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临床试验/NCT01912989
NCT01912989已完成不适用

Motivational Interviewing in NOURISH for Parents of Overweight Children

Virginia Commonwealth University2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
64
试验地点
2
主要终点
Number of sessions attended

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • non-ambulatory
  • 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

结局指标

主要结局

Number of sessions attended

时间窗: 8 weeks and 4-month follow up

次要结局

  • Baseline parent BMI and change in BMI(baseline, 8 weeks, 4-month post)
  • Baseline parent dietary intake and change in intake(baseline, 8 weeks, 4-month post)
  • Baseline child dietary intake and change in intake(baseline, 8 weeks, 4 month post)
  • Baseline child physical activity and change in activity(baseline, 8 weeks, 4-month post)
  • Baseline child BMI percentile and change in BMI(baseline, 8 weeks, 4-month post)
  • Baseline parent physical activity and change in activity(baseline, 8 weeks, 4-month post)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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