MedPath

Accelerating Implementation of Mindful Mood Balance for Moms

Not Applicable
Completed
Conditions
Perinatal Depression
Interventions
Behavioral: MMBFM program with clinician coach support
Behavioral: MMBFM program with peer coach support
Behavioral: Patient facing strategy intervention arm
Behavioral: Patient facing plus clinic facing strategy intervention arm
Registration Number
NCT04846504
Lead Sponsor
Kaiser Permanente
Brief Summary

The Mindful Mood Balance for Moms (MMBFM) study examines whether using an internet program called Mindful Mood Balance for Moms to deliver Mindfulness Based Cognitive Therapy (MBCT) over an 8-week time period, is effective for reducing depression symptoms among pregnant women with a history of prior depression, and studies the effects of implementation strategies on the reach of the MMBFM program. This study will enroll 470 women from Kaiser Permanente Colorado, Southern California, Georgia.

The investigators will compare clinical outcomes between those that receive mental health clinician coaching and those that receive peer coaching throughout the 8-week program. Survey data will be collected at 4 time points throughout the study (baseline, 12 weeks, 3rd trimester, and 3 months postpartum). The cost-effectiveness of both the clinical and peer coaching models at each health care system will be evaluated.

For the implementation portion of the study, 30 OB clinics across the 4 health systems will be randomized in equal numbers to provide clinician facing implementation strategies (e.g., recruitment flyers, script pads, electronic medical record prompts) to encourage engagement in the MMBFM program or to usual care where women are only recruited by the study team with no clinician involvement. The primary outcome for testing clinician facing implementation strategies is reach, the percentage of women outreached who initially engage in the MMBFM program.

Detailed Description

Specific Aims

Informed by the Consolidated Framework for Implementation Research, a leading implementation science framework, this hybrid type III effectiveness implementation study will evaluate specific implementation strategies for MMBFM. Consistent with a hybrid type III study, there are two goals: (1) compare the clinical effectiveness of MMBFM supported by mental health clinician vs. peer coaches in a randomized trial of 470 pregnant women; and (2) compare the reach of MMBFM across OB clinics for two sets of implementation strategies to facilitate access to and initial engagement in MMBFM: patient facing strategies (PFS - direct outreach to women following prenatal visits via secure patient portal, email, text, or mail) vs. patient facing strategies combined with clinician facing strategies (PFS+CFS - Electronic Medical Record (EMR)-embedded prompts for OB providers, printed prescription pads for providers, flyers). A cluster randomized design will be used, randomizing 30 OB clinics across 4 health systems to either of these two implementation conditions, to assess their impact on reach. The investigators will address the following specific aims:

Aim 1: Compare the clinical effectiveness (i.e. engagement and symptom reduction) of MMBFM supported by clinician vs. peer coaches among women with a history of prior depressive episodes. Hypothesis 1: Coaching delivered by mental health clinicians vs. peers with lived experience will be associated with equivalent reductions in depressive symptoms at 6 months post-randomization.

Aim 2: Examine specific mechanisms of action for MMBFM participants receiving clinician vs. peer coaching. Hypothesis 2a: MMBFM participants receiving peer coaching will report less self-stigma and social isolation than those receiving clinician coaching, and MMBFM participants receiving clinician coaching will report less ruminative response to negative affect and greater decentering at 6 months post-randomization than those receiving peer coaching. Hypothesis 2b: Any difference between peer and clinician coaching in depression outcomes will be mediated by treatment-specific targets - at least partially via increased engagement.

Aim 3: Examine the effects of specific implementation strategies on reach of the MMBFM program. Hypothesis 3: Clinician facing implementation strategies (CFS) in combination with patient facing strategies (PFS) will lead to higher rates of reach than patient facing strategies alone.

Aim 4: Estimate the cost-effectiveness of MMBFM supported by clinician vs. peer coaches. Hypothesis 4: MMBFM will be more cost-effective when supported by peer vs. clinician coaches.

The trials of implementation strategies at the individual and clinic levels will be conducted at four health systems representing diversity in geographic location and in racial and ethnic membership: Kaiser Permanente Colorado, Southern California, and Georgia, and HealthPartners in Minnesota. These sites include 95 clinics and more than 400 obstetric clinicians (OB physicians, nurse practitioners, midwives, nurses), providing prenatal care for 53,000 women annually. The implementation trial for Aims 1 and 2 will recruit 470 women following prenatal care visits total across the four health systems and randomize them in equal numbers to participate in one of the two coaching arms for the MMBFM program, lasting 8 weeks. The clinic-level implementation trial (Aim 3) will involve a cluster randomized design in which 30 OB clinics will be recruited from the four health systems and randomized in equal numbers to either the PFS or PFS+CFS intervention arms, lasting 6 months. The individual- and clinic-level trials will be conducted in parallel.

