (behavioural beliefs) and will be identified from focus groups.
The question asked to participants will be: In your opinion, what would be the disadvantages of participating in the NutriQuébec study?
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Baseline
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The persons most likely to approve the participant hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (normative beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The persons most likely to approve the participant hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (normative beliefs) and will be identified from focus groups. The question asked to participants will be: Among the people (groups or individuals) important to you, which ones would agree that you should participate in the NutriQuébec study? For what reasons? |
Baseline
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The persons most likely to disapprove the participant hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (normative beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The persons most likely to disapprove the participant hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (normative beliefs) and will be identified from focus groups.
The question asked to participants will be: Among the people (groups or individuals) important to you, which ones would not agree with the fact that you are participating in the NutriQuébec study?
For what reasons?
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Baseline
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The facilitators related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (control beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The facilitators related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (control beliefs) and will be identified from focus groups.
The question asked to participants will be: In your opinion, what would help you participate in the NutriQuébec study?
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Baseline
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The barriers related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (control beliefs) and will be identified from focus groups.
Time Frame: Baseline
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The barriers related to a hypothetical participation in the NutriQuébec study is based on the Theory of Planned Behaviour (control beliefs) and will be identified from focus groups.
The question asked to participants will be: In your opinion, what would prevent you from participating in the NutriQuébec study?
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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The preferences about the recruitment in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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The preferences about the recruitment in the NutriQuébec study will be identified from focus groups.
The question is: What ways would be effective to recruit you into the NutriQuébec study?
If we advertised the NutriQuébec study, how could you hear about us?
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Baseline
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The concerns about the security of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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The concerns about the security of the data in the NutriQuébec study will be identified from focus groups.
The question is: Do you have any concerns about the security of the data that will be collected using the web questionnaires?
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Baseline
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The concerns about the use of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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The concerns about the use of the data in the NutriQuébec study will be identified from focus groups.
The question is: Do you have any concerns about the use and sharing of data between different researchers, knowing that they will not have access to your personal data such as your name and health insurance number?
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Baseline
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The concerns about the share of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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The concerns about the share of the data in the NutriQuébec study will be identified from focus groups.
The question is: Do you have any concerns about the use and sharing of data between different researchers, knowing that they will not have access to your personal data such as your name and health insurance number?
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Baseline
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2018-042 A-1/18-05-2018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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