- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06234696
Cognitive Behavioral Therapy by Humor Based Psychoeducation
The Effect of Based Cognitive Behavioral Therapy by Humor Based Psychoeducation on Sense of Humour, Self Esteem and Depression Levels Patient in Diagnosed With Depression
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Aim: This study aims to reveal the effectiveness of based cognitive behavioral therapy by humor based psychoeducation on sense of humour, self esteem and depression level patient in diagnosed with depression .
Method: This study will be conducted as a randomized controlled experimental study by the researcher, who is a specialist psychiatric nurse, to the elderly patient in diagnosed with depression staying in the mardin traning and research hospital and kızıltepe state hospital. In the study, "power analysis" was performed and a total of 44 individuals, including 22 intervention people and 22 control group, were considered suitable for the sample size. It was decided to have 30 people in the groups, considering the high power of the test and the loses in the study. Accordingly, 30 people were determined as the intervention group and 30 people as the control group. In this study, personal ınformation form, coping humor scale, rosenberg self-esteem scale, beck depression scale, multidimensional sense of humor scale.
Findings: Aims to reveal the effectiveness of based cognitive behavioral therapy by humor based psychoeducation on sense of humour, self esteem and depression levels patient in diagnosed with depression .
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Mardin, Turkey, 47000
- Fatima
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Volunteering to participate in the study
- Not having any obstacle to communication
- Being between the ages of 18 and 65
- Being monitored on an outpatient basis with a diagnosis of depression according to the diagnostic and statistical manual of mental disorders criteria
- Being literate
- Not having undergone such training in the last 6 months
Exclusion Criteria:
- Serious factors that may prevent you from answering the survey
- Presence of physical and cognitive disability
- Refusing to participate in the study after being informed
- Having a comorbid psychiatric diagnosis
- A patient diagnosed with depression with psychotic features
- Having received any psychotherapy in the last 6 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: experimental group
The group consists of 30 people and this group will be given psychoeducation for 4 weeks. Training will be provided 2 days a week (monday and friday). |
The experimental group will be given psychoeducation for 4 weeks.
|
No Intervention: control group
The group consists of 30 people and this group will not be trained.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Data Collection Tools Personel İnformation Form
Time Frame: Between 1-3 months
|
Data Collection Tools Personel İnformation Form: form, organised by the researchers, includes 16 questions to determine the demograhic information of the participants.
|
Between 1-3 months
|
Coping humor scale
Time Frame: Between 1-3 months
|
Coping humor scale: The scale is a 4-point Likert-tybe scale (1: Strongly disagree - 4: Completely agree) consisting of 7 items.
The lowest score to be obtained from the scale 7 and the highest score is 28.
Rising scores indicate that individuals have a higher level of ability to use humor as a coping strategy in stressful situations.
|
Between 1-3 months
|
Multidimensional sense of humor scale
Time Frame: Between 1-3 months
|
Multidimensional sense of humor scale:The scale consists of a total of 24 items and four subscales.
The items in the scale are avaluated using 5- point likert tybe scale (0= strongly disagree, 4 = strongly agree) The lowest score to be obtained from the scale 0 and the highest score is 96.In addition to a general sense of humor score, the scale has 4 subscales: producing humor, coping using humor, attitude towards people who produce humor, and humor evaluation.
|
Between 1-3 months
|
Rosenberg self-esteem scale
Time Frame: Between 1-3 months
|
Rosenberg self-esteem scale: The scale consists of total 63 items and 12 subscales.In our study, only the part of the scale related to self-esteem will be used.
The self-esteem subscale is a Likert-type subscale consisting of 4 items and includes the first 10 items of the inventory.
Each statement contains 4-point Likert type options (4=very true, 3=true,2= false,1= very false).
When evaluating, in positive statements, the "very true" option is 4 points, the "very wrong" option is 1 point; For negative expressions, the calculation was made exactly the opposite.
Depending on the evaluation method of the scale, 0-6 points can be obtained.
Thus, the person who completes the test can get a maximum of 6 points in total.
5-6 points were determined as low self-esteem, 2-4 points as medium self-esteem, and 0-1 points as high self-esteem.
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Between 1-3 months
|
Beck depression scale
Time Frame: Between 1-3 months
|
Beck depression scale: This scale consists of 21 items and each item has four options.
The four options in each symptom category of the scale receive a score between 0 and 3.
The highest score that can be obtained from the scale is 63.
A high total score indicates a high level or severity of depression symptoms.10-17
points from the scale indicate mild depression, 18-29 points indicate moderate depression, and 30-63 points indicate severe depression.
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Between 1-3 months
|
Data Analysis
Time Frame: Between 1-3 months
|
Data Analysis: The data obtained from the study will be analysed in Statistical Packkage for Social Sciences 22 package programme.
Repeated Measures Analysis Of Variance was used to compare the scale scores and Fisher Least Significant Difference test was used for multiple comparisons of Group Time interaction
|
Between 1-3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: nurgül özdemir, 05332352154
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AIBU-SBF-FŞ-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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