Knowledge and awareness of Covid 19 and its impact on mental health

2020 ◽  
Vol 11 (SPL1) ◽  
pp. 807-815
Author(s):  
Pratheebha C ◽  
Gayatri Devi R ◽  
Gifrina Jayaraj

The coronavirus disease 2019 (COVID-19) pandemic—and the social distancing measures that many countries have implemented—have caused disruptions to daily routines. Mental health support and follow-up should be provided even six months after the release from isolation for those individuals with prior vulnerable mental health status. The main aim of the study is to create awareness and knowledge about COVID – 19 and its impact on the mental health of the public. The self-administered design was designed based on awareness. The questionnaire was distributed through google docs link to 100 numbers of the study population who were in lockdown irrespective of age. Methods of representation of each output variable were represented in the pie chart form. The measure that was taken to minimize the sampling bias was that the validity that was checked both internally and externally. The result was statistically analyzed using SPSS software. The participants were explained about the purpose of the study in detail. From the above Survey conducted, 58% of the total 100 participants' mental health being affected due to lockdown imposed due to COVID -19. This COVID 19 has created stress, anxious and nervous situations for 47% of the total participants. Educated people and health professionals are aware of this infection; they take possible preventive measures. They understand the importance of social distancing. So this lockdown is not affecting their mental health.

BMJ Open ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. e040610
Author(s):  
Renée O'Donnell ◽  
Melissa Savaglio ◽  
Debra Fast ◽  
Ash Vincent ◽  
Dave Vicary ◽  
...  

IntroductionPeople with serious mental illness (SMI) often fail to receive adequate treatment. To provide a higher level of support, mental health systems have been reformed substantially to integrate mental healthcare into the community. MyCare is one such community-based mental health model of care. This paper describes the study protocol of a controlled trial examining the effect of MyCare on psychosocial and clinical outcomes and hospital admission and duration rates for adults with SMI.Methods and analysisThis is a multisite non-randomised controlled trial with a 3, 6 and 12-month follow-up period. The study participants will be adults (18–64 years of age) with SMI recruited from Hobart, Launceston and the North-West of Tasmania. The treatment group will include adults who receive both the MyCare intervention and standard mental health support; the control group will include adults who receive only standard mental health support. The primary outcome includes psychosocial and clinical functioning and the secondary outcome will examine hospital admission rates and duration of stay. Mixed-effects models will be used to examine outcome improvements between intake and follow-up. This trial will generate the evidence needed to evaluate the effect of a community mental health support programme delivered in Tasmania, Australia. If MyCare results in sustained positive outcomes for adults with SMI, it could potentially be scaled up more broadly across Australia, addressing the inequity and lack of comprehensive treatment that many individuals with SMI experience.Ethics and disseminationThis study has been approved by the Tasmanian Health and Medical Human Research Ethics Committee. The findings will be disseminated to participants and staff who delivered the intervention, submitted for publication in a peer-reviewed journal and shared at academic conferences.Trial registration numberACTRN12620000673943.


2021 ◽  
Vol 16 (3) ◽  
pp. 131
Author(s):  
Lilis Banowati ◽  
Cucu Herawati ◽  
Wiwiet Indriyani

Background: The increasing number of positive patients with Covid-19, the social impact in the form of stigma from being shunned by neighbors and even families and the impact of mental health, namely causing major psychosocial stresses that can trigger anxiety. Purpose  this study was to determine the stigma and level of public anxiety about Covid- 19. Methods: This type of research is descriptive quantitative, the study population is all people in the UPTD Haurgeulis Puskesmas, Indramayu Regency, as many as 88,468 people. The number of samples was 100 respondents using purposive sampling technique. Data were analyzed statistically using univariate analysis and data presentation in the form of frequency distributions. Results: This study shows that people have a low stigma as much as 1% and those who experience a high stigma are as much as 99%. As well as people who do not experience anxiety as much as 14% and most of them experience mild anxiety as much as 86%. Conclusion: The public should be wiser in sorting out information related to Covid-19 from various sources and can manage anxiety with good self-coping management, for example by relaxation and positive thinking related to Covid-19.