The 8-session MMBFM program teaches mindfulness practice and cognitive behavioral skills to help reduce automatic, depressogenic modes of thoughts, emotions, and sensations. MMBFM is delivered in a mobile first digital format, accessible from desktop or mobile devices, and provided in an individually tailored manner that includes experiential practice, video-based vicarious learning, and didactic information.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
423
Inclusion Criteria
  • Aged 18 years or older, receiving prenatal care at one of the 4 participating health systems
  • 12-24 weeks gestation
  • >= 1 prior episode of major depressive disorder, self-reported
  • Current Patient Health Questionnaire 9-item (PHQ9) depression score <=9.
  • Have internet access through home computer, smart phone, or similar device
Exclusion Criteria
  • Non-English speaking
  • Past history of a psychotic, bipolar disorder, or substance misuse disorder within the past 6 months
  • Immediate risk of self-harm
  • PHQ9 score <5 or >9
  • Patients who are on the "do not call" list for research

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Patient facing strategy intervention armPatient facing strategy intervention armCentralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text, without direct involvement of OB providers.
MMBFM program with clinician coach supportMMBFM program with clinician coach supportTelephonic coaching provided by licensed mental health professionals to support and encourage participants' engagement in and completion of the 8-session online MMBFM program.
Patient facing strategy intervention armMMBFM program with clinician coach supportCentralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text, without direct involvement of OB providers.
MMBFM program with peer coach supportMMBFM program with peer coach supportTelephonic coaching provided by trained peers with lived experience of perinatal depression to support and encourage participants' engagement in and completion of the 8-session online MMBFM program.
Patient facing plus clinic facing strategy intervention armMMBFM program with clinician coach supportOB clinic providers' use of printed recruitment materials and/or electronic medical records prompts to recommend/refer women receiving prenatal care to access the MMBFM program. These clinic facing implementation strategies will be added to the patient facing strategies of centralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text
Patient facing strategy intervention armMMBFM program with peer coach supportCentralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text, without direct involvement of OB providers.
Patient facing plus clinic facing strategy intervention armMMBFM program with peer coach supportOB clinic providers' use of printed recruitment materials and/or electronic medical records prompts to recommend/refer women receiving prenatal care to access the MMBFM program. These clinic facing implementation strategies will be added to the patient facing strategies of centralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text
Patient facing plus clinic facing strategy intervention armPatient facing plus clinic facing strategy intervention armOB clinic providers' use of printed recruitment materials and/or electronic medical records prompts to recommend/refer women receiving prenatal care to access the MMBFM program. These clinic facing implementation strategies will be added to the patient facing strategies of centralized outreach and recruitment of women receiving prenatal care by study team using email, letter, or text
Primary Outcome Measures
NameTimeMethod
Change in Patient Health Questionnaire 9-item (PHQ-9) scores from baseline through 3 months postpartumBaseline, 3 months post-randomization, 3rd trimester, 3 months postpartum

Depression symptom severity, scores range from 0 (low) to 27 (high)

Reach6 months post-intervention involving patient facing vs. clinician facing implementation strategies

The percentage of participants who initially engage in the Mindful Mood Balance for Moms course.

Secondary Outcome Measures
NameTimeMethod
Change in Perceived Stress Scale scores from baseline through 3 months postpartumBaseline, 3 months post-randomization, 3rd trimester, 3 months post partum

Stress symptoms measured by a 10-item likert-type scores range from 0 to 40 with higher scores indicating higher perceived stress.

Client Satisfaction Questionnaire (CSQ)3 months post-randomization

The CSQ will measure satisfaction with the Mindful Mood Balance for Moms program. It is an 8-item questionnaire using different Likert-type responses for each item. Scores range from 8 to 32, with higher values indicating higher satisfaction.

Change in Attitudes Toward Motherhood (AToM) Scale scores from baseline through 3 months postpartumBaseline, 3 months post-randomization, 3rd trimester, 3 months post partum

Change in attitudes toward motherhood. The 12-item AToM will measure participants' attitudes toward their infants using likert-type responses. Scores range from 0 (positive attitudes) to 60 (negative attitudes).

Change in Short Form 12 (SF-12) scores from baseline through 3 months postpartumBaseline, 3 months post-randomization, 3rd trimester, 3 months post partum

The SF-12 is a 12-item measure of physical and mental functional status. Scores range from 0 (low functional status) to 100 (high functional status)

The TWente Engagement with Ehealth Technologies Scale (TWEETS)3 months post-randomization

TWEETS will measure user engagement with the Mindful Mood Balance for Moms program. TWEETS is a 9-item Likert-type scale with scores ranging from 9 (high engagement) to 45 (low engagement)

Change in Generalized Anxiety Disorder 7-item (GAD-7) questionnaire scores from baseline through 3 months postpartumBaseline, 3 months post-randomization, 3rd trimester, 3 months postpartum

Anxiety symptom severity, scores range from 0 (low) to 21 (high)

Trial Locations

Locations (4)

HealthPartners

🇺🇸

Bloomington, Minnesota, United States

Kaiser Permanente Colorado

🇺🇸

Denver, Colorado, United States

Kaiser Permanente Georgia

🇺🇸

Atlanta, Georgia, United States

Kaiser Permanente Southern California

🇺🇸

San Diego, California, United States

© Copyright 2025. All Rights Reserved by MedPath