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Feasibility of M-health Version of "What Were We Thinking" Intervention to Promote Maternal Postpartum Mental Health

Primary Purpose

Depression, Postpartum, Anxiety Disorders and Symptoms, Maternal Behavior

Status
Unknown status
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
m-health version of WWWT intervention
Treatment as usual
Sponsored by
Universidad del Desarrollo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Depression, Postpartum focused on measuring Feasibility Studies, Prevention, mHealth

Eligibility Criteria

18 Years - 64 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • First time mothers
  • Adult (18 -64 years old)
  • Having a healthy infant who is 6-8 weeks age
  • Receive medical care in a primary health centers
  • Having access to a mobile phone with instant messaging services (i.e., Whatsapp)
  • Fluent in Spanish

Exclusion Criteria:

  • Severe mental health problem (i.e. schizophrenia, mood disorder with suicidal ideation)
  • Cognitive disability
  • Actual substance abuse
  • High risk for presenting symptoms of depression (EPDS above cut-off score)
  • Severe psychosocial problem (i.e. domestic violence, sexual abuse).

Sites / Locations

  • Primary Health Center San LuisRecruiting
  • Primary Health Center Cardenal Silva HenríquezRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

m-health version of WWWT intervention

TREATMENT AS USUAL

Arm Description

Include: a) Psychoeducational information for understanding and managing infant behavior and on parenting. This information will be delivered through instant messaging service for mobile phones (i.e., Whatsapp) 3 times a week for four-week period. Each module will include a very brief video offering information regarding a specific topic, a proposed personal exercise and the invitation to assess the perceived usefulness of the information received. Some modules include links to external, complementary information from the Chilean Infancy Policy. b) Contact with the program facilitator. It will allow mothers to ask questions that arise from the topics addressed in the psychoeducational videos. The answers seek to promote the understanding and elaboration of the contents, and operate by providing expert support; c) A virtual group meeting.

TAU for children under one year of age include routine health checks by health professionals (nurse or doctor), every month from 0 to 4 months of age, and at 6, 8 and 12 months of age. The objective of the routine health care check is to carry out a comprehensive evaluation of the child's development and growth, guide parents and caregivers regarding child development, health and upbringing of the child. Also, promoting exclusive breastfeeding, healthy mother/child bonding (by detecting relevant alterations in this area) and encouraging paternal participation in upbringing and care of the child. Finally, in the health check-ups at 2 and 6 months of age of the child, Edinburgh Postpartum Depression Scale is used for screening depressive symptoms in mothers. At risk cases are referred for mental health assessment and care.

Outcomes

Primary Outcome Measures

Eligibility rate as feasibility indicator
Proportion of women who meet inclusion criteria compared with the total number of new mothers registered during the recruitment period in each participating primary health center
Recruitment rate as feasibility indicator
Proportion of mothers who accept the invitation to participate in the study respect to those meet eligibility criteria
Percentage of EG participants who receive the 12 psychoeducational modules, who attend the virtual meeting and who -at least- once established contact with the program facilitator
The feasibility to deliver the components of the intervention will be measured in terms of the percentage of participants of the EG who receive the 12 psychoeducational modules, who attend the virtual meeting and who -at least- once established contact with the program facilitator.
Percentage of participants who finished intervention by group as acceptability indicator
Proportion of participants who finished the intervention compared with a number of participant who began intervention in each group
Percentage of participant retention at follow-up by group as acceptability indicator
Proportion of participants who remain in the study at the 12 weeks follow up compared with a number of participant who began intervention in each group

Secondary Outcome Measures

Changes in maternal postnatal symptoms of depression, according to mean scores obtained with the Edinburgh Postnatal Depression Scale (EPDS)
The EPDS is a 10-item, self-report questionnaire used for screening current maternal symptoms of depression using a 4-point scale, total score ranging from 0 to 30 points. This scale has been validated in Chile.
Change in maternal postnatal symptoms of anxiety according to mean scores obtained with the Perinatal Anxiety Screening Scale (PASS)
The PASS is a 31-item, self-report questionnaire assesses maternal perinatal anxiety over the past month. A total score is calculated by adding all items that indicates level of severity: minimal (0-20 points), mild to moderate (21-41 points) and severe (42-93). The PASS includes four subscales, namely general worry and specific fears; perfectionism, control and trauma; social anxiety; and acute anxiety and adjustment.
Changes on perceived social support according to mean scores obtained with the multidimensional perceived social support scale (MSPSS)
The MSPSS is a 12 items self-report scale. It includes 3 subscales on perceived social support in three areas: family, friends and significant. Each item is rated on a 7-point Likert-scale (1 = very strongly disagree; 7 = very strongly agree). Three subscales' scores (range 4 to 28) and a total score (range 12 to 84) are estimated by adding the item scores. It has been translated and validated for the Chilean population.
Change in maternal self-efficacy according to mean scores obtained with the Parental Evaluation Scale (PEE)
The PEE is a 10-items self-report questionnaire to assess satisfaction and self-efficacy feelings about motherhood in women with children ages 0-2 years. Each item is rated on a 11-point scale (0=strongly disagree; 10=strongly agree) and the total score is estimated by adding item scores and then divided by 10