PLoS ONE ◽  
2021 ◽  
Vol 16 (11) ◽  
pp. e0260399
Author(s):  
Perla Werner ◽  
Aviad Tur-Sinai

Efforts to control the spread of the novel Coronavirus (COVID-19) pandemic include drastic measures such as isolation, social distancing, and lockdown. These restrictions are accompanied by serious adverse consequences such as forgoing of healthcare. The study aimed to assess the prevalence and correlates of forgone care for a variety of healthcare services during a two-month COVID-19 lockdown, using Andersen’s Behavioral Model of Healthcare Utilization. A cross-sectional study using computerized phone interviews was conducted with 302 Israeli Jewish participants aged 40 and above. Almost half of the participants (49%) reported a delay in seeking help for at least one needed healthcare service during the COVID-19 lockdown period. Among the predisposing factors, we found that participants aged 60+, being more religious, and reporting higher levels of COVID-19 fear were more likely to report forgone care than younger, less religious and less concerned participants. Among need factors, a statistically significant association was found with a reported diagnosis of diabetes, with participants with the disease having a considerably higher likelihood of forgone care. The findings stress the importance of developing interventions aimed at mitigating the phenomenon of forgoing care while creating nonconventional ways of consuming healthcare services. In the short term, healthcare services need to adapt to the social distancing and isolation measures required to stanch the epidemic. In the long term, policymakers should consider alternative ways of delivering healthcare services to the public regularly and during crisis without losing sight of their budgetary consequences. They must recognize the possibility of having to align medical staff to the changing demand for healthcare services under conditions of health uncertainty.


2018 ◽  
Vol 29 (1) ◽  
pp. 103-112 ◽  
Author(s):  
Cecilia Kjellgren

Purpose: This study explores outcomes of treatment provided by specialized units within the social welfare sector in Sweden to clients seeking help with hypersexual behavior. Method: The participants were 27 males and 1 female ( M = 40.3 years) who sought help from one of the three specialized units within social welfare in Sweden. A pretest–posttest group design was used to assess changes after treatment. Quantitative data were collected through interviews and self-report forms. Results: At posttreatment stage (on average a 10-month follow-up), mental health was significantly improved and hypersexual behavior reportedly reduced. The treatment at the specialized units appeared to help the clients. Conclusions: The specialized units seemed to deliver favorable service without shaming and stigmatizing participants. As this study can be considered a pilot study, it needs to be replicated.


2001 ◽  
Vol 88 (3_suppl) ◽  
pp. 981-986
Author(s):  
Crystale Purvis Cooper ◽  
Debra L. Roter

Psychological research is often criticized for routine use of a narrow and unrepresentative study population—college students. This study investigated the feasibility of recruiting research participants from U.S. jury pools, which by law must include a representative cross-section of the public. A questionnaire was mailed to the jury administrators in the 217 U.S. state court jurisdictions with populations of 250,000 or more. Court officials representing 79 jurisdictions in 30 states and the District of Columbia returned surveys (36% response rate). In addition, respondents who indicated in the mail survey that their court had previously allowed outside investigators to recruit jurors also completed a follow-up telephone interview. While the majority of jurisdictions (61%) opposed participation of jurors in research, 31 jurisdictions (39%) did not object to this practice. Only 8 of the nonopposed jurisdictions had been asked to host research, and 7 had agreed to do so. The jurisdictions that opened their jury pools to researchers employed a number of strategies to circumvent potential problems and generally reported that hosting research was a positive experience. Jury pools represent a viable and relatively untapped source of research participants. Many courts are open to the possibility of hosting research but have never been asked to do so. Both researchers and court officials should be reassured by the positive experiences of courts that have hosted research.


2006 ◽  
Vol 188 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Janet Meehan ◽  
Navneet Kapur ◽  
Isabelle M. Hunt ◽  
Pauline Turnbull ◽  
Jo Robinson ◽  
...  

BackgroundSuicide prevention is a health service priority. Suicide risk may be greatest during psychiatric in-patient admission and following discharge.AimsTo describe the social and clinical characteristics of a comprehensive sample of in-patient and post-discharge cases of suicide.MethodA national clinical survey based on a 4-year (1996–2000) sample of cases of suicide in England and Wales who had been in recent contact with mental health services (n=4859).ResultsThere were 754 (16%) current in-patients and a further 1100 (23%) had been discharged from psychiatric in-patient care less than 3 months before death. Nearly a quarter of the in-patient deaths occurred within the first 7 days of admission; 236 (31%) occurred on the ward, the majority by hanging. Post-discharge suicide was most frequent in the first 2 weeks after leaving hospital; the highest number occurred on the first day.ConclusionsSuicide might be prevented among in-patients by improving ward design and removing fixtures that can be used in hanging. Prevention of suicide after discharge requires early community follow-up and closer supervision of high-risk patients.


