scholarly journals COMMUNITY PERCEPTION AROUND HALFWAY HOUSE ABOUT CARE OF MENTAL DISORDERS

2021 ◽  
Vol 3 (1) ◽  
pp. 10
Author(s):  
Farah Aulia Nughraini ◽  
Ah Yusuf ◽  
Ni Ketut Alit Armini
Keyword(s):  
Mental Disorders ◽  
Phenomenological Approach ◽  
Community Response ◽  
Future Research ◽  
Community Perception ◽  
Halfway House ◽  
Mental Patients ◽  
Qualitative Research Design ◽  
Field Notes ◽  
Depth Interviews

Introduction: The high stigma in the community towards mental disorders does not only affect families and mental disorders patients but also on the patterns of care and care, for example, mental disorders patients are isolated so they do not interact with the community with shackles. The purpose of this research is perceptions in the community about how to treat patients with mental disorders.Method: This study used a qualitative research design with a phenomenological approach with ten participants. The technique of selecting participants was purposive sampling with the criteria of men and women aged > 17 years, living around halfway house and who had interacted with mental patients at halfway house. Retrieval of data on ten participants with in-depth interviews and field notes were then analyzed using the Colaizzi method.Results: In this study, 8 themes were identified, namely 5 themes (community understanding of mental disorders, community stigma, community response, community expectations and community experiences with mental patients) for the first specific purpose and 3 themes (treatment, form of care and caregiver factors nurse) for the second special purpose.Conclusion: Community perception is influenced by several factors including the factor of maintaining distance from mental patients, tolerance and support factors, social limitation factors, and factors of prejudice and misunderstanding. Future research can explore in-depth people's perceptions about the treatment of mental disorders patients, more specifically, for example, the care of mental patients in hospitals and at home.

scholarly journals Leprosy Resilience with Disabilities Due to Illness: A Qualitative Study

2020 ◽  
Vol 5 (2) ◽  
pp. 95
Author(s):  
Atika Jatimi ◽  
Ah Yusuf ◽  
Sestu Retno Dwi Andayani
Keyword(s):  
Data Collection ◽  
Sampling Technique ◽  
Psychosocial Problems ◽  
Phenomenological Approach ◽  
Active Coping ◽  
Positive Adaptation ◽  
Qualitative Research Design ◽  
Leprosy Patients ◽  
Field Notes ◽  
Depth Interviews

Introduction: Leprosy is an infectious disease that still causes complex problems. The problem in question is not only in medical and physical terms, such as disability, but extends to social, economic, and cultural problems. This study aims to explore the experience of leprosy sufferers with disabilities to achieve resilience. Methods: A descriptive qualitative research design with a phenomenological approach was used. The number of participants was eleven people affected by leprosy with grade 1 and 2 disabilities in Sumenep Regency obtained by a purposive sampling technique. Data collection used in-depth interviews with interview guides and field notes; the results of data collection were analyzed with theme analysis. Results: This study produced five main themes about the experience of leprosy patients in the process of achieving resilience, namely: 1) self-stigma as a stressor experienced by lepers, 2) psychosocial problems that arise in response to stressors, 3) active coping as a method of resolving stress, 4) positive adaptation as a form of self-adjustment, 5) characteristics of strong individuals. Conclusion: Lepers with disabilities identify self-stigma as a stressor that triggers the emergence of psychosocial problems. Individuals can form tough characteristics, such as responding positively to unexpected conditions, becoming more productive, and showing helping others behavior after overcoming stressors through the stages of active coping and positive adaptation.

scholarly journals “What Are The Challenges of Treating Mentally Impaired Patients in The Era of a Pandemic?” : Qualitative Exploration Caregivers

2021 ◽  
Author(s):  
Ah Yusuf ◽  
Joel Rey U. Acob ◽  
Roro Dian Tristiana ◽  
Intan Faizatun Nafisa ◽  
Verantika Setya Putri ◽  
...  
Keyword(s):  
Mental Disorders ◽  
Interpretative Phenomenological Analysis ◽  
Sampling Technique ◽  
Well Being ◽  
Daily Life Activities ◽  
Qualitative Research Design ◽  
Field Notes ◽  
Mentally Impaired ◽  
Qualitative Exploration ◽  
Depth Interviews

