A family-based behavioral group obesity randomized control feasibility trial across a clinical trials network: a focus on contact hours.

Publication date: Jan 29, 2025

This ancillary study’s purpose is to describe the relationship between dose of treatment and body mass index (BMI) outcomes in a tele-behavioral health program delivered in the IDeA States Pediatric Clinical Trials Network to children and their families living in rural communities. Participants randomized to the intervention were able to receive 26 contact hours (15 hr of group sessions and 11 hr of individual sessions) of material focused on nutrition, physical activity, and behavioral caregiver training delivered via interactive televideo. Dose of the intervention received by child/caregiver dyads (n = 52) from rural areas was measured as contact hours. The total doses of group, individual, and total contact hours were analyzed, and generalized linear mixed models were utilized to determine how dose received impacted BMI outcomes. The majority (64. 4%) of participants received the target of at least 80% (20. 8 hr) of the total intervention dose. Older children (9-11 years) achieved significantly less intervention dose than targeted (M = 19. 7; p = . 031); as did males (M = 17. 2; p 

Concepts Keywords
11years pilot/feasibility trial
Nutrition randomized controlled trial
Obesity school-age children
Rural
Televideo

Semantics

Type Source Name
disease MESH obesity
disease IDO intervention
disease MESH health disparities

Original Article

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