scholarly journals Quality of Life and Anxiety in Military Personnel

2019 ◽  
Vol 20 (2) ◽  
pp. 47-54
Author(s):  
Aleksandra Vojvodic ◽  
Gordana Dedic
Keyword(s):  
Quality Of Life ◽  
Physical Health ◽  
Social Relations ◽  
Military Personnel ◽  
Psychological Health ◽  
Mental Health Problems ◽  
Armed Forces ◽  
Life Assessment ◽  
World Health

Abstract The quality of life of military personnel represents their self-evaluation of the quality of their own mental and physical health, social relations, and the environment in which they live and work. The aim of our study was to evaluate the relationship between quality of life and anxiety levels in military personnel of the Serbian Armed Forces. The cross-sectional study included a total of 311 randomly selected professional military personnel (officers, non-commissioned officers and professional soldiers) between 23 and 53 years of age (mean, 35.3±7 years) without current mental health problems. For the purpose of this study, we used the World Health Organization Abbreviated Instrument for Quality of Life Assessment (WHOQOL-BREF) and the Beck Anxiety Inventory (BAI). The statistical analysis included parametric and non-parametric descriptive statistics. Professional military personnel showed high satisfaction with their quality of life in the categories of social relations (82.52), psychological health (82.10) and physical health (81.68), while the satisfaction scores in the category environment category were the lowest (62.77). The average value for the total BAI score was 4.83±5.66. Quality of life decreased, while anxiety increased, with increasing age of the military personnel. Higher BREF score values were associated with lower scores on the BAI questionnaires in all subscales (p<0.001). Military personnel of the Serbian Armed Forces showed a high degree of satisfaction with their own quality of life. Learning techniques to easily overcome everyday stress would reducedreduce anxiety and improve the quality of life in military personnel of the Serbian Armed Forces.

scholarly journals Age categories differences in subjective quality of life of women with physical disabilities

2021 ◽  
Vol 60 (2) ◽  
pp. 124-130
Author(s):  
Dagmar Nemček ◽  
Patrícia Shtin Baňárová ◽  
Petra Kurková
Keyword(s):  
Quality Of Life ◽  
Physical Health ◽  
Social Relations ◽  
Psychological Health ◽  
Physical Disabilities ◽  
Subjective Quality ◽  
Subjective Quality Of Life ◽  
The Social ◽  
Women With Physical Disabilities

Abstract Objective The objective of the study was to analyse and compare the subjective quality of life (S-QoL) of women with physical disabilities (PDs) through satisfaction with the quality of life domains and the overall quality of life assessment. Methods The sample comprised of women with PDs (n=137), divided into 4 age categories: 19-29 yrs. (n=53); 30-44 yrs. (n=25); 45-59 yrs. (n=24) and over 60 yrs. (n=35). The Subjective Quality of Life Analyses questionnaire and the WHO User Manual were used as a primary research method. The Wilcoxon Signed Rank Test was used to assess the differences between QoLDs, Kruskal Wallis test to assess differences in S-QoL among four independent groups and Mann Whitney U-test between two age categories. Results The highest satisfaction in all age categories of women was found in the social relations domain, and in the 19-29 yr-old women equally in the social relations and physical health domains. The highest dissatisfaction was reported with the psychological health and environment domains. The key finding is that the main differences are between the youngest category (aged 19-29 yrs) and the three older categories with regard to physical health, environment and overall QoL. Conclusions It is necessary to continue this line of research with a greater focus on exploring the ways in which the psychological health domain can be improved as an integral part of S-QoL, and to also focus on the QoL indicators that make up the environment domain and search for ways to enhance these.

scholarly journals Gender difference in quality of life (QoL) among outpatients with schizophrenia in a tertiary care setting

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Saleha Shafie ◽  
Ellaisha Samari ◽  
Anitha Jeyagurunathan ◽  
Edimansyah Abdin ◽  
Sherilyn Chang ◽  
...  
Keyword(s):  
Quality Of Life ◽  
Physical Health ◽  
Social Relationships ◽  
Clinical Features ◽  
Psychological Health ◽  
World Health ◽  
World Health Organization Quality ◽  
Significant Difference ◽  
Chinese Ethnicity

