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Keeping Well:Online Cognitive Behavioral Therapy (CBT) for Pregnant Women With Depressive Symptoms (OnCBTDep)

Primary Purpose

Anxiety, Mental Disorders, Postpartum Depression

Status
Withdrawn
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Online Cognitive Behavioral Therapy (CBT)
Treatment as usual
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety focused on measuring Pregnancy, symptoms of depression, anxiety, online CBT therapy, treatment as usual, maternal bonding, postnatal period

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • To be pregnant
  • Less than 20 weeks gestation,
  • To have symptoms of depression (EPDS between 12-22),
  • To be computer literate,
  • To have an online computer at home,
  • English speaking and writing,
  • Not being in psychiatric or psychological treatment,
  • Not having a twin pregnancy,
  • Not having undertaken an IVF (In vitro fertilization) procedure,
  • Not having the psychiatric problems (based on the patient's notes): psychosis, addiction, history of bipolar disorder, suicidality and other psychiatric diagnoses that do not fall into the affective disorders and/or anxiety disorders spectrum.

Exclusion Criteria:

  • Not pregnant
  • Having severe symptoms of depression (EPDS above 22),
  • Computer illiteracy,
  • No access to the internet,
  • Not speaking or reading English,
  • Already being in psychiatric or psychological treatment,
  • Twin pregnancy,
  • Having a medical disorder of pregnancy (including abnormal foetus),
  • Having undertaken an IVF (In vitro fertilization) procedure,
  • Psychiatric factors based on patient's notes: psychosis, addiction, history of bipolar disorder, suicidality and other psychiatric diagnoses that do not fall into the affective disorders and/or anxiety disorders spectrum.
  • After birth for baby data: baby born below 35 weeks, baby with any severe disorders. Mothers will continue to be treated if they want to.

Sites / Locations

  • Queen Charlotte's and Chelsea Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Treatment as usual (TAU)

Online Cognitive Behavioral Therapy

Arm Description

Patients randomized to the treatment as usual arm will follow advice by their GP(general practitioner), mental health midwife or perinatal psychiatric team concerning treatment.

CBT treatment: Patients randomized to the online treatment will have, in total, 10 real time individual sessions of 40min each, starting at the 20-23rd gestational week and lasting until 6 weeks postpartum. The therapy will be delivered every two weeks, with a break from the 36th gestational week until the 4th week postpartum.

Outcomes

Primary Outcome Measures

Changes in the Edinburgh Postnatal Depression Scale (EPDS)scores from 20 weeks antenatal to 10 weeks postnatal
The primary outcome will be the change in the EPDS scores from before to after intervention in the Cognitive Behavioral Therapy(CBT) online group compared with treatment as usual (TAU) conditions.

Secondary Outcome Measures

Compliance and dropout rates from 20 weeks antenatal to 4 weeks postnatal
Secondary outcome will be to assess the compliance and drop out rates in the CBT and TAU group
Changes in anxiety scores from 20 weeks antenatal to 10 weeks postnatal
Secondary outcome will be the changes in anxiety scores in the CBT and TAU group
Changes in bonding scores at 10 weeks postnatal
Secondary outcome will to check the differences in the bonding scores in the CBT and TAU group

Full Information

First Posted
July 2, 2013
Last Updated
June 21, 2022
Sponsor
Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT01909167
Brief Title
Keeping Well:Online Cognitive Behavioral Therapy (CBT) for Pregnant Women With Depressive Symptoms
Acronym
OnCBTDep
Official Title
A Randomized Controlled Trial of Internet Based Cognitive Behavioural Therapy (CBT) Versus Treatment as Usual (TAU) for Pregnant Women With Symptoms of Depression
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Withdrawn
Why Stopped
CI had other commitments
Study Start Date
June 1, 2020 (Anticipated)
Primary Completion Date
June 1, 2021 (Anticipated)
Study Completion Date
July 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Most depression during pregnancy is undetected and untreated although it is known to be harmful both to the woman herself and her future child. When these mental disorders are detected, psychotherapies remain difficult to access, especially in primary care, despite being effective.Also, prenatal depression is known to be a strong risk factor for postnatal depression and may prejudice the mother-infant relationship. This leads us to the following question: Will individual Cognitive Behavioral Therapy (CBT) delivered online be a more effective treatment for symptoms of depression in pregnant women, than treatment as usual (TAU)? The proposed randomized controlled trial aims at evaluating the efficacy of internet based cognitive behavioural therapy(CBT) delivered individually via "skype", using video and audio resources, by a fully trained psychotherapist, compared to treatment as usual, in women suffering from symptoms of depression in pregnancy. Hypothesis The internet based interventions will be more effective at reducing symptoms of depression in pregnant women than treatment as usual, in terms of rates of diagnoses and levels of self rated symptoms of depression.
Detailed Description
In the last hundred years there has been a great improvement in the physical care of pregnant women, with a corresponding decline in morbidity and mortality for both mother and child. This same is not true of their psychological and psychiatric care in pregnancy, and this is arguably one of the most important unmet aspects of current obstetrics. Previous research has shown that if a mother has high levels of depression or anxiety during pregnancy, including in later gestation,her child is at about double the risk for ADHD(attention deficit hyperactivity disorder), conduct disorder and emotional problems later in development, as well as increased risk for cognitive delay. Prenatal stress, depression and anxiety contribute an estimated 10-15% of the variance in these outcomes. High levels of antenatal anxiety and depression are frequently co-morbid and have been shown to increase risk for preterm delivery, low birth weight, as well as being a major risk factor for postpartum depression and recurrent maternal depression. This in turn, is also associated with increased risk of long-term emotional and behavioral problems in children. Over 80% of pregnant women with depression are currently undiagnosed and untreated. Most women prefer non pharmacological treatments during gestation and NICE(National Institute for Health and Care Excellence) clinical guidelines recommend Cognitive Behavioral Therapy (CBT) for the treatment of these disorders at this time. CBT has been shown to be effective for the treatment of depression in general; however there have been no randomized controlled trials with pregnant women. Since they may respond differently, they need to be studied directly. The most cost effective way of delivering personalized CBT is internet based and it can be offered online, individually and in real time. Computerized CBT programs have been developed to improve accessibility, but are inflexible, difficult to adapt to patient's specific needs and are associated to low rates of adherence. So, due to the real need of more accessible psychological therapies in primary care, it is crucial to investigate the efficacy of relatively low cost therapeutic tools to improve and broaden individual patient care in pregnancy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Mental Disorders, Postpartum Depression, Depressive Symptoms
Keywords
Pregnancy, symptoms of depression, anxiety, online CBT therapy, treatment as usual, maternal bonding, postnatal period

