NCT06892613 EFCT vs. BCT for Depression and Anxiety in Married Couples
| NCT ID | NCT06892613 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Beykoz University |
| Condition | Depression Anxiety Disorder |
| Study Type | INTERVENTIONAL |
| Enrollment | 150 participants |
| Start Date | 2025-01-01 |
| Primary Completion | 2025-08-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 150 participants in total. It began in 2025-01-01 with a primary completion date of 2025-08-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility Criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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 & Investigator
Eda Yılmazer, Phd
PRINCIPAL INVESTIGATOR
Beykoz University
Frequently Asked Questions
Who can join the NCT06892613 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Depression Anxiety Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06892613 currently recruiting?
Yes, NCT06892613 is actively recruiting participants. Contact the research team at edayilmazer@beykoz.edu.tr for enrollment information.
Where is the NCT06892613 trial being conducted?
This trial is being conducted at Istanbul, Turkey (Türkiye).
Who is sponsoring the NCT06892613 clinical trial?
NCT06892613 is sponsored by Beykoz University. The principal investigator is Eda Yılmazer, Phd at Beykoz University. The trial plans to enroll 150 participants.
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