跳至主要内容
临床试验/NCT05300646
NCT05300646招募中不适用

The Effect of an Adapted Mindfulness-Based Stress Reduction Program on Mental Health, Maternal Bonding and Birth Outcomes in Psycho-socially Vulnerable Pregnant Women: a Randomized Controlled Trial.

University of Aarhus3 个研究点 分布在 1 个国家目标入组 238 人开始时间: 2022年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
238
试验地点
3
主要终点
The World Health Organization - Five Well-Being Index (WHO-5)

研究概览

简要总结

The aim of the study is to address the need for a wider array of evidence-based and non-pharmacological options to improve mental health in a psycho-socially highly vulnerable group of pregnant women. In more detail, the primary outcome is to estimate the effect of prenatal Mindfulness-Based Stress Reduction (MBSR) as an add-on to usual care on mental well-being when compared to usual care alone. Second, to estimate the effect of prenatal MBSR on perceived stress and symptoms of depression and anxiety, and third to explore the effect on maternal bonding and childbirth, e.g. gestational age and experience of childbirth. Finally, to examine the mediating effect of mindfulness and self-compassion on the primary outcome.

详细描述

Background A history of psychopathology or psychosocial adversities are risk factors for mental disorders in the perinatal period. Mental disorders in pregnancy can adversely affect the developing fetus, which call for early prevention. Mindfulness-Based-Stress-Reduction (MBSR) is an acceptable intervention for pregnant women and has a growing evidence-base with meta-analyses consistently pointing to reductions in symptoms of stress, anxiety and depression. The aim of this study is to address the need for a wider array of evidence-based and non-pharmacological options to improve mental health in a psychosocially highly vulnerable group of pregnant women.

Methods/design Pregnant women (n = 238) referred to an outpatient clinic at Copenhagen University Hospital, Amager and Hvidovre, Denmark will be recruited for the study. The design is a single-center, parallel group, randomized controlled trial, with an adapted MBSR program as add on to usual care. The primary outcome is mental wellbeing. Secondary and exploratory outcomes include stress, anxiety, depression, mindfulness, compassion, antenatal attachment and childbirth experience. Participants will be randomized in a 1:1 ratio to prenatal MBSR or usual care.

Implications for perinatal mental health Teaching the skills of mindfulness meditation to a psychosocially vulnerable group of pregnant women could prove a viable and non-pharmacological approach to improve mental health during pregnancy, reduce stress and support the transition to parenthood. The MBSR program does not target a particular group, and results from the study is thus of potential relevance for pregnant women in general as a means of reducing stress and improving perinatal mental health.

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
Single (Outcomes Assessor)

盲法说明

Group affiliation will be concealed for the researcher performing the statistical analyses.

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

  • Estimated due date no sooner than three months from start of the intervention. This criterion is included in order for the women to be able to complete the intervention before their due date.
  • Eighteen + years of age.
  • Speak and write Danish.
  • Available for group intervention scheduled sessions. Being unavailable for two or more sessions is reason for exclusion from study participation.
  • Written informed consent to study criteria.

排除标准

  • Active substance dependence.
  • Psychotic disorders (e.g. schizophrenia or bipolar disorder).
  • Suicidality.

结局指标

主要结局

The World Health Organization - Five Well-Being Index (WHO-5)

时间窗: From baseline to 6 months after completion of the intervention.

The WHO-5 is a global rating scale measuring subjective well-being and consists of five statements and the respondent is asked to rate how well each of the statements applies to her when considering the last 14 days. Each item is scored from 5 "all of the time" to 0 "none of the time". Final scores range from 0 - 100 with higher scores representing greater well-being.

次要结局

  • The Self-Compassion Scale (SCS)(From baseline to 6 months after completion of the intervention.)
  • The Depression Anxiety Stress Scales (DASS-21)(From baseline to 6 months after completion of the intervention.)
  • The Five-Facet Mindfulness Questionnaire (FFMQ)(From baseline to 6 months after completion of the intervention.)
  • The Edinburgh Depression Scale (EDS)(From baseline to 6 months after completion of the intervention.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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