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Perinatal Mental HealthNCT07893210

Fathers and Babies (FAB) Research Study

A study testing Fathers and Babies Program and Mothers and Babies Program in people with Perinatal Mental Health and Fathers, run by Northwestern University at 1 site in United States.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The purpose of this study is to examine the effectiveness of the Fathers and Babies intervention (FAB). FAB aims to improve the mental health of fathers and provide strategies that help fathers support the mental health of their female partner. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Fathers and Babies Program and Mothers and Babies Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
624 participants
Where
1 siteUnited States
Study dates
8 Jan 2026to 31 Dec 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Must be in a fathering role with the mother of the index child (irrespective of whether he is biological father or co-residing with partner) and/or have a pregnant partner (mother of the child).
  • Be enrolled in a HV program OR have a partner (mother of the child) enrolled in an IL or TX HV program
  • Ability to speak English or Spanish
  • >18 years old
  • Be enrolled in a HV program OR have a partner (father of the child) enrolled in an IL or TX HV program
  • Ability to speak English or Spanish
Show all 10Show fewer
  • >18 years old
  • Must be a mother and/or are currently pregnant
  • Employed at a HV program in Illinois or Texas
  • Have an active caseload in which they deliver HV services can include roles such as home visitors, case workers, family support specialists, Doulas, parent educators or any other role that fits within the home visiting models and roles.

Who cannot join

  • Previously completed MB within the last 12 months
  • Father does not participate in the research study

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jocelyne Chavez, Master of Public Health contact

773-503-5050

jocelyne.chavez@northwestern.edu

United States1 site, 1 recruiting
  • Northwestern University

    Chicago, Illinois, 60611

    Jocelyne Chavez, Master of Public Health, 312-503-5050, jocelyne.chavez@northwestern.edu

    Darius Tandon

    Recruiting

Other trials in United States

About this study

Official title: Examining the Effectiveness of the Fathers and Babies Intervention During the Perinatal Period

The purpose of this study is to examine the effectiveness of the Fathers and Babies intervention (FAB). FAB aims to improve the mental health of fathers and provide strategies that help fathers support the mental health of their female partner. FAB was adapted from Mothers and Babies (MB), an evidence-based perinatal depression prevention intervention. FAB can be delivered as a standalone intervention or can be delivered alongside MB as a dyadic intervention to both fathers and mothers. In this longitudinal randomized controlled trial (RCT), the investigators will examine the effectiveness and implementation of the FAB intervention. To do this, the investigators will partner with Home Visiting (HV) programs in the state of Illinois (IL) and Texas (TX). Home visitors will be randomized to receive (intervention) or not to receive (controls) the FAB training. Home visitors that are randomized to receive FAB training will be trained and implement FAB or FAB with MB.

The specific aims include:

  1. To evaluate the effectiveness of FAB, delivered as a stand-alone intervention, in improving paternal mental health outcomes compared to a control group that does not receive the FAB intervention;
  2. To evaluate the effectiveness of FAB, when delivered in conjunction with MB, in improving paternal and maternal mental health outcomes compared to a control group that does not receive the FAB or MB intervention.
  3. To evaluate FAB implementation to inform future intervention delivery and scalability; the investigators will assess key implementation outcomes guided by the RE-AIM framework (feasibility, acceptability, barriers, facilitators, reach, adoption, implementation, and maintenance).
Read the detailed description

FAB was adapted from Mothers and Babies (MB), an evidence-based perinatal depression prevention intervention. Like MB, FAB was designed using principles from cognitive behavioral therapy (CBT) to help parents manage negative moods and emotions through pleasant activities, helpful ways of thinking and contact with others. MB and FAB can be delivered concurrently or as stand-alone interventions. MB and FAB are both delivered in nine sessions, with each session lasting 20-25 minutes. FAB can be implemented in-person, virtually, or via text message. MB has been found effective to prevent the onset of postpartum depression and reduce depressive symptoms through multiple randomized controlled trials (RCT). Home Visiting (HV) services target expectant parents and parents of young children to provide support in the home using evidence-based models that focus on children's development.

