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Willkommen Mutterglück: Online CBT for Pregnant and Postpartum Women With Depression and Anxiety

Primary Purpose

Prenatal Anxiety, Generalized Anxiety, Postpartum Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Online Cognitive Behavioural Therapy
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prenatal Anxiety focused on measuring generalized anxiety disorder, depression, cognitive behavioral therapy, web-based cognitive behavioural therapy, web-based CBT, pregnancy, prenatal depression, prenatal anxiety, postpartum anxiety, postpartum depression

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • pregnant women or women who had given birth in the last year
  • between 18 and 45 years old
  • minor to moderate depression and/or generalised anxiety disorder
  • fluent in German
  • having a computer, laptop or handheld device with internet access

Exclusion Criteria:

  • women with a severe medical disorder or a severe psychological disorder such as psychosis, drug addiction and other substance abuse
  • women taking psychotropic medication
  • women with current suicidality
  • women who are currently receiving psychological treatment for depression or anxiety

Sites / Locations

  • University of Zurich, Department of Psychology - Clinical Psychology and Psychotherapy

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Online Cognitive Behavioural Therapy

Arm Description

Screened participants diagnosed with minor to moderate anxiety and/or depression will receive online CBT therapy (8 interactive sessions) aiming to treat their symptomatology. Each session can be completed at one's own pace.

Outcomes

Primary Outcome Measures

Change of depressive symptoms at four measuring points from baseline to follow up
Measured with Beck's Depression Inventory (BDI)
Change of anxiety symptoms at four measuring points from baseline to follow up
Measured with Beck's Anxiety Inventory (BAI)
Change of severity of depressive symptoms at four measuring points from baseline to follow up
Measured with Patient Health Questionnaire (PHQ) Ranges from 0-27 (0-4=none-minimal; 5-9=mild; 10-14=moderate; 15-19=moderately severe; 20-27=severe)
Change of depression symptoms from baseline until follow-up
Measured with Edinburgh Postnatal Depression Scale (EPDS) Minimum score = 0, maximum score = 30. Cut off value is set at 12/13

Secondary Outcome Measures

Participant's satisfaction with the program and it's usability
This is reported with open-ended questions about satisfaction with the program and with self-report measure that assesses the patient's attitude on the overall usability to the program (System Usability Scale, SUS) The scores range from 0-100. It is agreed that score above 68 would be considered above average, whilst scores below 68 would be considered below average.
Program's evaluation of feasibility with prenatal and postpartum women
This is reported with user engagement, such as duration spent on web-intervention-site and number of log-ins into the intervention. These different measures should give an overview over how the participants perceive and evaluate the program and how they rate its feasibility.

Full Information

First Posted
April 11, 2018
Last Updated
November 28, 2019
Sponsor
University of Zurich
Collaborators
Ambulatorium für kognitive Verhaltenstherapie und Verhaltensmedizin - UZH, Lamprecht AG
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1. Study Identification

Unique Protocol Identification Number
NCT04183946
Brief Title
Willkommen Mutterglück: Online CBT for Pregnant and Postpartum Women With Depression and Anxiety
Official Title
Willkommen Mutterglück: A Controlled Trial of Internet Based Cognitive Behavioural Therapy (CBT) for Pregnant and Postpartum Women With Depression and Anxiety
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2020 (Anticipated)
Primary Completion Date
January 2022 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
Ambulatorium für kognitive Verhaltenstherapie und Verhaltensmedizin - UZH, Lamprecht AG