Abstract Introduction: Caregivers provide support for mental disorders in the form of care such as assistance in daily life activities, but during a pandemic it is a challenge in itself. Objective: To explore the caregiver's experience in caring for clients with mental disorders in remote areas during a pandemic. Methods: Using a phenomenological qualitative research design with 25 participants. The sampling technique used was purposive sampling with data collection techniques using in-depth interviews and field notes then analyzed using IPA (Interpretative Phenomenological Analysis). Results: This study found 6 themes, namely: Caregiver Workload and Tension, Threats to Caregivers' Physical and Psychological Well-Being, The Need for a Continuing Family Role, Holistic Care, Coping Strategy, Communication is getting harder.Conclusion: our research provides unique findings about the experience of treating mental disorders needs during the COVID-19 pandemic. Caregivers of mental disorders struggle with parenting difficulties during the pandemic, which poses a threat to their well-being and potential harm to the mental disorder survivor-caregiver relationship.

scholarly journals Could coronavirus 2019-infected disease patients get cope with the treatment?: A qualitative study

2021 ◽  
Vol 10 (4) ◽  
pp. 880
Author(s):  
Fery AM Mendrofa ◽  
Umi Hani ◽  
Yuni Nurhidayat
Keyword(s):  
Data Collection ◽  
Qualitative Study ◽  
Coping Strategies ◽  
Phenomenological Approach ◽  
Cross Infection ◽  
Psychological Aspect ◽  
Future Research ◽  
The World ◽  
Novel Coronavirus ◽  
Depth Interviews

A pandemic of a novel coronavirus-infected disease is currently ongoing in the world. Most patients have to be isolated due to the treatments. This study aimed to make sense of how patients with coronavirus-infected disease understand and experience infectious isolation. The research used a qualitative design with a phenomenological approach. Data collection was conducted with in-depth interviews of nine patients with coronavirus disease-2019 (COVID-19) confirmed who had been in the isolation room. The analysis was conducted on interview transcripts by organizing keywords found into categories, sub-themes, and themes based on Colaizzi's approach. The results indicated that the participants experienced fright due to the isolation and attempted to integrate their isolation experiences. Isolation highlighted a sense of threat posed by cross-infection, a threat that participants experienced as originating from others and from themselves to others. Participants described feeling changes experienced after several days of treatment. Participants reported various symptoms of the disease and received careful care while in isolation. They still communicate with family. Isolated patients are able to deal with the treatment by improving their coping strategies. Participants reported the most support from their families, even from a distance. Future research could explore experiences of isolation from family and staff perspectives and identify the psychological aspect in caring for the COVID-19 patients.

CHARACTERISTIC OF PARENTS’S ACCEPTANCE IN GETTING CHILD DIAGNOSIS AS AUTISM

2021 ◽  
Vol 5 (2) ◽  
pp. 186
Author(s):  
Rahma Furi Sagita ◽  
Ahmad Suryawan ◽  
Wahyul Anis
Keyword(s):  
Phenomenological Approach ◽  
Case Finding ◽  
Parental Acceptance ◽  
Coping Methods ◽  
Qualitative Research Design ◽  
Intervention Method ◽  
Child Diagnosis ◽  
Knowledge Age ◽  
Autism Interventions ◽  
Depth Interviews

 AbstractBackground: Autism is a child development disorder which usually late in case finding and intervention. It used to done in 30 month old of child. In Dr. Saiful Anwar Malang Regional Hospital, it was found that the average of case finding in 48 month of child. This study aims to determine how the acceptance of parents while getting diagnosis of their child and their action to give their child autism intervention. Method: This study used a qualitative research design with a phenomenological approach. Data colleted by in-depth interviews with 6 informants. Data analysis used Collaizi's (1978) Nine Steps method. Results: Most informants were late in recognizing the symptoms of autism in children, but they had a positive perception of the received diagnosis. All informants have felt bad feelings due to the diagnosis received, but have had coping methods for these feelings and have given autism interventions to children. Factors that influence parental acceptance include the level of education, knowledge, age, occupation, household harmony, social support, economic conditions, ethnicity, interaction between informants and experts, the clarity of symptoms shown by the child and the presence of siblings. Conclusion: Parental acceptance is a process from refusing, getting angry, bargaining, to accepting. In the process of being accepted, parents continue to make efforts to save children 

Structural Vulnerabilities, Personal Agency, and Caste: An Exploration of Child Sex Trafficking in Rural India

2020 ◽  
Vol 35 (3) ◽  
pp. 307-330
Author(s):  
Rochelle L. Dalla ◽  
Trupti Jhaveri Panchal ◽  
Sarah Erwin ◽  
Jessie Peter ◽  
Kaitlin Roselius ◽  
...  
Keyword(s):  
Sex Trafficking ◽  
Sexual Exploitation ◽  
Phenomenological Approach ◽  
Future Research ◽  
Sex Industry ◽  
Structural Factors ◽  
Personal Agency ◽  
Child Sex Trafficking ◽  
Vulnerability Theory ◽  
Depth Interviews

