MOVIN: a virtual program to support mental health during pregnancy and the early months after birth.
Official title: The Pregnancy and Postpartum Mental Health Optimization Virtual Intervention Network (MOVIN): Randomized Controlled Trial
Run by Women's College Hospital · NCT07066631 · Data updated 2026-11-12
This project will test a virtual collaborative-care program called MOVIN to see if it reduces depression and anxiety in pregnant and postpartum people with infants up to 6 months old who have elevated symptoms.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 570 (estimated) |
| Sponsor | Women's College Hospital Academic / other |
| Locations | 2 sites (Toronto, Ontario and 1 other locations) |
| Status | Recruiting |
| Started | October 29, 2025 |
| Main results expected | September 30, 2028 |
| Study ends | March 31, 2029 |
| Registry record updated | October 13, 2026 |
| Trial ID | NCT07066631 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults in Ontario who are pregnant or the primary parent of an infant 0–6 months old, have an EPDS score above 10, and can complete study activities in English and online.
✕Probably not a fit
People with active substance use disorder, mania or psychosis, an active suicide plan or intent, those planning to leave Ontario during the study, or those unable to complete online procedures are unlikely to benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
MOVIN delivers stepped, collaborative mental health care online, pairing participants with a care coordinator who co-develops personalized treatment plans and liaises with primary care clinicians and perinatal psychiatrists as needed. Eligible Ontario participants with elevated symptoms are randomized 1:1 to receive the MOVIN platform or enhanced usual care and are followed with systematic, measurement-based symptom tracking. The primary outcome is depressive symptoms measured by the Edinburgh Postnatal Depression Scale at 24 weeks post-randomization, with symptom remission (EPDS <10) as a main secondary outcome. The platform includes curated education, treatment resources, and direct referral pathways to support scalable perinatal mental health care.
Why it matters
Potential benefit: If successful, MOVIN could make it easier for pregnant and postpartum people to access timely, personalized mental health care and reduce depressive and anxiety symptoms.
How similar studies have gone: Collaborative care models have previously improved perinatal depression outcomes, but MOVIN's fully virtual, province-wide stepped-care delivery is a newer adaptation of that evidence base.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Adult (age 18 years or older) 2. Pregnant or postpartum and living with their infant 0-6 months old. This includes all individuals who identify as women, as well as those of female sex who do not identify as women (e.g., non-binary, trans) who are the primary parent for their infant. This includes via natural birth, adoption, or surrogacy. 3. EPDS score \>10 at eligibility screening. Exclusion Criteria: 1. Active alcohol or substance use disorder, mania or psychotic disorder (as these conditions are better managed in direct specialty care). 2. Active suicide plan or intent (as emergent hospital-based care is likely required), 3. Plan to move out of Ontario during the study. 4. Unable to complete relevant study procedures and measures online. For the few participants without access to devices/home internet, we will budget for tablets/data plans. 5. Unable to complete study activities in English. Note that Google translate is available for the intervention platform and language lines are available for participants so that they can be served in their language of choice, however we are unable to provide translations of all study assessment and questionnaire materials that participants will need to complete during the study. 6. No primary care clinician (required for collaborative mental health care delivery model). 7. Currently enrolled in a collaborative mental health care model.
Where it's running
-
Women's College Hospital
Toronto, Ontario, Canada Recruiting -
Women's College Hospital
Toronto, Ontario, Canada Recruiting
Study contacts
- Study coordinator: Simone Vigod
- Email: simone.vigod@wchospital.ca
- Phone: 416-323-6400
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Using external trigeminal nerve stimulation to treat migraines in pregnant women
This study is trying to see if a device that stimulates a nerve in the face can safely help pregnant women with migraines feel better.
-
Improving postpartum-to-primary care transitions for people with chronic conditions
This study tests whether embedding default PCP appointments, tailored reminder messages, and care recommendations into routine inpatient postpartum care helps people with chronic conditions connect with primary care after delivery.
-
Comparing high-intensity and moderate-intensity exercise during pregnancy and its effects on health and birth outcomes
This study tests whether high-intensity or moderate-intensity exercise during pregnancy can improve health and birth outcomes for moms and their babies.
-
Bonding Before Birth: A mobile program to support first-time expectant couples
A mobile app trial in Singapore tests short weekly exercises for first-time expectant couples to see if it helps reduce depression and improve emotional regulation during pregnancy.
-
Smartphone-supported single-session psychotherapy for postpartum depression
A single online therapy session plus four weeks of app-based support is being tested to see if it reduces depressive symptoms in postpartum women compared with a waitlist.
-
Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges
This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.