• 제목/요약/키워드: social suffering

검색결과 275건 처리시간 0.037초

황백(黃柏)의 신미(辛味)에 대한 고찰(考察) - 역수학파(易水學派) 의가(醫家)들과 주단계(朱丹溪)의 활용 방식의 비교를 중심으로 - (A Study on the Pungent Taste of Huangbo (Phellodendri Cortex) - Based on Comparison of Its Application by the Yishui School and Zhu Danxi -)

  • 辛相元
    • 대한한의학원전학회지
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    • 제35권4호
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    • pp.97-114
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    • 2022
  • Objectives : Background research on the history of Huangbo's taste being written as 'pungent' was undertaken, after which its clinical meaning was examined from the medical perspective that was behind the medicinal's taste designation. Furthermore, through various understandings on the 'pungent' taste within the process of clinical application, the meaning of 'pungent' in Korean medicinal research was re-evaluated. Methods : Description of Huangbo's taste as 'pungent' as written in medical texts were chronologically examined to determine its origin. The clinical meaning of the pungent taste of Huangbo was examined within the broad medical perspective of doctors who were behind these descriptions. Results & Conclusions : The pungent taste of Huangbo was first described by Zhang Yuansu, followed by doctors of the Yishui School such as Li Dongyuan, Wang Haogu, etc., during which such knowledge was established and contributed to recognition of Huangbo's effect as tonifying Kidney deficiency and treatment of fire within water, after reaching the Kidney. Li Dongyuan understood the meaning of Huangbo's pungent taste as eliminating Yin fire and restoring the upward direction, ultimately restoring the general 'Rising-Falling-Floating-Sinking' mechanism within the context of his inner damage treatment. On the other hand, Zhu Danxi interpreted the pungentness of Huangbo based on his understanding of the nature of fire and action towards it. It seems as Huangbo's effects were understood within a relatively narrow frame, application of its pungent taste became vague, which gave rise to criticism by later period doctors, ultimately leading to an ambiguous understanding of the pungent taste of Huangbo.

교육 소외계층 학생과 일반학생의 컴퓨팅 사고력 비교분석 연구 (A Comparative Study of Computational Thinking Competency Between Underprivileged Students and General Students)

  • 이재호;최승윤;장준형
    • 창의정보문화연구
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    • 제5권1호
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    • pp.25-34
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    • 2019
  • 4차 산업혁명으로 인한 사회 변화에 따라 2015 개정교육과정부터 SW교육이 정규 교육과정에 편입되었고, SW교육의 궁극적 목표는 컴퓨팅 사고력의 계발이다. 현장에서 SW교육이 성공적으로 정착하기 위해서는 교육 수혜자인 학생들의 수준을 정확히 진단하고 이에 맞는 교육과정과 교수학습 방법을 적용해야한다. 현재까지 일반학생이나 영재학생을 대상으로 한 컴퓨팅 사고력 관련 연구는 진행되었으나, 교육 소외 계층 학생을 대상으로 한 연구는 미비한 실정이다. 본 연구에서는 교육 소외계층 학생 135명과 일반학생 201명을 대상으로 컴퓨팅 사고력을 측정하고 비교 분석하는 연구를 진행하였다. 교육 소외계층 학생은 남양주 지역아동센터 15곳을 방문해 모집하였고, 비교집단인 일반학생은 남양주 소재 B 초등학교 학생을 모집하였다. 두 집단 간 컴퓨팅 사고력을 다각도로 비교 분석한 결과 교육 소외계층 학생의 컴퓨팅 사고력이 일반학생에 비해 저조한 것으로 나타났고 이를 통해 몇 가지 시사점을 제언하였다.

치매노인과의 관계개선을 위한 중풍노인 이야기치료 집단상담 사례 연구 (A Qualitative Case Study of the Narrative therapy group work on the elderly with palsy to solve conflict with the elderly with dementia)

