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E-health Intervention for Improving Mental Health During Pregnancy Using Virtual Reality

Primary Purpose

Anxiety Depression, Pregnancy Related

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Immersive Virtual Reality (IVR)
Sponsored by
Hospital Mutua de Terrassa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Depression focused on measuring Pregnancy, Anxiety, Depression, Virtual Reality, Midwifery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: All women who control their pregnancy in the primary care centers of the Sexual and Reproductive Health Care (ASSIR; Atención a la Salut Sexual i Reproductiva) of Mutua Terrassa, Barcelona (Spain) The women must present a positive value in the mental health screening performed at the beginning of the pregnancy (weeks 12-14 of gestation). Verbal and written literacy understanding of Spanish ≥18 years old. Exclusion Criteria: Women with diagnosed psychiatric pathology who are already being followed by the mental health team Women victims of gender-based violence who tested positive in the partner violence screen

Sites / Locations

  • Fundació Assitencial Mutua TerrassaRecruiting
  • Hospital Universitari Mútua TerrassaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Virtual Reality

Routine care

Arm Description

The intervention will consist of an Immersive Virtual Reality (IVR) application with virtual reality goggles Oculus GO, to reduce anxiety during pregnancy. This application lasts 14 minutes by the use of mindfulness techniques based on breathing, mindfulness and passive muscle relaxation.

The control group will receive the usual follow-up pregnancy monitoring, without the e-health intervention.

Outcomes

Primary Outcome Measures

Depression in pregnand women
Edingburg depression Scale (>9)
Anxiety in pregnand women
State trait anxiety inventory (>75%)

Secondary Outcome Measures

Symptom checklist -90-R
Anxiety symptoms (>60%)

Full Information

First Posted
February 8, 2023
Last Updated
February 23, 2023
Sponsor
Hospital Mutua de Terrassa
Collaborators
University of Barcelona
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1. Study Identification

Unique Protocol Identification Number
NCT05756205
Brief Title
E-health Intervention for Improving Mental Health During Pregnancy Using Virtual Reality
Official Title
A Randomized Controlled Low-intensity E-health Intervention by Midwives for Improving Mental Health in Pregnant Women
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2022 (Actual)
Primary Completion Date
February 1, 2024 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Mutua de Terrassa
Collaborators
University of Barcelona

