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

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

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Recruitment Status

COMPLETED

Total Enrollment

1 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-17

Study Completion Date

2022-01-24

Brief Summary

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This trial studies how the Three-Factor Eating Questionnaire works in measuring eating behavior in adolescent and young adult survivors of central nervous system (CNS) tumors. The Three-Factor Eating Questionnaire is comprised of three factors, including cognitive restraint, uncontrolled eating, and emotion eating. The Eating Questionnaire - Ecological Momentary Assessment method measures a patient's recent experiences and behavior, such as eating behavior, as they continue their daily living. Giving the Three-Factor Eating Questionnaire and the Eating Questionnaire - Ecological Momentary Assessment may help researchers measure eating behaviors more effectively in adolescent and young adult survivors of CNS tumors.

Detailed Description

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PRIMARY OBJECTIVES I. Evaluate whether the factor structure of the adapted Eating Questionnaire-Ecological Momentary Assessment (EQ-EMA), which has been modified for real time assessment, will be similar to the factor structures for cognitive restraint (CR) and uncontrollable eating (UE) factors assessed by the Three Factor Eating Questionnaire-R18v2 (TFEQ-R18v2) in a sample of adolescent and young adult (AYA) survivors of childhood central nervous system (CNS) tumors in the United States (US).

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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Cancer Survivor

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

Intervention Type OTHER

Complete dietary intake assessment

Questionnaire Administration

Intervention Type OTHER

Complete TFEQ-R18v2 questionnaire

Questionnaire Administration

Intervention Type OTHER

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

Intervention Type OTHER

Complete dietary intake assessment

Questionnaire Administration

Intervention Type OTHER

Complete TFEQ-R18v2 questionnaire

Questionnaire Administration

Intervention Type OTHER

Complete EQ-EMA questionnaire

Interventions

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Nutritional Assessment

Complete dietary intake assessment

Intervention Type OTHER

Questionnaire Administration

Complete TFEQ-R18v2 questionnaire

Intervention Type OTHER

Questionnaire Administration

Complete EQ-EMA questionnaire

Intervention Type OTHER

Other Intervention Names

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Dietary Assessment dietary counseling nutritional counseling

Eligibility Criteria

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Inclusion Criteria

* Adolescent or young adult (AYA) who has survived a primary CNS tumor
* 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 in foster care
* 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
Minimum Eligible Age

15 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Related Links

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http://www.mdanderson.org

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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