- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07679204
Type D Personality and Life Satisfaction in Bipolar Disorder Type 2 and Major Depressive Disorder
Examination of Type D Personality and Factors Associated With Life Satisfaction in Parents of Patients Diagnosed With Bipolar Disorder Type 2 and Major Depressive Disorder
Bipolar Disorder Type II (BD-II) and Major Depressive Disorder (MDD) are common mood disorders associated with substantial psychological distress, impaired functioning, and reduced quality of life. BD-II is characterized by recurrent major depressive episodes and hypomanic episodes, whereas MDD is characterized by one or more major depressive episodes without a history of mania or hypomania. Both disorders have a significant genetic component, and family studies suggest that first-degree relatives may exhibit subclinical affective traits, personality characteristics, and psychosocial vulnerabilities related to these conditions. The aim of this cross-sectional study was to examine Type D personality traits and life satisfaction among patients with BD-II and MDD and parents of patients. The study recruited/will recruit 30 patients with BD-II; 30 patients with MDD; 30 healthy control subjects; mothers and/or fathers of 30 healthy control subjects, mothers and/or fathers of 30 patients with BD-II, and mothers and/or fathers of 30 patients with MDD who are in remission and receiving follow-up care at the Psychiatry Outpatient Clinic of Elazığ Fethi Sekin City Hospital, Turkey (By Dilek ÖRÜM -Associate Professor of Psychiatry, dr.dilekulukan@gmail.com). Sociodemographic characteristics, Type D personality traits, general psychiatric symptoms, and life satisfaction assessed/will be assessed using validated self-report measures, including the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
The primary objective was/is to compare Type D personality characteristics and life satisfaction levels between patients with MDD and BD-II and between their parents. Secondary objectives included/include investigating the associations between Type D personality traits, psychiatric symptom severity, and life satisfaction. The findings may contribute to a better understanding of familial psychological characteristics associated with mood disorders and may help identify potential psychosocial targets for preventive and supportive interventions among family members of affected individuals.
Study Overview
Status
Detailed Description
Bipolar Disorder Type II (BD-II) and Major Depressive Disorder (MDD) are chronic mood disorders that contribute substantially to global disability, psychosocial impairment, and reduced quality of life. BD-II is characterized by recurrent major depressive episodes and at least one hypomanic episode, whereas MDD is characterized by recurrent depressive episodes without a history of mania or hypomania. Although both disorders share several clinical features, they differ in course, prognosis, treatment approaches, and familial aggregation patterns. Family and twin studies have consistently demonstrated that genetic and familial factors contribute significantly to the development of mood disorders. Consequently, first-degree relatives of individuals with mood disorders may exhibit subclinical affective traits, maladaptive personality characteristics, and psychosocial difficulties even in the absence of a diagnosable psychiatric disorder.
Type D ("distressed") personality is a stable personality construct characterized by the coexistence of two major traits: negative affectivity and social inhibition. Individuals with Type D personality tend to experience persistent negative emotions while simultaneously suppressing emotional expression in social interactions. Previous studies have shown that Type D personality is associated with increased psychological distress, anxiety, depressive symptoms, poorer coping abilities, lower quality of life, and adverse health outcomes. Similarly, life satisfaction is an important indicator of subjective well-being and psychological adjustment, and it may be influenced by both personality characteristics and familial vulnerability factors.
Although Type D personality has been investigated in patients with various psychiatric disorders, including mood disorders, little is known about the prevalence and clinical significance of Type D personality traits among parents of individuals diagnosed with BD-II or MDD. Furthermore, no study has directly compared Type D personality characteristics, psychiatric symptom severity, and life satisfaction among parents of patients with these two mood disorders. Understanding these familial psychological characteristics may provide important insights into the broader psychosocial and hereditary dimensions of mood disorders.
The present study was designed as a cross-sectional observational study conducted at the Psychiatry Outpatient Clinic of Elazığ Fethi Sekin City Hospital, Turkey. All participants included in the study were/will be recruited by MD Dilek ÖRÜM (Associate Professor of Psychiatry, dr.dilekulukan@gmail.com). The study recruited/will recruit 30 patients with BD-II; 30 patients with MDD; 30 healthy control subjects; mothers and/or fathers of 30 healthy control subjects, mothers and/or fathers of 30 patients with BD-II, and mothers and/or fathers of 30 patients with MDD who are in remission and receiving follow-up care at the Psychiatry Outpatient Clinic of Elazığ Fethi Sekin City Hospital, Turkey. The psychiatric diagnoses were made according to Text Revision of Fifth Edition of Diagnostic and Statistical Manual of Mental Disorders (DSM-5-TR) criteria. To minimize the influence of acute illness-related factors, only parents of patients who are currently in remission will be included. Parents with active psychiatric disorders, a history of major psychiatric illness, significant neurological disorders affecting cognition, or severe medical illnesses will be excluded.
