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临床试验/NCT07127731
NCT07127731尚未招募不适用

REACH BP: REmote Physical ACtivity Intervention for High Blood Pressure Postpartum

Northwestern University0 个研究点目标入组 60 人开始时间: 2027年4月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Feasibility of Recruitment

研究概览

简要总结

The purpose of this intervention is to help new mothers who had elevated blood pressure during pregnancy become more physically active after birth. The investigators will connect data from FitBits to the electronic health record. Women will then get weekly messages with feedback and goals to help them stay active. The investigators will test if the intervention improves step counts and blood pressure after pregnancy. The investigators will also test if the intervention is feasible and enjoyed by postpartum women.

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
Double (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Delivery of a live birth at Northwestern Medicine 6-12 weeks prior
  • Systolic blood pressure 120-139 or diastolic blood pressure 80-89 during the first 20 weeks of gestation
  • Low self-reported physical activity levels
  • Able to access the internet at least weekly
  • Have patient portal account or willing to set one up
  • Willing to wear a FitBit
  • Spoken and written English or Spanish language fluency

排除标准

  • Medical contraindications to participating in a structured physical activity program
  • Currently participating in a structured physical activity or weight loss program
  • Hypertensive disorder of pregnancy (e.g., preeclampsia, gestational hypertension, eclampsia)

结局指标

主要结局

Feasibility of Recruitment

时间窗: From enrollment to the end of the 24 week intervention

Number of participants enrolled in the intervention

Feasibility of Participant Retention

时间窗: At study weeks 12 and 24

Percent of enrolled participants who continue to participate in the intervention

Acceptability of the Intervention

时间窗: Study week 24

Participants will fill out a survey to assess the extent to which they were satisfied with individual intervention components including FitBit usage, portal messaging, blood pressure and weight assessments, surveys, intervention length and intervention delivery. Each component will be rated on a 5-point Likert Scale in which 1 represents very dissatisfied (lowest score) and 5 represents very satisfied (highest score).

Feasibility of FitBit+EHR linkage

时间窗: From enrollment to the end of the 24 week intervention

Percent of intervention days FitBit data are linked to the Electronic Health Record

Feasibility of Intervention Messaging

时间窗: From enrollment to the end of the 24 week intervention

Percent of weekly messages that are read by participants

次要结局

未报告次要终点

研究者

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

Natalie Cameron

Instructor

Northwestern University

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