How Does Mindful Mood Balance for Moms Work?

Sponsor
University of Colorado, Boulder (Other)
Overall Status
Completed
CT.gov ID
NCT05000879
Collaborator
(none)
60
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2
9.1
6.6

Study Details

Study Description

Brief Summary

The purpose of this investigation is to conduct a randomized trial comparing a web-based Mindful Mood Balance for Moms course without coaching support to waitlist control among pregnant or early parenting women with depression histories.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: MMB for Moms
N/A

Detailed Description

Mindfulness-based cognitive therapy (MBCT) prevents depressive relapse and reduces residual depression symptoms among adults with recurrent depression not currently in episode. Women in perinatal or early parenting years constitute a significant portion of this at-risk population with a history of depression for whom MBCT was designed. Novel delivery formats that provide access to core knowledge and skills of MBCT could increase public health impact-particularly for perinatal or early parenting women-but it is unclear whether such formats have comparable mental health outcomes and changes in putative targets as in-person MBCT.

In the present study, we planned to randomize 60 pregnant or early parenting women with a history of major depression and current residual depressive symptoms to MMB for Moms, a web-based course that teaches skills from MBCT customized specifically for pregnant and postpartum women, or waitlist control. We planned to address the following specific aims:

Aim 1. We evaluated the extent to MMB for Moms was associated with significant reduction in residual depression symptoms as compared to WLC. We predicted the rate of change in depression symptoms across the study would be greater on average for participants randomized to MMB for Moms relative to those randomized to WLC.

Aim 2. We evaluated the extent to MMB for Moms significantly engaged the putative target of decentering as compared to WLC. We predicted the rate of change in decentering across the study would be greater on average for participants randomized to MMB for Moms relative to participants randomized to WLC.

Aim 3. We evaluated the extent to MMB for Moms significantly engaged the putative target of self-compassion as compared to WLC. We predicted the rate of change in self-compassion across the study would be greater on average for participants randomized to MMB for Moms relative to participants randomized to WLC.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
A Randomized Controlled Trial of Mental Health Outcomes and Putative Targets of an Online Mindfulness Program for New and Expectant Mothers
Actual Study Start Date :
Nov 16, 2018
Actual Primary Completion Date :
Aug 20, 2019
Actual Study Completion Date :
Aug 20, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: MMB for Moms

Subjects will receive digital delivery of Mindful Mood Balance for Moms for 12 weeks. Subjects will be unconstrained in the types of treatments or other wellness activities they could receive while participating in the study.

Behavioral: MMB for Moms
12-week program that emphasizes mindfulness and cognitive behavioral skills

No Intervention: Waitlist Control

Subjects will be unconstrained in the types of treatments or other wellness activities they could receive while participating in the study.

Outcome Measures

Primary Outcome Measures

  1. Rate of change in depression symptoms [Through 6-month follow-up]

    Change in the severity of depressive symptoms will be evaluated by the Patient Health Questionnaire-9 (PHQ-9)

  2. Rate of change in decentering [Through 6-month follow-up]

    Change in decentering will be evaluated by the Experiences Questionnaire-Decentering subscale

  3. Rate of change in self-compassion [Through 6-month follow-up]

    Change in self-compassion will be evaluated by the Self-Compassion Scale (SCS)

  4. Depressive Relapse Status [Through 6-month follow-up]

    Rate of depressive relapse will be assessed using the Lifetime Depression Assessment Self-report (LIDAS), adapted to reference the past 3 or 6 months based on survey completion.

  5. Rate of change in anxiety symptoms [Through 6-month follow-up]

    Change in the severity of anxiety symptoms will be evaluated by the 3. Generalized Anxiety Disorder-7 (GAD-7)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. female,

  2. pregnant or having had a child within the past 36 months, *

  3. 18 years of age or older,

  4. having a history of one or more prior major depressive episode (as assessed by a single question, "Have you had a history of mood concerns or major depression?")

  5. a current PHQ-9 score of <= 14, and

  6. endorses ability to read and write fluently in English.

Exclusion Criteria:
  1. meeting criteria for current moderately severe depression symptoms (as assessed by the PHQ-9 >= 15),

  2. current imminent suicidality (as assessed by the PHQ-9), and

  3. indication of other disorders or symptoms that necessitate priority treatment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado Boulder Boulder Colorado United States 80309

Sponsors and Collaborators

  • University of Colorado, Boulder

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
CHRISTINA METCALF, Senior Instructor, University of Colorado, Boulder
ClinicalTrials.gov Identifier:
NCT05000879
Other Study ID Numbers:
  • 18-0402
First Posted:
Aug 11, 2021
Last Update Posted:
Aug 11, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 11, 2021