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AzTrials

SurveyNCT03847584

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

An observational study of Survey, run by Laval University at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Populations with low socioeconomic status (SES) are more likely to develop diseases across lifespan and are frequently underrepresented in large cohort studies. The aim of this study is to examine beliefs, preferences and concerns towards participating in an e-cohort prospective study on nutrition (NutriQuébec) among… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Survey
What is being tested?
Survey
How many people
418 participants
Where
1 siteCanada
Study dates
11 Oct 2018to 20 Oct 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Adults with low/middle/high socioeconomic status

Who may be able to join

  • Adult (18 years of age or older)
  • Living in the province of Québec
  • Have access to the Internet and have an active email address
  • Be able to answer questionnaires in French

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Laval University

    Québec, G1V 0A6

Other trials in Canada

About this study

Official title: Recruiting Participants With Low Socioeconomic Status in the NutriQuébec Study: Using Survey to Explore Their Beliefs, Preferences and Concerns

Populations with low socioeconomic status (SES) are more likely to develop diseases across lifespan and are frequently underrepresented in large cohort studies. The aim of this study is to examine beliefs, preferences and concerns towards participating in an e-cohort prospective study on nutrition (NutriQuébec) among this population.

A cross-sectional survey will be completed by 418 adults in the Province of Québec (Canada), including individuals with low SES (high school or less and gross annual household income < $55,000 canadian). The survey is based on the Theory of Planned Behaviour and assesses intention to participate in NutriQuébec as well as attitude, subjective norm, and perceived behavioural control. The survey also assesses preferences regarding the recruitment.

Read the detailed description

A cross-sectional survey will be completed by 418 participants from several administrative regions of Québec (Canada). A special effort will be made to recruit men and women with low socioeconomic status (SES), but without rejecting adults from middle/high SES. First, 325 adults from low SES (high school or less and gross annual household income < $55,000 canadian) and from several administrative regions of Québec will be identified by a survey firm. In addition, an e-mail mailing list from the Institute of Nutrition and Functional Food (INAF, Laval University) will be used to distribute the recruitment ad to complete our sample (n=93 from all SES).

The survey is based on the Theory of Planned Behaviour and assesses intention to participate in NutriQuébec as well as attitude, subjective norm, and perceived behavioural control. The salient beliefs underlying the determinants of individual's intention to participate in the NutriQuébec study most frequently cited in the focus groups (from a preliminary elicitation study: 2018-042 A-1/18-05-2018) were used to develop the survey questions. The survey also assesses the preferences regarding the recruitment. Sociodemographic questions are also asked.

Conditions
Survey
Being tested
Survey
Keywords
Low socioeconomic status population, Web-based prospective cohort study, Survey, Recruitment, Attitude, Subjective norms, Perceived behavioural control, Intention
Medical subject headings
Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • SurveyOther

    The survey is based on the Theory of Planned Behaviour and assesses intention to participate in NutriQuébec as well as attitude, subjective norm, and perceived behavioural control. The salient beliefs underlying the determinants of individual's intention to participate in the NutriQuébec study most frequently cited in the focus groups (from a preliminary elicitation study: 2018-042 A-1/18-05-2018) were used to develop the survey questions. The survey also assesses the preferences regarding the recruitment. Sociodemographic questions are also asked.

Study groups in NCT03847584
Study groupRoleWhat they receive
Adults-low socioeconomic statusSurvey completed by adults with low socioeconomic status
Receives: Other: Survey
Adults-middle/high socioeconomic statusSurvey completed by adults with middle/high socioeconomic status
Receives: Other: Survey

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The intention to participate to the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour.

    Intention will be calculated as the mean of three questions on a five point bipolar Likert scale. The three questions are: 1) I intend to participate in the NutriQuébec study : 1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely; 2) The chances that I participate in the NutriQuébec study are : 1=very small, 2=rather small, 3=neither high nor small, 4=rather high, 5=very high; 3) I will participate in the NutriQuébec study: 1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely). Thus, the mean score for intention ranges from 1 to 5, with higher values reflecting a greater likelihood for participation in the NutriQuébec study.