Full Information

First Posted
April 5, 2021
Last Updated
September 29, 2021
Sponsor
Universidad del Desarrollo
Collaborators
Instituto Milenio para Investigación en Depresión y Personalidad, Peñalolén County Corporation, Chile
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1. Study Identification

Unique Protocol Identification Number
NCT04847076
Brief Title
Feasibility of M-health Version of "What Were We Thinking" Intervention to Promote Maternal Postpartum Mental Health
Official Title
Preliminary Evaluation of the Effectiveness of the Intervention And Now What? to Promote Maternal Mental Health in the Postpartum Period in the Primary Health System in Chile.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 3, 2021 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad del Desarrollo
Collaborators
Instituto Milenio para Investigación en Depresión y Personalidad, Peñalolén County Corporation, Chile

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
The purpose of this study is to assess the feasibility, acceptability and preliminary effectiveness of "What Were We Thinking" (WWWT) a psychoeducational intervention -delivered remotely via communication technologies- to prevent symptoms of postpartum depression and anxiety in new mothers; which has been shown to be effective in primary health settings. WWWT was developed in Australia and has been culturally adapted to be used in Chile. The m-health version of the Chilean adaptation of WWWT for the current study includes: Psychoeducational modules on issues relevant to mothers during the post-partum period; contact with the program facilitator through instant messaging services available on mobile phones and a virtual group meeting. This pilot study will use a mixed design. The quantitative component will consist of a before-after design with control group including 90 adult mothers of child aged 6-8 weeks who receive health care in a primary health centers in Santiago, Chile. Mothers will be randomized into the experimental (EG) or control groups (CG) in a rate of 1:1. Both EG and CG will receive usual treatment provided by primary health centers (TAU), and only de EG will receive the m-health adapted version of the WWWT. The qualitative component considers 12 users semi-structured interviews. The maximum variation sampling strategy will be used according to the completion of m-health version of WWWT. An open coding of Grounded Theory will be used to data analysis. The feasibility of m-health version of WWWT intervention will be evaluated in terms of eligibility rates, recruitment rates and reasons for study refusals, feasibility to deliver the three components of the intervention, data attrition and follow-up rates by treatment condition. Their acceptability considers participant completion of the intervention rates, and a qualitative assessment of the users' acceptability of and satisfaction. Secondary outcomes will include changes on maternal levels of depressive and anxiety symptoms, maternal self-efficacy and perceived social support. And differences in mother-infant quality of interaction between intervention and control groups.
Detailed Description
Mental health symptoms are common in new mothers. Despite the availability of effective screening and referral in the primary health system in Chile, very few women access treatment due to diverse barriers (i.e., long waiting lists and insufficient knowledge about postnatal depression and treatment). This highlights the importance of using a preventive approach. Currently in Chile there are no universal preventive interventions, although they are available internationally. Thus, this study seeks to assess if it's feasible and acceptable to offer an alternative intervention that can be delivered remotely by mobile phones, to support women in the early postpartum period by promoting confidence and reducing distress in first time mothers. By doing so, it will increase the number of available interventions to promote and prevent children´s early adverse experiences related to maternal mental health problems. This study accounts for the feasibility, acceptability and preliminary effectiveness of "What Were We Thinking" (WWWT) a psychoeducational intervention -delivered remotely via communication technologies- to prevent symptoms of postpartum depression and anxiety in new mothers. WWWT was developed in Australia and has been culturally adapted to be used in Chile. The m-health version of the Chilean adaptation of WWWT includes: Psychoeducational information for understanding and managing infant behavior and about parenting. Modules on understanding and managing infant behavior include information on: infant temperament, including such as differences in the reactivity, responsivity and regulation of young infants; amount and known and unknown reasons for infant crying; stimulation, over-stimulation and soothing; infant sleep needs and optimal sleep habits; the use of settling strategies to achieve these while supporting breastfeeding; and establishing sustainable routines of daily care: the feed, play, sleep routine. Modules on matters relating to parents include: gendered differences in the losses and gains of parenthood; differences in