Three-Factor Eating Questionnaire in Measuring Eating Behavior in Adolescent and Young Adult Survivors of CNS Tumors
NCT ID: NCT01682824
Last Updated: 2022-02-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1 participants
OBSERVATIONAL
2013-05-17
2022-01-24
Brief Summary
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Detailed Description
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SECONDARY OBJECTIVES I. To validate the original TFEQ-R18v2 in a sample of AYA survivors of childhood CNS tumors in the US.
II. To determine the association of the original TFEQ-R18v2 with self-reported body mass index (BMI).
III. To determine the association of the original TFEQ-R18v2 with fruits and vegetables, fiber, and fat intake.
IV. To determine the association of EQ-EMA with self-reported BMI. V. To determine the association of EQ-EMA with fruits and vegetables, fiber, and fat intake.
OUTLINE: Patients are randomized to 1 of 2 groups.
GROUP I: Patients complete the TFEQ-R18v2 questionnaire, a dietary intake assessment, and the EQ-EMA questionnaire online.
GROUP II: Patients complete the EQ-EMA questionnaire, a dietary intake assessment and the TFEQ-R18v2 questionnaire.
Conditions
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Study Groups
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Group I (questionnaire, nutritional assessment)
Patients complete the TFEQ-R18v2 questionnaire, a dietary intake assessment, and the EQ-EMA questionnaire online.
Nutritional Assessment
Complete dietary intake assessment
Questionnaire Administration
Complete TFEQ-R18v2 questionnaire
Questionnaire Administration
Complete EQ-EMA questionnaire
Group II (questionnaire, nutritional assessment)
Patients complete the EQ-EMA questionnaire, a dietary intake assessment and the TFEQ-R18v2 questionnaire.
Nutritional Assessment
Complete dietary intake assessment
Questionnaire Administration
Complete TFEQ-R18v2 questionnaire
Questionnaire Administration
Complete EQ-EMA questionnaire
Interventions
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Nutritional Assessment
Complete dietary intake assessment
Questionnaire Administration
Complete TFEQ-R18v2 questionnaire
Questionnaire Administration
Complete EQ-EMA questionnaire
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Has been off therapy without relapse for at least 6 months
* Able to speak, write, and read in English
* Has access to the internet
* Has telephone access
* Currently lives in the United States
Exclusion Criteria
* Is experiencing severe cognitive impairments that do not allow them to engage in basic conversations (excluding individuals who may experience severe cognitive impairments because participants will need to provide assent \[if \< 18 years old\] or consent \[if \>= 18 years old\] and will need to have the ability to independently complete the TFEQ-R18v2, Multifactor screener, and EQ-EMA. Through the phone screening conducted by the M D Anderson Cancer Center \[MDACC\] graduate research assistant \[GRA\], a person is determined to not be severely cognitive impaired if the participant is able to respond to basic questions such as their age, whether or not they have internet access, and telephone.)
* Is incarcerated at the time of enrollment
15 Years
39 Years
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Karen Basen-Engquist
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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M D Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2018-02536
Identifier Type: REGISTRY
Identifier Source: secondary_id
2012-0628
Identifier Type: OTHER
Identifier Source: secondary_id
2012-0628
Identifier Type: -
Identifier Source: org_study_id
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