Early Childhood Obesity Prevention Program (ECHO)

Connecticut Children's Medical Center

Status: Completed

Conditions: Body Weight Changes

Treatments: Behavioral: Experimental

Study type: Interventional

Funder types: Other

Identifiers

NCT02052518

HD073966-02

Details and patient eligibility

About

This study is proposed on behalf of the Hartford Childhood Wellness Alliance, a 107 member, 35 group organization whose goal is to improve the health of children in Hartford, CT. In a randomized control trial, the primary aim of this study is to test the initial efficacy of a program of enhanced home visitation with neighborhood and community support to change maternal behaviors related to infant nutrition (sweetened beverage/juice consumption, breastfeeding and introduction of solids), parenting skills (establishing routines around sleep, reading cues for hunger, satiety, television time) and family wellness (improving the home food environment, enhancing physical activity). The investigators hypothesize that at 12 months of age, infants in the intervention arm will drink less sugar sweetened beverages/juices, will have ingested solids at an older age, will have been breastfed longer and more exclusively than infants in the control arm and will have less TV viewing, more established sleep routines and greater soothability (primary outcomes).

Full description

See Manuscript: 125. Cloutier MM, Wiley J, Wang Z, Grant A, Gorin AA. The Early Childhood Obesity Prevention Program (ECHO): An ecologically-based intervention delivered by home visitors for newborns and their mothers. BMC Public Health, 15:584 PMID 26073106, 2015.

Enrollment: 57 patients

Sex: All

Ages: Under 1 month old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Enrolled in the Nurturing Families Network Program
• Singleton birth >34 weeks gestation
• Any race or ethnicity
• ECHO neighborhood
• Mothers and their newborns

Exclusion criteria

• Mothers or newborns with special health care needs
• Infant with major malformation
• Small for Gestational Age/low birth weight

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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57 participants in 2 patient groups, including a placebo group

Enhanced NFN Home Program

Experimental group

Description:

Education and Skill set training with materials to implement the behaviors recommended. Using a motivational interviewing framework, intervention participants will receive dietary and activity counseling, develop a Family Wellness Plan and will be linked to community resources.

Treatment:

Behavioral: Experimental

Nurturing Family Network Home Visitation

Placebo Comparator group

Description:

Mothers will receive the standard of care from the Nurturing Families Network Home Visitation program

Treatment:

Behavioral: Experimental