scholarly journals The Impact of Psychological Interventions on the Quality of Life of Diabetes Mellitus Patient

2014 ◽  
Vol 21 (4) ◽  
pp. 301-311
Author(s):  
Dana Sonia Oieru ◽  
Amorin Remus Popa ◽  
Ionuţ Vlad

AbstractBackground and aims: The theory regarding the psychological factors as etiologic agents that trigger the somatic diseases has gained more and more ground in the past few years, successfully repeating that the human being is a bio-psycho-social entity. In order to render the psychological interventions more efficient in the management of the psychosomatic diseases, this research aims to detect and modify, even treat throught psychological interventions those configurations of the early maladaptive schemes and coping styles that stick form together in the so-called acquired vulnerability which makes the person liable to an inappropriate reaction against stress, and also to track the effects of these changes on somatic indicators of diabetes mellitus. Material and methods: Analysis of variance (ANOVA) and paired T-test were used for analysing subjects` responses at three psychological instruments, evolution of blood pressure, body mass index, drug units, hospitalisation days, medical leave days, depressive symptoms before and after 10-12 psychological interventions sessions. Results: Results draw the attention once again upon the multiple directions of intervention and especially of prevention in case of the psychosomatic disease, in particular diabetes mellitus. Conclusions: Psychological intervention in the early stages of diabetes is a major contributor to the management of this disease.

2015 ◽  
Vol 9 (1) ◽  
pp. 46-52
Author(s):  
Dana Sonia Oieru ◽  
Remus Amorin Popa

Regarding the psychological factors as etiologic agents that trigger the somatic diseases has gained more and more ground in the past few years, successfully repeating that the human being is a bio-psycho-social entity. In order to render the psychological interventions more efficient for the management of the diabetes mellitus diseases, we must detect and modify those configurations of the early maladaptive schemes and coping styles that stick together in the so-called acquired vulnerability which makes the person liable to an inappropriate reaction against stress.


2020 ◽  
Vol 30 (2) ◽  
pp. 140-143
Author(s):  
Anahli Patel ◽  
Yelena Chernyak

Transplant recipients have significant psychosocial stressors due to unique posttransplant sequela that results in an increased incidence of psychopathology. Posttransplant psychological interventions, especially in lung transplant recipients, are understudied, as the focus of prior research has emphasized pretransplant interventions. However, posttransplant psychological stability affects medical outcomes. The importance of posttransplant psychological intervention is highlighted. Recommendations exist which call for attention to specific psychological domains in the posttransplant recovery period and highlight the impact of psychological rehabilitation on overall wellness and success in recovery. A novel psychological rehabilitation intervention is outlined as a response to posttransplant intervention recommendations to demonstrate implementation.


SAGE Open ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 215824402093251
Author(s):  
Hua Li

Psychological intervention has a positive impact on the competitive psychological ability and performance of athletes, while there are few studies on this subject. To improve the psychological ability of athletes’ mood and coping styles and promote the smooth progress of the competition, a single-subject experimental design model is used carry out psychological intervention on four high-level athletes for 8 months. According to the characteristics of Wushu routines, the psychological measurement and social validity evaluation are combined to explore the effect of psychological intervention. The results show that the mood state of four athletes improved obviously with the same trend. The coping styles showed a positive upward trend after psychological intervention. The results of three athletes also improved in the City Games. In addition, the results of “social validation” obtained from the coaches and athletes support the effectiveness of the intervention. Psychological intervention can effectively improve the bad mood and negative coping style of Wushu routine athletes so as to improve the competition of athletes.


