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Testing Doula Link, a Multi-Component Intervention to Improve Perinatal Mental Health

Doula Link for Perinatal Mental Health - Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07217561
Acronym
Doula Link
Enrollment
90
Registered
2025-10-16
Start date
2025-10-21
Completion date
2027-06-30
Last updated
2025-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perinatal Anxiety, Perinatal Depression

Keywords

Doulas, Perinatal mental health, Depression

Brief summary

Doulas are trained individuals who offer informational, emotional, and physical support to their pregnant, birthing, and postpartum clients. The goal of this clinical trial is to learn if a new intervention (called Doula Link) is feasible to implement and acceptable to both doulas and their clients. The main questions it aims to answer are: * Is Doula Link feasible to implement and acceptable to doulas and their clients? * What are the preliminary differences in depression and anxiety between individuals working with doulas who received Doula Link compared to those who did not receive Doula Link? Researchers will compare Doula Link to usual doula practice to see if Doula Link is feasible and has potential to improve mental health outcomes in postpartum individuals. Doulas will be randomly assigned to either receive Doula Link or continue with their practice as usual. Participating doulas assigned to Doula Link will receive training mental health and implementing an intervention called Our Babies and Us; receive access to a toolkit; receive access to perinatal psychiatrists and referral specialists for consultations; receive access to a support group All participating doulas will be invited to complete surveys about their experience with Doula Link (if assigned to that group) and their experience providing care for their clients. All participating clients (pregnant and postpartum individuals) will be invited to complete surveys about their experiences with their doulas, their own mental health, and their experiences with the health system.

Detailed description

Many people experience anxiety, depression, or other mental health concerns during the pregnancy, birth, and the postpartum periods. Despite interventions that work to prevent and treat, most perinatal depression and anxiety is unprevented and untreated. Doulas are trained professionals who offer emotional, educational, and physical support during this period. Their support has been shown to improve health outcomes for pregnant and postpartum individuals. This study will pilot test a multi-component intervention, called Doula Link for Perinatal Mental Health (Doula Link), that gives doulas the tools to directly support mental health. Through Doula Link, doulas will receive: 1. a doula-specific mental health toolkit adapted from MCPAP for Moms, a statewide psychiatry access program; 2. training to implement an evidence-based, stress-reduction program called Our Babies and Us; 3. access to expert consultations and client referrals with perinatal psychiatric specialists through MCPAP for Moms. 4. training on perinatal mental health 5. access to doula support groups By bringing together clinicians, doulas, and families, the goal of Doula Link is to support doulas to support their clients' mental health. Investigators hypothesize that building a program with doulas to provide direct support and link health system and community resources is an attainable intervention to expand access to mental health support.

Interventions

BEHAVIORALDoula Link

1\) a doula-specific mental health toolkit; 2) training to implement an evidence-based, stress-reduction program called Our Babies and Us; 3) training for, and access to expert consultations with perinatal psychiatric specialists through MCPAP for Moms; 4) training on perinatal mental health; 5) access to doula support groups

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* For doulas: currently providing prenatal or postpartum support to at least one client; plant to provide prenatal or postpartum support to at least three clients in the next six months; work in Massachusetts; did not participate in development of the intervention; available to participate in in-person training; English language fluency * For clients: Pregnant or no more than 12 weeks postpartum at enrollment; served by one of the 30 study doulas; live in, and plan to give birth in Massachusetts; fluency in either English or Spanish

Exclusion criteria

* Not meeting inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of Intervention Measure32-weeks gestation and 6 weeks postpartum postpartum for clients. Directly following, 6-months after, and 12-months after training for doulas.Perception among postpartum individuals in the Doula Link arm that Doula Link is agreeable and perception among postpartum individuals in the Doula Link arm that Doula Link and its individual components is agreeable. The Acceptability of Intervention Measure (AIM) will be used. This is a four-question scale scored on a range from 1-5 with higher values indicating better acceptability.
Feasibility of InterventionDirectly following, 6-months after, and 12-months after doula trainingHow well Doula Link and its individual components can be successfully delivered to doulas. The Feasibility of Intervention Measure (FIM) will be used. This is a four-question scale scored on a range from 1-5 with higher values indicating better feasibility.

Secondary

MeasureTime frameDescription
Fidelity of implementation of Our Babies and UsEvery two weeks after client enrollment for a total of six time points.The degree to which the Our Babies and Us component of Doula Link is implemented by the doulas to each client. This will be measured using the Our Babies and Us fidelity scale, which measures each topic across three dimensions. Possible scores range from 0 to 6 with higher scores indicating higher fidelity.
Reach of Our Babies and Us componentAt 6 weeks postpartumThe proportion of clients who receive part or all of the Our Babies and Us component of the intervention.
Symptoms of depression32-weeks gestation, 6-weeks postpartum, and 16-weeks postpartumClient scores on the Edinburgh Postnatal Depression Scale (EPDS). Possible range of scores is 0 to 30 with higher scores indicating a worse outcome.
Appropriateness of Intervention32-weeks gestation and 6 weeks postpartum for clients. Directly following, 6-months after, and 12-months after training for doulas.The perceived fit and relevance of Doula Link and its individual components among doulas and their clients in the Doula Link arm. The Appropriateness of Intervention Measure (IAM) will be used. This is a four-question scale scored on a range from 1-5 with higher values indicating better appropriateness.
Symptoms of anxiety32-weeks gestation and 6- and 16-weeks postpartumSymptoms of anxiety as measured by the generalized anxiety scale (GAD-7). The possible range of scores is 0 to 21 with higher scores indicating a worse outcome.
Feasibility of Our Babies and UsDirectly following, 6-months after, and 12-months after doula trainingHow well doulas can implement the our Babies and Us component to their clients. The Feasibility of Intervention Measure (FIM) will be used. This is a four-question scale scored on a range from 1-5 with higher values indicating better feasibility.
Reach of MCPAP for Moms componentAt the completion of the doula interventionThe proportion of doulas who call to access the MCPAP for Moms component of the intervention.

Other

MeasureTime frameDescription
Help-seeking32-weeks gestation and 6- and 16-weeks postpartumClients scores on the barriers to access to care evaluation scale (BACE). The possible range of scores on the BACE is 0 to 90 with higher scores indicating a worse outcome, i.e. more barriers to access to care.
Treatment participation32-weeks gestation and 6- and 16-weeks postpartumProportion of individuals who have symptoms of depression (denominator) who report accessing treatment (numerator) in the past six weeks. Denominator is defined as a score of 10 or higher on the Edinburgh Postpartum Depression Scale (EPDS), indicating any thoughts of self-harm on the EPDS, or having been diagnosed with depression by a clinician. Numerator is defined as having seen a mental health professional or been prescribed medication to treat a perinatal mental health disorder.
Skills used32-weeks gestation, 6-weeks postpartum, and 16-weeks postpartumOur babies and us stress reduction skill used. The Mothers and Babies Skills Utilization Scale will be used. This 11-item scale assesses aspects of skills using a five-point frequency Likert scale. The full scale has a possible range of 0 to 44 with higher scores indicating a better outcome, i.e. more skills used.

Countries

United States

Contacts

Primary ContactElysia Larson
elarson@bidmc.harvard.edu617-667-4051

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026