Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05533138

Internet CBT for Antenatal Depression

Led by Karolinska Institutet · Updated on 2024-06-25

415

Participants Needed

1

Research Sites

357 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

R

Region Stockholm

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Internet CBT for Antenatal Depression

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Mild to moderate major depression
  • Pregnant at treatment start
  • Regular contact with maternity mental health clinic
  • Older than 18 years
  • Able to start treatment between gestational week 8 and week 30
  • Stable medication for depression or other psychiatric conditions for at least 3 weeks
  • Able to participate throughout treatment and have internet and mobile phone access during treatment
  • Able to understand spoken and written Swedish
Not Eligible

You will not qualify if you...

  • Montgomery-�c5sberg Depression Rating Scale score below 15 or above 35
  • High risk of self harm or suicide
  • Psychiatric comorbidity, disability, somatic disorder, or pregnancy complications that prevent treatment participation or pose fetal risk
  • Ongoing psychological treatment with similar content

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Psychiatry Southwest, Department of CL Psychiatry & Internetpsychiatry

Stockholm, Sweden, 141 86

Actively Recruiting

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Research Team

M

Marie Bendix, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

4

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