Work ◽  
2021 ◽  
pp. 1-15
Author(s):  
Zhe Liu ◽  
Malizia King

BACKGROUND: For family caregivers, sudden stroke events and heavy caring works are stressful events. At present, controversies about the factors affecting caregivers’ stress response and their correlation with coping styles still exist. OBJECTIVE: To explore the influencing factors and coping styles of mental health stress responses of stroke caregivers and promote caregivers to adopt positive coping styles for diseases and caring works. METHODS: The convenience sampling method is used to select stroke caregivers as the research objects. The general information questionnaires, Relative Stress Scale (RSS), General Self-Efficacy Scale (GSES), Social Support Rate Scale (SSRS), Positive and Negative Affect Schedule (PANAS), and Simplified Coping Style Questionnaire (SCSQ) are utilized for investigation. RESULTS: 205 valid questionnaires are returned. Analysis suggests that the influential factors of mental health stress responses of stroke caregivers include the course of the disease, the impact of the disease on economic conditions, obligation to take care of other family members, understanding of stroke-associated diseases, and whether the patient is at risk. Social support and self-efficacy are negatively correlated with stress responses, while negative coping style is significantly positively correlated with stress responses. CONCLUSIONS: By increasing social support and self-efficacy, medical workers can guide stroke caregivers to take positive coping styles, thereby reducing their mental health stress responses.


Author(s):  
Natal’ya Ye. Kharlamenkova

The investigation results of the disease representation and its relationship with the coping styles in adolescents (n = 43) with tumour of the musculoskeletal system are discussed. The data obtained before and after surgery for the removal of the musculoskeletal tumour were compared. The results expected in accordance with the hypothesis that estimates of physical and emotional states dominate in adolescents disease representations have not been confirmed. It is shown that disease representation correlates with the social support and coping resources (motivation for recovery) and practically does not include the characteristics of the child’s physical and emotional states. A comparison of the relationship between disease representation and coping styles in subgroups of adolescents with different levels of stress revealed the following differences: with a low level of stress, the motivation for recovery as the child’s internal resource is correlated with an active search for social support which at the stage after surgery, begins to be supported by different styles of coping behaviour – solving the problem and reference to others; intense experience of stress significantly limits the possibilities of a teenager which correlates its disease with the physical and emotional problems solved by passively waiting for help from loved ones. Own resources to cope with difficult life situations in adolescents with high levels of stress are not widely available.


2016 ◽  
Vol 17 (3) ◽  
pp. 254-264 ◽  
Author(s):  
Caterina Romaniello ◽  
Chiara Simoni ◽  
Marina Farinelli ◽  
Erik Bertoletti ◽  
Vincenzo Pedone ◽  
...  

The literature about the care givers of patients with Disorders of Consciousness (DOCs) has highlighted the impact on both mental and physical dimensions of quality of life. This study aimed to: (1) describe emotional burden, quality of life, and coping styles in care givers of hospitalized patients with DOCs, compared to Italian normative data; (2) explore the relationships between these variables and their associations with socio-demographic features; and (3) describe their changes over time.Fifteen care givers of patients with DOCs, mostly middle-aged women, were assessed using the Family Strain Questionnaire, the SF-36 Health Survey, and the Coping Orientation to Problems Experienced – Nuova Versione Italiana. Eleven subjects were also assessed after 6 and 12 months. Data were analysed through descriptive statistics, correlations, and nonparametric tests of group differences.Compared to the Italian normative data, our sample showed a worse outcome in mental health, social functioning, global mental component, and emotional role functioning. Furthermore, subjects with high emotional burden had more thoughts of death compared to subjects with low emotional burden. Follow-up analyses revealed no variables changed over time.These results highlight the need for psychological interventions and support, since care givers represent an important part of an all-embracing support and care network for patients with DOCs.


