跳至主要内容
临床试验/NCT05186272
NCT05186272进行中(未招募)3 期

mHealth Mindfulness Intervention for Pregnant Black and Latina Women at Risk of Postpartum Depression

Kaiser Permanente1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2022年6月14日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
600
试验地点
1
主要终点
Patient Health Questionnaire-9

研究概览

简要总结

Postpartum depression (PPD) is associated with significant health consequences for mothers and children, and the current COVID-19 pandemic has had a major impact on the mental health of particularly vulnerable populations including pregnant Black and Latina women. There is an urgent need for evidence-based, accessible, and scalable mental health care options for these high-risk, vulnerable women. This study aims to: (a) compare the effectiveness of two digitally-delivered self-paced stress reduction programs in pregnant Black and Latina women at increased risk of PPD; and (b) examine barriers and facilitators to implementation within a large healthcare system.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Age ≥18 years
  • Current Kaiser Permanente Permanente Northern California (KPNC) member
  • Pregnant woman receiving prenatal care at KPNC
  • Gestational age <30 weeks
  • Singleton pregnancy
  • Self-identify as Black and/or Latina
  • Moderate to moderately severe depressive symptoms (PHQ-9 score between 10 and 19) and no indication of suicidality
  • Owns a device with internet access
  • English- or Spanish-speaking

排除标准

  • Regular stress reduction practice with a mindfulness component (e.g., meditation or yoga more than twice a week)
  • Acting as gestational carrier/surrogate

研究组 & 干预措施

Intervention

Experimental

Use of mHealth stress reduction program 'A' app 5-20 min daily for 6 weeks

干预措施: Stress reduction program 'A' (Behavioral)

Active control

Active Comparator

Use of mHealth stress reduction program 'B' app 5-20 min daily for 6 weeks

干预措施: Stress reduction program 'B' (Behavioral)

结局指标

主要结局

Patient Health Questionnaire-9

时间窗: 7 weeks postpartum

Depression scale; total score range of 0-27; higher scores indicate higher depression.

Patient Health Questionnaire-9

时间窗: Baseline

Depression scale; total score range of 0-27; higher scores indicate higher depression.

Patient Health Questionnaire-9

时间窗: 6-week follow-up

Depression scale; total score range of 0-27; higher scores indicate higher depression.

次要结局

  • Perceived Stress Scale(7 weeks postpartum)
  • Generalized Anxiety Disorder 7-item scale(7 weeks postpartum)
  • Promis Sleep Disturbance - Short Form 6a(7 weeks postpartum)
  • Perceived Stress Scale(Baseline)
  • Perceived Stress Scale(6-week follow-up)
  • Generalized Anxiety Disorder 7-item scale(Baseline)
  • Generalized Anxiety Disorder 7-item scale(6-week follow-up)
  • Promis Sleep Disturbance - Short Form 6a(Baseline)
  • Promis Sleep Disturbance - Short Form 6a(6-week follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验