- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02459925
MOMS Hubs- CT Dept of Social Services Block Grant (MOMS-Hubs)
MOMS Partnership-Community-Based Hubs for Maternal Mental Health and Workforce Development, New Haven MOMS Partnership- CT Dept of Social Services Block Grant
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The MOMs workforce program will involve teaching, coaching, and supportive services for participants as they navigate their journeys to sustainable employment that pays a family-supporting wage. Participants will be guided through an individualized progression of services designed to increase their employability, to increase their ability to earn higher incomes in career-track employment, and to improve their chances of retaining jobs and advancing in them.
The MOMS Mental Health program centers around a manualized Stress Management Course 8-class group treatment, delivered once per week. The course was adapted from "The Mother and Child Course" by Munoz and Le (2011) for the population of New Haven mothers who are served by the MOMS Partnership.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Connecticut
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New Haven, Connecticut, United States, 06510
- Boys & Girls Club of New Haven
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New Haven, Connecticut, United States, 06510
- Center for Wellbeing of Women and Mothers, Dept. of Psychiatry, Yale University
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New Haven, Connecticut, United States, 06510
- Stop & Shop
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New Haven, Connecticut, United States, 06510
- West Rock Author's Academy
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria are as follows:
- Participant is a woman raising a child or adolescent under 18 years of age. The child/adolescent may be her biological offspring or in her custody due to adoption or foster care. Care arrangements may be legally sanctioned or informal, as is common in New Haven families. Thus, the eligible participant may be a sister, aunt, grandmother, or other female responsible for the daily care of children.
- Participant currently resides within the city limits of New Haven, CT.
- Participant resided within County of New Haven, CT on October 29, 2012.
- Participant's income is at or below 325% of the Federal poverty income.
- Participant is a U.S. citizen.
- Participant's score on CES-D > 16.
Exclusion criteria are as follows:
- Signs or symptoms of active psychosis or active suicidality will be a basis for exclusion in the study.
- Lack of proficiency in English.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: CBT- Mental Health Program
Cognitive Behavioral Therapy.
Manualized Stress Management class; brief individual behavioral counseling.
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Manualized Stress Management class; brief individual behavioral counseling.
|
|
Active Comparator: MOMS GROW
MOMS GROW (Generating Real Opportunities for Work) Teaching, coaching, and supportive services for participants as they navigate their journeys to sustainable employment that pays a family-supporting wage.
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MOMS GROW (Generating Real Opportunities for Work) Teaching, coaching, and supportive services for participants as they navigate their journeys to sustainable employment that pays a family-supporting wage.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in Center for Epidemiologic Studies Depression (CED-D) Scale
Time Frame: 6 months
|
Reduced CES-D Score (CES-D score goal <16)
|
6 months
|
|
Improvement in work readiness skills
Time Frame: 6 months
|
Reduced CASAS score
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Megan V Smith, DrPH, Yale University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1409014610
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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