mHealth Intervention to Prevent Postpartum Depression and Anxiety in Chilean Women (WWWT)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversidad del Desarrollo

About this trial

The goal of this clinical trial is to evaluate the effectiveness of a digital psychoeducational intervention, "What Were We Thinking" (WWWT), to prevent the development of postpartum depression and anxiety symptoms in first-time mothers in Chile. The study includes adult women with a healthy, full-term infant younger than two months who are receiving care in primary health centers.

The main questions it aims to answer are:

* Does participation in the WWWT intervention reduce depressive and anxiety symptoms at 3 months after the end of the intervention compared to usual care? * Does participation in the intervention improve maternal self-efficacy, perceived social support, and coparenting relationship quality compared to usual care? Researchers will compare an experimental group receiving the full WWWT intervention with a control group receiving usual care to determine the effectiveness of the intervention.

Participants will:

* Complete self-report questionnaires assessing depressive symptoms, anxiety symptoms, maternal self-efficacy, perceived social support, and coparenting at baseline and at 3-month follow-up * Be randomly assigned to either the intervention group or the control group * Receive the WWWT intervention between 4 and 10 weeks postpartum (intervention group), including:

* Fourteen psychoeducational video modules (3-5 minutes each) delivered via text messaging over 4-5 weeks * Individual contact with a trained facilitator through text messaging * One virtual group session with other mothers and a facilitator * Continue receiving usual care in primary health services (control group) and receive a shortened version of the intervention after the follow-up assessment

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

First-time mothers (primiparous women)

Aged 18 years or older

Having a healthy, full-term infant younger than 2 months of age

Receiving prenatal or postnatal care at participating primary health centers in Chile

Disqualifiers

Severe symptoms of depression or anxiety at baseline requiring immediate specialized mental health treatment

Severe psychosocial problems (e.g., substance abuse, domestic violence, significant cognitive impairment)

Infant born preterm or with severe medical conditions (e.g., genetic disorders or serious neonatal complications)

Inability to provide informed consent or participate in study procedures due to language or cognitive barriers

Trial design

Design model

Parallel

Treatments tested in this trial

  • What Were We Thinking (WWWT) mHealth Intervention

    Behavioral

    The "What Were We Thinking" (WWWT) is a psychoeducational, preventive mHealth intervention designed for first-time mothers to reduce the risk of postpartum depression and anxiety. The intervention targets modifiable risk factors, including maternal self-efficacy in infant care and perceived social support. It is delivered between 4 and 10 weeks postpartum and includes three components: (1) fourteen psychoeducational video modules (3-5 minutes each) delivered via text messaging over 4-5 weeks, accompanied by reflective prompts; (2) asynchronous support from a trained facilitator via text messaging; and (3) one virtual group session led by the facilitator. Facilitators are trained health professionals and can refer participants to primary care services when needed.

Treatment groups

220 Participants
are divided into 2 treatment groups
Group A: WWWT InterventionExperimental treatment 1 intervention
Group B: Usual CareNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Postpartum depressive symptoms

Depressive symptoms assessed using the Edinburgh Postnatal Depression Scale (EPDS)

Time frame
Baseline and 3 months after completion of the intervention
2

Postpartum anxiety symptoms

Anxiety symptoms assessed using the Depression, Anxiety and Stress Scales (DASS-21)

Time frame
Baseline and 3 months after completion of the intervention

Secondary outcomes

1

Maternal self-efficacy

Maternal self-efficacy assessed using the Escala de Evaluación Parental (EEP)

Time frame
Baseline and 3 months after completion of the intervention
2

Perceived social support

Perceived social support assessed using the Multidimensional Scale of Perceived Social Support (MSPSS)

Time frame
Baseline and 3 months after completion of the intervention
3

Satisfaction with coparenting

Satisfaction with coparenting assessed using the Escala de Evaluación Parental (EEP)

Time frame
Baseline and 3 months after completion of the intervention

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Universidad del Desarrollo

Lead sponsor

University of Barcelona

Collaborator

This trial is not recruiting at the moment. You can still explore other options: