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临床试验/NCT04114734
NCT04114734进行中(未招募)不适用

Park Rx, Physical Activity and Other Health Benefits Among Low-income Children

Kaiser Permanente2 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2020年3月27日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
500
试验地点
2
主要终点
Change in Physical Activity

研究概览

简要总结

This study is a randomized controlled trial to evaluate ParkRx, a clinic-based counseling intervention in which health care providers prescribe park visits at a specific frequency, duration, and includes instructions for physical activity in the parks. We will assess whether prescribing visits to specific parks changes physical activity levels and improves health and mental health outcomes among low-income pediatric patients.

详细描述

Park prescriptions are formal clinical encouragements for patients to engage in more physical activity outdoors. From the beginning, ParkRx has been perceived as a common-sense solution to physical inactivity and to increasing the time children might be spending outdoors in nature. In spite of a lack of rigorous evidence that it is effective, the ParkRx concept is currently being widely disseminated and has been embraced by multiple national organizations. Unity Health, a federally qualified community health center in Washington, DC, is currently implementing park prescriptions for its largely low-income and minority population, a group at high risk of chronic diseases, physical inactivity and obesity. In partnership with Unity Health, we propose to conduct a randomized controlled trial (RCT) to prospectively evaluate Park Rx's impact on physical activity, as well as other secondary health outcomes in pediatric patients. Our specific aims are: 1) to test whether Park Rx will increase park visits and accelerometry-measured physical activity among children; 2) to identify any biological impacts of Park Rx on health, including impact on hypercholesterolemia, hypertriglyceridemia, HbA1C, overweight and obesity, for those patients with relevant diagnoses; 3) to explore impacts on mental health, including stress and measures of cognitive functioning; and 4) to determine whether there are age and gender differences in adherence to and impact of Park Rx. The results of this study will quantify the effectiveness of Park Rx and inform its future dissemination.

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
6 Years 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • ages >6 and <16 with one or more diagnoses of chronic conditions that usually require two or more routine health care provider visits per year.
  • Overweight or obesity, or
  • hypertriglyceridemia or
  • hypercholesterolemia, or
  • pre-diabetes or
  • Type 2 diabetes. AND
  • Likely to live in the Washington DC area in the next 2 years.

排除标准

  • Individuals who have previously been given a park prescription

结局指标

主要结局

Change in Physical Activity

时间窗: Baseline, 3 months, 6 months 12 months and 2 years

Accelerometer measured

次要结局

  • Change in Cognition(Baseline, 3 months, 6 months 12 months and 2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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