Abstract Background Patients with mental illness report lower quality of life (QoL) compared to the general population. Prior research has found several differences in clinical features and experiences of male and female patients with schizophrenia. Given these differences, it is also important to explore if there are any gender differences in terms of their QoL. This study aimed to investigate differences in QoL between and within each gender among outpatients with schizophrenia in Singapore. Methods A total of 140 outpatients were recruited through convenience sampling at the Institute of Mental Health, Singapore. QoL was measured using the brief version of World Health Organization Quality of Life (WHOQOL-BREF) which consists of four domains: physical health, psychological health, social relationships, and environment. QoL scores of males and females were compared using independent t-tests, and multiple linear regressions were used to examine sociodemographic correlates of QoL in the overall sample and within each gender. Results There was no significant difference in QoL domain scores between genders. Among males, Indian ethnicity (versus Chinese ethnicity) was positively associated with physical health (β=3.03, p=0.018) while males having Technical Education/ Diploma/ A level education (versus Degree and above) were positively associated with social relationships domain (β=2.46, p=0.047). Among females, Malay ethnicity (versus Chinese ethnicity) was positively associated with physical health (β=1.95, p=0.026) psychological health (β=3.21, p=0.001) social relationships (β=2.17, p=0.048) and environment (β=2.69, p=0.006) domains, while females who were separated/divorced (versus single) were inversely associated with psychological health (β=− 2.80, p=0.044) and social relationships domains (β=− 4.33, p=0.011). Females who had Secondary and below education (versus Degree and above) were inversely associated with social relationships (β=− 2.29, p=0.028) and environment domains (β=− 1.79, p=0.048). Conclusions The findings show the importance of treatments targeting QoL to attend to both the clinical features of the illness as well patient’s sociodemographic characteristics.

scholarly journals Procrastination at the Core of Physical Activity (PA) and Perceived Quality of Life: A New Approach for Counteracting Lower Levels of PA Practice

2020 ◽  
Vol 17 (10) ◽  
pp. 3413
Author(s):  
Nuria Codina ◽  
José V. Pestana ◽  
Rafael Valenzuela ◽  
Nuria Giménez
Keyword(s):  
Quality Of Life ◽  
Physical Activity ◽  
Psychological Health ◽  
Perceived Quality ◽  
Life Assessment ◽  
World Health ◽  
World Health Organization Quality ◽  
Time Investment ◽  
Perceived Quality Of Life

Faced with the demonstrated need to engage in physical activity (PA), lack of time is the argument commonly used to justify low or non-existent levels of PA. Underlying this argument, the accomplishment of procrastination behaviour seems to be related to the less time dedicated to practicing PA and the low perception of the quality of life. With this in mind, the purpose of this study is to show that dedicating different amounts of time to PA affects the perceived quality of life and the widespread problem of procrastination. We hypothesise that greater time investment in PA is related to greater perceived quality of life and less procrastination. In all, 621 practitioners of PA (347 men, 274 women) between 18 and 83 years old (M = 35.43, SD = 14.45) filled out validated versions of the World Health Organization quality of life assessment (WHOQOL-BREF) and the Pure Procrastination Scale. Results showed that people who do enough PA have a more positive perception of the quality of life in the domains of physical and psychological health; this perception, in turn, is related to lower levels of procrastination. Likewise, socio-demographic characteristics such as gender and the main activity presented significant associations with various quality of life domains and procrastination. In sum, the benefits of improvements in quality of life and reductions in procrastination identified in this study are sensitive to the time spent on PA, which suggests that a strategy to promote the practice of PA would improve time management and, thus, counteract procrastination.

scholarly journals Subjective quality of life of Slovak men with physical disabilities: An age categories differences

2021 ◽  
Vol 84 (3) ◽  
pp. 275-287
Author(s):  
Dagmar Nemček
Keyword(s):  
Quality Of Life ◽  
Physical Health ◽  
Psychological Health ◽  
Physical Disabilities ◽  
Research Field ◽  
Subjective Quality ◽  
World Health ◽  
Future Research ◽  
Subjective Quality Of Life