emotional needs and the potential for adverse reproductive events to have lasting psychological effects on women after the birth of a baby; and developing strategies to assist couples to address these in a non-confrontational manner. This information will be delivered through instant messaging services for mobile phones (i.e., Whatsapp) 3 times a week for four-week period. Each module will include a very brief video offering information regarding a specific topic, a proposed personal exercise and the invitation to assess the perceived usefulness of the information received. Some modules include links to external, complementary information from the Chilean Infancy Policy. Contact with the program trained facilitator. It will allow mothers to ask questions that arise from the topics addressed in the psychoeducational videos and share their personal experiences. The facilitator responses will focus on aiding the understanding and elaboration of the contents. This will be done through instant messaging service for mobile phones (i.e., Whatsapp). In the present study, the facilitator will be a mental health professional of the research team, that has been trained on the intervention model. Group virtual meeting. A virtual group meeting will take place with mothers and their partners (or significant others) and the program facilitator. The group meeting seeks to offer an instance were new mothers and fathers can share their experiences regarding their parenthood and the changes it has involved in their daily lives, as well as providing the opportunity for developing support networks among them. This pilot study will use a mixed design. The quantitative component will consist of a before-after design with control group including 90 adult mothers of child aged 6-8 weeks who receive health care in a primary health centers in Santiago. Mothers will be randomized into the experimental (EG) or control groups (CG) in a rate of 1:1. Mothers in the EG will receive the m-health version of WWWT intervention plus the usual treatment that primary health centers (TAU) provided to children. Participants in the CG will be subject to TAU. TAU for children under one year of age include routine health checks by health professionals (nurse or doctor), every month from 0 to 4 months of age, and at 6, 8 and 12 months of age. The objective of the routine health care check is to carry out a comprehensive evaluation of the child's development and growth, guide parents and caregivers regarding child development, health and upbringing of the child. Also, promoting exclusive breastfeeding, healthy mother/child bonding (by detecting relevant alterations in this area) and encouraging paternal participation in upbringing and care of the child. Finally, in the health check-ups at 2 and 6 months of age of the child, Edinburgh Postpartum Depression Scale is used for screening depressive symptoms in mothers. At risk cases are referred for mental health assessment and care. A waiting list procedure will allow the delivery of the intervention to control women once the data collection for the study has been completed. The participating mothers will be contacted in coordination with the health providers of two public primary health centers after the first newborn health check. All women who meet the inclusion criteria will be contacted by the research assistant to participate of the research project. Women who wish to participate will be randomly assigned to the EG or CG. Both groups will receive informed consent and will be assessed regarding sociodemographic characteristics, mother's symptoms of anxiety and depression, maternal self-efficacy and perceived social support. The participants in both groups will be assessed a week before the start of the intervention (baseline) and three months after its completion (follow-up). After the intervention is completed, the qualitative component of the study will be carried out to access of the users' acceptability and satisfaction. It considers 12 semi-structured interviews to members of the EG group. The maximum variation sampling strategy will be used according to the completion of the intervention. An open coding of Grounded Theory will be used to data analysis. The feasibility of m-health version of WWWT will be evaluated in terms of eligibility rates, recruitment rates and reasons for study refusals, feasibility to deliver the three components of the intervention, data attrition and follow-up rates by treatment condition. Their acceptability considers participant completion of the intervention rates, and a qualitative assessment of the users' acceptability and satisfaction. Quantitative indicators of feasibility and acceptability will be presented on frequency and/or percentage. Secondary outcomes will include: changes in maternal postnatal symptoms of depression and anxiety, change in parenting self-efficacy and perceived social support in both groups. Mixed-ANOVA analysis will be used to examine this variables differences between EG and CG whilst subjecting participants to repeated measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Postpartum, Anxiety Disorders and Symptoms, Maternal Behavior
Keywords
Feasibility Studies, Prevention, mHealth

