Brief Inhibitory Training for Eating - Intervention
BITE-I
Inhibitory Control Training for Adolescents
1 other identifier
interventional
36
0 countries
N/A
Brief Summary
The purpose of this study is to conduct a proof-of-concept intervention of daily inhibitory control (IC) training. Aim 1 is to examine the feasibility, acceptability, and barriers of an IC training EMI in adolescents' daily life. Aim 2 is to evaluate the efficacy of IC training for modifying the hypothesized intervention mechanism: food-related IC and eating regulation. In the study, participants will: Complete questionnaires and cognitive tasks Receive a short nutrition education Complete three weeks of daily brain games on your phone
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable obesity
Started May 2026
Shorter than P25 for not_applicable obesity
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 6, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedFirst Posted
Study publicly available on registry
May 18, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 10, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 10, 2027
May 18, 2026
May 1, 2026
7 months
April 6, 2026
May 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Inhibitory control
Go-No/Go Task with food cues
1 month
Eating self-regulation
Self-Regulation of Eating Behaviour Questionnaire
1 month
Secondary Outcomes (2)
Binge-eating symptoms
1 month
Diet Quality
1 month
Study Arms (1)
Inhibitory control training
EXPERIMENTALInterventions
Children will first complete a short nutrition education then complete daily 10-minute inhibitroy control training each day for 10 minutes across 3 weeks
Eligibility Criteria
You may qualify if:
- years old
- Have obesity (BMI-z≥95th percentile)
- Have a smartphone
- Can read and speak English
- Interest in improving one's diet.
You may not qualify if:
- Not currently in eating disorder or weight loss treatment or receiving pharmacological/surgical treatment for obesity in the past four weeks
- Not meeting criteria for atypical anorexia nervosa or bulimia nervosa
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tyler Mason, PhD
George Mason University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
April 6, 2026
First Posted
May 18, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
December 10, 2026
Study Completion (Estimated)
March 10, 2027
Last Updated
May 18, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, ICF
- Time Frame
- June 2027 for an indefinite time period
- Access Criteria
- Anyone
All IPD collected throughout the trial