Abstract The objective of the study was to analyze and compare the subjective quality of life (S-QOL) of Slovak men with physical disabilities through satisfaction with the quality of life domains (QOLDs) and the overall quality of life (QOL) assessment. The sample comprised of men with physical disabilities (n = 132), divided into 4 age categories: 19–29 yrs. (n = 59); 30–44 yrs. (n = 26); 45–59 yrs. (n = 24) and over 60 yrs. (n = 23). The Subjective Quality of Life Analysis (S-QUA-L-A) and The World Health Organisation Quality of Life User Manual (WHOQOL User Manual) were used as primary research methods. The findings of this study confirm differences in S-QOL in one QOLD as well as in the overall QOL between two from four age categories of men with physical disabilities. The 19–29 yrs. old men were significantly more satisfied in their lives with the Physical health domains and declared significantly higher overall QOL compare to 45–59 yrs. men. There were no significant differences found in S-QOL between other pair comparisons of the age categories of men with physical disabilities. The highest satisfaction in all age categories of men was declared by the domains of Social relation and Physical health and the highest dissatisfaction by the Psychological health and Environment domains. It is necessary to continue this line of this research field with stress on exploring the ways of psychological health increase as an integral part of S-QOL in men with physical disabilities. Future research should focus on life indicators that saturate the Environment domain, which should be positively affected in mens’ life.

scholarly journals Gambaran Kualitas Hidup Penderita Kanker Serviks Setelah Pengobatan di Rumah Sakit Islam Faisal Makassar Tahun 2016

2019 ◽  
Vol 1 (1) ◽  
Author(s):  
Besse Ainul Mardiyah Kadir ◽  
Rini Fitriani
Keyword(s):  
Quality Of Life ◽  
Cervical Cancer ◽  
Cancer Patient ◽  
Physical Health ◽  
Social Relations ◽  
Psychological Health ◽  
Cervical Cancer Patient ◽  
Health Quality ◽  
Health Quality Of Life

Pendahuluan penelitian gambaran kualitas hidup penderita kanker serviks setelah pengobatan di Rumah Sakit Islam Faisal Makassar bertujuan untuk mengetahui gambaran kualitas hidup penderita kanker serviks setelah pengobatan dari aspek kesehatan fisik, psikologis, sosial, dan lingkungan.Metode penelitian ini merupakan survay deskriptif, untuk mengetahui gambaran kualitas hidup penderita kanker serviks setelah pengobatan di Rumah Sakit Islam Faisal Makassar dengan jumlah sampel 42 orang yang dilaksanakan pada bulan Oktober – Desember 2016.Hasil penelitian gambaran kualitas hidup penderita kanker serviks setelah pengobatan dari segi kesehatan fisik kualitas hidup cukup sebanyak15 responden (35,7%) dan responden yang memiliki kualitas hidup kurang sebanyak 27 responden (64,3%), dari segi kesehatan psikologis kualitas hidup cukup sebanyak 29 responden (69%) dan kualitas hidup kurang sebanyak 13 responden (31%), dari segi hubungan sosial kualitas hidup baik sebanyak 18 responden (42,8%), kualitas hidup cukup sebanyak 23 responden (54,8%), dari segi lingkungan kualitas hidup cukup sebanyak 3 responden (7,1%) dan kualitas hidup kurang sebanyak 39 responden (92,9%).Kesimpulan dari empat aspek terdapat kualitas hidup baik 18 responden (42,8%) dari segi hubungan sosial,  kualitas hidup cukup 29 responden (69%) dari segi kesehatan psikologis, kualitas hidup kurang 39 responden (92,9%) dari segi kesehatan lingkungan, dan dari segi kesehatan fisik sebanyak 27 responden (64,3%) kualitas hidup kurang.ABSTRACTIntroduction research picture of quality of life of cervical cancer patient after treatment at Islamic Hospital Faisal Makassar aims to know  picture  quality  of  life  of  cervical cancer patient after treatment from aspect of physical health, psychological, social, and environment.Method this research is descriptive survey, to know the picture of quality of life of cervical cancer patient after treatment at Faisal Makassar Islamic Hospital with total sample 42 people conducted in October - December 2016.The results of the study of the quality of life of cervical cancer patients after treatment in terms of physical health quality of life is quite as much as 15 respondents (35.7%) and respondents who have quality of life less as much as 27 respondents (64.3%), in terms of psychological health quality of life is enough As many as 29 respondents (69%) and quality of life less 13 respondents (31%), in terms of social relations quality of life both as many as 18 respondents (42.8%), quality of life is quite as much as 23 respondents (54.8%), In terms of quality of life environment is quite as much as 3 respondents (7.1%) and quality of life is less as much as 39 respondents (92.9%). From  the  four  aspects,  there  is  a good quality of life of 18 respondents (42.8%) in terms of social relations, quality of life is enough 29 respondents (69%) in terms of psychological health, quality of life is less 39 respondents (92.9%) in terms of environmental health, And in terms of physical health as much as 27 respondents (64.3%) poor quality of life.

