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临床试验/NCT06445556
NCT06445556已完成不适用

Uplifting Equitable Park Use and Promoting Physical Activity Among African American Families in Minnesota: A Culturally-Responsive, Community-Engaged Approach

University of Minnesota1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2024年5月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
13
试验地点
1
主要终点
Pre-/post-intervention changes in physical activity (PA)

研究概览

简要总结

Social injustices, such as the absence of racial representation and culturally tailored programs in parks, may further discourage African American families from accessing and using these spaces. 10 Studies are needed to investigate how exposure to more equitable greenspace environments may support physical activity (PA) among African American families. Justice-focused, park-based PA interventions hold high promise for reducing health disparities and future cardiovascular diseases (CVD) and related chronic conditions (RCC) risk, thus carrying significant implications for the fields of public health, family medicine, and urban planning.

This pilot study is a two-arm, parallel randomized controlled trial that will be conducted in partnership with community stakeholders from the Three River Park District (TRPD); TRPD parks are located in the Twin Cities region of Minnesota. This trial aims to evaluate the changes in PA, psychological health, sleep, and blood pressure among a cohort of African American parent-child dyads who will be randomized to two intervention conditions. The intervention conditions are: (1) a culturally tailored, nature-based program offered at the TRPD (hereafter, "NatureUplift"), and (2) NatureUplift plus a supplementary walking/hiking educational component (hereafter, "NatureUplift+Active"). Participant dyads will be randomized to NatureUplift or NatureUplift+Active.

研究设计

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

入排标准

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

入选标准

  • •Inclusion criteria for adult parents/caregivers are:
  • •Able and willing to provide informed consent for child
  • •Are the child's primary caregiver, i.e., they are the adult who spends the largest proportion of time caring for the child (e.g., cleaning, feeding, etc.) or they spent an exactly equal proportion to another caregiver (e.g., parents each with 50% of childcare responsibilities)
  • •Are able to read and speak English
  • •Self-reported Black/African American
  • •Live in the Twin Cities area
  • •Participating in less than 60 min/day and 150 min/week of PA, assessed via a modified a Godin-Shephard Leisure Time Physical Activity Questionnaire
  • •No contraindications to engaging in PA, assessed via the Physical Activity Readiness Questionnaire (PAR-Q+)
  • •Parents need to own a smartphone or a tablet to synchronize both their Fitbit and their children's Fitbit with the Fitbit application.
  • •Inclusion criteria for youth are:
  • •Able and willing to provide informed assent and to comply with study requirements
  • •Child aged 8-12 years
  • •Live with the consenting parent/caregiver at least 50% of the time
  • •Are able to read and speak English

排除标准

  • •Exclusion criteria for adult parents/caregivers are:
  • •Currently engaged in ≥150 min/week of PA.
  • •Individuals with contraindications to exercise participation as indicated by the PAR-Q+.
  • •A self-reported physical/mental disability that would prevent them from being able to adhere to the intervention.
  • •Currently pregnant or planning to become pregnant during the study period.
  • •Currently breastfeeding.
  • •Unwilling to be randomized to a study group.
  • •Exclusion criteria for youth are:
  • •Currently engaged in >60 min of MVPA per day
  • •Individuals with contraindications to exercise participation as indicated by the PAR-Q+.
  • •Evidence of significant cognitive deficits or a severe, persistent psychiatric disorder (self-reported by the caregiver) that may interfere with comprehension of survey and adhere to the intervention.

研究组 & 干预措施

NatureUplift

Active Comparator

Parent-child dyads randomized to NatureUplift group

干预措施: NatureUplift (Behavioral)

NatureUplift+Active

Experimental

Parent-child dyads randomized to NatureUplift+Active group

干预措施: NatureUplift+Active (Behavioral)

结局指标

主要结局

Pre-/post-intervention changes in physical activity (PA)

时间窗: 12 weeks

ActiGraph GT9X will be used to measure primary outcomes (time spent in light- (LPA), moderate- (MPA), and vigorous-intensity (VPA)) Fitbits are also used, but mostly to monitor compliance and not necessarily to report on the outcome.

次要结局

  • Pre-/post-intervention changes in psychological health(12 weeks)
  • Pre-/post-intervention changes in blood pressure(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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