- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05587335
Project Harmony 2.0: Relationship Education for Couples
October 18, 2022 updated by: University of Central Florida
Project Harmony 2.0: A Relationship Education Intervention for Couples
Project Harmony directly addresses prioritized areas identified by Administration of Children and Families, emphasizing healthy marriage promotion activities and career advancement opportunities for adults.
Included in service provisions are elements of: [a] marriage and relationship education/skills, [b] marriage enhancement, [c] divorce reduction and [d] job and career advancement.
The targeted service population for Project Harmony includes married/committed couples in the greater Orlando metro area.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The primary program consists of 12 hours of relationship education.
The investigators seek to conduct an impact evaluation utilizing a randomized control trial (RCT) to compare outcomes of couples enrolled in either face to face relationship education or web-based relationship education to assess the impact of program structure on outcomes.
By offering both face to face and online versions of evidenced based curricula, the investigators are directly addressing requests from ongoing needs assessments of our targeted population.
The project is designed for couples 18 years and older; all participants in the face-to-face group will receive the Prevention and Relationship Education Program (PREP) 8.0 + Career Pathways Program (CPP) curricula whereas couples in the online group will receive the OurRelationship Intervention + CPP curricula.
Study Type
Interventional
Enrollment (Anticipated)
1800
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 Contact
- Name: Sejal Barden
- Phone Number: 4078231748
- Email: sejal.barden@ucf.edu
Study Locations
-
-
Florida
-
Orlando, Florida, United States, 32816
- Recruiting
- University of Central Florida
-
Contact:
- Sejal Barden, PhD
- Phone Number: 407-823-1748
- Email: sejal.barden@ucf.edu
-
-
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
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Must be 18 years older and be in a committed relationship, must attend with partners
Exclusion Criteria:
-
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: In person
Couples will be assigned into in person relationship intervention.
|
Relationship intervention to improve communication and conflict resolution for couples
|
|
Experimental: Online
Couples will be assigned into online relationship intervention.
|
Relationship intervention to improve communication and conflict resolution for couples
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Revised Dyadic Adjustment Scale
Time Frame: 6 months
|
The Revised Dyadic Adjustment Scale (RDAS) is a self report questionnaire that assesses seven dimensions of couple relationships.
The RDAS includes only 14 items, ranging from 0 to 69 with higher scores indicating greater relationship satisfaction and lower scores indicating greater relationship distress.
The cut-off score for the RDAS is 48 such that scores of 48 and above indicate non-distress and scores of 47 and below indicate marital/relationship distress.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 1, 2022
Primary Completion (Anticipated)
April 1, 2025
Study Completion (Anticipated)
September 29, 2025
Study Registration Dates
First Submitted
September 22, 2022
First Submitted That Met QC Criteria
October 18, 2022
First Posted (Actual)
October 20, 2022
Study Record Updates
Last Update Posted (Actual)
October 20, 2022
Last Update Submitted That Met QC Criteria
October 18, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- UCFloirda
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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