Though HV programs tend to focus on mothers, there have been increasing efforts to engage fathers in HV services. Evidence-based models vary in their approach to reaching fathers, though most models place an emphasis on the promotion of responsible fatherhood. Efforts to include fathers in these programs stem from the increasing knowledge that father involvement is associated with positive child development outcomes, like peer relationships, increased self-esteem, and fewer externalizing and internalizing behaviors. Furthermore, fathers involved in HV services with their partners show increased knowledge of child development and more responsive parenting practices.

More attention has been recently directed toward fathers' perinatal mental health, with epidemiological evidence indicating an unmet need for the treatment of paternal depression and anxiety. Paternal depression in the United States has a reported prevalence of 8.4% during pregnancy and the postpartum period, though the prevalence between three and six months postpartum can be as high as 13%. Postpartum depression disproportionately affects low-income men across racial and ethnic groups. However, men across racial and ethnic groups are less likely to seek mental health services compared to women. Fathers with worse mental health outcomes during the perinatal period are less likely to have nurturing relationships with their children, which can negatively affect child outcomes from infancy through adolescence. Despite the prevalence of paternal depression, few interventions have targeted fathers during the perinatal period to address their mental health. To address this gap, FAB was developed to address the mental health of fathers during the perinatal period.

FAB was developed in collaboration with infant mental health consultants, academics, home visitors, fatherhood experts, and fathers. In the pilot study, FAB was concurrently delivered with MB, and tested among 30 mother-father dyads. Data from the pilot study showed that FAB led to reductions in anxiety and depressive symptoms, and perceived stress among fathers receiving the intervention. Additionally, 88% of fathers indicated that FAB gave them skills to help manage their mood and stress and 82% indicated that FAB helped them and their partner talk about stress and parenting. All pilot participants indicated that they would recommend FAB to other fathers.

In this longitudinal RCT, the investigators will examine the effectiveness and implementation of the FAB intervention. To do this, the investigators will partner with HV programs in the state of Illinois (IL) and Texas (TX). Home visitors will be randomized to receive (intervention) or not to receive (controls) the FAB training. Home visitors that are randomized to receive FAB training will be trained and implement the FAB or FAB with MB. Home visitors randomized to serve as controls will continue to deliver their normal home visiting services during the study and refer fathers or fathers and their partners (mother of the child).

Being tested
Fathers and Babies Program, Mothers and Babies Program
Keywords
fathers, perinatal mental health, paternal depression, home visiting, parenting

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Fathers and Babies ProgramBehavioural

    FAB is a 9-session intervention divided into four modules: Introduction, Pleasant Activities, Thoughts, and Contact with Others. Fathers will be provided with a participant workbook that contains skill-based worksheets relevant to each session. Fathers will be able to choose how they would like to receive FAB: 1-on-1 delivered by a home visitor, text-based, or a combination of both. Home visitors will deliver FAB or FAB with MB based on participants' preference. FAB or FAB with MB must be delivered within 18 weeks. In the 1-on-1 modality, fathers will receive FAB through 9 in-person or virtual sessions with their home visitor. Each session lasts 20-25 minutes. The 9 sessions may occur on a weekly or bi-weekly basis. FAB content can also be delivered in a text-based format, with an initial in-person or virtual session with a home visitor to deliver session 1. The HealthySMS online platform will be used to deploy the text messages and track FAB completion by session for each father.

  • Mothers and Babies ProgramBehavioural

    Mothers offered MB as part of their study participation will receive the intervention in conjunction with FAB. In the 1-on-1 MB modality, mothers will receive MB through 9 in-person or virtual sessions with their home visitor. Each session will last 20-25 minutes. The nine sessions must be delivered within 18 weeks. The MB content is divided into four modules: Introduction, Pleasant Activities, Thoughts and Contact with Others. Mothers will be provided with a participant workbook that contains skill-based worksheets relevant to each session.