All participants completed/will complete a sociodemographic data form and a battery of validated psychometric instruments. Type D personality characteristics will be assessed using the Type D Personality Scale (DS14), which evaluates negative affectivity and social inhibition. General psychiatric symptom severity will be evaluated using the Brief Psychiatric Rating Scale (BPRS). Subjective well-being and life satisfaction will be assessed using the Adult Life Satisfaction Scale (ALSS). Sociodemographic variables including age, sex, marital status, and educational level will also be collected.
The primary objective of the study was/is to compare Type D personality traits and life satisfaction levels between patients with BD-II-MDD and parents of patients with BD-II and parents of patients with MDD. Secondary objectives include/d examining the relationships between Type D personality dimensions, psychiatric symptom severity, and life satisfaction within each group and across the entire sample. The study additionally aims to identify demographic and clinical factors associated with life satisfaction among parents of individuals with mood disorders.
The study hypothesizes/d that parents of patients with BD-II will demonstrate higher levels of Type D personality traits and lower levels of life satisfaction than parents of patients with MDD. It was/is also hypothesized that greater Type D personality characteristics was associated/will be associated with increased psychiatric symptoms and lower life satisfaction.
Statistical analyses will be performed using SPSS 26.version software. Descriptive statistics will summarize demographic and clinical characteristics. Group comparisons will be conducted using chi-square or Fisher's exact tests for categorical variables and independent-samples t-tests or Mann-Whitney U tests for continuous variables, depending on data distribution. Correlation and regression analyses will be performed to investigate associations between Type D personality traits, psychiatric symptoms, and life satisfaction. Statistical significance will be set at p < 0.05.
The findings of this study may contribute to a better understanding of the familial psychological characteristics associated with mood disorders and may help identify potential targets for preventive, supportive, and psychosocial interventions among family members of affected individuals. By exploring the relationship between Type D personality and life satisfaction in parents of patients with BD-II and MDD, this study seeks to expand current knowledge regarding familial vulnerability factors and psychosocial outcomes related to mood disorders.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Mehmet Hamdi Örüm, MD, Associate Professor
- Phone Number: +905382207558
- Email: mhorum@hotmail.com
Study Contact Backup
- Name: Dilek Örüm, MD, Associate Professor
- Phone Number: +905453681686
- Email: dr.dilekulukan@gmail.com
Study Locations
-
-
-
Elâzığ, Turkey (Türkiye), 23200
- Recruiting
- Elazığ Fethi Sekin City Hospital
-
Contact:
- Dilek Örüm, MD Associate Professor
- Phone Number: +905453681686
- Email: dr.dilekulukan@gmail.com
-
Contact:
- Mehmet Hamdi Örüm, MD Associate Professor
- Phone Number: +905382207558
- Email: mhorum@hotmail.com
-
Sub-Investigator:
- Dilek Örüm, Associate Professor, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
For Bipolar Disorder Type II (BD-II) Group:
*Inclusion Criteria:
- Diagnosis of BD-II according to DSM-5-TR
- Remission period
- Age ≥ 18 years
- Provided informed consent
For Bipolar Disorder Type II (BD-II) Group:
*Exclusion Criteria:
- Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Primary psychiatric disorders other than BD-II and not in remission for BD-II
- Alcohol/drug/substance use
For Major Depressive Disorder (MDD) Group:
*Inclusion Criteria:
- Diagnosis of MDD according to DSM-5-TR
- Remission period
- Age ≥ 18 years
- Provided informed consent
For Major Depressive Disorder (MDD) Group:
Exclusion Criteria:
- Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Primary psychiatric disorders other than MDD and not in remission for MDD
- Alcohol/drug/substance use
For Healthy Control (HC) Group:
*Inclusion Criteria:
- No psychiatric diagnosis
- No systemic or immunological illness
- Medication-free for at least one month
- Age ≥ 18 years
- Provided informed consent
For Healthy Control (HC) Group:
*Exclusion Criteria:
- Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Having psychiatric disorders
- Alcohol/drug/substance use
For Healthy Father and/or Mother of Bipolar Disorder Type II (BD-II) Group:
*Inclusion Criteria:
- No psychiatric diagnosis
- No systemic or immunological illness
- Medication-free for at least one month
- Age ≥ 18 years
- Provided informed consent
For Healthy Father and/or Mother of Bipolar Disorder Type II (BD-II) Group:
*Exclusion Criteria:
• Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Having psychiatric disorders
- Alcohol/drug/substance use
For Healthy Father and/or Mother of Major Depressive Disorder (MDD) Group:
*Inclusion Criteria:
- No psychiatric diagnosis
- No systemic or immunological illness
- Medication-free for at least one month
- Age ≥ 18 years
- Provided informed consent
For Healthy Father and/or Mother of Major Depressive Disorder (MDD) Group:
*Exclusion Criteria:
• Hypertension
• Diabetes mellitus
• Chronic kidney disease
• Rheumatoid arthritis
• Systemic lupus erythematosus
• Cardiac illness
• Severe neurological disorders
- Immunological or systemic illness
- Having psychiatric disorders
- Alcohol/drug/substance use
For Healthy Father and/or Mother of Healthy Control (HC) Group:
*Inclusion Criteria:
• No psychiatric diagnosis
• No systemic or immunological illness
- Medication-free for at least one month
- Age ≥ 18 years
- Provided informed consent
For Healthy Father and/or Mother of Healthy Control (HC) Group:
*Exclusion Criteria:
- Hypertension
- Diabetes mellitus
- Chronic kidney disease
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Cardiac illness
- Severe neurological disorders
- Immunological or systemic illness
- Having psychiatric disorders
- Alcohol/drug/substance use
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Bipolar Disorder Type II (BD-II)
Adult patients diagnosed with Bipolar Disorder Type II (BD-II) according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria.
