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Clinical Trials in Turkey / NCT07484789
Starting soon Not applicable

Effect of Mindfulness-based Psychoeducation in Depression

NCT07484789 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-04-01
Last updated
2026-03-20

Condition(s) studied

Depression - Major Depressive DisorderMindfulness Based Stress ReductionPsychiatric Nursing

Investigational drug(s) / intervention(s)

Mindfulness-based psychoeducation

Mindfulness-based psychoeducation: The experimental group will receive an 8-session mindfulness-based psychoeducation program, administered twice a week for four weeks. Each session of the eight-week program will be 45-60 minutes long. Sessions will be conducted in groups. Following an initial face-to-face meeting to inform the experimental group about the program and schedule meetings, the sessions will continue in person. Each group will consist of 7 people, with a total of 5 groups. Patients will be contacted by phone before each session to remind them of the program time. Immediately after the program sessions are completed, the experimental group will take a post-test. Additionally, follow-up tests will be administered two months after the program is completed. The control group will receive a pre-test followed by no intervention; a post-test will be administered two months later, and follow-up tests two months after the post-test.

Study summary

Major depression is a mental illness that seriously threatens public health, leading to disability, reduced quality of life, economic burden, and premature death. It is estimated that 18.4% of the world's population lived with depression between 2005 and 2015, and it is projected to be a leading cause of global disease burden by 2030. Major depressive disorder manifests with symptoms such as decreased interest and desire, a depressed mood, increased or decreased sleep and appetite, feelings of worthlessness and guilt, decreased energy, suicidal thoughts and attempts, leading to significant impairment in functioning. Choosing the appropriate treatment for depression and taking measures to improve the individual's functionality quickly, shorten hospital stays, and reduce the number of hospitalizations are crucial. In addition to pharmacological treatment, clinical guidelines recommend the combined use of pharmacological and psychosocial interventions in the treatment of depression. The mindfulness-based cognitive therapy, which forms the basis of the psychoeducation planned for this study, was developed as an 8-week group approach. Theoretical studies examining emotion regulation mechanisms have indicated that mindful awareness is a fundamental mechanism for emotion regulation. The literature suggests a negative correlation between mindful awareness and the severity of depressive symptoms and difficulty in emotion regulation. Furthermore, despite numerous descriptive, correlational, and experimental studies on major depression, no studies have been found demonstrating the effect of mindful awareness-based psychoeducation on emotion regulation difficulties, distress tolerance, and symptom severity in patients diagnosed with major depression. This study, therefore, differs from existing research and will make a significant contribution to the literature.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Volunteering to participate in the study * Residing in Gaziantep city center * Not having any communication impediments * Being between 18 and 65 years of age * Being followed up as an outpatient with a diagnosis of depression according to DSM-V criteria * Having been receiving treatment for depression for at least 6 months * Being literate * Not having been enrolled in such an educational program related to their illness within the last 5 years Exclusion Criteria: * Those diagnosed with another comorbid mental illness * Patients with mental conditions that make cooperation impossible, such as intellectual disability or dementia * Those who are illiterate * Patients who do not consent to the interview * Those receiving inpatient treatment

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gaziantep Üniversitesi Gaziantep şehitkamil

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07484789 on ClinicalTrials.gov ↗ ← All trials in Turkey