  • 이경욱
    • 한국노년학
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    • 제29권3호
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    • pp.1123-1140
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    • 2009
  • 본 연구는 주간보호센터의 중풍노인이 이야기치료 집단상담을 통해 치매노인과의 갈등을 해결하는 과정을 탐색하는 연구이다. 중풍노인에 대한 이야기치료 집단상담을 7회 동안 실시한 과정을 사례연구방법을 통해 분석하였다. 분석결과 첫째, 중풍 노인들이 집단상담을 통해 치매노인을 '문제'가 아니라 '치매로 고통받는 사람'으로 보고, 치매노인을 비난하는 대신 도와줄 방법을 적극적으로 찾게 되었으며, 둘째, 자신들을 '치매노인의 피해자'가 아니라 '유능한 사람 으로 규정하게 되었고, 셋째, 중풍노인들끼리 협력적이고 친밀한 관계가 되었으며, 넷째, 중풍노인들이 주간보호센터 운영에 적극적으로 참여하게 된 것으로 나타났다. 이러한 변화에 이야기치료의 문제와 사람을 분리시키기, 클라이언트를 자기 문제의 전문가로 존중하기, 독특한 결과 찾기 등이 도움이 된 것으로 분석되었다. 이러한 결과를 바탕으로 장기요양보호대상자에게 보호를 제공할 뿐만 아니라 참여 기회를 확대하고, 이야기치료를 노인에게 적용할 것을 제안하였다.

학업부진 전문대학생을 위한 지원 프로그램의 효과 연구 (A Study on the Effectiveness of the Support Program for Underachieving Junior College Students)

  • 조채영;김경미
    • 문화기술의 융합
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    • 제10권1호
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    • pp.395-402
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    • 2024
  • 본 연구의 목적은 학업부진 전문대학생을 위한 집중 지원 프로그램이 학생들의 학습동기 및 자기학습효능감에 미치는 효과를 검증하고 의미를 탐색하는 것이다. 본 연구는 부산광역시 D대학교 교수학습개발센터가 학사경고자 및 성적부진 학생들을 대상으로 지원한 JUMP-UP 프로그램에 참여한 46명의 학생을 대상으로 진행되었다. 본 연구의 연구문제는 첫째, JUMP-UP 프로그램은 전문대학생의 학습동기 강화에 영향을 미치는가? 둘째, JUMP-UP 프로그램은 전문대학생의 자기학습효능감에 영향을 미치는가?이다. JUMP-UP 프로그램 참여 전·후 설문조사를 실시하여 효과성을 살펴본 결과 JUMP-UP 프로그램은 참여 학습자의 학습동기와 자기학습효능감 모든 항목에서 통계적으로 유의미한 변화를 나타내었다. 이를 통하여 JUMP-UP 프로그램과 같은 집중 지원 프로그램은 학업부진을 겪는 전문대학생의 학습동기 및 자기학습효능감 향상에 적합한 지원 프로그램으로 가치가 있다는 것을 알 수 있다.

뇌졸중환자 가족의 간호요구 (A Study on the Care Needs of Family-Caregivers to the Patients with Stroke)

  • 김미희
    • 기본간호학회지
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    • 제4권2호
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    • pp.175-192
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    • 1997
  • The purpose of this study was to identify the care needs of family-caregivers to the patients with stroke. Subjects were 115 family-caregivers caring for the patients while they were in-patients or out-patients with stroke in two general hospitals and one oriental medicine hospital located in Seoul and Kwang-Ju. The instrument used for this study was made by the researcher on the basis of results of literature review and interviews with family-caregivers, composed of 35 items. Internal validity by calculation of cronbach's alpha with data of respondents was 0.91, which was regarded as high. The Data were analyzed by SAS program, with percentage, mean, t-test, and ANOVA. Factor structures of care needs of family-caregivers were elicited by factor analysis(PCA, Varimax rotation). Datum collection had been from July 1 to August 14, 1997. The results of this study were as follows : 1. The mean score of the sum of the care needs of family-caregivers was 3.96 and the highest-mean item was 'need for immediate care(M=4.77)', and the lowest-mean item was 'need for chaplian's visit (M=2.82)'. 2. Care needs of the family-caregivers were : Need to be informed of the disease, treatment and care ; need of education and assistance related to physical functional level ; need of social support and consultation ; need of management of nursing problem related to immobility ; need of appreciation ; need of the way to communicate with patients ; need of immediate care and help. The highest mean factor was the 'need for immediate care and help(M=4.74)', and the lowest mean factor was the 'need of appreciation(M=3.58)'. 3. The variables influencing the degree of care needs perceived by family-caregivers to the patients with stroke were as follows : There were significant differences between need to be informed of the disease, treatment and care and general characteristic factors, which were family caregiver's sex (p=.0178), caring period(p=.0223) and patient's suffering period(p=.0244). There were significant differences between need of education and assistance related to physical functional level and general characteristic factors, which were patient's paralysis(p=.0177), patient's ADL dependency(p=.0032). There were significant differences between need of social support and consultation and general characteristic factors, which were family caregiver's sex(p=.0055), occupation(p=.0159), religion(p=.0093) and patient's sex(p=.0134). There was significant difference in the degree of need of management of nursing problem related to immobility, according to the patient's ADL dependency(p=.0493). There were significant differences between need of appreciation and general characteristic factors, which were family caregiver's age(p=.0107), sex(p=.0133), and patient's age(p=.0338). There were significant differences between need of the way to communicate with patient and general characteristic factors, which were patient's paralysis(p=.0002) and aphasia(p=.0001). There were significant differences between need of immediate care and help and general characteristic factors, which were family caregiver's caring period(p=.0162) and patient's suffering period(p=.0116). 4. The mean score of patient's ADL dependency was 3. 38 and the highest-mean item was 'ascending and descending stairs(M=4.12)', and the lowest-mean item was 'drinking(M=2.60)'. There was no significant difference in the degrees of care needs related to the patient's ADL dependency. 5. The highest information source of family-caregivers was from the doctors about the disease, treatment and care(26.1%). The second highest one was from mass media(20.8%), and the third one was from the nurses. The above findings may be used as the basic data to seek more efficient way of elevating nursing practice and quality for family-caregivers to the patients with stroke.

