Evaluation of the Refugee Family Strengthening (RFS) Program

April 27, 2020 updated by: US Committee for Refugees and Immigrants

Evaluation of the U.S. Committee for Refugees and Immigrants (USCRI): Refugee Family Strengthening (RFS) Program

The US Committee for Refugees and Immigrants (USCRI) will be conducting an evaluation of a healthy marriage and relationship program developed by USCRI titled Refugee Family Strengthening (RFS) Program. This program is funded through an initiative of the Administration for Children and Families, Office of Family Assistance (OFA).

The study is intended to measure if the identified interventions improve the well-being of individuals and families within the refugee and immigrant population served by USCRI. Outcomes to be measured include behavioral outcomes and perceptual changes towards healthy relationships, family development, and positive home environment. The study will examine the following:

  1. Participants will identify utilizing healthy marriage and relationship skills.
  2. Participants will report an increase in satisfaction with conflict management with others after completion of the relationship workshop series.
  3. Participants will report an increase in quality and time spent with children.
  4. Participants will report an increase in economic stability.

Study Overview

Detailed Description

The US Committee for Refugees and Immigrants (USCRI) will be conducting an evaluation of a healthy marriage and relationship program developed by USCRI titled Refugee Family Strengthening (RFS) Program. This program is funded through an initiative of the Administration for Children and Families, Office of Family Assistance (OFA).

The Refugee Family Strengthening (RFS) Program builds on literature and existing research from the healthy marriage and relationship initiatives developed by ACF over the last 10 years, in particular the Supporting Healthy Marriage Program initiative that established a randomized clinical trial. In addition, marriage and relationship education/ enrichment literature and research has expanded dramatically over the past 35 years. The most glaring shortcoming of this database is the limited types of populations that are sampled and included in studies. USCRI's RFS program will provide important data about a diverse group of subjects that is currently unavailable.

The aim of the evaluation is to determine the effect of participating in two interventions on the population of refugee and immigrant couples, families, and individuals, served by USCRI. The program will target individuals ages 16 and older using a randomized control design. The program will be implemented with individuals, couples, and families. RFSP will recruit 9,350 individuals over the 5 year tenure of the project, 3115 of which will serve as control subjects, the remaining 6,235 subjects will be randomly assigned to intervention groups at each of the 11 selected sites that are participating in the project. Control subjects will not receive the intervention workshops, only case management.

The intervention is to be delivered as follows:

Group I: Intro to Relationship Enhancement (RE) (8 hours), Family Stress & Conflict Management (8 hours), and case management Group II: Intro to Relationship Enhancement (RE) (8 hours), & Financial Management (8 hours), and case management Group III: Case management ONLY

Data will be collected and analyzed across 3 collection points: Pre-test immediately before the start of the interventions, Post-test immediately upon completion of the interventions, and again at 6 months following the pre-test date.

Results will be analyzed to determine gains towards the following research questions:

When participating in the RFS program:

  1. Do individuals who participate in the two RFS interventions demonstrate favorable impact in the four program outcomes as compared to those who participate in the control?
  2. What are the differences in gains for subjects who participate in the two different interventions?
  3. What are the long-term effects of participation in the RFS interventions on individuals?

The local evaluation is expected to reflect progress toward project outcomes and is anticipated to demonstrate significant results that will be highlighted and prepared for dissemination.

Study Type

Interventional

Enrollment (Actual)

5365

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • California
      • Los Angeles, California, United States, 90033
        • International Institute of Los Angeles
    • Iowa
      • Des Moines, Iowa, United States, 50314
        • USCRI Des Moines
    • Michigan
      • Dearborn, Michigan, United States, 48126
        • USCRI Detroit
    • Missouri
      • Kansas City, Missouri, United States, 64110
        • Jewish Vocational Services
      • Saint Louis, Missouri, United States, 63118
        • International Institute of St. Louis
    • New York
      • Albany, New York, United States, 12204
        • USCRI Albany
    • North Carolina
      • Raleigh, North Carolina, United States, 27609
        • USCRI North Carolina
    • Pennsylvania
      • Erie, Pennsylvania, United States, 16504
        • International Institute of Erie
      • Philadelphia, Pennsylvania, United States, 19107
        • Nationalities Services Center
    • Texas
      • Houston, Texas, United States, 77057
        • YMCA International Services
    • Vermont
      • Colchester, Vermont, United States, 05446
        • Vermont Refugee Resettlement Program

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Refugee or Immigrant

Exclusion Criteria:

  • Individuals under the age of 16
  • Individuals that are not identified as refugees or immigrants

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group I
Participants in Group I will receive the following interventions: Intro to Relationship Enhancement (8 hours), Family Stress and Conflict Management (8 hours), and case management
Relationship Enhancement is a curriculum based program provided by a facilitator over an 8 hour skill-based education intervention.
Family Stress and Conflict Management is a curriculum based program provided by a facilitator over an 8 hour skill-based education intervention.
Experimental: Group II
Participants in Group II will receive the following interventions: Intro to Relationship Enhancement (8 hours), RE & Financial Management (8 hours), and case management
Relationship Enhancement is a curriculum based program provided by a facilitator over an 8 hour skill-based education intervention.
Family Management is a curriculum based program provided by a facilitator over an 8 hour skill-based education intervention.
No Intervention: Group III
Participants in Group III will receive the the standard care of all participants, case management ONLY

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Healthy Relationship Skills
Time Frame: At program enrollment-during registration, immediately after completing 8 hour Relationship Enhancement intervention and at 6 month follow up.
Questionnaire developed for intervention to measure change from before 8 hour intervention to after intervention
At program enrollment-during registration, immediately after completing 8 hour Relationship Enhancement intervention and at 6 month follow up.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Conflict Management Skills
Time Frame: At program enrollment-during registration, immediately after completing 8 hour Conflict Resolution intervention and at 6 month follow up.
Questionnaire developed for intervention to measure change from before 8 hour intervention to after intervention
At program enrollment-during registration, immediately after completing 8 hour Conflict Resolution intervention and at 6 month follow up.
Economic Stability
Time Frame: At program enrollment-during registration, immediately after completing 8 hour Financial Literacy intervention and at 6 month follow up.
Questionnaire developed for intervention to measure change from before 8 hour intervention to after intervention
At program enrollment-during registration, immediately after completing 8 hour Financial Literacy intervention and at 6 month follow up.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jennifer Salerno, DNP, Possibilities for Change

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2016

Primary Completion (Actual)

March 31, 2020

Study Completion (Actual)

March 31, 2020

Study Registration Dates

First Submitted

June 29, 2016

First Submitted That Met QC Criteria

July 7, 2016

First Posted (Estimate)

July 12, 2016

Study Record Updates

Last Update Posted (Actual)

April 28, 2020

Last Update Submitted That Met QC Criteria

April 27, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 90FM0092-01-00

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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