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临床试验/NCT02150681
NCT02150681已完成1 期

MBCT for Perinatal Women With Mood Disorders

University of California, Los Angeles4 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2012年10月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
39
试验地点
4
主要终点
Change in Self-Rated Depression from Pretreatment to Post-treatment to 1- and 6- months post-treatment

研究概览

简要总结

This study will investigate the effectiveness of mindfulness-based cognitive therapy (MBCT) for mood stabilization in perinatal women (preconception, pregnant, and postpartum) with a history of mood disorders. MBCT is a short-term group psychotherapy that has shown effectiveness in preventing depressive relapse. MBCT teaches mindfulness practices and cognitive-behavioral techniques.

详细描述

Approximately 10-15% of women experience depression following the birth of a child. Depression during pregnancy is also common. Women with a history of depression or bipolar disorder are at increased risk of depressive relapse or exacerbation of mood symptoms during the perinatal period. Perinatal depression is associated with a host of negative consequences that can affect the mothers, infants, and families. Women with perinatal depression may have trouble with parenting, marital quality, and employment. Children of mothers with perinatal depression may suffer intellectually or emotionally. These children are also more likely to develop a mood disorder or other psychiatric disorders throughout their lifetimes compared to children whose mothers have not been depressed. Prevention efforts during the preconception, pregnancy, and postpartum periods are of considerable public health benefit. However, perinatal women are often reluctant to start or continue psychotropic medications due to concerns about their influence on the developing fetus or nursing infant. Therefore, psychosocial treatments that modify key vulnerability factors, without medication side effects, are likely to be of strong interest to women who might otherwise remain untreated.

This study will investigate the effectiveness of mindfulness-based cognitive therapy (MBCT) for mood stabilization in perinatal women (preconception, pregnant, and postpartum) with a history of mood disorders. MBCT is a short-term group psychotherapy that has shown effectiveness in preventing depressive relapse. MBCT teaches mindfulness practices and cognitive-behavioral techniques. Mindfulness is the practice of cultivating a non-judgmental awareness of internal experiences (thoughts, feelings, and body sensations) and external experiences. Cognitive-behavioral techniques focus on identifying maladaptive thoughts and behaviors before they spiral into a depressive episode. MBCT teaches observational skills and helpful techniques for responding to distorted or dysfunctional thoughts and behaviors, thereby preventing an impending depressive relapse.

The investigators plan to (1) recruit 20 perinatal women at each of two sites with a history of major depressive disorder or bipolar disorder (currently in remission or partial remission), (2) ascertain their diagnoses and eligibility, (3) collect baseline data (e.g., demographic information, mood and anxiety symptoms), and (4) conduct open-trial MBCT groups with 10-12 women in each group. The investigators examine the feasibility of identifying, enrolling, and retaining perinatal women at high risk for mood episodes in an 8-week MBCT group psychotherapy. Treatment effectiveness, acceptability, and satisfaction will be assessed at the end of treatment, at 1 month post-treatment, and 6 months post-treatment.

This study will contribute to the field's understanding of non-pharmacological prevention options for perinatal and postnatal women at risk for mood episode relapse. MBCT could fill an urgently needed gap in services for preconception, pregnant, and postpartum women who are at increased risk for relapse, and who wish to learn efficacious prevention skills. Given the long-term adverse consequences of untreated perinatal mood episodes for women and their children; low rates of treatment seeking; and concerns associated with pharmacological treatments, the development of a viable psychosocial intervention may have significant benefits for women, children, and society at large.

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 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Eligible women for this study
  • will be planning pregnancy within the forthcoming year, are pregnant, or within one year postpartum
  • will meet criteria for at least one prior Diagnostic and Statistical Manual of Mental Disorders, 4th Ed., Revised major depressive, hypomanic, or manic episode,
  • has met lifetime Diagnostic and Statistical Manual criteria for bipolar I, II, or not otherwise specified disorder or major depressive disorder;
  • are available for group intervention scheduled meetings,
  • speak and read English,
  • age 18 or older.

排除标准

  • schizophrenia, schizoaffective disorder, or current psychosis;
  • organic mental disorder or pervasive developmental delay
  • current eating disorder;
  • current substance abuse or dependence;
  • imminent suicide or homicide risk;
  • history of violent behaviors toward others;
  • current thoughts of harm to an unborn or recently born child; or
  • currently experiencing a mood episode that meets full Diagnostic and Statistical Manual criteria.

结局指标

主要结局

Change in Self-Rated Depression from Pretreatment to Post-treatment to 1- and 6- months post-treatment

时间窗: Pretreatment to Post-treatment (2 months), 1 month post-treatment, and 6 months post-treatment

The primary outcome is self-rated Beck Depression Inventory, II scores at the pretreatment baseline and again at Post-treatment (8 weeks), and then at 1- month and 6-months post-treatment

次要结局

  • Change in Observer-Rated Depression from Pretreatment to Post-treatment to 1- and 6 months post-treatment(Pretrreatment to Post-treatment; one-month post-treatment and 6-months post-treatment)
  • Changes in Anxiety Symptoms(Pretreatment to 6 months post-treatment)
  • Changes in mania symptoms(Pretreatment to 6 months post-treatment)

研究者

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

David J. Miklowitz, Ph.D.

Professor of Psychiatry

University of California, Los Angeles

研究点 (4)

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