EFCT vs. BCT for Depression and Anxiety in Married Couples
EFCT-BCT
A Comparison of the Effectiveness of Emotion-Focused Couples Therapy and Behavioral Couples Therapy in Reducing Depression and Anxiety Symptoms in Married Couples
1 other identifier
interventional
150
1 country
1
Brief Summary
This study compares the effectiveness of Emotion-Focused Couples Therapy (EFCT) and Behavioral Couples Therapy (BCT) in reducing depression and anxiety symptoms in married couples. A total of 150 married couples aged 18-65 will be screened, and 60 couples with high depression and anxiety levels will be selected. These couples will be randomly assigned to one of three groups: EFCT, BCT, or a control group. Therapy sessions will be conducted weekly for 12 weeks, with assessments before therapy, after the 6th and 12th sessions, and at a 3-month follow-up. The study aims to determine which therapy is more effective in improving mental health outcomes in couples.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedFirst Submitted
Initial submission to the registry
February 16, 2025
CompletedFirst Posted
Study publicly available on registry
March 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2025
CompletedMarch 25, 2025
March 1, 2025
7 months
February 16, 2025
March 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
The Beck Depression Inventory-II (BDI-II)
The Beck Depression Inventory-II (BDI-II) will be used to measure changes in depression symptoms over time. Scores range from 0 to 63, with higher scores indicating more severe depressive symptoms.
Baseline, after the 6th session (6 week), after the 12th session (12 week), and at 3-month follow-up (24 week)
The Beck Anxiety Inventory (BAI)
The Beck Anxiety Inventory (BAI) will be used to measure changes in anxiety symptoms over time. Scores range from 0 to 63, with higher scores indicating more severe anxiety symptoms.
Baseline, after the 6th session (6 week), after the 12th session (12 week), and at 3-month follow-up (24 week)
Study Arms (3)
Emotion-Focused Couples Therapy (EFCT) Group
EXPERIMENTALParticipants in this group will receive Emotion-Focused Couples Therapy, consisting of 12 weekly 50-minute sessions focused on emotional expression, attachment needs, and improving emotional bonds between partners.
Behavioral Couples Therapy (BCT) Group
EXPERIMENTALParticipants in this group will receive Behavioral Couples Therapy, consisting of 12 weekly 50-minute sessions focused on modifying maladaptive behaviors, enhancing communication, and developing problem-solving strategies.
Control Group
NO INTERVENTIONParticipants in this group will receive no therapeutic intervention during the study period but will be offered therapy after the study is completed.
Interventions
EFCT is a structured approach to couples therapy that focuses on helping partners understand and express their emotions, address attachment insecurities, and strengthen their emotional connection.
BCT is a form of therapy that aims to improve relationship satisfaction through behavioral change, communication training, and problem-solving techniques.
Eligibility Criteria
You may qualify if:
- Married couples aged between 18 and 65 years
- Married for at least one year
- No current psychiatric diagnosis or history of psychiatric treatment
- Not receiving any form of psychological therapy at the time of recruitment
- Ability to provide informed consent
- Willingness to participate in all therapy sessions and assessments
You may not qualify if:
- Current or past psychiatric diagnosis (excluding mild transient conditions)
- Ongoing psychological therapy or psychiatric treatment
- Severe mental health disorders (e.g., schizophrenia, bipolar disorder), Substance abuse or dependency
- Severe medical conditions that may interfere with participation
- Refusal to participate in follow-up assessments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Beykoz Universitylead
- Uskudar Universitycollaborator
- Istanbul Nisantasi Universitycollaborator
Study Sites (1)
Beykoz University
Istanbul, Istanbul, 34820, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eda Yılmazer, Phd
Beykoz University
- PRINCIPAL INVESTIGATOR
Metin Çınaroğlu, Phd
Istanbul Nisantasi University
- PRINCIPAL INVESTIGATOR
Selami VArol Ülker, Phd
Üsküdar University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Primary Investigator
Study Record Dates
First Submitted
February 16, 2025
First Posted
March 25, 2025
Study Start
January 1, 2025
Primary Completion
August 1, 2025
Study Completion
September 15, 2025
Last Updated
March 25, 2025
Record last verified: 2025-03