The commercial sexual exploitation of children (CSEC) is considered normative and expected among some Indian castes. Focusing on the Bedia specifically, we sought to identify factors responsible for the intergenerational continuation of CSEC as well as opportunities for prevention. To this end, three questions were posed, including: (a) What structural factors perpetuate CSEC among the Bedia? (b) What are the mechanisms by which Bedia children enter the commercial sex industry (CSI)? and (c) To what extent do Bedia women have personal agency in exiting the CSI and in keeping their children from entering? Guided by structural vulnerability theory and a phenomenological approach, in-depth interviews were conducted with 31 Bedia women engaged in (or exited from) the CSI. Results indicate that girls as young as 12 are “selected” to enter the CSI; once involved, they carry the burden of familial financial sustainability and exit only comes when they are no longer able to attract paying clients and younger female kin able to assume the primary breadwinner role. Ability to keep female children from entry is minimal. Implications for future research, practice, and policy are discussed.

scholarly journals MANAGEMENT STRES, COPING STRES PADA REMAJA DAN DAMPAK PADA PEMBANGUNAN EKONOMI DAERAH KOTA TERNATE

2019 ◽  
Vol 2 (1) ◽  
pp. 185
Author(s):  
Nurlaila Nurlaila
Keyword(s):  
Qualitative Method ◽  
Phenomenological Approach ◽  
Research Subjects ◽  
Social Psychological ◽  
Field Notes ◽  
Psychological Maturity ◽  
Age Limit ◽  
Younger Generation ◽  
Depth Interviews

Adolescence is a period where the transition from childhood to adulthood, not only that they also do not form physical maturity (hacking) but will also lead to social-psychological maturity, among others, towards maturity and independence (Ruwaida, 2006 ) This study uses a qualitative method to describe stress management coping in adolescents as a result of parental divorce through a phenomenological approach which focuses on finding facts of human behavior based on the informant's perspective. Methods of collecting data through in-depth interviews and completed with field notes. The research subjects were teenagers whose parents divorced with the age limit (15-22 years) the number of subjects in this case study was 14 (fourteen) people in Ternate City. The behavior and culture of life of informants due to not being able to manage stress and accept family conditions, there is no visible achievement of the informants for regional economic development. very influential in regional development considering that the younger generation is the successor of the nation and state development. The results of this research indicate the condition of adolescents who experience problems such as this affect the development of development when viewed from the achievements that should be owned by the younger generation.  

scholarly journals Conducting In-Depth Interviews via Mobile Phone with Persons with Common Mental Disorders and Multimorbidity: The Challenges and Advantages as Experienced by Participants and Researchers

2021 ◽  
Vol 18 (22) ◽  
pp. 11828
Author(s):  
Azadé Azad ◽  
Elisabet Sernbo ◽  
Veronica Svärd ◽  
Lisa Holmlund ◽  
Elisabeth Björk Brämberg
Keyword(s):  
Mental Disorders ◽  
Mobile Phone ◽  
Common Mental Disorders ◽  
Qualitative Interviews ◽  
Self Disclosure ◽  
Telephone Interviews ◽  
Illness Experiences ◽  
Research Interviews ◽  
Field Notes ◽  
Depth Interviews

Qualitative interviews are generally conducted in person. As the coronavirus pandemic (COVID-19) prevents in-person interviews, methodological studies which investigate the use of the telephone for persons with different illness experiences are needed. The aim was to explore experiences of the use of telephone during semi-structured research interviews, from the perspective of participants and researchers. Data were collected from mobile phone interviews with 32 individuals who had common mental disorders or multimorbidity which were analyzed thematically, as well as field notes reflecting researchers’ experiences. The findings reveal several advantages of conducting interviews using mobile phones: flexibility, balanced anonymity and power relations, as well as a positive effect on self-disclosure and emotional display (leading to less emotional work and social responsibility). Challenges included the loss of human encounter, intense listening, and worries about technology, as well as sounds or disturbances in the environment. However, the positive aspects of not seeing each other were regarded as more important. In addition, we present some strategies before, during, and after conducting telephone interviews. Telephone interviews can be a valuable first option for data collection, allowing more individuals to be given a fair opportunity to share their experiences.

