Actively Recruiting
The Effect of Mindfulness-Based Psychoeducation
Led by University of Gaziantep · Updated on 2024-05-16
60
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is a randomized controlled experimental study conducted to determine the effect of mindfulness-based psychoeducation on levels of mindfulness, cognitive defusion, and depression in patients with depression. The sample of the study will consist of 60 patients (30 experimental, 30 control) diagnosed with major depression, recruited from a state hospital. Mindfulness-based psychoeducation will be applied to the experimental group once a week for a total of 8 weeks in the form of group sessions. No intervention other than routine treatment will be applied to the control group. The primary questions that the study aims to answer are as follows: Does mindfulness-based psychoeducation increase levels of mindfulness and cognitive defusion in depression patients? Does mindfulness-based psychoeducation decrease levels of depression in depression patients?
CONDITIONS
Official Title
The Effect of Mindfulness-Based Psychoeducation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be literate
- Willing to participate in the study voluntarily
- No communication barriers
- Aged between 18 and 65 years
- Outpatients diagnosed with major depressive disorder according to DSM-5 criteria
- Have not participated in a mindfulness-based psychoeducation program for depression in the last 5 years
You will not qualify if you...
- Diagnosed with other comorbid psychiatric disorders
- Have intellectual impairment or cognitive conditions like dementia making cooperation impossible
- Have psychotic symptoms along with depression
- Illiterate individuals
- Do not consent to interview
- Currently receiving inpatient treatment
AI-Screening
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Trial Site Locations
Total: 1 location
1
Gaziantep University
Gaziantep, Turkey (Türkiye)
Actively Recruiting
Research Team
R
Rabia ARPACI, Student
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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