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Behavioral Weight Loss Treatment for Individuals With Food Addiction

Behavioral Weight Loss Treatment for Individuals With Food Addiction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04311450
Acronym
FA Pilot
Enrollment
50
Registered
2020-03-17
Start date
2021-03-01
Completion date
2022-06-30
Last updated
2022-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Food Addiction, Overweight and Obesity, Weight Loss

Brief summary

The purpose of this research study is to examine how well an existing weight loss treatment works for individuals with food addiction. Treatment will consist of a preliminary 12-week RCT pilot of the feasibility and effectiveness of behavioral weight loss (BWL) compared to a waitlist control.

Interventions

This therapy is a weekly treatment which focuses on making gradual and modest lifestyle changes with goals of establishing regular patterns of eating, setting weekly goals, decreasing caloric intake, developing coping skills, and increasing physical activity.

Sponsors

Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* BMI 25-50 kg/m2 * Meets criteria for Food Addiction (based on the self-report score from the Yale Food Addiction Scale) * Available for the duration of the treatment (3 months) * Read, comprehend, and write English at a sufficient level to complete study-related materials. * Availability of internet to participate in study interventions (i.e., electronic SMART scales)

Exclusion criteria

* Co-existing psychiatric condition that requires hospitalization or more intensive treatment (e.g., bipolar mood disorders, psychotic illnesses, severe depression). * Reports active suicidal or homicidal ideation * Current anorexia or bulimia nervosa * Endorsing current or history of heart trouble/chest pain. * Breast-feeding or pregnant, or planning to become pregnant during the study. * History of stroke or myocardial infarction. * Current or recent (within 12 months) drug or alcohol dependence * Currently receiving effective treatment for eating or weight loss, including individual who received bariatric surgery within the past five years * Currently participating in another clinical study.

Design outcomes

Primary

MeasureTime frameDescription
Weight (e.g., change in percent weight loss)Up to 12 weeks
Food addiction (change in food addiction scores)Up to 12 weeksYale Food Addiction Scale scores will be assessed by self-report (range of scores 0-7, higher score reflect greater food addiction symptoms)

Secondary

MeasureTime frameDescription
Food Craving (change in food craving scores)Up to 8 weeksFood Craving Inventory scores will be assessed by self-report (range of score 0-185, higher scores reflect greater food cravings).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026