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment as usual (TAU)
Arm Type
Active Comparator
Arm Description
Patients randomized to the treatment as usual arm will follow advice by their GP(general practitioner), mental health midwife or perinatal psychiatric team concerning treatment.
Arm Title
Online Cognitive Behavioral Therapy
Arm Type
Active Comparator
Arm Description
CBT treatment: Patients randomized to the online treatment will have, in total, 10 real time individual sessions of 40min each, starting at the 20-23rd gestational week and lasting until 6 weeks postpartum. The therapy will be delivered every two weeks, with a break from the 36th gestational week until the 4th week postpartum.
Intervention Type
Behavioral
Intervention Name(s)
Online Cognitive Behavioral Therapy (CBT)
Intervention Description
CBT treatment: Patients randomized to the online treatment will have, in total, 10 real time individual sessions of 40min each, starting at the 20-23rd gestational week and lasting until 6 weeks postpartum. The therapy will be delivered every two weeks, with a break from the 36th gestational week until the 4th week postpartum.
Intervention Type
Other
Intervention Name(s)
Treatment as usual
Intervention Description
Patients randomized to the treatment as usual arm will be advised by their GP,perinatal psychiatric team or mental health midwife concerning treatment.
Primary Outcome Measure Information:
Title
Changes in the Edinburgh Postnatal Depression Scale (EPDS)scores from 20 weeks antenatal to 10 weeks postnatal
Description
The primary outcome will be the change in the EPDS scores from before to after intervention in the Cognitive Behavioral Therapy(CBT) online group compared with treatment as usual (TAU) conditions.
Time Frame
Prenatal: 20, 28, 36weeks.Postnatal: 4 and 10 weeks
Secondary Outcome Measure Information:
Title
Compliance and dropout rates from 20 weeks antenatal to 4 weeks postnatal
Description
Secondary outcome will be to assess the compliance and drop out rates in the CBT and TAU group
Time Frame
Prenatal: 20, 28, 36 weeks.Postnatal: 4 and 10 weeks
Title
Changes in anxiety scores from 20 weeks antenatal to 10 weeks postnatal
Description
Secondary outcome will be the changes in anxiety scores in the CBT and TAU group
Time Frame
Prenatal: 20, 28, 36 weeks.Postnatal: 4 and 10 weeks
Title
Changes in bonding scores at 10 weeks postnatal
Description
Secondary outcome will to check the differences in the bonding scores in the CBT and TAU group
Time Frame
Postnatal: 10 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: To be pregnant Less than 20 weeks gestation, To have symptoms of depression (EPDS between 12-22), To be computer literate, To have an online computer at home, English speaking and writing, Not being in psychiatric or psychological treatment, Not having a twin pregnancy, Not having undertaken an IVF (In vitro fertilization) procedure, Not having the psychiatric problems (based on the patient's notes): psychosis, addiction, history of bipolar disorder, suicidality and other psychiatric diagnoses that do not fall into the affective disorders and/or anxiety disorders spectrum. Exclusion Criteria: Not pregnant Having severe symptoms of depression (EPDS above 22), Computer illiteracy, No access to the internet, Not speaking or reading English, Already being in psychiatric or psychological treatment, Twin pregnancy, Having a medical disorder of pregnancy (including abnormal foetus), Having undertaken an IVF (In vitro fertilization) procedure, Psychiatric factors based on patient's notes: psychosis, addiction, history of bipolar disorder, suicidality and other psychiatric diagnoses that do not fall into the affective disorders and/or anxiety disorders spectrum. After birth for baby data: baby born below 35 weeks, baby with any severe disorders. Mothers will continue to be treated if they want to.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martin Kammerer, PhD
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Charlotte's and Chelsea Hospital
City
London
ZIP/Postal Code
W12 0NN
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
16938144
Citation
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Citation
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Citation
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Citation
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Citation
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Results Reference
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Citation
National Institute for Clinical Health Excellence (NICE) (2008). Technology appraisal 97: Computerized cognitive behavioural therapy for depression and anxiety (Review of technology appraisal 51), NICE, London.
Results Reference
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PubMed Identifier
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Citation
Oates MR. Adverse effects of maternal antenatal anxiety on children: causal effect or developmental continuum? Br J Psychiatry. 2002 Jun;180:478-9. doi: 10.1192/bjp.180.6.478. No abstract available.
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Keeping Well:Online Cognitive Behavioral Therapy (CBT) for Pregnant Women With Depressive Symptoms

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