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to intervention or control groups at a 1:1 ratio.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
m-health version of WWWT intervention
Arm Type
Experimental
Arm Description
Include: a) Psychoeducational information for understanding and managing infant behavior and on parenting. This information will be delivered through instant messaging service for mobile phones (i.e., Whatsapp) 3 times a week for four-week period. Each module will include a very brief video offering information regarding a specific topic, a proposed personal exercise and the invitation to assess the perceived usefulness of the information received. Some modules include links to external, complementary information from the Chilean Infancy Policy. b) Contact with the program facilitator. It will allow mothers to ask questions that arise from the topics addressed in the psychoeducational videos. The answers seek to promote the understanding and elaboration of the contents, and operate by providing expert support; c) A virtual group meeting.
Arm Title
TREATMENT AS USUAL
Arm Type
Other
Arm Description
TAU for children under one year of age include routine health checks by health professionals (nurse or doctor), every month from 0 to 4 months of age, and at 6, 8 and 12 months of age. The objective of the routine health care check is to carry out a comprehensive evaluation of the child's development and growth, guide parents and caregivers regarding child development, health and upbringing of the child. Also, promoting exclusive breastfeeding, healthy mother/child bonding (by detecting relevant alterations in this area) and encouraging paternal participation in upbringing and care of the child. Finally, in the health check-ups at 2 and 6 months of age of the child, Edinburgh Postpartum Depression Scale is used for screening depressive symptoms in mothers. At risk cases are referred for mental health assessment and care.
Intervention Type
Behavioral
Intervention Name(s)
m-health version of WWWT intervention
Intervention Description
m-health version of Chilean adaptation of WWWT intervention: a) Psychoeducational information for understanding and managing infant behavior and on parenting. b) Contact with the program facilitator. c) A virtual group meeting
Intervention Type
Other
Intervention Name(s)
Treatment as usual
Intervention Description
TAU for children under one year of age include routine health checks by health professionals (nurse or doctor), every month from 0 to 4 months of age, and at 6, 8 and 12 months of age
Primary Outcome Measure Information:
Title
Eligibility rate as feasibility indicator
Description
Proportion of women who meet inclusion criteria compared with the total number of new mothers registered during the recruitment period in each participating primary health center
Time Frame
At the baseline assessment during the recruitment period.
Title
Recruitment rate as feasibility indicator
Description
Proportion of mothers who accept the invitation to participate in the study respect to those meet eligibility criteria
Time Frame
At the baseline assessment during the recruitment period.
Title
Percentage of EG participants who receive the 12 psychoeducational modules, who attend the virtual meeting and who -at least- once established contact with the program facilitator
Description
The feasibility to deliver the components of the intervention will be measured in terms of the percentage of participants of the EG who receive the 12 psychoeducational modules, who attend the virtual meeting and who -at least- once established contact with the program facilitator.
Time Frame
At 4-weeks from beginning intervention (when intervention finished)
Title
Percentage of participants who finished intervention by group as acceptability indicator
Description
Proportion of participants who finished the intervention compared with a number of participant who began intervention in each group
Time Frame
At 4-weeks from beginning intervention (when intervention finished).
Title
Percentage of participant retention at follow-up by group as acceptability indicator
Description
Proportion of participants who remain in the study at the 12 weeks follow up compared with a number of participant who began intervention in each group
Time Frame
At 12-weeks after the completion of the intervention (follow-up measurement).
Secondary Outcome Measure Information:
Title
Changes in maternal postnatal symptoms of depression, according to mean scores obtained with the Edinburgh Postnatal Depression Scale (EPDS)
Description
The EPDS is a 10-item, self-report questionnaire used for screening current maternal symptoms of depression using a 4-point scale, total score ranging from 0 to 30 points. This scale has been validated in Chile.
Time Frame
At baseline (a week before the intervention starts) and 12-weeks after the completion of the intervention (follow-up measurement).
Title
Change in maternal postnatal symptoms of anxiety according to mean scores obtained with the Perinatal Anxiety Screening Scale (PASS)
Description
The PASS is a 31-item, self-report questionnaire assesses maternal perinatal anxiety over the past month. A total score is calculated by adding all items that indicates level of severity: minimal (0-20 points), mild to moderate (21-41 points) and severe (42-93). The PASS includes four subscales, namely general worry and specific fears; perfectionism, control and trauma; social anxiety; and acute anxiety and adjustment.
Time Frame
At baseline (a week before the intervention starts) and 12-weeks after the completion of the intervention (follow-up measurement).
Title
Changes on perceived social support according to mean scores obtained with the multidimensional perceived social support scale (MSPSS)
Description
The MSPSS is a 12 items self-report scale. It includes 3 subscales on perceived social support in three areas: family, friends and significant. Each item is rated on a 7-point Likert-scale (1 = very strongly disagree; 7 = very strongly agree). Three subscales' scores (range 4 to 28) and a total score (range 12 to 84) are estimated by adding the item scores. It has been translated and validated for the Chilean population.
Time Frame
At baseline (a week before the intervention starts) and 12-weeks after the completion of the intervention (follow-up measurement).
Title
Change in maternal self-efficacy according to mean scores obtained with the Parental Evaluation Scale (PEE)
Description
The PEE is a 10-items self-report questionnaire to assess satisfaction and self-efficacy feelings about motherhood in women with children ages 0-2 years. Each item is rated on a 11-point scale (0=strongly disagree; 10=strongly agree) and the total score is estimated by adding item scores and then divided by 10
Time Frame
At baseline (a week before the intervention starts) and 12-weeks after the completion of the intervention (follow-up measurement).
Other Pre-specified Outcome Measures:
Title
Reasons for study refusals as a feasibility indicator
Description
A list will be made containing the different reasons given by women who refused to participate, the results will be aggregated in terms of percentages.
Time Frame
At the baseline assessment during the recruitment period.
Title
Acceptability and satisfaction of the intervention from EG mothers' perspective
Description
EG mothers' acceptability and satisfaction with the intervention, assessed through qualitative semi-structured interviews
Time Frame
During a 12 weeks period following the completion of the intervention

