Key takeaways:
- Lifestyle changes remain first-line for pediatric obesity, but caregivers facing food insecurity report significant barriers and limited effectiveness.
- Caregivers’ past experiences with diet-based interventions strongly influence openness to GLP-1 receptor agonist use.
- Trust in medication—including safety concerns and media influence—plays a major role in decision-making for children.
- Beliefs about prioritizing physical health versus socioemotional wellbeing shape preferences for lifestyle-only care or medication.
- Shared decision-making that incorporates family values and structural challenges is critical for equitable pediatric obesity treatment.
Exploring barriers to lifestyle change, building understanding around treatment options, and aligning care with family values are the 3 key points for shared decision-making about using glucagon-like peptide-1 receptor agonists (GLP-1 RAs) in children of caregivers with food insecurity, according to a recent study published in JAMA Network Open.1
Lifestyle modifications have remained the first-line method for managing obesity, but limited efficacy has been reported, especially among low-income populations.2 GLP-1 RAs have been highlighted as a potential option for addressing barriers and improving health equity among children with obesity.1
“As new pediatric clinical practices surrounding the use of GLP-1 RAs take shape, it is essential to incorporate the voices of families affected by food insecurity,” wrote investigators.
Assessing the decision-making process
The qualitative study was conducted to analyze the caregiver decision-making process about GLP-1 RA use among caregivers of obese children with food insecurity. Electronic medical records of pediatric gastroenterology visits between January 1, 2022, and October 31, 2023, were assessed for eligible patients.
Participants included caregivers of a pediatric patient with obesity attending at least 2 months of routine physician-recommended dietary changes. These patients also had moderate to high household food insecurity risk and were aged at least 18 years so they could give consent. Family reports were assessed for participant race and ethnicity data.
The semistructured interviews lasted 45 minutes and were conducted by a pediatric gastroenterologist with qualitative research training and a research analyst. These discussions occurred over telephone or video from December 1, 2023, to April 30, 2024, and were structured around the Capability, Opportunity, Motivation–Behavior framework.
Data collection and participant demographics
Interviews were also structured around the Theoretical Domains Framework. These frameworks included multiple questions about treatment knowledge, healthy food access, and motivation for sustaining lifestyle change. The Brief Health Literacy Screen and a demographic survey were also administered to participants.
There were 20 caregivers aged a mean 40.5 years included in the final analysis, with 95% of interviews conducted with a mother and 5% with a mother and father together. Being born outside the United States was reported in 90% of caregivers, using a language besides English for medical care in 75%, and being at the lowest health literacy level in 70%.