How Does Mindful Mood Balance for Moms Work?
Primary Purpose
Depression, Pregnancy Related, Antenatal Depression
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MMB for Moms
Sponsored by
About this trial
This is an interventional other trial for Depression
Eligibility Criteria
Inclusion Criteria:
- female,
- pregnant or having had a child within the past 36 months, *
- 18 years of age or older,
- 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?")
- a current PHQ-9 score of <= 14, and
- endorses ability to read and write fluently in English.
Exclusion Criteria:
- meeting criteria for current moderately severe depression symptoms (as assessed by the PHQ-9 >= 15),
- current imminent suicidality (as assessed by the PHQ-9), and
- indication of other disorders or symptoms that necessitate priority treatment.
Sites / Locations
- University of Colorado Boulder
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
MMB for Moms
Waitlist Control
Arm Description
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.
Subjects will be unconstrained in the types of treatments or other wellness activities they could receive while participating in the study.
Outcomes
Primary Outcome Measures
Rate of change in depression symptoms
Change in the severity of depressive symptoms will be evaluated by the Patient Health Questionnaire-9 (PHQ-9)
Rate of change in decentering
Change in decentering will be evaluated by the Experiences Questionnaire-Decentering subscale
Rate of change in self-compassion
Change in self-compassion will be evaluated by the Self-Compassion Scale (SCS)
Depressive Relapse Status
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.
Rate of change in anxiety symptoms
Change in the severity of anxiety symptoms will be evaluated by the 3. Generalized Anxiety Disorder-7 (GAD-7)
Secondary Outcome Measures
Full Information
NCT ID
NCT05000879
First Posted
August 5, 2021
Last Updated
August 5, 2021
Sponsor
University of Colorado, Boulder
1. Study Identification
Unique Protocol Identification Number
NCT05000879
Brief Title
How Does Mindful Mood Balance for Moms Work?
Official Title
A Randomized Controlled Trial of Mental Health Outcomes and Putative Targets of an Online Mindfulness Program for New and Expectant Mothers
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
November 16, 2018 (Actual)
Primary Completion Date
August 20, 2019 (Actual)
Study Completion Date
August 20, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Colorado, Boulder
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Pregnancy Related, Antenatal Depression, Depression, Postpartum
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MMB for Moms
Arm Type
Experimental
Arm Description
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.
Arm Title
Waitlist Control
Arm Type
No Intervention
Arm Description
Subjects will be unconstrained in the types of treatments or other wellness activities they could receive while participating in the study.
Intervention Type
Behavioral
Intervention Name(s)
MMB for Moms
Intervention Description
12-week program that emphasizes mindfulness and cognitive behavioral skills
Primary Outcome Measure Information:
Title
Rate of change in depression symptoms
Description
Change in the severity of depressive symptoms will be evaluated by the Patient Health Questionnaire-9 (PHQ-9)
Time Frame
Through 6-month follow-up
Title
Rate of change in decentering
Description
Change in decentering will be evaluated by the Experiences Questionnaire-Decentering subscale
Time Frame
Through 6-month follow-up
Title
Rate of change in self-compassion
Description
Change in self-compassion will be evaluated by the Self-Compassion Scale (SCS)
Time Frame
Through 6-month follow-up
Title
Depressive Relapse Status
Description
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.
Time Frame
Through 6-month follow-up
Title
Rate of change in anxiety symptoms
Description
Change in the severity of anxiety symptoms will be evaluated by the 3. Generalized Anxiety Disorder-7 (GAD-7)
Time Frame
Through 6-month follow-up
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
female,
pregnant or having had a child within the past 36 months, *
18 years of age or older,
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?")
a current PHQ-9 score of <= 14, and
endorses ability to read and write fluently in English.
Exclusion Criteria:
meeting criteria for current moderately severe depression symptoms (as assessed by the PHQ-9 >= 15),
current imminent suicidality (as assessed by the PHQ-9), and
indication of other disorders or symptoms that necessitate priority treatment.
Facility Information:
Facility Name
University of Colorado Boulder
City
Boulder
State/Province
Colorado
ZIP/Postal Code
80309
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified data and accompanying documentation will be available for use by other investigators upon request.
IPD Sharing Time Frame
Data will become available after study completion.
IPD Sharing Access Criteria
Interested investigators will be asked to submit a proposal form, which will be reviewed by the principal investigators for scientific integrity and adherence to ethical guidelines.
Citations:
PubMed Identifier
26654212
Citation
Dimidjian S, Goodman SH, Felder JN, Gallop R, Brown AP, Beck A. Staying well during pregnancy and the postpartum: A pilot randomized trial of mindfulness-based cognitive therapy for the prevention of depressive relapse/recurrence. J Consult Clin Psychol. 2016 Feb;84(2):134-45. doi: 10.1037/ccp0000068. Epub 2015 Dec 14.
Results Reference
background
Learn more about this trial
How Does Mindful Mood Balance for Moms Work?
We'll reach out to this number within 24 hrs