4. Oversight

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

5. Study Description

Brief Summary
This intervention study aims to evaluate the effectivity of web-based cognitive therapy in reducing depression and anxiety in pregnant and postpartum women. Moreover, it aims to assess treatment feasibility and usability of the treatment in the same population. After an initial screening to determine the eligibility to participate, all participants fulfilling the inclusion criteria will receive their personal access login in order to start the intervention.
Detailed Description
Introduction: Evidence has shown that 10-20% of women suffer from depression during gestation and after birth (Barnes, 2014; Zaers, Waschke & Ehlert, 2008), while 7-21% present clinically relevant anxiety levels prenatally and following delivery (Grant, McMahon & Austin, 2008). Previous research has shown that if a woman has high levels of depression or anxiety during pregnancy her child is at about double the risk for attention deficit hyperactivity disorder, conduct disorders, difficult temperament and behavioural problems later in development (O'Connor et al., 2002). High levels of prenatal anxiety and depression are frequently comorbid (Amiel Castro et al., 2016) and together with stress have been shown to increase risk for preterm delivery, low birth weight, impaired memory and cognitive function among others (Talge, Neal & Glover, 2007). The important biopsychological changes brought by the perinatal period (Ehlert et al., 1990) require constant attention from health workers since they carry relevant risk factors for the mother's health and for the infant's neurodevelopment (Schetter & Tanner, 2012). Current depression interventions are not deliverable to a large number of individuals (Andersson & Titov, 2014). As seen worldwide, the difficulty to receive proper treatment for depression and anxiety is also evident in Switzerland. About half of people suffering from depression and/or anxiety are not diagnosed and consequently do not receive any sort of psychological or pharmaceutical treatment (Baer et al., 2013). The internet offers an opportunity to deliver tailored interventions such as those based on cognitive behavioural therapy (CBT) to a large audience, cost-effectively, while preserving intervention fidelity and anonymity. The potential effectiveness of the internet is indicated by research demonstrating the successful delivery of CBT by computer and the use of the internet in the delivery of CBT treatment (Andrews et al., 2010). Recent reviews of the evidence have recommended further research that includes long-term follow-up and evaluation of novel treatment modalities such as the ones provided by internet (Dennis et al., 2012). Moreover, online interventions have been widely explored for different mental health problems (Sourander et al., 2016) suggesting its potential to increase access to and uptake of services for women with a perinatal disorder. The "Willkommen Mutterglück" program is an 8-session, interactive web-based cognitive behavioural intervention for prenatal and postpartum depression and anxiety. Given the prevalence rates of depression and anxiety during the perinatal period and the rates of untreated patients, it is important to propose treatment alternatives. Several reviews on the area emphasize that topics such as type and amount of CBT material incorporated to the program, length and frequency of sessions, amount of homework given and frequency of minimal therapist intervention are related to effectivity of online interventions and warrant further research. Also, it is unclear whether therapist contact focusing on motivation to complete the program is more effective than non-therapist contact in the treatment of the disorders. Therefore, routine use of this online intervention for depressed and anxious mothers is only possible if this program/the effects are is scientifically evaluated with biomarkers. The primary goal of this project is to investigate the effectiveness of an online cognitive behavioural intervention specifically tailored to pregnant and postpartum women in reducing depression and anxiety symptoms. The secondary goal is to assess the feasibility and usability of this intervention on the treatment of depression and anxiety. Method: The investigators aim to recruit N=300 patients from the first gestational trimester to one year after birth. The eight intervention sessions are administered online via audio and video images. The participants are asked to actively participate during their weekly session through exercises and quizzes. Each weekly session has a duration of 40-50 minutes. A SCID interview for screening will be conducted by a trained clinical psychologist and an experienced psychiatrist from a trusted Outpatient Clinic will verify the diagnosis. Screened and consented participants will then fill in some baseline questionnaires, provide sociodemographic information and receive a private login to access the program in order to start the intervention. After completing the second, fourth and eight intervention session participants will fill in the same and other psychological questionnaires. Throughout the intervention, the investigators will frequently monitor patient's progress and potential worsening of depressive and anxiety symptoms. The investigating team will be particularly attentive to suicidal ideation. Patients identified with suicidal thoughts will be immediately contacted by the study team and advised to an appropriate course of action. Moreover, in all online pages of the "Willkommen Mutterglück" intervention participants can find an SOS button, providing contact information of emergency psychiatric units and suicide hotlines. During the online intervention, participants will be contacted three times by telephone by coaches (psychotherapists in training). The content of coaching calls will adhere to a manualized script with defined aims of reviewing patient's progress, problem solving, encourage skill acquisition and introducing topics in upcoming sessions. Coaches will be trained with a specific manual developed by the investigation team. Training for the coaching role will involve reading the coach manual, knowledge of the program content and explanations from a senior researcher about the role and the tasks involved. Importance: In view of the substantial challenge posed by the global burden of depression and anxiety, it is relevant to investigate how a disorder, which is a leading cause of disability worldwide, may affect mothers and mothers-to-be. Pregnant and postpartum women are often reluctant to take medication due to concerns about breast milk transmission or potential side effects. Therefore, non-pharmacologic interventions are a desirable first-line treatment option for this population. Given that despite frequent interactions with health workers during pregnancy and postpartum, rates of treatment for perinatal disorders are low, online therapy may be a viable treatment alternative. The planned longitudinal study is relevant in investigating the feasibility of an interactive CBT online intervention including minimal psychotherapist involvement and tailored specifically for this population. At the same time, it assesses the effectiveness of it in reducing depression and/or anxiety in pregnant and postpartum women. The results will help to better understand if an intervention (online program with coaching) with few barriers (e.g. no travel, no childcare costs, reduced stigma), may serve as an effective treatment option for pregnant and postpartum women who experience significant stigma or are underresourced in their local community.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prenatal Anxiety, Generalized Anxiety, Postpartum Depression, Major Depressive Disorder