Study groups in NCT07893210
Study groupRoleWhat they receive
Fathers (Intervention)ExperimentalFAB is a 9-session intervention divided into four modules: Introduction, Pleasant Activities, Thoughts, and Contact with Others. Fathers will be provided with a participant workbook that contains skill-based worksheets relevant to each session. Fathers will be able to choose how they would like to receive FAB: 1-on-1 delivered by a home visitor, text-based, or a combination of the two. Home visitors will deliver FAB or FAB in conjunction with MB based on participants' preference. FAB or FAB in conjunction with MB must be delivered within 18 weeks. In the 1-on-1 modality, fathers will receive FAB through 9 in-person or virtual sessions with their home visitor. Each session lasts 20-25 minutes. The nine sessions may occur on a weekly or bi-weekly basis. FAB content can also be delivered in a text-based format, with an initial in-person or virtual session with a home visitor to deliver session 1. The remaining 8 sessions are delivered through text messages.
Receives: Behavioral: Fathers and Babies Program
Fathers (Control)No interventionControl father participants will not receive the FAB intervention and will continue receiving normal home visiting services.
Mothers (Intervention)ExperimentalMothers offered MB as part of their study participation will receive the intervention in conjunction with FAB. In the 1-on-1 MB modality, mothers will receive MB through 9 in-person or virtual sessions with their home visitor. Each session will last 20-25 minutes. The nine sessions must be delivered within 18 weeks. The MB content is divided into four modules: Introduction, Pleasant Activities, Thoughts and Contact with Others. Mothers will be provided with a participant workbook that contains skill-based worksheets relevant to each session.
Receives: Behavioral: Mothers and Babies Program
Mothers (Control)No interventionControl mother participants will not receive the FAB with MB intervention and will continue receiving normal home visiting services.
Home Visitor (Intervention)ExperimentalHome visitors randomized to the intervention arm will receive the FAB training. After training, intervention home visitors will recruit and refer study participants (fathers and mothers) who will receive either FAB or FAB with MB. If FAB is delivered with MB, the father and mother dyad would receive the FAB and MB intervention concurrently. MB can be delivered in person, virtually, or via phone. FAB can be delivered in person or via text messages. Home visitors will deploy the FAB text-messages on the HealthySMS online platform, in which they will also track their FAB implementation completion by session for each father participant.
Receives: Behavioral: Fathers and Babies Program; Behavioral: Mothers and Babies Program
Home Visitor (Control)No interventionHome visitors randomized to the control arm will not receive FAB training or implement FAB/FAB with MB. Although they will not deliver the FAB or MB intervention initially as part of this study, these home visitors will still be responsible for identifying and referring eligible study participants to the research team who will be recruited as control participants. Control group home visitors will continue to deliver standard HV services. After all study activities are completed, control group home visitors will receive FAB training and will be able to deliver FAB.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mental Health Outcomes: Stress

    The Perceived Stress Scale will be used to assess perceived stress in father and mother participants. assigning values from 0 to 4 to each of its 10 questions ("Never" = 0, "Almost never" = 1, "Sometimes" = 2, "Fairly often" = 3, "Very often" = 4). Reverse scoring is applied to the four positive items (items 4, 5, 7, and 8) where 0=4, 1=3, 2=2, 3=1, and 4=0. All scores are then summed. Scores between 14-26 indicate moderate stress. Scores between 27-40 indicate high perceived stress.

    Measured: All father and mother participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB or FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  2. Mental Health Outcome: Depression

    The Edinburgh Postpartum Depression Scale will be used to assess depression symptoms. The Edinburgh Postnatal Depression Scale (EPDS) is a 10-item self-report questionnaire scored from 0 to 30. Questions 1, 2, and 4 score 0 to 3 sequentially, while questions 3 and 5-10 are reverse-scored (3 to 0). A total score of 13 flags a possible depressive risk requiring clinical evaluation, and any positive response to question 10 regarding self-harm requires immediate safety assessment.

    Measured: All father and mother participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB or FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  3. Mental Health Outcome: Anxiety

    The Generalized Anxiety Disorder Scale will be used to assess anxiety symptoms. The GAD-7 (Generalized Anxiety Disorder-7) is a seven-question tool used to measure anxiety severity. Each question is scored from 0 to 3 based on how often symptoms occurred over the past two weeks. A score of 10 or higher suggests probable clinical anxiety.

    Measured: All father and mother participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB or FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

Secondary outcomes (5)
  1. Mental Health Outcome: Mood Regulation

    The Negative Mood Regulation Scale will be used to asses mood regulation. The Negative Mood Regulation (NMR) Scale is a 30-item questionnaire measuring a person's belief that their actions or thoughts will help change a negative mood. Total scores range from 30 to 150, calculated by summing all item responses on a 5-point Likert scale. Higher scores mean stronger confidence in managing negative moods.

