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临床试验/NCT06671652
NCT06671652已完成不适用

Adaptation and Implementation of a Cherokee-based Participatory Research Project to Reduce CVD Risk

University of Missouri-Columbia1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2023年9月24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
42
试验地点
1
主要终点
Blood Pressure

研究概览

简要总结

This is a two phase project. Phase I is an online convenience sample to collect health and preference data for the intervention phase, as well as a partnership with community to co-create an intervention; Phase II. Phase II is an intervention to improve community connection and historical knowledge within Cherokee communities within the Cherokee Nation reservation involving consultation with Cherokee cultural and historical experts.

详细描述

  1. Identify necessary program enhancements to maximize reach and acceptability of the intervention for primary prevention of CVD in Cherokee Nation adults. The new intervention will have a broad reach, and thus, potentially greater public health impact. By building on the well-established and popular intervention, RTR, the goal is to maximize the likelihood that this intervention will be culturally acceptable, logistically feasible, and financially sustainable.
  2. Conduct a pilot study (n = 40) to demonstrate acceptability and feasibility of the adapted intervention and research methods. The expectation is that the intervention will be culturally acceptable to participants, and retention and data collection protocols will support feasibility of a larger randomized controlled trial.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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
是

入选标准

  • •Citizen of Cherokee tribe

排除标准

  • •Under the age of 18

研究组 & 干预措施

Intervention

Experimental

Participants will take part in a community building program in which Cherokee cultural, linguistic, and historical experts will met with the self-selected community groups approximately 1 x month for 5 months. Participants will complete homework assignments for each meeting and will complete a final presentation on the history and culture of their families and communities.

干预措施: Duyugoda igalenisodi (Starting again the right way) (Behavioral)

结局指标

主要结局

Blood Pressure

时间窗: Pre; Post (study completion; within 6 months)

Systolic and Diastolic blood pressure measured through millimeters of mercury (mmHG)

Weight

时间窗: Pre;Post

Weight was gathered from participants using a digital scale and measured in pounds.

次要结局

  • Keyes Mental Health Continuum, Short Form (Also Known as "Positive Mental Health Scale")(Pre; Post (study completion; within 6 months))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Melissa Lewis

Associate Professor

University of Missouri-Columbia

研究点 (1)

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