scholarly journals PENGALAMAN KELUARGA DALAM MERAWAT DEKUBITUS

2017 ◽  
Vol 2 (1) ◽  
pp. 11
Author(s):  
Rita Sari
Keyword(s):  
Family Members ◽  
Deep Understanding ◽  
Phenomenological Approach ◽  
Pressure Sores ◽  
The Family ◽  
Long Time ◽  
Field Notes ◽  
Written Questions ◽  
Depth Interviews ◽  
At Home

Immobilization is a problem faced by patients with chronic illness, the patients is very weak and paralyzed patients in a long time. This study have purpose  to gain a deep understanding of the experience of families in caring for family members is immobilized with pressure sores at home. This study used qualitative methods. Participants are families who care for patients at home who are immobilized with pressure sores. Collecting data with in-depth interviews by means of instrument is the researcher's own self, written questions as an interview, used recording devices and used field notes.  Criterion sampling by taking 6 participants. Analysis of data used a phenomenological approach. The results showed that the family had a positive experience; Can be more patient, and assume that caring for a sick family member has its own challenges, being able to be with other families in caring for patients, being able to give affection and obligation as a child to parents can help take care of it. There was also an unpleasant (negative) family experience during the care of sick family members, the family felt tired, not strong and bored during patient care. The conclusion of the study is that families have positive and negative experiences in caring for family members with decubitus

scholarly journals CREATION OF COMPASSION" - FAMILY EXPERIENCE IN CARING FOR PATIENT WITH MENTAL DISORDERS

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Nining Wuri Lestari ◽  
Setyawati Soeharto ◽  
Dwi Windarwati
Keyword(s):  
Qualitative Research ◽  
Mental Disorders ◽  
Interpretative Phenomenological Analysis ◽  
Phenomenological Approach ◽  
Structured Interview ◽  
Phenomenological Analysis ◽  
Family Experience ◽  
Family Experiences ◽  
The Family ◽  
Depth Interviews

Background: Caring for people with post-pasung (post seclusion and restraint of patient) mental disorders can provide special experience for families who act as caregivers. Objective: To explore family experiences in rehabilitating people with post-pasung mental disorders in Trenggalek Regency. Methods: This research is a qualitative research with an interpretive phenomenological approach. Data were obtained through in-depth interviews using semi-structured interview guidelines. Participants in this study were twelve in number who treated people with post-pasung mental disorders in Trenggalek Regency. Results: Analysis of data using IPA (Interpretative Phenomenological Analysis), found eight themes, namely having compassion for patients, having the responsibility of caring for patients, repaying the kindness of patients and others who have helped, having the hope that patients can recover, feel the need to supervise the independence of patients, realize the condition of mental patients, resigned to accept, thankful that the patient can improve and upset. Conclusion: Family is a determinant of the success of rehabilitation in people with post-pasung mental disorders. Family compassion and attention support the patient's recovery. The family hopes that the patient can recover and be independent in self-care, take medicine and work so that it does not depend on the family. This study produced eight themes and answered the research objectives.

Social innovation camps: an analysis of participants’ experiences

2019 ◽  
Vol 12 (1) ◽  
pp. 99-110
Author(s):  
Karen Milner
Keyword(s):  
Design Methodology ◽  
Social Innovation ◽  
Group Processes ◽  
Group Facilitation ◽  
Content Type ◽  
Qualitative Research Design ◽  
Innovative Thinking ◽  
Field Notes ◽  
Depth Interviews

Purpose The purpose of this paper is to document and analyse the processes underpinning the Southern African Social Innovation Camp (the Camp). This paper details the theoretical basis on which the Camp was designed and assesses the ways in which the participants experienced the camp in light of these theoretical principles. Design/methodology/approach A qualitative research design was used with four sources of data: participant reviews of the Camp, in-depth interviews with stakeholders, the researcher’s field notes and a reflective blog posted online by one of the participants. Data were analysed using thematic content analysis. Findings Three themes emerged from the analysis. The Camp as a foreign but safe space that moves people out of their comfort zones, enabling innovative thinking; the importance of discipline and rigour in self-organising groups; and the interplay of diversity feedback and trust/mistrust. The theoretical principles which informed the design of the Camp were clearly evident in these themes. Research limitations/implications No evaluation of the degree of innovativeness/quality of the prototypes. While the focus of the study was on participants’ experiences, a clearer indicator of the innovativeness and usefulness of the prototypes would have provided greater insight. Originality/value The study describes a theoretical framework for designing innovation groups and establishes the usefulness of the framework for analysing the group processes. Based on the results, recommendations for effective functioning in innovation groups are proposed: group diversification; discipline and rigour in group facilitation; vigilance in eliminating hierarchy; and managing the interplay between diversity, feedback and trust.

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