Receiving Genetic Information: A Quantitative Survey

October 11, 2018 updated by: St Mary's University College

The Public's Response to Receiving Genetic Information Via an Electronic Platform: A Quantitative Survey

This study will evaluate the public's response to receiving genetic information via an electronic platform. It will comprise of an internet run quantitative survey.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

There is currently a high prevalence of obesity in the UK. Diets personalised to an individual's genetics could help to reduce the prevalence. However, how the public will respond to this information is unknown. The use of technology is very common and could provide an accessible platform to communicate genetic results to the public. Therefore, this study will evaluate the public's response to receiving genetic information via an electronic platform.

This study will comprise of an internet run quantitative survey. The survey will be circulated using relevant websites, internet forums, emails and social media. Participants will be required to complete the survey once which will take around 10 minutes. The participants will not be required to complete the survey in a controlled setting, it may be complete wherever the participant feels comfortable. Data analysis will take place at St Mary's University.

Study Type

Observational

Enrollment (Anticipated)

370

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

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 to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

UK citizens between the ages of 18 and 65 years

Description

Inclusion Criteria:

UK citizens between the ages of 18 and 65 years

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
Whole Cohort
UK Citizens, aged 18-65 years
Other: Survey
Survey

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
BMI against response.
Time Frame: October - November 2018
If BMI and socioeconomic status differs between participants who show a positive response to receiving genetic information to those that show a negative response.
October - November 2018
Socioeconomic status versus response.
Time Frame: October - November 2018
If socioeconomic status and socioeconomic status differs between participants who show a positive response to receiving genetic information to those that show a negative response.
October - November 2018

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

St Mary's University College

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 (ANTICIPATED)

October 31, 2018

Primary Completion (ANTICIPATED)

November 30, 2018

Study Completion (ANTICIPATED)

November 30, 2018

Study Registration Dates

First Submitted

September 10, 2018

First Submitted That Met QC Criteria

September 10, 2018

First Posted (ACTUAL)

September 11, 2018

Study Record Updates

Last Update Posted (ACTUAL)

October 16, 2018

Last Update Submitted That Met QC Criteria

October 11, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • SMEC_2017-18_140

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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