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Women is selected, since only they have the biological capacity to have children
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First time mothers Adult (18 -64 years old) Having a healthy infant who is 6-8 weeks age Receive medical care in a primary health centers Having access to a mobile phone with instant messaging services (i.e., Whatsapp) Fluent in Spanish Exclusion Criteria: Severe mental health problem (i.e. schizophrenia, mood disorder with suicidal ideation) Cognitive disability Actual substance abuse High risk for presenting symptoms of depression (EPDS above cut-off score) Severe psychosocial problem (i.e. domestic violence, sexual abuse).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Soledad Coo
Phone
56968417262
Email
scoo@udd.cl
First Name & Middle Initial & Last Name or Official Title & Degree
Carola Perez
Phone
56997051989
Email
janetperez@udd.cl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Soledad Coo
Organizational Affiliation
Universidad del Desarrollo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Primary Health Center San Luis
City
Santiago
State/Province
RMN
ZIP/Postal Code
7931091
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felipe Guajardo, MD
Email
fguajardo@cormup.cl
First Name & Middle Initial & Last Name & Degree
Constanza Delpino, Nurse
Email
cdelpino.fernandez@cormpup.cl
Facility Name
Primary Health Center Cardenal Silva Henríquez
City
Santiago
State/Province
RM
ZIP/Postal Code
7910652
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francisco Peláez, MD
Email
fpelaez.quintana@cormup.cl
First Name & Middle Initial & Last Name & Degree
Natalia Fuenzalida, MPsych
Email
nfuenzalida.coloma@cormup.cl

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual quantitative participant data that underlie the reported results, after deidentification (text, tables and figures).
IPD Sharing Time Frame
Beginning 3 months and ending 5 years following article publication.
IPD Sharing Access Criteria
These data will be available to researchers who provide a methodologically sound proposal for the purposes of achieving specific aims outlined in that proposal. Proposals should be directed to Soledad Cood and J. Carola Pérez via email (scoo@udd.cl; janetperez@udd.cl) and will be reviewed by both researchers. Requests to access data to undertake hypothesis-driven research will not be unreasonably withheld. To gain access, data requesters will need to sign a data access agreement and to confirm that data will only be used for the agreed purpose for which access was granted and this these data will be not shared to other people.
Citations:
PubMed Identifier
36300324
Citation
Perez JC, Aldoney D, Garcia MI, Olhaberry M, Fernandez O, Alamo N, Franco P, Perez F, Fisher J, Rowe H, Coo S. Online intervention to prevent postnatal depression and anxiety in Chilean new mothers: Protocol for a feasibility trial. Health Informatics J. 2022 Oct-Dec;28(4):14604582221135440. doi: 10.1177/14604582221135440.
Results Reference
derived

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Feasibility of M-health Version of "What Were We Thinking" Intervention to Promote Maternal Postpartum Mental Health

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