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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05702736
Other study ID # 20-3T/42
Secondary ID 20-3T/42
Status Completed
Phase N/A
First received
Last updated
Start date March 4, 2020
Est. completion date September 4, 2022

Study information

Verified date January 2023
Source Ege University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

The research was conducted to examine the effect of logotherapy-based intervention practiced to depressed patients on depression, psychological pain and meaning of life. The research is in a quasi-experimental research design with pre-test post-test follow-up measurement, control group. Sample selection was carried out in two stages, and in the first stage, 48 patients diagnosed with depression between September 2020 and September 2022 were referred to the researcher by the polyclinic physician. The patients were evaluated within the scope of the inclusion criteria of the study, and 32 patients with a diagnosis of depression, aged 18-65 years, voluntarily aged between 18-65, who scored 17 points or more from the Beck Depression Inventory, were accepted into the study. Patients were assigned to intervention and control groups, respectively. A total of 28 patients, 12 intervention and 16 control groups, completed the study. "Descriptive Information Form", "Beck Depression Inventory", "Psychache Scale" and "Meaning of Life Questionnaire" were used as data collection tools in the study. Online logotherapy-based intervention was administered to the individuals in the intervention group as a total of eight sessions, once a week. In order to evaluate the effect of logotherapy-based intervention, Beck Depression Inventory, Psychache Scaleand Meaning of Life Questionnaire were administered to all individuals in the sample group at time series points (pretest, posttest, follow-up test at 3rd month). In the analysis of the data, descriptive statistics, independent t-test, chi-square analysis, analysis of variance in repeated measurements, Bonferroni correction were applied.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date September 4, 2022
Est. primary completion date February 4, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
logotherapy-based intervention
Logotherapy-based intervention was administered to the individuals in the intervention group as a total of eight sessions, once a week.

Locations

Country Name City State
Turkey Ege University Faculty of Nursing Izmir

Sponsors (1)

Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary "Beck Depression Inventory" scores Decreased "Beck Depression Inventory"scores of intervention group in post test and follow-up measurements after logotherapy-based intervention A total of five months of logotherapy-based practice for each patient
Primary "Psychache Scale" scores Decreased "Psychache Scale" scores of the intervention group in post test and follow-up measurements after logotherapy-based intervention A total of five months of logotherapy-based practice for each patient
Primary "Meaning of Life Questionnaire" scores Increased "Meaning of Life Questionnaire" scores of intervention group in post test and follow-up measurements after logotherapy-based intervention A total of five months of logotherapy-based practice for each patient
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