Cognitive Behavioral Therapy by Humor Based Psychoeducation

January 28, 2024 updated by: Fatima Ozdemir Sigva, University of Gaziantep

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

This study aims to reveal the effectiveness of based cognitive behavioral therapy by humor based psychoeducation on sense of humour, self-esteem and depressıon level patient in diagnosed with deppression .

Study Overview

Status

Active, not recruiting

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

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Mardin, Turkey, 47000
        • Fatima

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
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.
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

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: nurgül özdemir, 05332352154

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 30, 2022

Primary Completion (Estimated)

June 1, 2024

Study Completion (Estimated)

July 1, 2024

Study Registration Dates

First Submitted

January 4, 2024

First Submitted That Met QC Criteria

January 28, 2024

First Posted (Actual)

January 31, 2024

Study Record Updates

Last Update Posted (Actual)

January 31, 2024

Last Update Submitted That Met QC Criteria

January 28, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • AIBU-SBF-FŞ-1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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