scholarly journals The Effect of Mental Health Status on the Quality of Life of Faculty of Medicine Students during the Pandemic Coronavirus Disease 2019 Period

2021 ◽  
Vol 9 (E) ◽  
pp. 645-652
Author(s):  
Agustina Arundina Triharja Tejoyuwono ◽  
Rangga Putra Nugraha ◽  
Faisal Kholid Fahdi
Keyword(s):  
Quality Of Life ◽  
Mental Health ◽  
Health Status ◽  
Physical Health ◽  
Social Relationships ◽  
Psychological Health ◽  
Mental Health Problems ◽  
Mental Health Status ◽  
Cross Sectional Survey

BACKGROUND: The spread of Coronavirus Disease 2019 (COVID-19) disease which has not been balanced with effective protocols can create mental health problems which could affect the quality of life; as of today, there is not any research that examines the influence of both factors. AIM: This study purpose was to analyze the mental health status on the quality of life amongst medicine students during COVID-19 period. METHODS: This is a cross-sectional survey on 361 students from Faculty of Medicine Tanjungpura University. This study was conducted from June 2019 to November 2020 by spreading Depression Anxiety Stress Scale questionnaire and a WHOQOL-BREF questionnaire through online. The data analysis was administered using Kruskal–Wallis statistics. RESULT: The students’ mental health status was dominantly on the normal category with depression domain by 323 students (89.5%), anxiety domain by 311 students (86.1%), and stress domain by 343 students (95%). The quality of life measurement was in category medium in all domains which are physical health (88.6%), psychological health (92.5%), social relationships (50.7%), and environment (78.7%). There was significant effect of mental health status of depression and anxiety toward the aspect of physical health, psychological health, and social relationships (p < 0.05). Stress significantly influenced all domains of quality of life, and there was no significant effect of mental health status domain depression (p = 0.051) and anxiety (p = 0.881) toward the environment aspect. CONCLUSION: Students’ mental health status in this research belongs to the category normal with moderate level in quality of life. To compare, there was a significant effect of mental health status toward the quality of life domains. The good application of self-coping mechanisms and the social encouragement from the environment is suitable intervention strategies during the pandemic COVID-19 period.

scholarly journals The quality of life in patients with diabetes mellitus type 2

2012 ◽  
Vol 69 (10) ◽  
pp. 858-863 ◽  
Author(s):  
Dragana Bosic-Zivanovic ◽  
Milica Medic-Stojanoska ◽  
Branka Kovacev-Zavisic
Keyword(s):  
Quality Of Life ◽  
Diabetes Mellitus ◽  
Physical Health ◽  
Social Relations ◽  
Psychological Health ◽  
Self Control ◽  
Daily Activities ◽  
Dm Type 2

