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E-health Cognitive Behavioral Therapy in Women Treated by in Vitro Fertilization (IVF)

Primary Purpose

Depression, Anxiety, Infertility

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Digicoach
Sponsored by
University Medical Center Nijmegen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depression focused on measuring in vitro fertilization, e-health, cognitive behavioral therapy, psychosocial risk profile, emotional maladjustment

Eligibility Criteria

18 Years - 42 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • women screened as 'at risk' for emotional maladjustment after In vitro fertilization (IVF) by a screening tool

Exclusion Criteria:

  • impossibility to use Internet
  • impossibility to write or read the Dutch language
  • high screening scores requiring immediate intervention

Sites / Locations

  • Radboud University Nijmegen Medical Centre, department of obstetrics and gynecology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Digicoach

Control

Arm Description

Women randomized in the Digicoach group will be treated by the Digicoach therapy. Digicoach is an e-health cognitive behavioral therapy with 4-12 weekly sessions especially developed for in vitro fertilization (IVF) women. Digicoach is facilitated by an e-therapist. The investment for the weekly home work assignments is about one and a half hour. Digicoach consist of different modules (e.g. stress reduction, acceptance). Digicoach starts before the hormonal down regulation as the start of the IVF procedure and ends three weeks after the pregnancy test.

Women in the control group will get the usual treatment, there will be no additional intervention.

Outcomes

Primary Outcome Measures

scores on anxiety and depression
anxiety and depression rates three weeks after an unsuccessful IVF cycle, scored by the Hospitality Anxiety Depression Scale (HADS), we also measure the scores during the IVF cycle and three months after the IVF cycle.

Secondary Outcome Measures

(para)medical consumption
by questionnaires
process evaluation of the webbased cognitive behavioral therapy (CBT)
process evaluation will be investigated by the individual's use of Digicoach (page view registration) and the patients' and professionals' experiences with Digicoach (questionnaires).
productivity loss
by questionnaires
health related quality of life
by questionnaire using FertiQol (Fertility Quality of Life questionnaire), a validated screening instrument measuring quality of life related to fertility treatment
IVF outcome
by questionnaire and medical record viewing
economical evaluation
cost effectiveness of the e-health cognitive behavioral therapy

Full Information

First Posted
January 21, 2011
Last Updated
November 14, 2013
Sponsor
University Medical Center Nijmegen
Collaborators
Stichting Nuts Ohra
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1. Study Identification

Unique Protocol Identification Number
NCT01283607
Brief Title
E-health Cognitive Behavioral Therapy in Women Treated by in Vitro Fertilization (IVF)
Official Title
Treatment of Depression and Anxiety by an E-health Cognitive Behavioral Therapy (Digicoach) in Women Treated by in Vitro Fertilization (IVF)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Center Nijmegen
Collaborators
Stichting Nuts Ohra

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Yearly, 15,000 Dutch in vitro fertilization (IVF) cycles are performed for subfertility with a pregnancy rate of 26%. A failed cycle has great emotional impact; 20-25% of the women has relevant forms of depression/anxiety even after 6 months. For such maladjustment a risk profile has been identified and translated into a screening tool. Identification of women at risk enables a timely and tailored (individual's needs) cognitive behavioral therapy (CBT), which reduces more serious maladjustment and corresponding costs. Aim: To investigate the effectiveness of an e-health CBT (digital coaching, Digicoach) in women ongoing IVF and having been screened at risk. Design: A single-centered randomised controlled trial comparing Digicoach (intervention) with standard care (control). Digicoach: an e-health CBT with 4-12 weekly sessions starting before an IVF cycle, following a woman's IVF course and covering in modules the main problems: depressed mood, anxiety, strong focus on child wish and acceptance. Main outcome measures: anxiety and depression occurrence rate 3 weeks after an unsuccessful IVF cycle. Secondary outcome measures: 1. (para)medical consumption, 2. quality of life, 3. productivity loss and 4. IVF outcome. Data are collected by questionnaires, diaries, medical record audit and page view registrations. Process evaluation: Individual's use (e.g. module progress, completion rate), experiences, (e.g. satisfaction and usability) and potential barriers for implementation are evaluated. Economic evaluation: studied during the Digicoach exposures from a societal perspective. Incremental costs (costs/%avoidance of depression/anxiety) are determined by comparing both study groups. Power/data analysis: To detect a 29% difference in the depression/anxiety occurrence rates (alfa=0.05 and beta=0.80) 58 unpregnant IVF women are evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety, Infertility
Keywords
in vitro fertilization, e-health, cognitive behavioral therapy, psychosocial risk profile, emotional maladjustment

