Testing the FLASHE Survey

NCT ID: NCT01661036

Last Updated: 2018-04-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

36 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-07-23

Study Completion Date

2015-08-07

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cognitive Testing Interview Survey

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

11 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Cancer Institute (NCI)

NIH

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Linda C Nebeling

Role: PRINCIPAL_INVESTIGATOR

National Cancer Institute (NCI)

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

National Cancer Institute (NCI), 9000 Rockville Pike

Bethesda, Maryland, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

12-C-N176

Identifier Type: -

Identifier Source: secondary_id

999912176

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Senior Health Clinic Study
NCT05634239 UNKNOWN NA
The Kunshan Elderly Health Study
NCT05141565 ACTIVE_NOT_RECRUITING
Food at Home Study
NCT06286514 RECRUITING