Background/Aim. Through its various activities, World Health Organization (WHO) contributed to increasing the understanding of the concept of quality of life. People with diabetes have a lower quality of life than people without chronic illnesses. The aim of this study was to examine the differences in the quality of life, related to health, in patients with diabetes mellitus (DM) type 2 by age, gender and type of therapy. Methods. We performed a cross-sectional study at the outpatient department of the Clinical Center in Novi Sad and the Health Center Ruma - General Practice. The group consisted of 90 patients with DM type 2, 41 men and 49 women. The age of respondents was from 40 to 80 years and they were classifed into four groups according to the ten-year age intervals. We applied WHO Quality of life questinnaire - BREF 100 composed of four domains: physical health, psychological health, social relationships and environment. The general questionnaire asks questions about socio-demographic data, duration of diabetes, the last value of blood glucose and glycosylated hemoglobin, training for self-control and its implementation, informing patients about their disease, therapy and its impact on daily activities and the presence of comorbidity. In statistical analysis the following tests were used: Student?s t-test, Ftest, ANOVA (one way). Results. The average duration of DM type 2 was 11.2 ? 9.2 years. Most of the patients (76%) were trained to self-control and 91% received enough information about their disease. Oral hypoglycemic preparations were used by 49%, insulin by 21%, and oral drugs and insulin by 29% patients while 1% were on a special regime of a diet therapy. Daily activities were performed without difficulties by over 29%, with some difficulties by 41% and 30% of patients who could not perform daily activities. The patients with DM type 2 had significantly lower scors in all 4 domains of quality of life (physical health, psychological health, social relations, environment). The biggest influence was on physical domains (51.31). Education level had an impact on physical and psychological domains. Comorbidity was found in 83% of the respondents. The most common were: arterial hypertension (63%), chronic cardiovascular disease (46%), neuropathy (23%), impaired vision 24%, elevated blood lipids (39%) and amputation of toes or feet (2.2%). The average value HbA1C in the group with comorbidity was 8.47% and in the group without comorbidity 6.46%. The subjects with comorbidity had low quality of life assessment in relation to the group without comorbidity: the domain of physical health (45.64 vs 79.66), psychological health (50.3 vs 76.86), social relations (52.97 vs 75.46) and environment (52.7 vs 75.06). Conclusion. Diabetes mellitus type 2 has negative influence on the quality of life. It contributes to the presence of comorbidity. The occurrence of comorbidity was associated with higher glucosylated HbA1C values. There was no difference in the assessment of quality of life regarding gender, age, or the type of therapy used. The quality of life was assessed as low in patients with comorbidity. However, certain personality characteristics play a decisive role in self-evaluation.

scholarly journals Quality of life of schizophrenic patients in a tertiary care hospital in Bangladesh

2017 ◽  
Vol 29 (1) ◽  
pp. 30-34 ◽  
Author(s):  
Mir Hasan Shakil Mahmud ◽  
Bushra Yeasmin ◽  
Shipra Mandal
Keyword(s):  
Quality Of Life ◽  
Physical Health ◽  
Environmental Health ◽  
Social Relationship ◽  
World Health ◽  
P Value ◽  
Health Domain ◽  
Schizophrenic Patients ◽  
Physical Health Domain

Schizophrenia is one of the major mental disorders which affect individual’s thinking ability, social interaction or attention. It affects person’s entire quality of life. The purpose of the study was to find out the quality of life of schizophrenic patient in Bangladesh. Cross sectional study design was used to conduct this study. The convenient sampling procedure was used throughout the process of participant’s selection and the numbers of respondents were 83. The study was carried out at National Institute of Mental Health and Hospital (NIMH), Dhaka. Data was collected by using face to face interview with a structured questionnaire WHOQOL-BREF (The World Health Organization Quality of Life- BREF) scale. It was found that most of the participants lead poor to moderate quality of life in four domains of the WHOQOL-BREF scale. Results showed that mean scores were for physical health (mean 2.7, SD+0.106); psychological health (mean 2.108, SD +0.0787); social relationship (mean 2.226; SD+0.116) and environmental health (mean 2.47; SD+0.077).This study indicated that, quality of life poor on psychological domain. It was also found statistically significance with age and social relationship domain (p value 0.005< 0.05); marital status and physical health domain (p value 0.004<0.05); educational level and physical health domain (p value 0.005<0.05) and environmental health domain (p value 0.025<0.05). There were no statistically significant difference between gender and other variables. Schizophrenia affects all aspects of person’s life such as physically, psychologically, socially and economically. Schizophrenic patients as well as their family members led very poor quality of life.Bang J Psychiatry June 2015; 29(1): 30-34

scholarly journals Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members

Medicina ◽  
2021 ◽  
Vol 57 (1) ◽  
pp. 43
Author(s):  
Esme Brittain ◽  
Nina Muirhead ◽  
Andrew Y. Finlay ◽  
Jui Vyas
Keyword(s):  
Quality Of Life ◽  
Chronic Fatigue Syndrome ◽  
Physical Health ◽  
Family Members ◽  
Chronic Fatigue ◽  
Myalgic Encephalomyelitis ◽  
World Health ◽  
Life Questionnaire ◽  
Fatigue Syndrome