    Measured: All father participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB or FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  2. Mental Health Outcomes: Behavioral Activation Depression Scale

    The Behavioral Activation for Depression Scale (BADS) is a 25-item self-report instrument scored on a 7-point Likert scale from 0 ("not at all") to 6 ("completely"). It uses four subscales (Activation, Avoidance/Rumination, Work/School Impairment, Social Impairment) where subscale items are summed directly, and a total score is computed by reverse-scoring the avoidance and impairment subscales. Higher total scores reflect healthier behavioral activation and less overall depressive disengagement.

    Measured: All father participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB and FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  3. Parenting Outcome: The Fatherhood Research and Practice Network (FRPN) Father Engagement Scale

    The Fatherhood Research and Practice Network (FRPN) Father Engagement Scale is a free, validated research tool designed to assess the frequency of a father's involvement and engagement with his children. The scale is divided into four distinct age-based versions. This study will use version 1 and 2 (version 1: children 1 month to 1 year old; version 2: children 1 year, 1 month to 6 years old).

    Measured: All father participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB and FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  4. Relationship Satisfaction: Revised Dyadic Adjustment Scale

    The Revised Dyadic Adjustment Scale (RDAS) is a 14-item questionnaire scored by summing all item values to yield a total score from 0 to 69. Higher scores mean better relationship adjustment, while a total score of 48 or less indicates relationship distress.

    Measured: All father and mother participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB and FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

  5. Social Support: Social Support Effectiveness Survey

    The Social Support Effectiveness Questionnaire (SSE-Q), yields full-scale scores ranging from 0 to 80, with each subscale ranging from 0 to 20. Higher scores reflect more effective and adaptive social support.

    Measured: All father and mother participants will complete this measure at baseline, 20 and 32 weeks after completing the 1st FAB and FAB with MB session (if intervention randomized) or at baseline, 20 and 32 weeks after study enrollment (if control participants).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Oct 2026
  2. Study start8 Jan 2026
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
624 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07893210
Sponsor's protocol ID
STU00224192
Status last verified
Oct 2026
First submitted
12 Aug 2026
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Tandon SD, Hamil J, Gier EE, Garfield CF. Examining the Effectiveness of the Fathers and Babies Intervention: A Pilot Study. Front Psychol. 2021 Jul 15;12:668284. doi: 10.3389/fpsyg.2021.668284. eCollection 2021.

    PubMed 34335380
  • Muñoz R. F., Le H., Ippen C., Diaz M., Urizar G., Soto J., et al. (2007). Prevention of postpartum depression in low-income women: development of the Mamás y Bebés/mothers and babies course. Cogn. Behav. Pract. 14 70-83. 10.1016/j.cbpra.2006.04.021

  • Figueroa CA, Hernandez-Ramos R, Boone CE, Gomez-Pathak L, Yip V, Luo T, Sierra V, Xu J, Chakraborty B, Darrow S, Aguilera A. A Text Messaging Intervention for Coping With Social Distancing During COVID-19 (StayWell at Home): Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2021 Jan 14;10(1):e23592. doi: 10.2196/23592.

    PubMed 33370721
  • Aguilera A, Bruehlman-Senecal E, Demasi O, Avila P. Automated Text Messaging as an Adjunct to Cognitive Behavioral Therapy for Depression: A Clinical Trial. J Med Internet Res. 2017 May 8;19(5):e148. doi: 10.2196/jmir.6914.

    PubMed 28483742
  • Lovett E, Smith A. Mental Health, Declining Physical Activity and Social Connection during Transitions into Fatherhood in the UK. Int J Environ Res Public Health. 2024 Jul 9;21(7):890. doi: 10.3390/ijerph21070890.

    PubMed 39063466
  • Panter-Brick C, Burgess A, Eggerman M, McAllister F, Pruett K, Leckman JF. Practitioner review: Engaging fathers--recommendations for a game change in parenting interventions based on a systematic review of the global evidence. J Child Psychol Psychiatry. 2014 Nov;55(11):1187-212. doi: 10.1111/jcpp.12280. Epub 2014 Jul 1.

    PubMed 24980187

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