Patients with BD-II must have a history of at least one hypomanic episode and one major depressive episode and must be in remission at the time of study participation, with no current hypomanic, depressive, or mixed episode.
Patients with active psychiatric disorders, a history of major psychiatric disorders, significant neurological disorders affecting cognitive functioning, or severe medical illnesses excluded/will be excluded.
Participants evaluated/will be evaluated once in a cross-sectional assessment.
No intervention assigned/will be assigned by the study protocol.
Assessments will include a sociodemographic data form, the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
|
|
Major Depressive Disorder (MDD)
Adult patients diagnosed with Major Depressive Disorder (MDD) according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria.
Patients with MDD must have a history of at least one major depressive episode and must be in remission at the time of study participation, with no current major depressive episode.
Patients with a current or lifetime diagnosis of bipolar disorder, schizophrenia spectrum or other psychotic disorders, active psychiatric disorders requiring immediate treatment, significant neurological disorders affecting cognitive functioning, or severe medical illnesses excluded/will be excluded.
Participants evaluated/will be evaluated once in a cross-sectional assessment.
No intervention assigned/will be assigned by the study protocol.
Assessments will/included a sociodemographic data form, the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
|
|
Healthy Control (HC)
Healthy control (HC) adult participants without any current or past psychiatric disorder enrolled/will be enrolled in the study.
No intervention was administered/will be administered as part of the research protocol.
Participants undergo/will undergo a baseline clinical evaluation.
Clinical assessments in the HC group included/will include the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
Sociodemographic and clinical data was recorded/will be recorded for all participants.
|
|
Healthy Father and/or Mother of Bipolar Disorder Type II (BD-II) Participant
Adult participants without any current or past psychiatric disorder enrolled/will be enrolled in the study.
No intervention was administered/will be administered as part of the research protocol.
Participants undergone/will undergo a baseline clinical evaluation.
Clinical assessments in the this group included/will include the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
Sociodemographic and clinical data was recorded/will be recorded for all participants.
|
|
Healthy Father and/or Mother of Major Depressive Disorder (MDD) Participant
Adult participants without any current or past psychiatric disorder enrolled/will be enrolled in the study.
No intervention was administered/will be administered as part of the research protocol.
Participants undergone/will undergo a baseline clinical evaluation.
Clinical assessments in the this group included/will include the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
Sociodemographic and clinical data was recorded/will be recorded for all participants.
|
|
Healthy Father and/or Mother of Healthy Control (HC) Participant
Adult participants without any current or past psychiatric disorder enrolled/will be enrolled in the study.
No intervention was administered/will be administered as part of the research protocol.
Participants undergone/will undergo a baseline clinical evaluation.
Clinical assessments in the this group included/will include the Type D Personality Scale (DS14), the Brief Psychiatric Rating Scale (BPRS), and the Adult Life Satisfaction Scale (ALSS).
Sociodemographic and clinical data was recorded/will be recorded for all participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Type D Personality Scale (DS14)
Time Frame: At hospital admission (baseline)
|
The Type D Personality Scale (DS14) was developed by Denollet in 2005.
The validity and reliability of the Turkish version among Turkish hemodialysis patients were established by Alçelik et al.
The DS14 is a 14-item self-report instrument consisting of two 7-item subscales that assess Negative Affectivity (NA) (items 2, 4, 5, 7, 9, 12, and 13) and Social Inhibition (SI) (items 1, 3, 6, 8, 10, 11, and 14).
