Parent/Caregiver Conference Attendance Feasibility

February 25, 2021 updated by: University of Florida
This study will assess and evaluate conference attendance feasibility and will gather feedback about preferences and barriers to attendance at the American Society for Nutrition annual conference.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study will use a survey provided on the American Society for Nutrition Family Support Grant application webpage for those who are registering to attend the American Society for Nutrition annual meeting and who are applying for this particular grant. The survey will take about 10 minutes to complete and will provide detailed information for assessment and evaluation of conference attendance feasibility and will also provide feedback about preferences and barriers related to attendance and this annual meeting.

Study Type

Observational

Enrollment (Actual)

84

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

  • United States
    • Florida
      • Gainesville, Florida, United States, 32610
        • University of Florida

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

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Applicants for the Family Support Grant to the American Society for Nutrition annual conference that takes place in June 2018

Description

Inclusion Criteria:

  • Must be an applicant for the Family Support Grant to the American Society for Nutrition annual conference that takes place in June 2018

Exclusion Criteria:

-

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Family Support Grant applicants
Participants include applicants for the Family Support Grants that will be provided for the American Society for Nutrition annual meeting who are willing to complete the applicant survey.
Behavioral: Applicant Survey
This survey will ask a few brief demographic questions and will assess feedback from participants about preferences and barriers to conference attendance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participant likelihood of attendance to the American Society for Nutrition annual meeting if provided with a family support grant
Time Frame: 20 minutes to complete survey
5-point scale
20 minutes to complete survey

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Grant option most likely to be used by participants
Time Frame: 20 minutes to complete survey
4 options provided for participants to select. This will be tallied to determine which of the four options were most likely to be pursued.
20 minutes to complete survey
Participants' opinion of greatest value of a family support grant should it be provided
Time Frame: 20 minutes to complete survey
Participants will be asked to describe the greatest value of the family grant support. Potentially the top 7 selections will be recorded.
20 minutes to complete survey
Participants' greatest barrier to attending the American Society for Nutrition annual meeting
Time Frame: 20 minutes to complete survey
Participants will be asked to describe the greatest barrier to attending the American Society for Nutrition annual meeting. Potentially the top 10 selections will be recorded.
20 minutes to complete survey
Most significant factor influencing the participant's decision to attend the American Society for Nutrition annual meeting
Time Frame: 20 minutes to complete survey
Participants will be asked to describe the most significant factor influencing the participant's decision to attend the American Society for Nutrition annual meeting. Potentially the top 10 selections will be recorded.
20 minutes to complete survey

Collaborators and Investigators

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

Sponsor

University of Florida

Collaborators

American Society for Nutrition

Investigators

  • Principal Investigator: Michelle Cardel, PhD, RD, University of Florida

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

February 21, 2018

Primary Completion (Actual)

September 1, 2020

Study Completion (Actual)

September 1, 2020

Study Registration Dates

First Submitted

January 29, 2018

First Submitted That Met QC Criteria

February 7, 2018

First Posted (Actual)

February 14, 2018

Study Record Updates

Last Update Posted (Actual)

February 26, 2021

Last Update Submitted That Met QC Criteria

February 25, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • IRB201800142

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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