    Measured: Baseline

  2. The attitude related to a hypothetical participation in the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour.

    The attitude will be calculated as the mean of three questions on a five point bipolar Likert scale. The three questions are: 1) For me, participating in the NutriQuébec study would be...: 1=very unpleasant, 2=rather unpleasant, 3=neither pleasant nor unpleasant, 4=rather pleasant, 5=very pleasant; 2) For me, participating in the NutriQuébec study would be...: 1=very useless, 2=rather useless, 3=neither useful nor useless, 4=rather useful, 5=very useful; 3) For me, participating in the NutriQuébec study would be…: 1=very unsatisfactory, 2=rather unsatisfactory, 3=neither satisfactory nor unsatisfactory, 4=rather satisfactory, 5=very satisfactory. Thus, the mean score for attitude ranges from 1 to 5, with higher values reflecting a more positive attitude towards a participation in the NutriQuébec study.

    Measured: Baseline

  3. The subjective norm related to a hypothetical participation in the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour.

    The subjective norm will be calculated as the mean of three questions on a five point bipolar Likert scale. The three questions are: 1) The people most important to me might think that I should participate in the NutriQuébec study:1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely; 2) Many people I know may be interested in participating in the NutriQuébec study: 1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely; 3) If I participated in the NutriQuébec study, most people who are important to me could...: 1= strongly disapprove, 2= slightly disapprove, 3=neither approve nor disapprove, 4= slightly approve, 5=strongly approve. Thus, the mean score for the subjective norm ranges from 1 to 5, with higher values representing perceptions that important others expect the participant to participating in the NutriQuébec study.

    Measured: Baseline

  4. The perceived behavioural control related to a hypothetical participation in the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour.

    The perceived behavioural control will be calculated by the mean of three questions on a five point bipolar Likert scale. The three questions are: 1) I feel able to participate in the NutriQuébec study: 1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely; 2) I am confident that I can overcome any obstacles that may prevent me from participating in the NutriQuébec study: 1=very unlikely, 2=rather unlikely, 3=neither likely nor unlikely, 4=rather likely, 5=very likely; 3) For me, participating in the NutriQuébec study would be....: 1=very difficult, 2=rather difficult, 3=neither easy nor difficult, 4=rather easy, 5=very easy. Thus, the mean score for the perceived behavioural control ranges from 1 to 5, with higher values representing a greater perceived behavioural control towards a participation in the NutriQuébec study.

    Measured: Baseline

  5. The determinants to the intention to participate to the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour.

    Determinants to the intention to participate in the NutriQuébec study will be identified with a multiple linear regression using constructs that will be found significant in influencing the intention to participate in the NutriQuébec study (e.g. attitude, subjective norm, perceived behavioural control).

    Measured: Baseline

Secondary outcomes (1)
  1. The preferences about the recruitment in the NutriQuébec study will be assessed by a questionnaire

    The preferences about the recruitment in the NutriQuébec study will be assessed by a questionnaire. The question is: By which means of communication would advertising about the NutriQuébec study be most likely to capture your attention?: 1=Television, 2=Social networks (Facebook, Instagram, YouTube, etc.), 3=The Internet (other than social networks), 4=Newspapers, 5=Posters in public places (hospitals, community centres, etc.), 6=Flyers, 7=Postal mail, 8=None.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2019
  2. Study start11 Oct 2018
  3. Primary completion20 Oct 2018
  4. Study completion20 Oct 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
418 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03847584
Sponsor's protocol ID
2018-042 A-2/10-09-2018
Status last verified
Aug 2024
First submitted
10 Jan 2019
Last updated
20 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Survey, run by Laval University at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The intention to participate to the NutriQuébec study will be assessed by a questionnaire based on the Theory of Planned Behaviour. (time frame: Baseline). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2024.

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