- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01795963
ePREP for Community Couples
February 19, 2013 updated by: Scott R. Braithwaite, Ph.D., Brigham Young University
The purpose of the present study is to examine the impact of ePREP when it is administered to couples.
More specifically, investigators will test whether--compared to placebo controls--participants who receive ePREP will experience better outcomes for relationship relevant variables.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
104
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
-
-
Florida
-
Tallahassee, Florida, United States, 32309
- Florida State University
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Only those who are married or who have been in a committed romantic relationship for six months or longer will be invited to participate.
Exclusion Criteria:
- The only exclusionary criteria were inability to read study questionnaires and unwillingness to access the internet to receive e-mail instructions on weekly homework assignments.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Placebo Control
Participants in the control condition will view a presentation that teaches inert information about anxiety, depression, and relationships such as definitions, prevalence rates, common problems associated with these conditions and available forms of treatment.
This presentation was used initially in Cuckrowicz & Joiner (2007) and has since been shown to be effective as a placebo in two previous ePREP studies (Braithwaite & Fincham, 2007; Braithwaite & Fincham, 2008).
This presentation is identical to the ePREP intervention in its set up, the only difference being, there is no information included in this presentation that teaches specific skills or strategies for improving relationships, depression or anxiety.
|
Participants in the control condition will view a presentation that teaches inert information about anxiety, depression, and relationships such as definitions, prevalence rates, common problems associated with these conditions and available forms of treatment.
This presentation was used initially in Cuckrowicz & Joiner (2007) and has since been shown to be effective as a placebo in two previous ePREP studies (Braithwaite & Fincham, 2007; Braithwaite & Fincham, 2008).
This presentation is identical to the ePREP intervention in its set up, the only difference being, there is no information included in this presentation that teaches specific skills or strategies for improving relationships, depression or anxiety.
|
Active Comparator: ePREP
The ePREP intervention teaches individuals how to recognize and combat dynamic risk factors that lead to relationship distress.
|
The ePREP intervention teaches individuals how to recognize and combat dynamic risk factors that lead to relationship distress.
Specifically, it teaches communication techniques and problem-solving skills that help couples to effectively deal with conflict.
It also teaches couples how to enhance positive aspects of their relationship by fostering fun and friendship.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Revised Conflict Tactics Scale (CTS-2)
Time Frame: Change across three time-points: baseline, 6-week follow up and 1-year follow up
|
Change across three time-points: baseline, 6-week follow up and 1-year follow up
|
Communication Patterns Questionnaire (CPQ)
Time Frame: Change across three time-points: baseline, 6-week follow up and 1-year follow up
|
Change across three time-points: baseline, 6-week follow up and 1-year follow up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Scott R Braithwaite, Ph.D., Brigham Young University
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
June 1, 2009
Primary Completion (Actual)
August 1, 2010
Study Completion (Actual)
August 1, 2010
Study Registration Dates
First Submitted
February 15, 2013
First Submitted That Met QC Criteria
February 19, 2013
First Posted (Estimate)
February 21, 2013
Study Record Updates
Last Update Posted (Estimate)
February 21, 2013
Last Update Submitted That Met QC Criteria
February 19, 2013
Last Verified
February 1, 2013
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2009.2841
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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