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Using Artificial Intelligence to Optimize Delivery of Weight Loss Treatment

Using Artificial Intelligence to Optimize Delivery of Weight Loss Treatment

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05231824
Acronym
ReLearn
Enrollment
301
Registered
2022-02-09
Start date
2022-03-22
Completion date
2025-02-28
Last updated
2026-09-04

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

Conditions

Obesity, Weight Loss

Keywords

Obesity, Weight Loss, Behavioral treatment, Artificial intelligence

Brief summary

Project ReLearn is testing the efficacy and cost-effectiveness of an Artificial Intelligence system for optimizing weight loss coaching. Participants are randomized to a 1-year weekly gold standard behavioral weight loss remote (video) group treatment or the AI-optimized treatment, which is made up of a combination of remote group treatment, short video call and automated message. In the AI-optimized condition, the system monitors outcomes (via wireless scale, mobile phone app, and wristworn tracker) and, each week, assigns each participant the treatments they have responding to the best, within certain time constraints.

Interventions

Behavioral weight loss treatment is the current gold standard treatment for obesity.

BEHAVIORALAI-optimized Behavioral Weight Loss Treatment

AI-optimized Behavioral Weight Loss Treatment will continuously vary intensity (automated text message, videoconference group, individual coaching call) and coach type (paraprofessional or MS-level expert) based on continuously-monitored participant digital data.

Sponsors

Oregon Research Institute
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Individuals must be of overweight or obese BMI (27-50 kg/m) * Individuals must be adults (aged 18-70) * Able and willing to engage in the remote program * Able to engage in physical activity (defined as walking two city blocks without stopping) * Individuals must also provide consent for the research team to contact their personal physician if necessary, to provide clearance or to consult about rapid weight loss * Access and willingness to use an Apple or Android smartphone * Satisfactory completion of all enrollment procedures

Exclusion criteria

* Medical condition (e.g., cancer, type I diabetes, psychosis, full-threshold eating disorder) that may pose a risk to the participant during intervention or cause a change in weight * Currently pregnant, breastfeeding, or planning to become pregnant in the next 12 months * Recently began or changed the dosage of medication that can cause significant change in weight * History of bariatric surgery * Weight loss of \> 5% in the previous 3 months

Design outcomes

Primary

MeasureTime frameDescription
Weight changeBaseline, 1-month, 6-month, and 12-month assessmentWeight will be measured using the Fitbit Aria Air wireless scale, which is accurate to 0.2 kg. In order to maximize accuracy, we will (1) provide instructions (e.g., place scale on flat, hard surface; weigh upon waking, without clothes, after using the bathroom), (2) require participants to confirm that they are following instructions at each assessment point, (3) use an average of 5 consecutive daily weights for each timepoint, (4) remove errant weights (e.g., \>1 kg change in 1 day).
CostsBaseline, 1-month, 6-month, and 12-month assessmentAll time spent training counselors, participants and supervising counselors, will be tracked by the project coordinator, as will time counselors spend delivering individual and group treatment. The web portal will track counselor time on the portal, e.g., reviewing food records and texting. While the basic time commitments are pre-set by condition, several factors will vary including participant no-shows, participant drop-outs, and counselor adherence to time limits.

Secondary

MeasureTime frameDescription
Physical ActivityBaseline, 1-month, 6-month, and 12-month assessmentMinutes of moderate to vigorous physical activity (MVPA) will be measured via Fitbit, a consumer-grade wrist-worn activity tracker which has superior compliance and close-to-equivalent accuracy as a research-grade accelerometer. Number of days meeting MVPA goal will be used by the AI system, with MVPA minutes as a secondary outcome.
Calorie intakeBaseline, 1-month, 6-month, and 12-month assessmentSeven days of calorie intake as derived from the Fitbit app's food log will be used as a secondary outcome. Participants will already be tracking their consumption using the app because data are used by both the coaches (per standard treatment) and the AI system.
Acceptability as Measured by Likert Self-report Scale6-month and 12-month assessmentParticipants will be asked to rate satisfaction with and perceived effectiveness of the program. Counselors will rate effectiveness and ease of use.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATOREvan M Forman, PhD

Drexel University Center for Weight, Eating and Lifestyle Science

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026