N/A
Completed N=32
The Effect of Logotherapy-Based Intervention on Depression Patients on Depression,Psychological Pain and Meaning of Life
Source: ClinicalTrials.gov NCT05702736 ↗Enrolled (actual)
32
Serious AEs
—
Results posted
Apr 2025
Primary outcomePrimary: "Beck Depression Inventory" Scores — 17.75; 30.62; 13.58; 31.18 score on a scale
Summary
The goal of this interventional study is to compare in logotherapy-based intervention practiced to depressed patients on depression, psychological pain and meaning of life. The main questions it aims to answer are:
* Is the logotherapy-based intervention practiced in addition to the standard treatment in depression patients effective in reducing the depression levels of the patients?
* Is the logotherapy-based intervention practiced in addition to the standard treatment in depression patients effective in reducing the psychological pain levels of the patients?
* Is the logotherapy-based intervention practiced in addition to the standard treatment in depression patients effective in increasing the patients' level of meaning to life? Participants will be done online interview once a week for eight sessions. Researchers will compare intervention and control groups to see if logotherapy-based intervention practiced effect depression, psychological pain and meaning of life levels.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY "Beck Depression Inventory" Scores |
17.75; 30.62; 13.58; 31.18 | — |
| PRIMARY "Psychache Scale" Scores |
27.83; 45.81; 27.83; 46.25 | — |
| PRIMARY "Meaning of Life Questionnaire" Scores |
42.83; 39.25; 50.25; 37.81 | — |
Eligibility Criteria
Inclusion Criteria
- Be between the ages of 18-65
- Having been diagnosed with depression
- A score of 17 or higher on the Beck Depression Inventory
- Willingness and willingness to participate in the research
- Completed at least six interviews
Exclusion Criteria
- Having an active risk of suicide
- Having psychotic symptoms
- Having a psychiatric comorbidity
- Using antipsychotic medication
Data sourced from ClinicalTrials.gov (NCT05702736). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.