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临床试验/NCT01699958
NCT01699958已完成不适用

A Pilot Study of the "Healthy Living Study," a Randomized Controlled Trial of a Brief Outpatient Problem-solving Intervention to Promote Healthy Eating and Activity Habits in Adolescents.

Stanford University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2011年6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
50
试验地点
2
主要终点
Feasibility to conduct a brief problem-solving intervention in a busy academic outpatient setting.

研究概览

简要总结

The purpose of this study is to refine, evaluate the feasibility, and to estimate the effect of the "healthy Living Study," a brief outpatient problem-solving intervention to promote healthy eating and activity habits in adolescents.

详细描述

This study will refine, evaluate the feasibility, and estimate the effect of a brief problem-solving intervention to promote healthy eating and activity habits in adolescents. Intervention participants will receive 2 sessions of individual behavioral counseling on problem-solving skills utilizing educational videos, handouts, and worksheets. Intervention participants will be asked to generate unique health goals and practice utilizing problem-solving skills to achieve these goals.Control participants will receive standard of care. Outcomes will explore the ability to shorten the intervention, integrate the intervention into busy outpatient clinics, and estimate the effect of the intervention on confidence to maintain or improve healthy habits and to improve problem-solving skills.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 13-18 years old
  • Able to read and speak English
  • Patient of the Lucile Packard Children's Hospital teen clinic, weight clinic, or mobile teen van

排除标准

  • History of purging within the prior 12 months

结局指标

主要结局

Feasibility to conduct a brief problem-solving intervention in a busy academic outpatient setting.

时间窗: From recruitment of the first participant to completion of the intervention by the last participant, anticipated duration of time: 7-8 months

Feasibility will be measured in the following ways: 1. Refinement of the intervention by the end of the study to a reasonable length to compliment average patient clinic visits with a goal of 30 minutes or less 2. Minimal disruption of clinic flow measured through clinic provider and staff satisfaction surveys and qualitative comments during the course of the intervention

次要结局

  • Change in problem-solving skills(Change from baseline to 1-2 months)
  • Change in confidence to maintain or improve healthy eating habits(Change from baseline to 1-2 months)
  • Sufficient recruitment and retention rates(From recruitment of the first participant to completion of the intervention by the last participant, anticipated duration of time: 7-8 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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