Testing the FLASHE Survey

Survey Clinical Trial

Official title:

Cognitive Testing of the Family Life, Activity, Sun, Health, and Eating (FLASHE) Survey

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01661036
• Other study ID #: 999912176
• Secondary ID: 12-C-N176
• Status: Completed
• First received: August 7, 2012
• Last updated: April 4, 2018
• Start date: July 23, 2012
• Est. completion date: August 7, 2015

Study information

• Verified date: August 7, 2015
• Source: National Institutes of Health Clinical Center (CC)
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Background:

• The Family Life, Activity, Sun, Health, and Eating (FLASHE) Survey is designed to look at health-related topics. It is being developed for the Department of Health and Human Services. Researchers want to see how easy or difficult the FLASHE survey questions are to understand and answer. They will interview parents and teenagers to test the survey questions.

Objectives:

• To test the FLASHE survey questions on teenagers and their parents.

Eligibility:

• Adolescents between 11 and 18 years of age.

• Parents of the participating adolescents.

Design:

• Participants will have a one-on-one interview to test the survey questions. The interview will last up to an hour and a half. Participants will be allowed to skip any questions that they do not wish to answer.

• Participants will receive financial compensation for their time.

Description:

The National Cancer Institute s (NCI) Division of Cancer Control and Population Sciences (DCCPS), Behavioral Research Program (BRP) proposes conducting formative research as an integral part of the development of a new data collection instrument, the Family Life, Activity, Sun, Health, and Eating (FLASHE) survey. Specifically, NCI proposes conducting cognitive testing with the objective of identifying potential sources of measurement or response errors within the questionnaires. Many of the questions are new questions that have not been previously tested, or previously-used questions that have never been used with a teenage population.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: August 7, 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 11 Years to 100 Years

Eligibility

• INCLUSION AND EXCLUSION CRITERIA:

The DCCPS contractor, Westat, will be conducting the study. Participants for the cognitive interviews will be recruited from the general population, and will include dyads of a parent or caregiver, and his/her teenage child between the ages of 11 and 18. Neither the contractor who will be coordinating the research (Westat) or NCI employees will be eligible to participate in the cognitive interviews. Westat will recruit respondents using a variety of methods including use of Westat s current database of potential participants and advertising on CraigsList in the local DC area under the Jobs postings within the subheading Et Cetera. Westat's digital media team will reach out to 100 local DC area (including lower Pennsylvania) publishers such as mommy and papi bloggers, health websites, giveaway publishers, and Facebook and Twitter users.

Related Conditions & MeSH terms

• Cognitive Testing
• Interview
• Survey

Locations

Country	Name	City	State
United States	National Cancer Institute (NCI), 9000 Rockville Pike	Bethesda	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Survey Development		At time of interview