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병원종사자의 직업성 스트레스에 관한 연구 - 서울시내 500병상 이상 병원종사자를 중심으로 - (Occupational Stress of Hospital Workers)

  • 이우천
    • 한국병원경영학회지
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    • 제3권1호
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    • pp.1-33
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    • 1998
  • The purpose of this thesis is to study theoretical access to the methods that have been used for the research of occupational stress, thereby providing management methods of occupational stress of hospital workers. With a stress model of hospital workers set up from the viewpoint of organization management, 929 sets of questionnaires were collected from intern doctors, resident doctors, nurses, nursing aides, pharmacists, medical technicians, workers in patient affairs(reception and medical insurance workers), administrators and clerks from the 8 hospitals in Seoul with more than 500 beds. Upon variance analysis, correlation analysis and regression analysis of the collected questionnaires, this work examined how differences in stress caused by specific occupations and formulated a method of stress management for the hospital workers. The results are as follows. 1) If some duties of the nurses suffering from role-overloaded stress are transferred to the nursing aides dissatisfied with insufficient role, the two grunting groups can be satisfied at the same time. It is also necessary to transfer some jobs of the overloaded workers in patient affairs to the administrators, or the other way around. To reduce stress of conflict and ambiguity of role caused by the obscure division of roles between the workers, the role of each occupation should be delineated and the clear division of roles should be translated into action strictly according to that delineated. 2) Stress of inefficiency of organization from which the student doctors suffer can be relieved by management of participation. If they have access to the process of decision-making in general hospital affairs and consequently their understanding and the autonomy of job performance are promoted, such stress will be reduced. 3) To cope with stress of career development from which nurses, medical technicians, administrators, workers in patient affairs suffer, it is necessary to establish whether they have a chance to revive their careers, whether there are any ways of remotivation for less contributive workers, and whether they encourage each other to develope their careers. If they are given a chance to develope their careers, such stress will be relieved. 4) Pharmacists, suffering from stresses of living and personal relations, have strong cohesive power among themselves and organize a well-integrated team; thereby reducing the stress of personal relations and increasing productivity. 5) For administrators and student doctors confined to lesser social supports and for nurses and workers in patient affairs whose recognition of stress and job satisfaction are affected by social supports, emotional and informational supports for job performance help alleviate an individual's mental, and physical stress. 6) In addition to the above-mentioned stress-management methods, if an organizational coping strategy is provided according to the types of stress from the general viewpoint of the whole group of hospital workers, it would be of great help to managing stress. For example, the redesign of jobs, the management of objective, the improvement of working environment, the formation of an autonomous working group and various working plans can be set up for those who suffer from stress related to inappropriate role, while career counseling and development of career process can be provided for those dissatisfied with career development. Participation in the process of decision-making and the restructuring of the organization are needed for those who suffer from stress of malfunctioning organization, whereas creation of a supportive organizational atmosphere is desired for those who feel stressed due to personal relations. As well, such organizational coping strategies. as the increase of welfare facilities, seminars and educational programs and provision of health-promotion facilities can be provided.