2019 ◽  
Vol 1 (1) ◽  
pp. 55-65
Author(s):  
Abid Hussain ◽  
Zareen Atta Memon ◽  
Rakhshan Ahsan ◽  
Syeda Khushbakht Hussain

The study was accomplished through correlational research design. The purpose was comprised of investigating the impact of psychological burden on patients’ level of their marital life. The convenient sampling technique was utilized to approach 139 patients with diabetes mellitus as a sample. The data was collected through questionnaires as a source of measurement. The permission was taken to keep information confidential. The collected data was entered into SPPS for analysing. Inferential statistics were used to test hypothesis with the help of the following tests; linear regression and t-test for independent sample designs. The results of the study reflect that the psychological burden of diabetic patients influences their degree of marital satisfaction significantly. In addition, the difference of psychological burden (stress, depression and anxiety) and marital satisfaction was found significant with respect to demographic characteristics of the participants; gender, type of disease, education and working status. Female patients are reported with a greater level of psychological burden but they were observed with a poor degree of marital satisfaction as compared to males. Psychological burden and satisfaction associated with marital life due to diabetes was discussed as significant between working and non-working, type 1 and type 2 diabetes mellitus, and educated and uneducated patients. In the future, there is a need to investigate the coping styles as mediator between psychological disturbance and marital satisfaction.


2020 ◽  
Vol 6 (2) ◽  
pp. 388-414
Author(s):  
Fernando Oliveira Pereira

Conciousness is decisive in attributing meanings to the manifestations of life. The impact of diabetes mellitus on patients` psychic and psychosocial functionality depends on the understanding of the disease. Objective: to study the dynamics of changes in psychic and psychosocial functionality in patients with diabetes mellitus, before and after diagnosis. Participants: 50 subjects of both sexes, with diabetes mellitus (30 - 88 years) and 50 subjects with the same socio-demographic characteristics, who do not suffer from the disease. Methodology: Clinical-psychological interview; Socio-demographic questionnaire; Clinical-dynamic disease questionnaire; Self-assessment questionnaire on psychic, family, social and work functionality. Results: Diabetes mellitus patients in the period of life “after diagnosis”, compared to the period “before diagnosis”, show statistically significant differences of greater expressiveness psychic functionality (nervousness, anxiety, irritability, depression, pessimism and fatigue) and lower in psychosocial and work activities (work capacity, availability to socialize with friends and family). In the comparison “before diagnosis” and “current moment” there are significant differences in all categories, but if comparing “after diagnosis” and “current moment”, significant differences only exist in work capacity, fatigue, availability to live together with friends; lower values at the present time. Conclusion: The intrusion of diabetes mellitus and the patient's knowledge of the diagnosis cause changes in the dynamics of psychic functionality and psychosocial activity, aggravating the levels of nervousness, anxiety, irritability, depression, pessimism, feeling of fatigue, less work capacity, availability to socialize with friends and family. Diabetes has a negative impact on the functionality of patients, affecting well-being and quality of life.


2020 ◽  
Vol 22 (1) ◽  
pp. 11-28 ◽  
Author(s):  
Wai Kwong Tang ◽  
Lisha Wang ◽  
George Kwok Chu Wong ◽  
Gabor S. Ungvari ◽  
Fumihiko Yasuno ◽  
...  

Background and Purpose Depression is common and debilitating illness accompanying many neurological disorders including non-traumatic subarachnoid hemorrhage (SAH). The aim of this systematic review was to identify and critically appraise all published studies that have reported the frequency, severity and time course of depression after SAH, the factors associated with its development and the impact of depression on patients’ quality of life after SAH.Methods The PubMed database was searched for studies published in English that recruited at least 40 patients (>18 years old) after SAH who were also diagnosed with depression.Results Altogether 55 studies covering 6,327 patients met study entry criteria. The frequency of depression ranged from 0% to 61.7%, with a weighted proportion of 28.1%. Depression remained common even several years after the index SAH. Depression after SAH was associated with female sex, premorbid depression, anxiety, substance use disorders or any psychiatric disorders, and coping styles. Comorbid cognitive impairment, fatigue, and physical disability also increased the risk of depression. Aneurysmal SAH and infarction may be related to depression as well. Depression reduces the quality of life and life satisfaction in patients after SAH.Conclusions Depression is common after SAH and seems to persist. Further research is needed to clarify its time course and identify the neuroendocrine and neurochemical factors and brain circuits associated with the development of post-SAH depression. Randomized controlled treatment trials targeting SAH-related depression are warranted.


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