- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03568565
Automated & Coached Web-based Programs to Improve and Strengthen Romantic Relationships
Web-based Marriage Preparation/Enrichment and Divorce Prevention for Low-Income Couples
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Nationwide, lower-income (LI) couples (those with household incomes <200% of the federal poverty level) - many of whom are also African American, Hispanic/Latino, or rural couples - face numerous challenges to their relationships. Chief amongst those challenges are: 1) higher risk of relationship problems and 2) lack of access to effective relationship services to prevent or intervene with relationship distress. Compared to higher-income couples, LI married and cohabiting couples are significantly more likely to divorce or separate and report lower relationship quality. Unfortunately, LI couples are least likely to receive interventions to prevent or solve relationship problems. To overcome these barriers, we propose to test the effectiveness of two effective web-based curricula - OurRelationship and PREP Online.
A total of 1,246 LI couples will be recruited nationwide and randomly assigned to the ePREP program, the OurRelationship program, the ePREP program plus a coach, the OurRelationship program plus a coach, or a wait-list control group and followed for six months. Once randomly assigned to group, couples will be assessed at one month, two months, four months, and six months following randomization. After couples randomized to the wait-list control group finish their waiting period, they will be able to select the program they would like to complete (OurRelationship or ePREP) but will not complete research assessments during or following their participation in the program.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Florida
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Coral Gables, Florida, United States, 33146
- University of Miami
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- They are married, engaged, or have been cohabiting with their partner for at least six months
- They are both located in the United States
- Both partners are willing to participate in the study
- Both partners are between the ages of 18 and 64 (inclusive)
- Couples report a household income at or below 200% of the Federal Poverty Level.
Exclusion Criteria:
- Severe domestic violence
- Inadequate internet connection
- Previous participation in OR, PREP-O, in-person PREP, or its variants
- Current participation in other relationship programs
- Current participation in an evaluation funded by Administration for Children and Families
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ePREP Program
The ePREP program is based on the in-person Prevention and Relationship Enhancement Program.
The ePREP program consists of six sections of material.
In each section, new information and skills are presented, videos demonstrate real couples practicing the skills, participants are encouraged to discuss the information in the context of their own relationship, and a multiple choice quiz reiterates and summarizes the section.
In addition to the core educational materials, couples are asked to complete six additional online and offline homework assignments (one per week), each lasting approximately one hour.
Participants who do not complete activities in a timely manner will be re-randomized to either continue without a coach or to receive a coach.
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see arm descriptions
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Experimental: ePREP Program plus Coach
The ePREP program is based on the in-person Prevention and Relationship Enhancement Program.
The ePREP program consists of six sections of material.
In each section, new information and skills are presented, videos demonstrate real couples practicing the skills, participants are encouraged to discuss the information in the context of their own relationship, and a multiple choice quiz reiterates and summarizes the section.
In addition to the core educational materials, couples are asked to complete six additional online and offline homework assignments (one per week), each lasting approximately one hour.
Couples also have four, brief video or phone calls with a coach throughout the program.
|
see arm descriptions
|
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Experimental: OurRelationship Program
The OurRelationship program is based on Integrative Behavioral Couple Therapy and encourages couples to select, understand, and solve a relationship problem.
Partners complete the majority of the web-based program on their own and come together for three key conversations with their partner.Participants who do not complete activities in a timely manner will be re-randomized to either continue without a coach or to receive a coach.
|
see arm descriptions
|
|
Experimental: OurRelationship Program plus Coach
The OurRelationship program is based on Integrative Behavioral Couple Therapy and encourages couples to select, understand, and solve a relationship problem.
Partners complete the majority of the web-based program on their own and come together for three key conversations with their partner.
The first conversation between partners centers on discussing possible core relationship issues and jointly deciding on the problem(s) to focus on during the program.
During the second conversation, both partners' previous written responses are displayed on the screen and conversation is encouraged.
During the final conversation, couples share their strategies to decrease stress, improve patterns of communication, and engage in problem-solving exercises specific to their core issue(s).
Couples also have four, brief video or phone calls with a coach throughout the program.
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see arm descriptions
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No Intervention: Waitlist
Participants are assessed at 1, 2, 4, and 6 months after randomization; however, no active intervention is given during the waitlist period.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Relationship Satisfaction
Time Frame: Baseline, 2 months after baseline, and 6 months after baseline
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Four-item Couple Satisfaction Index (CSI) self-report measure.
Range of scores 0 to 21, with higher scores indicating greater satisfaction.
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Baseline, 2 months after baseline, and 6 months after baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Communication Conflict
Time Frame: Baseline, 2 months after baseline, and 6 months after baseline
|
7-item scale; self-report of communication conflict.
Range of scores 7 to 28, with higher scores indicating greater conflict.
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Baseline, 2 months after baseline, and 6 months after baseline
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Relationship break-up potential
Time Frame: Baseline, 2 months after baseline, and 6 months after baseline
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3-item self-report measure of likelihood of relationship ending in the near future.
Range of scores 3 to 15, with higher scores indicating greater potential for the relationship to end.
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Baseline, 2 months after baseline, and 6 months after baseline
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brian D Doss, Ph.D., PROFESSOR
Publications and helpful links
Helpful Links
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 (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
- 20160451-R
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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