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Motivational Interviewing in NOURISH for Parents of Overweight Children

Motivational Interviewing in NOURISH for Parents of Overweight Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01912989
Acronym
NOURISH+MI
Enrollment
64
Registered
2013-07-31
Start date
2013-01-31
Completion date
2015-08-31
Last updated
2015-09-24

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

Conditions

Overweight and Obesity

Keywords

motivational interviewing, obesity, parent

Brief summary

The purpose of this study is to investigate if a brief, motivational interviewing intervention (NOURISH+MI) can improve retention and treatment adherence for parents enrolled in an intervention for their child's overweight (NOURISH+). The investigators hypothesize that children whose parents participate in NOURISH+MI will demonstrate lower attrition and greater adherence with NOURISH+, ultimately leading to greater treatment effects, compared with children whose parents are randomized to NOURISH+ or a control group.

Detailed description

There is an urgent need for innovative approaches to pediatric obesity prevention and treatment. There is also a demand for targeted strategies that reduce attrition and improve compliance with obesity treatment. Intervening exclusively with parents of overweight children is a novel treatment approach, with demonstrated efficacy in reducing child body mass index (BMI) percentile. Motivational interviewing (MI), a brief communication style for exploring and resolving ambivalence about change, may enhance treatment engagement when implemented as part of obesity interventions. Further research investigating MI within pediatric obesity treatments is needed. In the current application, the investigators are examining whether MI implemented with parents for the treatment of their children's overweight can improve treatment effects. NOURISH+, a recently funded R01 (Nourishing Our Understanding of Role modeling to Improve Support and Health; PI, Mazzeo), is a culturally tailored parent intervention for overweight children ages 5-11. NOURISH+ targets lower-income, African American participants, a group at increased risk for pediatric overweight and associated complications, and builds on pilot work which yielded significant reductions in child BMI percentile. The investigators are adding an MI treatment into NOURISH+. Specifically, we will randomly select 60 parents at enrollment and investigate if adding two brief MI sessions prior to the NOURISH+ group intervention will enhance treatment effects. The investigators will be able to compare NOURISH+MI with participants from the two R01 treatment conditions (NOURISH+ and Control), matched on child ethnicity and gender. The investigators hypothesize that children whose parents participate in NOURISH+ MI will demonstrate lower attrition and greater compliance with NOURISH+, ultimately leading to greater treatment effects, compared with children whose parents are randomized to NOURISH+ or a control group.

Interventions

BEHAVIORALLifestyle counseling

Parents will participate in one telephone and one in person session of motivational interviewing prior to their participation in an 8 week parent-exclusive treatment focusing on parenting skills to improve their child's overweight.

Sponsors

American Heart Association
CollaboratorOTHER
Virginia Commonwealth University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* parents/caregivers must be at least 18 years old * have a child between the ages of 5 and 11 * have a child with a BMI \> the 85th%ile * the eligible child primarily resides in the caregiver's home * English speaking

Exclusion criteria

* non-ambulatory * pregnant * have a medical condition that might be negatively impacted by exercise have a psychiatric diagnosis that would impair their ability to respond to assessments or participate in a group * Parents whose children have a medical or developmental condition that precludes weight loss using conventional diet and exercise methods are also ineligible

Design outcomes

Primary

MeasureTime frame
Number of sessions attended8 weeks and 4-month follow up

Secondary

MeasureTime frame
Baseline child physical activity and change in activitybaseline, 8 weeks, 4-month post
Baseline child BMI percentile and change in BMIbaseline, 8 weeks, 4-month post
Baseline child dietary intake and change in intakebaseline, 8 weeks, 4 month post
Baseline parent dietary intake and change in intakebaseline, 8 weeks, 4-month post
Baseline parent physical activity and change in activitybaseline, 8 weeks, 4-month post
Baseline parent BMI and change in BMIbaseline, 8 weeks, 4-month post

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026