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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01795963
Other study ID # 2009.2841
Secondary ID
Status Completed
Phase N/A
First received February 15, 2013
Last updated February 19, 2013
Start date June 2009
Est. completion date August 2010

Study information

Verified date February 2013
Source Brigham Young University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 104
Est. completion date August 2010
Est. primary completion date August 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
ePREP
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.
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.

Locations

Country Name City State
United States Florida State University Tallahassee Florida

Sponsors (3)

Lead Sponsor Collaborator
Brigham Young University Department of Health and Human Services, Florida State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Revised Conflict Tactics Scale (CTS-2) Change across three time-points: baseline, 6-week follow up and 1-year follow up Yes
Primary Communication Patterns Questionnaire (CPQ) Change across three time-points: baseline, 6-week follow up and 1-year follow up No
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