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Park Rx and Physical Activity Among Low-income Children

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04114734
Acronym
ParkRx
Enrollment
500
Registered
2019-10-03
Start date
2020-03-27
Completion date
2025-07-31
Last updated
2023-03-13

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

Conditions

Mental Health Wellness 1, Physical Activity

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALPark Rx

Participants will be advised to visit a specific park at a specific frequency and duration

Sponsors

Unity Health
CollaboratorOTHER
Kaiser Permanente
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be assigned to get Park Rx or to receive care as usual.

Eligibility

Sex/Gender
ALL
Age
6 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

* 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. * ADHD, or * 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.

Exclusion criteria

\- Individuals who have previously been given a park prescription

Design outcomes

Primary

MeasureTime frameDescription
Change in Physical ActivityBaseline, 3 months, 6 months 12 months and 2 yearsAccelerometer measured

Secondary

MeasureTime frameDescription
Change in CognitionBaseline, 3 months, 6 months 12 months and 2 yearsWe will use the NIH toolbox A)The Flanker Inhibitory Control Test; B) Dimensional Change Card Sort Test C) List Sorting Working Memory Test

Other

MeasureTime frameDescription
Change in BMI percentile2 yearsWe will review the electronic health record for BMI
Change in Lipids2 yearsEHR review

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026