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
Pregnancy-related anxiety and depression has received considerable attention worldwide. Mental health problems in pregnant women already since early weeks of gestation may have important consequences for the fetus. Current literature recommends the use of interventions based on new technologies for the treatment of mood disorders, already during the prenatal period. Adult pregnant women (weeks 12-14 of gestation) will be recruited and screened from different primary care centres in Catalonia, Spain. Women who pass the initial mental screening will be randomly allocated to the relaxation virtual reality intervention or control group. The intervention aims to improve mental state of pregnant women during pregnancy, work through breathing, mindfulness and muscle relaxation techniques.
Detailed Description
Background: Pregnancy-related anxiety and depression has received considerable attention worldwide. Mental health problems in pregnant women already since early weeks of gestation may have important consequences for the fetus. The necessity for more effective health care pathways, including some early interventions that reduce the overall burden of the childbearing situation, appears a key factor for a successful birth and care of the baby. The few studies focalized in interventions, are focused on delivery and post-partum, without taking into account the whole maternity process. Current literature recommends the use of interventions based on new technologies for the treatment of mood disorders, already during the prenatal period. There have been scarce well-designed intervention studies that test technological low-intensity interventions by midwives to address pregnant women's mental health, diminishing anxiety and depression during pregnancy. Methods/design: Adult pregnant women (weeks 12-14 of gestation) will be recruited and screened from different primary care centres in Catalonia, Spain. Women who pass the initial mental screening will be randomly allocated to the relaxation virtual reality intervention or control group. The intervention aims to improve mental state of pregnant women during pregnancy, work through breathing, mindfulness and muscle relaxation techniques. Women in the control group will receive standard care offered by the public funded maternity services in Catalonia. The primary outcome measures will include the Edinburg Postnatal Depression (EPDS), State Trait Anxiety Inventory (STAI), Symptom Checklist-90 (SCL-90), and the Cambridge Worry Scale (CWS) instruments. Secondary outcome measures will include the Temperament and Character Inventory-Revised (TCI-R) and the Whooley and Generalized Anxiety Disorder-2 (GAD-2) questions. Routinely, pregnancy monitoring measures will also be evaluated. Discussion: This study aims to test the efficacy of a low-intensity, midwife-led e-health intervention based on new technologies to work on women's anxiety and depression during pregnancy. The hypothesis is that that low-intensity mental health intervention during pregnancy, using an e-health (virtual reality) as a support tool, will be effective in reducing of anxiety, depressive symptoms, and improving satisfaction with pregnancy follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Depression, Pregnancy Related
Keywords
Pregnancy, Anxiety, Depression, Virtual Reality, Midwifery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This will be a two-arm prospective, randomized, parallel-controlled clinical trial. 150 women will be recruited and screened during their pregnancy
Masking
Participant
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual Reality
Arm Type
Experimental
Arm Description
The intervention will consist of an Immersive Virtual Reality (IVR) application with virtual reality goggles Oculus GO, to reduce anxiety during pregnancy. This application lasts 14 minutes by the use of mindfulness techniques based on breathing, mindfulness and passive muscle relaxation.
Arm Title
Routine care
Arm Type
No Intervention
Arm Description
The control group will receive the usual follow-up pregnancy monitoring, without the e-health intervention.
Intervention Type
Device
Intervention Name(s)
Immersive Virtual Reality (IVR)
Intervention Description
The intervention will consist of an Immersive Virtual Reality (IVR) application with virtual reality goggles Oculus GO, to reduce anxiety during pregnancy. This application lasts 14 minutes by the use of mindfulness techniques based on breathing, mindfulness and passive muscle relaxation. It consists of three modules that can be chosen completely or separately. The aspects that conform this intervention will be: information about, the most common perinatal mental health problems, exercises based on attention to breathing (mindfulness-relaxation), 6 weeks of duration, for 14 minutes a day, knowledge from involved personnel of the number of times the woman has connected and the time she has done the exercise, satisfaction questions to pregnant women after pregnancy, alerts to notify the principal investigator if there is a problem with e-health, and, finally, an email address to contact the principal investigator.
Primary Outcome Measure Information:
Title
Depression in pregnand women
Description
Edingburg depression Scale (>9)
Time Frame
6 weeks
Title
Anxiety in pregnand women
Description
State trait anxiety inventory (>75%)
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Symptom checklist -90-R
Description
Anxiety symptoms (>60%)
Time Frame
6 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All women who control their pregnancy in the primary care centers of the Sexual and Reproductive Health Care (ASSIR; Atención a la Salut Sexual i Reproductiva) of Mutua Terrassa, Barcelona (Spain) The women must present a positive value in the mental health screening performed at the beginning of the pregnancy (weeks 12-14 of gestation). Verbal and written literacy understanding of Spanish ≥18 years old. Exclusion Criteria: Women with diagnosed psychiatric pathology who are already being followed by the mental health team Women victims of gender-based violence who tested positive in the partner violence screen
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marta Jimenez Barragan, RN, RM
Phone
+34937365050
Ext
41707
Email
mjimenezb@mutuaterrassa.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Pilar Arcusa
Phone
+34937365050
Email
parcusa@mutuaterrassa.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marta Jimenez Barragan, RN, RM
Organizational Affiliation
Fundació Assistencial Mutua Terrassa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fundació Assitencial Mutua Terrassa
City
Terrassa
State/Province
Barcelona
ZIP/Postal Code
08221
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marta Jimenez-Barragan, MA
Phone
+34686698651
Email
mjimenezb@mutuaterrassa.cat
First Name & Middle Initial & Last Name & Degree
Marta Jimenez Barragan, MA
First Name & Middle Initial & Last Name & Degree
Olga Monistrol Ruano, PhD
First Name & Middle Initial & Last Name & Degree
Gemma Falguera Puig, PhD
First Name & Middle Initial & Last Name & Degree
Amparo del Pino, PhD
Facility Name
Hospital Universitari Mútua Terrassa
City
Terrassa
State/Province
Barcelona
ZIP/Postal Code
08221
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marta Jimenez-Barragan, MA
Phone
+34686698651
Email
mjimenezb@mutuaterrassa.cat
First Name & Middle Initial & Last Name & Degree
Marta Jimenez Barragan, MA
First Name & Middle Initial & Last Name & Degree
Olga Monistrol Ruano, PhD
First Name & Middle Initial & Last Name & Degree
Gemma Falguera Puig, PhD
First Name & Middle Initial & Last Name & Degree
Amparo del Pino, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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E-health Intervention for Improving Mental Health During Pregnancy Using Virtual Reality

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