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临床试验/NCT05533138
NCT05533138招募中不适用

Guided-internet Cognitive Behavioral Therapy for Antenatal Depression - Treatment Effects, Assessment Modalities and Extra Support.

Karolinska Institutet2 个研究点 分布在 1 个国家目标入组 415 人开始时间: 2021年2月25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
415
试验地点
2
主要终点
Change in Montgomery Asberg Depression Rating Scale, self-rating version (MADRS-S)

研究概览

简要总结

Pregnant women in pregnancy week 8-29 screening positive for antenatal depression will be randomized to either choose or to be allotted by chance to different forms of diagnostic assessment; i.e. telephone, video or face-to-face assessment.

Those diagnosed with mild to moderate major depression will then be randomized to treatment with therapist-guided Internet-delivered Cognitive Behavioral Therapy (ICBT) adapted for women suffering from antenatal depression or to the same treatment with addition of up to three contacts with extra support by a midwife or experienced perinatal mental health nurse.

The primary aim is to assess whether extrasupport in addition to internet-guided pregnancy adapted ICBT decreases depressive symptoms more than internet-guided pregnancy adapted ICBT only. Secondary aims include effects of extrasupport and assessment mode on treatment satisfaction, fidelity and credibility.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Participants are blinded for allocation to perinatal extra support in addition to therapist-guided internet CBT treatment.

Outcome is assessed by an independent assessor who is blind for whether patient chose or was allocated to assessment modality and whether patient received extra-support or not.

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

  • Mild to moderate major depression
  • Pregnant at treatment start
  • Regular contact with maternity mental health clinic
  • > 18 years old
  • Being able to start the treatment earliest in gestational week 8 and latest in gestational week 30
  • Stable medication for depression and/or other psychiatric conditions for at least 3 weeks.
  • Being able to participate in the treatment during the treatment time and having access to and being able to use the internet and mobile phone during the treatment time
  • Being able to understand the Swedish language orally and in writing

排除标准

  • Montgomery-Åsberg Depression Rating Scale-Self report version (MADRS-S) score below 15 (symptoms of depression to low) or above 35 (severe depression)
  • High risk of self harm or suicide (based on semi-structured clinical suicide risk assessment)
  • Psychiatric comorbidity, disability, somatic disorder, or pregnancy complications that prevent treatment participation or that can be negatively affected or compose a risk for the fetus by treatment participation
  • Ongoing psychological treatment with similar content

结局指标

主要结局

Change in Montgomery Asberg Depression Rating Scale, self-rating version (MADRS-S)

时间窗: Baseline to post-treatment (10 weeks) and to 8-10 weeks post-partum

A 9-item self-rated measure of depression severity that also screens for suicidality (Montgomery \& Asberg, 1979). Scores range from 0 to 54 points with 13-19 points indicating mild depression, 20-34 points indicating moderate depression and 35-54 points indicating severe depression

次要结局

  • Remission of major depression (DSM-5)(8-10 weeks postpartum.)
  • Change in Work and Social Adjustment Scale (WSAS)(Baseline to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in Euroqol (EQ-5D-5L)(Screening to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in Prenatal Attachment Inventory (PAI)(Screening to post-treatment (10 weeks))
  • Change in Edinburgh Postnatal Depression Scale (EPDS)(Baseline to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in Multidimensional Scale of Perceived Social Support (MSPSS)(Screening to 8-10 weeks post-partum)
  • Change in Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry (TIC-P)(Baseline to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in Clinical Global clinical global improvement (CGI-I)(Post-assessment and post treatment (after week 10).)
  • Change in Generalized Anxiety Disorder-7 (GAD-7)(Screening to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in self-rated Insomnia Severity Index (ISI)(Baseline to post-treatment (10 weeks) and to 8-10 weeks post-partum)
  • Change in Experience of close relationships (ENR)(Screening to 8-10 weeks post-partum)
  • Change in Valentine Scale(Screening to 8-10 weeks post-partum)
  • Change in Fear of birth scale (FOBS)(Screening to post-treatment (after 10 weeks) and to 8-10 weeks post-partum)
  • Change in Clinical Global Impression Severity Scale (CGI-S)(Post-assessment and post treatment (after week 10).)

研究者

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

Marie Bendix

Principal investigator

Karolinska Institutet

研究点 (2)

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