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미혼 양육모의 양육 결정 체험 : 현상학적 연구 (The Experience in Deciding for Childcare of Unmarried Lone Mother : Phenomenological Research)

  • 김혜선;김은하
    • 한국사회복지학
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    • 제58권1호
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    • pp.373-393
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    • 2006
  • 본 연구는 미혼 양육모가 체험하고 있는 양육결정 경험을 이해하고 그 체험의 본질을 심층적으로 탐색하여 개입 방안에 필요한 기초 자료를 제시하고자 현상학적 연구방법 중 꼴라쥐(Colazzi)의 분석방법을 적용하였다. 연구 참여자는 미혼양육모를 위안 '미혼모 중간의 집'에서 거주하고 있는 20대 초반에서 30대 초반의 미혼 양육모 7명이었으며, 2003년 11월부터 2005년 2월까지 평균 2차례에 걸쳐 "당신이 체험한 양육 결정 경험은 무엇인가?" 에 대한 질문을 가지고 대상자를 만나 개별적으로 심층 면담하여 자료를 수집하였다. 대상자의 기술을 읽어서 구, 문장으로부터 의미 있는 진술을 도출한 후 이를 좀더 일반적인 형태로 제 진술하고 구성된 의미를 주제(Theme), 주제묶음(Theme clusters), 범주(Categories)로 분석한 결과, 22개의 주제와 '임신으로 인해 혼란스러워 짐', '홀로 겪는 현실이 모질게 느껴짐', '아이에게 정을 느낌', '아이 양육에 대해 갈등', '아이 양육을 마음으로 정', '스스로의 결정을 다짐함', '회생의 희망을 가짐'의 7개의 주제 묶음을 통해서 아이를 양육하고 있는 미혼모의 양육 결정 체험의 의미가 '회생(回生)'임을 발견할 수 있었다. 본 연구가 현상학적 연구로 연구결과를 일반화시킬 수 없다는 한계점을 가지고 있지만 본 연구의 결과를 바탕으로 우리 사회에서도 미혼모 모자세대들을 하나의 가족 형태로 받아들여 바르게 이해하고 그들의 권리를 되찾아 주어야 할 필요성을 인식하고 미혼 양육모에 대한 개입 방안의 기초 자료를 제시하였다는 데 그 의의를 찾을 수 있다.

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뇌성마비아 부모의 스트레스와 대처방안에 대한 연구 (Stress and Coping in Parents of Cerebral Palsy Children)

  • 송영화
    • The Journal of Korean Physical Therapy
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    • 제6권1호
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    • pp.49-60
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    • 1994
  • Stress is experienced when a person tries to maintain stability in the face of life change but is not able to meet the adaptive demands of change. This can be especially true for the parents who has a cerebral palsy childs who needs long term rare, where parents, are the primary source of care and responsibility. Successful coping leads to maintenance of the parents role and this has an effect on the health status of the child. This descriptive study was attempted to identify stress factors, levels and helpful coping patterns for parents who must take care of cerebral palsy children. Data were collected from 43 subjects who were parents of children diagnosed with cerebral palsy The informations gathered from March 25, 1994 to April 14, 1994 by means of structured questionnaires were analyzed. Two instruments were used to collect the data 1) Lee's stress questionnaire consisted of 33 stress factors and measured by four point Likert scale. 2) Modified Chronic Health Inventory for parents: The modified CHIP included 43 items of coping methods with four point Likert scale. The results of this study were as follows: 1) Stress items could have a maximum score of three points, for a total possible score of 132 points. The mean score for the total was 92.02 points. The item mean score was 2.85 points showing that the parents were experiencing moderate to much stress. 2) The items with the highest stress items were 16 items. The stress items with the lowest mean scores were 10 items. 3) Of the stress categories: The highest stress category was related to changes in the illness status of the child and difficulty in taking rare of the child. The second stressful category was related to the prognosis of the child's condition. The least stress was noticed to social-personal relationships and the responsibility of the care givers. 4) Items measuring coping in the parents had a maximum score of three points each with a total possible roping score of 172 points. The mean score for the total was 103,9 paints. The item mean score was 2.42 points indicating that there were responses of little helpful to moderately helpful on each coping pattern. 5) The most helpful coping items were 7 items. The least helpful coping items were 2 items. 6) Effectiveness of the coping for each patterns was examined : Understanding the illness condition from communication with parents of children with the same condition and consultation with the medical team was the most helpful coping pattern. Family's coorperation and integration and optimism were a moderately helpful coping pattern. Social support psychological stability and self esteem were the least helpful toping pattern. In conclusion, the highest stress for parents of children with cerebropalsy was found to be very stressful changes in the illness of the child and to taking care of a child who is suffering. The parents were helped by the coping methods using understanding of the illness condition through consultation with the medical learn and communication with parents in the same situation. Based on the knowledge, care could develop intervention strategies appropriate for them, help them to develop their effective coping patterns, and give support them in the process of coping with their stress.

