- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05299138
Restoring Empowerment and Choosing Hope (REACH) (REACH)
Restoring Empowerment and Choosing Hope (REACH) in Sarasota Florida
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
REACH will serve a minimum of 337 individual adults during each full year of the five-year grant term in Sarasota, Manatee, and Charlotte counties on the Gulf Coast of Florida. REACH will target individual participants and, in cases where both members of a couple are interested in participating, will deliver services to each partner individually. The primary target population for REACH is low-income, at-risk individuals.
Coupled with its successful history of providing healthy marriage programming, JFCS is well-positioned to help families in crisis become more stable and self-sufficient. Understanding the inextricable link between financial security and family stability, REACH is targeting and reaching the most vulnerable individuals based solely on economic risk factors. REACH will incorporate a comprehensive employment program combining both job and career advancement. This will help families in crisis reach improved financial stability, which will in turn improve the ability of individual participants to be better parents and better partners, furthering the goal of promoting healthy marriages and reducing local divorce rates.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Kathleen A Moore, PhD
- Phone Number: 813-485-6977
- Email: katkeeley1122@gmail.com
Study Contact Backup
- Name: Andrew Truman, BS
- Phone Number: 9412564130
- Email: atruman@jfcs-cares.org
Study Locations
-
-
Florida
-
Sarasota, Florida, United States, 34237
- Recruiting
- Jewish Family and Children Service
-
Contact:
- Megan Sicks, BA
- Phone Number: 104 9413662224
- Email: msicks@jfcs-cares.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- adults age 18 or older
- interested in education about strengthening their current marriage or committed relationship
- reside in Sarasota, Manatee, and Charlotte counties on the Gulf Coast of Florida
Exclusion Criteria:
- under age 18
- do not reside in Sarasota, Manatee, and Charlotte counties
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Marriage and Relationship Enhancement Skills (MRES) Intervention
The Intervention group will be assigned a Case Manager and begin Marriage and Relationship Enhancement Skills (MRES) class weekly and meet with their Case Manager as needed.
|
The Intervention group will be assigned a Case Manager and placed in the next available Marriage and Relationship Enhancement Skills (MRES) class that is convenient for their schedule.
Intervention participants will attend classes weekly and meet with their Case Manager weekly, bi-weekly, or monthly, as needed.
Study measures will be gathered from intervention participants at baseline, 10 weeks after baseline, and then 22 weeks after baseline.
The following tools will be utilized at baseline and follow-up assessment: (1) REACH program eligibility screening (only conducted at baseline), (2) Information, Family Outcomes, Reporting, and Management (nFORM) system, (3) Family Environment Scale (FES), (4) Revised Dyadic Adjustment Scale (RDAS), and (5) Economic Self-Sufficiency Scale (ESS).
|
|
No Intervention: Wait list control
The Control group will be placed on a wait-list and offered services as soon as they complete the study's final 22-week follow-up measures.
Control participants will not be assigned a Case Manager and will not receive any comparable services from our agency until they complete their 22-week measures.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Family Environment Survey (FES)
Time Frame: 22 weeks after baseline
|
The FES was developed to measure social and environmental characteristics of families.
Face and content validity are supported by clear statements about family situations that relate to subscale domains, and the measure can differentiate between distressed and normal family samples.
|
22 weeks after baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Revised Dyadic Adjustment Scale (RDAS)
Time Frame: 22 weeks after baseline
|
The RDAS is a 32-item self-report standardized measure with 4 subscales (Dyadic Consensus, Dyadic Satisfaction, Affectional Expression, Dyadic Cohesion) in addition to a total score.
|
22 weeks after baseline
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Economic Self-Sufficiency Scale (ESS)
Time Frame: 22 weeks after baseline
|
The ESS includes the following subscales with demonstrated reliability and validity: 1) Financial Management Attitudes Scale, 2) Scale of Economic Self-Sufficiency, 3) Financial Knowledge Scale, 4) Family Empowerment Scale, and 5) Financial Management and Planning Behaviors.
|
22 weeks after baseline
|
Collaborators and Investigators
Investigators
- Study Director: Katelyn Kopakin, MA, Jewish Family Children's Services of the Suncoast, Inc.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20220208
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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