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Effects of Thai Food-Specific Inhibition Control Training on Psychophysiological Outcomes in Thai Adults With Obesity

NCT07928817, Not applicable, Enrolling by invitation, Burapha University

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleEffects of Thai Food-Specific Inhibition Control Training on Psychophysiological Outcomes in Thai Adults With ObesityClinicalTrials.gov
NCT numberNCT07928817ClinicalTrials.gov
StatusEnrolling by invitationClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment72 participants, estimatedClinicalTrials.gov
Lead sponsorBurapha UniversityClinicalTrials.gov
ConditionsObesity & Overweight, Obesity (Disorder)ClinicalTrials.gov
InterventionsThai Food-Specific Inhibition Control Training, General Inhibition Control TrainingClinicalTrials.gov
First posted2026-11-10ClinicalTrials.gov
Last updated2026-11-10ClinicalTrials.gov

Registered outcomes 11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in Body WeightBaseline, Week 8, and Week 12.Body weight measured in kilograms using a weighing scaleClinicalTrials.gov
PrimaryChange in Body Mass IndexBaseline, Week 8, and Week 12.BMI calculated as body weight in kilograms divided by height in meters squared.ClinicalTrials.gov
PrimaryChange in Waist CircumferenceBaseline, Week 8, and Week 12.Waist circumference measured in centimeters using a measuring tape.ClinicalTrials.gov
SecondaryChange in Eating BehaviorBaseline, Week 8, and Week 12. Specify total or subscale scores and scoring range.Measured using the Dutch Eating Behavior Questionnaire (DEBQ)ClinicalTrials.gov
SecondaryChange in Power of Food Scale ScoreBaseline, Week 8, and Week 12. Specify scoring range and interpretationMeasured using the Power of Food Scale (PFS)ClinicalTrials.gov
SecondaryChange in Eating Inhibition Control Behavior ScoreBaseline, Week 8, and Week 12Measured using the 54-item Eating Inhibition Control Behavior Questionnaire (EICB). Total score ranges from 54 to 270; higher scores indicate better eating inhibition control behaviorClinicalTrials.gov
SecondaryChange in Health-Related Quality of LifeBaseline, Week 8, and Week 12. Specify the eight domain scores or prespecified summary scores.Measured using the SF-36 Health SurveyClinicalTrials.gov
SecondaryChange in Mental HealthBaseline, Week 8, and Week 12. Specify psychological distress and well-being scoring.Measured using the Mental Health Inventory-38 (MHI-38)ClinicalTrials.gov
SecondaryChange in Self-EsteemBaseline, Week 8, and Week 12. Confirm scoring convention.Measured using the 10-item Rosenberg Self-Esteem Scale (RSE-10)ClinicalTrials.gov
SecondaryChange in N2 Event-Related Potential AmplitudeBaseline and Week 8. Confirm electrode, task condition, and latency windowN2 amplitude measured in microvolts (µV) during the inhibitory control taskClinicalTrials.gov
SecondaryChange in P3 Event-Related Potential AmplitudeBaseline and Week 8. Confirm electrode, task condition, and latency windowP3 amplitude measured in microvolts (µV) during the inhibitory control taskClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)