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NCT05635019
FoodRx for Obesity Treatment
Conditions: Obesity, Food Insecurity
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 105
Sponsor: University of Pennsylvania
Location: United States
Summary
This study is a 3-group, parallel design, randomized controlled trial (RCT) in 105 adults with obesity and food insecurity that will compare BWL-Alone (including standard-of-care referral and connection with community food resources; n=35) to BWL plus food supplementation with either food vouchers (BWL+VOUCHER; n=35) or home-delivered, medically tailored groceries consistent with BWL recommendations (BWL+HOME; n=35).
All groups will have BWL treatment provided for 24 weeks per clinical guidelines.
Food vouchers and HOME will be provided for 24 weeks of treatment.
Assessments will be conducted at baseline, and weeks 12 and 24.
Eligibility Criteria
Inclusion Criteria:Provision of signed and dated informed consent formStated willingness to comply with all study procedures and availability for the duration of the studyAge >18 yearsBMI >30 kg/m2 at screening visitScreening positive for food insecurity using a score of >3 on the 10-item US Adult Food Security Survey Module109Completion of baseline assessmentsAbility to engage in physical activity (i.e., can walk at least 2 blocks)Willing and able to provide pictures of food receipts to study team (or mail actual receipts)Ability to reliably receive packages at a consistent location in a timely mannerTelephone or internet service to communicate with study staffFor females of reproductive potential: agreement to use of highly effective contraception for during study participationExclusion Criteria:Serious medical conditions (e.g., type 1 or type 2 diabetes, renal failure) that may pose a risk to the participant during intervention, cause a change in weight, or limit ability to adhere to the program's behavioral recommendationsSignificant psychiatric conditions (e.g., active substance abuse, schizophrenia) that may pose a risk to the participant during intervention, cause a change in weight, or limit ability to adhere to the program's behavioral recommendationsBreastfeeding, pregnant or planning pregnancy in the next 6 monthsPlanned move from the Philadelphia area in the next 6 monthsWeight loss of >5 kg in the previous 90 daysRecently began a course of or changed the dosage of medication that can cause significant weight change (±5 kg)Previous or planned obesity treatment with surgery (excluding lap band if removed for >1 year) or a weight-loss deviceUse of prescription or over the counter medications for chronic weight management in the past 3 monthsHousehold member already participating in study due to potential contamination effectsLack of stable residence and ability to store and prepare food
Source: ClinicalTrials.gov (NCT05635019). StuddyBuddy aggregates publicly available trial information.