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Digicoach
Arm Type
Active Comparator
Arm Description
Women randomized in the Digicoach group will be treated by the Digicoach therapy. Digicoach is an e-health cognitive behavioral therapy with 4-12 weekly sessions especially developed for in vitro fertilization (IVF) women. Digicoach is facilitated by an e-therapist. The investment for the weekly home work assignments is about one and a half hour. Digicoach consist of different modules (e.g. stress reduction, acceptance). Digicoach starts before the hormonal down regulation as the start of the IVF procedure and ends three weeks after the pregnancy test.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Women in the control group will get the usual treatment, there will be no additional intervention.
Intervention Type
Behavioral
Intervention Name(s)
Digicoach
Intervention Description
Digicoach is an e-health cognitive behavioral therapy with 4-12 weekly sessions especially developed for IVF women. Digicoach is facilitated by an e-therapist. The investment for the weekly home work assignments is about one and a half hour. Digicoach consist of different modules (e.g. stress reduction, acceptance). Digicoach starts before the hormonal down regulation as the start of the IVF procedure and ends three weeks after the pregnancy test.
Primary Outcome Measure Information:
Title
scores on anxiety and depression
Description
anxiety and depression rates three weeks after an unsuccessful IVF cycle, scored by the Hospitality Anxiety Depression Scale (HADS), we also measure the scores during the IVF cycle and three months after the IVF cycle.
Time Frame
three months after an in vitro fertilization (IVF) cycle.
Secondary Outcome Measure Information:
Title
(para)medical consumption
Description
by questionnaires
Time Frame
during the IVF cycle
Title
process evaluation of the webbased cognitive behavioral therapy (CBT)
Description
process evaluation will be investigated by the individual's use of Digicoach (page view registration) and the patients' and professionals' experiences with Digicoach (questionnaires).
Time Frame
after the IVF cycle
Title
productivity loss
Description
by questionnaires
Time Frame
during the IVF cycle
Title
health related quality of life
Description
by questionnaire using FertiQol (Fertility Quality of Life questionnaire), a validated screening instrument measuring quality of life related to fertility treatment
Time Frame
before, during, three weeks and three months after the IVF cycle
Title
IVF outcome
Description
by questionnaire and medical record viewing
Time Frame
three weeks after the IVF cycle
Title
economical evaluation
Description
cost effectiveness of the e-health cognitive behavioral therapy
Time Frame
three months after the IVF cycle

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: women screened as 'at risk' for emotional maladjustment after In vitro fertilization (IVF) by a screening tool Exclusion Criteria: impossibility to use Internet impossibility to write or read the Dutch language high screening scores requiring immediate intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jan A Kremer, Ph.D. M.D.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Chris M Verhaak, Ph.D.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Willianne L Nelen, Ph.D. M.D.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Radboud University Nijmegen Medical Centre, department of obstetrics and gynecology
City
Nijmegen
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
15817584
Citation
Verhaak CM, Smeenk JM, van Minnen A, Kremer JA, Kraaimaat FW. A longitudinal, prospective study on emotional adjustment before, during and after consecutive fertility treatment cycles. Hum Reprod. 2005 Aug;20(8):2253-60. doi: 10.1093/humrep/dei015. Epub 2005 Apr 7.
Results Reference
background
PubMed Identifier
20228392
Citation
Verhaak CM, Lintsen AM, Evers AW, Braat DD. Who is at risk of emotional problems and how do you know? Screening of women going for IVF treatment. Hum Reprod. 2010 May;25(5):1234-40. doi: 10.1093/humrep/deq054. Epub 2010 Mar 13.
Results Reference
background
PubMed Identifier
26965429
Citation
van Dongen AJ, Nelen WL, IntHout J, Kremer JA, Verhaak CM. e-Therapy to reduce emotional distress in women undergoing assisted reproductive technology (ART): a feasibility randomized controlled trial. Hum Reprod. 2016 May;31(5):1046-57. doi: 10.1093/humrep/dew040. Epub 2016 Mar 10.
Results Reference
derived

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E-health Cognitive Behavioral Therapy in Women Treated by in Vitro Fertilization (IVF)

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