- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05662137
The Effect of Recognition and Expression of Emotions Program Applied to Schizophrenia Patients
The Effect of Recognition and Expression of Emotions Program Applied to Schizophrenia Patients Applying to Community Mental Health Center on Alexithymia and Emotion Expression
As a result of the positive and negative symptoms that occur in schizophrenia, patients with schizophrenia may experience negative emotions more frequently than individuals with other mental problems. Since these emotions can trigger psychotic symptoms, there is a need to develop effective emotion regulation strategies to be applied to patients with schizophrenia.
Aim: In this study, it was aimed to examine the effect of emotion recognition and expression program on alexithymia and emotion expression in patients with schizophrenia.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Sinop, Turkey, 57000
- Sinop Community Mental Health Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patient who had received a diagnosis of schizophrenia and comes to the Community Mental Health Center regularly,
- Being able to read and communicate
- Being 18 years of age or older,
- Not having mental retardation,
- Not having insight, understanding, hearing problems,
- Being in remission,
- Volunteering to study
Exclusion Criteria:
- Not diagnosed with clinical schizophrenia,
- Being under the age of 18,
- Having mental retardation,
- Having no insight,
- Not understanding and hearing,
- Not in remission
- Refusing to participate in the study
- Stop studying at any stage of the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
At the beginning of the study, data collection tools Personal Information Form, Expression of Emotions Scale, Toronto Alexithymia Scale, Positive and Negative Syndrome Scale will be applied to the control group. No intervention will be made in the control group. Measurement tools will be applied for the posttest. Emotional Expression Scale, Toronto Alexithymia Scale and Positive and Negative Syndrome Scale will be reapplied 1 month after the last session. |
|
|
Experimental: Experimental group
Emotion recognition and expression program is aimed to be carried out in 8-week sessions for schizophrenia patients included in the experimental group. Personal Information Form, Expression of Emotions Scale, Toronto Alexithymia Scale, Positive and Negative Syndrome Scale will be applied to the experiment. The principal investigator will lead the structured group sessions as the group leader. The principal investigator will lead the structured group sessions as the group leader. Each group is planned to be 60-90 minutes. Before sessions, participants are taken from their previous session's emotions so far. Homework is discussed by providing recall of the topic from the previous session, and then the current topic is moved on. At the end of each session, a general summary and evaluation is made. After the sessions in the research, measurement tools will be applied for the posttest. It will be reapplied 1 month after the last session. |
Emotion recognition and expression program consisting of 8 sessions will be used.
In this program, patients will have the opportunity to describe their emotions, explain emotions that are difficult to express such as anger, sadness, shame, guilt, and discuss the consequences of suppressed emotions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emotion Recognition and Expression
Time Frame: One day
|
Expression of Emotions Scale is used to measure the state of expression of emotions.
The scale was developed by King and Emmons (1990), and its Turkish validity and reliability were verified by Kuzucu (2011).
The measurement tool consists of a total of 16 items and 3 sub-dimensions.
It has positive, negative and closeness sub-dimensions.
It is a 7-point Likert type scale .The scores to be taken from the scale vary between 15 and 105, and as the scores obtained increase, it is seen that the tendency of the individual to express emotion increases.
The scale provides information about expressing emotions both in interpersonal relationships and independent of interpersonal relationships.
A high score indicates a high tendency to express emotions.
|
One day
|
|
Alexithymia
Time Frame: One day
|
Toronto Alexithymia Scale (TAS): The scale was developed by Bagby et al. (1994) Güleç et al. (2009) adapted into Turkish.
The scale consists of 20 items, has three sub-dimensions and is in a 5-point Likert type.
High scores indicate high alexithymic level.
There are sub-dimensions of difficulty in recognizing emotions, difficulty in putting emotions into words, and extroverted thinking.
|
One day
|
|
Positive and Negative Syndrome
Time Frame: One day
|
Positive and Negative Syndrome Scale (PANNS): The scale evaluating positive and negative symptoms in schizophrenia was developed by Kay et al (1987) and Kostakoğlu et al.
It was adapted into Turkish by (1999).
Consisting of 30 items, the scale has three sub-dimensions.
A 7-point severity assessment is carried out.
Seven of the items of the scale belong to the positive symptoms subscale, seven to the negative symptoms subscale, and the remaining sixteen to the general psychopathology subscale.
|
One day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Adeviye AYDIN, PhD, Sinop University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- sınopUadeviye-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.