Background and objectives: To explore the impacts that Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has on the patient and their family members using the WHOQOL-BREF (Abbreviated World Health Organisation Quality of Life questionnaire) and FROM-16 (Family Reported Outcome Measure-16) quality of life assessments. Materials and Methods: A quantitative research study using postal questionnaires was conducted. A total of 39 adult volunteers expressed an interest in participating in the study: 24 returned appropriately completed questionnaires. Patients with ME/CFS completed the WHOQOL-BREF and up to four of their family members completed the FROM-16 questionnaire. Results: ME/CFS negatively affects the quality of life of the patient (median scores WHOQOL-BREF: Physical health = 19, Psychological = 44, Social relationships = 37.5, Environment = 56, n = 24) and their family members’ quality of life (FROM-16: Emotional = 9.5, Personal and social = 11.5, Overall = 20.5, n = 42). There was a significant correlation between the patient’s reported quality of life scores and their family members’ mean FROM-16 total scores. Conclusions: This study identifies the major impact that having an adult family member with ME/CFS has on the lives of partners and of other family members. Quality of life of ME/CFS patients was reduced most by physical health compared to the other domains. Quality of life of family members was particularly impacted by worry, family activities, frustration and sadness. This highlights the importance of measuring the impact on the lives of family members using tools such as the FROM-16 in the ME/CFS clinical encounter and ensuring appropriate support is widely available to family members.

scholarly journals Three Strategies for Describing Social Interactions of Adolescents in a Multicultural Environment—Indicators for the Quality of Life Research

2021 ◽  
Vol 18 (15) ◽  
pp. 8166
Author(s):  
Alicja Szerląg ◽  
Arkadiusz Urbanek ◽  
Kamila Gandecka
Keyword(s):  
Quality Of Life ◽  
Social Interactions ◽  
Social Relationships ◽  
Social Relations ◽  
Living Environment ◽  
Life Assessment ◽  
Multicultural Environment ◽  
Multicultural Community ◽  
The Social

Background: The analysis has involved social interactions in a multicultural environment. The social context has been defined by the Vilnius region (Lithuania), where national, religious, and cultural differences exist across generations (multicultural community). The space of “social relationships”, as one of the modules of the WHO quality of life assessment, has been studied. An innovation of the research has been related to the analysis of the phenomenon of community of nationalities and cultures as a predictor of quality of life (QoL). The social motive of the research has been the historical continuity (for centuries) of the construction of the Vilnius cultural borderland. Here, the local community evolves from a group of many cultures to an intercultural community. Interpreting the data, therefore, requires a long perspective (a few generations) to understand the quality of relationships. We see social interactions and strategies for building them as a potential for social QoL in multicultural environments. Methods: The research has been conducted on a sample of 374 respondents, including Poles (172), Lithuanians (133), and Russians (69). A diagnostic poll has been used. The respondents were adolescents (15–16 years). The research answers the question: What variables form the interaction strategies of adolescents in a multicultural environment? The findings relate to interpreting the social interactions of adolescents within the boundaries of their living environment. The description of the social relations of adolescents provides an opportunity to implement the findings for further research on QoL. Results: An innovative outcome of the research is the analysis of 3 interaction strategies (attachment to national identification, intercultural dialogue, and multicultural community building) as a background for interpreting QoL in a multicultural environment. Their understanding is a useful knowledge for QoL researchers. The data analysis has taken into account cultural and generational (historical) sensitivities. Therefore, the team studying the data has consisted of researchers and residents of the Vilnius region. We used the interaction strategies of adolescents to describe the category of “social relationships” in nationally and culturally diverse settings.

Sign in / Sign up

Export Citation Format

Share Document