2016 ◽  
Vol 33 (S1) ◽  
pp. S443-S443
Author(s):  
E. Perju ◽  
E. Gallois

IntroductionThe intention of this study is to show the frequency of the burnout syndrome among the population seen at psychiatric ER for the most severe complication of the burnout, the suicide attempt.Objective(a) To demonstrate the frequency of burnout among the population examined at psychiatric ER for suicide attempt.(b) To establish a correlation between the frequency of burnout and:– the socio-demographic characteristics;– the psychiatric follow-up;– the type of personality found.MethodsDescriptive study on a sample of 92 patients examined at psychiatric ER between 01/02/2014 and 01/06/2014 after a suicide attempt, seen by a single doctor. The patients received the Maslach Burnout inventory (MBI).ResultsThe frequency of burnout among the population consulted for suicide attempts is 8.7%. The limitations of this study were: the use of MBI questionnaire only by one doctor and a collection of data carried on a certain period of time.I managed to characterize the population seen after the suicide attempt induced by the burnout: 88% women; 25% foreign population working in a context with many responsibilities; the predominance of obsessive personality – 50%, followed by anxious personality type – 25%; the suicide attempt was done by a population without psychiatric history and without psychiatric follow-up – 75%; the studied population is divided between patients working in a high responsibility environment – 36% and patients working in the social or the public environment – 63%.Eighty-eight percent of patients were brought in after their first suicide attempt.ConclusionDespite the fact that until now a unanimous definition has not been formulated on the CIM-10, the burnout syndrome is one of the most popular disorders.The problematic is real, considering that this syndrome, which starts with a psychological distress, can escalade to a self-aggressive behaviour.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2020 ◽  
Vol 16 (2) ◽  
Author(s):  
Sally Hett

I was excited. When I started working I was excited about the social impact mandate inherent in the public sector – how good! Then, as my work led me into the depths of the public sector’s limitations, I was swallowed by despair. As an advisor on the Government Inquiry into Mental Health and Addiction I was a sponge to the pain of the country. I heard the pain in young people, solo mothers, whänau, refugees of not being heard, seen or supported. The reality of slow, siloed, under-resourced and overly risk-averse agencies was undeniable.


2020 ◽  
Author(s):  
Gunn Pungpapong ◽  
Rasmon Kalayasiri

Abstract Background: Stressors introduced to adolescents by COVID-19 social distancing measures may cause mental health problems to (re)surface. We studied depression, anxiety and stress among adolescents experiencing lockdown. Methods: From May-June 2020, secondary school students were enrolled in an online cross-sectional survey through social media. We assessed presence and severity of depression (PHQ-9), anxiety (GAD-7) and stress (PSS-10) in the last month, demographics, degree of social distancing, and other associated issues.Results: Of 392 respondents (56.4% male, 43.1% female), mostly from Thailand (59.2%) and UK (26.5%). We identified depressive symptoms in 58.7%, anxiety in 40.3% and high levels of stress in 9.7%. We found, by multivariate analysis, significant associations between being female and depression and anxiety, being in late secondary school years and depression, and changes in patterns of substance use and anxiety and stress.Conclusions: We propose that girl-centred mental health support platforms should be readily available and tailored to fit specific countries’ contexts. Schools must closely monitor and act upon any concerns which arise from their students and must also monitor mental health wellbeing as changes in academic routine due to COVID-19 could be drastic for some. Harm reduction services must adapt and utilise innovative telemedicine interventions, tailored towards adolescent users.


Author(s):  
Colin P. Neufeldt

This article examines the role that Mennonites played in the establishment and management of kolkhozy in the two largest Mennonite settlements (Khortytsia and Molochansk) in Soviet Ukraine during dekulakization and collectivization (1928-1934).  More specifically, it investigates the social and ethnic criteria used in selecting Mennonites to be kolkhoz chairmen; the duties and daily routines of chairmen; the conflicted relationships that chairmen had with local authorities and kolkhoz members; the numerous challenges that chairmen encountered during the 1932-33 famines; and the mechanisms that local authorities and kolkhoz members used to control, embarrass, and discipline chairmen.  It also discusses the negative repercussions that the rise of Nazi Germany had for Mennonite chairmen, and how political, economic, agricultural, social, and ethnic policies and conditions made it impossible for Mennonite chairmen to succeed.


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