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临床试验/NCT05796648
NCT05796648已完成不适用

Preparing a Food is Medicine Intervention to Promote Healthy Eating and Blood Pressure Control in Black Women with Hypertension and Obesity

University of Illinois at Chicago2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Number of participants who complete the 12 week intervention

研究概览

简要总结

Hypertension and obesity are both major risk factors for cardiovascular disease (CVD), a leading cause of death for Black women in the United States. The investigators propose examining the feasibility and acceptability of the 12-week RN-CHeFRx (Real Nourishment and Cooking Healthy Food is Rx) intervention - grocery delivery, cooking classes, and nutrition education - for Black women with hypertension and obesity to improve nutritious eating habits and blood pressure control.

详细描述

The objective of this study is to conduct the RN-CHeFRx (Real Nourishment and Cooking Healthy Food is Rx) for 12 weeks among Black women who are obese and hypertensive living Chicago. We propose to 1) Pilot the RN-CHEFRx intervention and measures that will be used to assess blood pressure, BMI status, and sodium intake with 20 Black women diagnosed with hypertension and BMI ≥ 30. We will assess the efficacy of the evaluation tools to be used in a future clinical trial at three-time points (baseline, 12 weeks, and 6 months); and 2) Assess the feasibility and acceptability of the RN-CHeFRx intervention using interviews, surveys, and documentary analysis. Findings from this study will inform a larger efficacy trial of RN-CHeFRx to improve dietary behaviors and blood pressure control among Black women with hypertension and obesity.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • self-identified as Black or of African descent
  • ≥ 18 years old
  • baseline blood pressure ≥130/85 or diagnosed with hypertension and BMI ≥ 30

排除标准

  • inability to cook in their homes
  • cognitive deficits impeding the ability to participate or provide informed consent
  • current treatment for cancer
  • liver or renal disease
  • pregnancy
  • lack of English language proficiency

结局指标

主要结局

Number of participants who complete the 12 week intervention

时间窗: Up to 12 weeks

Completion will be measured by class attendance

Acceptability of the intervention

时间窗: Up to 12 weeks

Assessed via participant feedback

dietary intake during intervention

时间窗: Baseline to 12 weeks

Dietary intake at baseline and 12 weeks

Number of participants recruited

时间窗: Up to 12 weeks

Patients recruited, screened, eligible and consented to participate in the study

Number of participants who complete data collection visits

时间窗: Baseline to 4 months

Completion measured by participants completing surveys, blood pressure measurements, and those who provide blood biospecimens

Change in mean blood pressures (mmHg) during intervention

时间窗: Baseline to 12 weeks

Change will be measured by comparing blood pressures from baseline to 12 weeks

次要结局

  • Change in body weight during intervention(Up to 12 weeks)
  • Change in body weight at 6 months(12 weeks to 24 weeks)
  • Change in blood pressure at 6 months(12 weeks to 24 weeks)
  • Dietary intake during post-intervention(12 weeks to 24 weeks)

研究者

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

Saria Lofton

Assistant Professor

University of Illinois at Chicago

研究点 (2)

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