Keywords
generalized anxiety disorder, depression, cognitive behavioral therapy, web-based cognitive behavioural therapy, web-based CBT, pregnancy, prenatal depression, prenatal anxiety, postpartum anxiety, postpartum depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Online Cognitive Behavioural Therapy
Arm Type
Other
Arm Description
Screened participants diagnosed with minor to moderate anxiety and/or depression will receive online CBT therapy (8 interactive sessions) aiming to treat their symptomatology. Each session can be completed at one's own pace.
Intervention Type
Behavioral
Intervention Name(s)
Online Cognitive Behavioural Therapy
Other Intervention Name(s)
Willkommen Mutterglück: Online CBT program for pre-postnatal depression & anxiety
Intervention Description
The "Willkommen Mutterglück" program is an 8-session, interactive web-based CBT intervention for prenatal and postpartum depression and anxiety. The sessions are administered online via audio and video images. Each weekly session has a duration of 40-50 minutes during which the participants are asked to actively participate through exercises and quizzes. A SCID interview for screening will be conducted by a trained clinical psychologist and an experienced psychiatrist from our outpatient clinic will verify the diagnosis. Screened and consented participants will answer baseline questionnaires, provide sociodemographic information and receive a private login to access the program. After completing the 2nd, 4th and 8th intervention session participants will fill in psychological questionnaires. During the intervention, participants will be contacted three times by telephone by coaches (psychotherapists in training) who follow a manualized script.
Primary Outcome Measure Information:
Title
Change of depressive symptoms at four measuring points from baseline to follow up
Description
Measured with Beck's Depression Inventory (BDI)
Time Frame
At baseline, during week 4, 8, 16 of the intervention and at one month after completing intervention.
Title
Change of anxiety symptoms at four measuring points from baseline to follow up
Description
Measured with Beck's Anxiety Inventory (BAI)
Time Frame
At baseline, during week 4, 8, 16 of the intervention and at one month after completing intervention.
Title
Change of severity of depressive symptoms at four measuring points from baseline to follow up
Description
Measured with Patient Health Questionnaire (PHQ) Ranges from 0-27 (0-4=none-minimal; 5-9=mild; 10-14=moderate; 15-19=moderately severe; 20-27=severe)
Time Frame
At baseline, during week 4, 8, 16 of the intervention and at one month after completing intervention.
Title
Change of depression symptoms from baseline until follow-up
Description
Measured with Edinburgh Postnatal Depression Scale (EPDS) Minimum score = 0, maximum score = 30. Cut off value is set at 12/13
Time Frame
At baseline and during week 16 of the intervention
Secondary Outcome Measure Information:
Title
Participant's satisfaction with the program and it's usability
Description
This is reported with open-ended questions about satisfaction with the program and with self-report measure that assesses the patient's attitude on the overall usability to the program (System Usability Scale, SUS) The scores range from 0-100. It is agreed that score above 68 would be considered above average, whilst scores below 68 would be considered below average.
Time Frame
At week 16 of the intervention
Title
Program's evaluation of feasibility with prenatal and postpartum women
Description
This is reported with user engagement, such as duration spent on web-intervention-site and number of log-ins into the intervention. These different measures should give an overview over how the participants perceive and evaluate the program and how they rate its feasibility.
Time Frame
From baseline until 1 month follow-up of the intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: pregnant women or women who had given birth in the last year between 18 and 45 years old minor to moderate depression and/or generalised anxiety disorder fluent in German having a computer, laptop or handheld device with internet access Exclusion Criteria: women with a severe medical disorder or a severe psychological disorder such as psychosis, drug addiction and other substance abuse women taking psychotropic medication women with current suicidality women who are currently receiving psychological treatment for depression or anxiety
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rita Amiel Castro, Dr. phil.
Phone
+41 44 635 73 42
Email
r.castro@psychologie.uzh.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Ulrike Ehlert, Prof. Dr.
Phone
+41 44 635 73 50
Email
u.ehlert@psychologie.uzh.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ulrike Ehlert, Prof. Dr.
Organizational Affiliation
University of Zurich, Department of Psychology - Clinical Psychology and Psychotherapy
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rita Amiel Castro, Dr. phil.
Organizational Affiliation
University of Zurich, Department of Psychology - Clinical Psychology and Psychotherapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Zurich, Department of Psychology - Clinical Psychology and Psychotherapy
City
Zürich
ZIP/Postal Code
8050
Country
Switzerland
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rita Amiel Castro, Dr. phil.
Phone
+41 44 635 73 42
Email
r.castro@psychologie.uzh.ch

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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28540597
Citation
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Links:
URL
http://www.ichbinschwanger.ch
Description
Pregnancy related research by the University of Zurich

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Willkommen Mutterglück: Online CBT for Pregnant and Postpartum Women With Depression and Anxiety

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