Using Focus Groups to Explore Perceptions of Adults With Low Socioeconomic Status Regarding the NutriQuébec Study

February 19, 2019 updated by: Laval University

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

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Four focus groups will be conducted in three community centers (n=6 to 8 participants/group; n=28 participants). First, all participants will read and sign the consent form. They will also complete a sociodemographic questionnaire. Then, 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 behavioral 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. The focus groups will be recorded and transcribed. Two coders will perform the codification independently using NVivo 10.

Study Type

Observational

Enrollment (Actual)

28

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

      • Québec, Canada, G1V 0A6
        • Laval University

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

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adults with low socioeconomic status

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

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
Intervention / Treatment
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.
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.

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
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?
Baseline
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
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?
Baseline
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

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
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
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?
Baseline
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
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?
Baseline
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
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?
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The preferences about the recruitment in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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?
Baseline
The concerns about the security of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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?
Baseline
The concerns about the use of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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?
Baseline
The concerns about the share of the data in the NutriQuébec study will be identified from focus groups.
Time Frame: Baseline
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?
Baseline

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 (Actual)

May 22, 2018

Primary Completion (Actual)

June 12, 2018

Study Completion (Actual)

June 12, 2018

Study Registration Dates

First Submitted

January 10, 2019

First Submitted That Met QC Criteria

February 19, 2019

First Posted (Actual)

February 21, 2019

Study Record Updates

Last Update Posted (Actual)

February 21, 2019

Last Update Submitted That Met QC Criteria

February 19, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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