Items 1 and 3 are reverse scored.
Each item is rated on a 5-point Likert scale ranging from 0 ("false") to 4 ("true"), with the intermediate response options being "rather false," "neutral," and "rather true."
Scores for each subscale range from 0 to 28, and a score of ≥10 on each subscale is considered the established cutoff value.
In the Turkish validation study, the Cronbach's alpha coefficients were 0.82 for the Negative Affectivity subscale and 0.81 for the Social Inhibition subscale.
The test-retest reliability coefficients were 0.84 and 0.78, respectively.
|
At hospital admission (baseline)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brief Psychiatric Rating Scale (BPRS)
Time Frame: At hospital admission (baseline)
|
The Brief Psychiatric Rating Scale (BPRS) is an 18-item Likert-type clinician-administered instrument with established validity and reliability in Turkish.
It is used to assess the severity of psychiatric symptoms following a brief clinical interview and to evaluate treatment response over time.
Higher scores indicate greater psychiatric symptom severity.
The BPRS is widely used to measure the severity and changes in psychotic symptoms, as well as certain depressive symptoms, in individuals with schizophrenia, bipolar disorder, and other psychotic disorders, and to assess the effectiveness of psychiatric treatment.
|
At hospital admission (baseline)
|
|
Adult Life Satisfaction Scale (ALSS)
Time Frame: At hospital admission (baseline)
|
The Adult Life Satisfaction Scale (ALSS) is a 21-item self-report instrument developed within the Turkish cultural context to assess life satisfaction in adults.
The scale uses a 5-point Likert-type response format and comprises five dimensions: general life satisfaction, relationship satisfaction, self-satisfaction, satisfaction with the social environment, and job satisfaction.
Total scores range from 21 to 105, with higher scores indicating greater perceived life satisfaction and more positive evaluations of one's own life.
In the present study, the overall internal consistency of the ALSS was high, with a Cronbach's alpha coefficient of 0.87.
|
At hospital admission (baseline)
|
Collaborators and Investigators
Investigators
- Study Director: Mehmet Hamdi Örüm, Associate Professor, MD, Elazığ Mental Health and Diseases Hospital
Publications and helpful links
General Publications
- Mahmoud JS, Staten R, Hall LA, Lennie TA. The relationship among young adult college students' depression, anxiety, stress, demographics, life satisfaction, and coping styles. Issues Ment Health Nurs. 2012 Mar;33(3):149-56. doi: 10.3109/01612840.2011.632708.
- Kim S, Choi M, Lee J, Kim H, Song K, Park HJ. Type D personality, cognitive illness perception, depression, approach coping, and self-management among older adults in long-term care hospitals: Structural equation modeling. Geriatr Nurs. 2022 Nov-Dec;48:150-157. doi: 10.1016/j.gerinurse.2022.09.011. Epub 2022 Oct 8.
- Kendler KS, Ohlsson H, Sundquist J, Sundquist K. Risk for Mood, Anxiety, and Psychotic Disorders in Individuals at High and Low Genetic Liability for Bipolar Disorder and Major Depression. JAMA Psychiatry. 2022 Nov 1;79(11):1102-1109. doi: 10.1001/jamapsychiatry.2022.2873.
- Ilhan RS, Senturk Cankorur V. [Clinical and cognitive predictors of psychosocial functioning during the euthymic period in bipolar disorder type II]. Turk Psikiyatri Derg. 2015 Spring;26(1):13-20. Turkish.
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- EMHDH-2024-BD-MDD-TYPE-D
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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.
Clinical Trials on Major Depressive Disorder (MDD)
-
Yonggui YuanNot yet recruitingMajor Depressive Disorder (MDD)China
-
King's College LondonCardiff and Vale University Health Board; South London and Maudsley NHS Foundation... and other collaboratorsRecruitingMajor Depressive Disorder (MDD)United Kingdom
-
Supernus Pharmaceuticals, Inc.RecruitingMajor Depressive Disorder (MDD)United States
-
University of PennsylvaniaRecruiting
-
Daniel LindqvistLund University; KetabonActive, not recruitingMajor Depressive Disorder (MDD)Sweden
-
University of PretoriaNot yet recruitingMajor Depressive Disorder (MDD)Saudi Arabia
-
Shanghai Mental Health CenterLingang National LaboratoryNot yet recruitingMajor Depressive Disorder (MDD
-
Tel Aviv UniversityNot yet recruitingMajor Depressive Disorder (MDD)Israel
-
Sichuan Purity Pharmaceutical Technology Co., Ltd.Recruiting
-
Instituto Mexicano del Seguro SocialCompleted