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정치 PR 전략으로서의 SNS 메시지 : 21대 총선을 중심으로 (SNS Message as an Political PR Campaign Strategy: Focusing on the 21st General Election)

  • 차영란
    • 한국콘텐츠학회논문지
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    • 제20권9호
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    • pp.208-223
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    • 2020
  • 이번 2020년 4.15에 치른 21대 총선에서는 코로나 19와 맞물리면서 선거 캠페인으로써의 SNS에 대한 중요성이 더욱 두드러졌다. 이에 본 연구에서는 선거 캠페인으로서의 SNS 전략을 수립하기 위해 다양한 연구를 진행하였다. 본 연구는 선거 캠페인 도구로서의 SNS(페이스북, 트위터, 유튜브) 활동을 살펴보고자 2020년 제21대 국회의원 선거 기간 동안에 서울시 종로구 후보인 이낙연 후보와 황교안 후보의 SNS상의 메시지에 관한 내용 분석을 실시하였다. 자료 수집은 각 후보들의 공식계정의 올라온 글들을 위주로 분석했으며 조사방법은 R 프로그램을 활용하여 텍스트 분석을 했으며, 텍스트 분석 중 워드 클라우드, 비교 분석, q-graph 분석, LDA, STM 분석 등을 사용하였다. 그리고 분석결과는 상관관계 분석을 통하여 통계적으로 유의미한지를 확인하였다. 연구 결과 이낙연 후보의 선거 내용을 살펴보면 코로나, 국민, 문제, 위기, 고통, 지혜 등이 있는데, 이는 코로나로 인한 위기 문제를 지혜를 짜내어 극복해야 한다는 메시지를 나타내고 있다. 반면 황교안 후보의 선거 내용은 문재인, 정권, 살리다, 조국, 심판, 경제 등이 있는데, 이는 현재의 문재인 정권과 조국에 대한 심판과 더불어 나라를 살려야 한다는 메시지를 전달하고 있다. 그리고 정치홍보 관점에서 이낙연 후보는 칭송(acclaim)을 많이 하였고 반면에 황교안 후보는 공격(attack)을 많이 하였으며, 메시지 논제는 두 후보 모두 이미지보다는 정책에 대한 부분을 강조하였다.

한국 30대~40대 여성의 이중돌봄 현실과 돌봄경험의 다중성에 관한 연구 (A Study on Double-Care and Multiplicity of Caring Experiences among Women Aged 30s to 40s in Korea)

  • 송다영
    • 한국사회복지학
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    • 제66권3호
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    • pp.209-230
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    • 2014
  • 본 논문은 30대 부터 40대까지의 여성들 가운데 6세 이하의 자녀를 양육하는 시기와 부모/노부모를 동시에 돌봐야 하는 이중돌봄의 문제가 상당히 광범위하게 존재하고 있음을 보여주면서, 돌봄이 특정 시기의 특정 연령대에 분절적으로 일어나는 것이 아니라 생애주기의 어느 시점에도 발생할 수 있는 일상성에 주목하였다. 또한 돌봄은 부담으로서 뿐만 아니라 즐거움이나 보람을 동시에 주고 있으며, 돌봄제공자-돌봄대상자-돌봄보조자의 관계에 의하여 다양한 층위의 경험으로 분화될 수 있음을 드러내었다. 연구결과, 6세 이하 아동돌봄과 노인돌봄을 동시에 하는 이중돌봄 가구는 전체의 38%에 달했고, 향후 이중돌봄이 예상된다는 가구까지 합하면 54.9%에 이르러 이중돌봄이 상당히 보편적임을 보였다. 돌봄의 즐거움과 부담을 분석한 결과, 돌봄의 즐거움은 아동돌봄>부모돌봄>시부모돌봄 순이었으며 부담은 역순으로 나타났다. 그러나 돌봄제공자와 대상자간 관계는 돌봄 자체의 즐거움이나 부담에 영향을 미치는 주요한 요인으로 나타났다. 구체적으로 며느리-시부모간 돌봄도, 딸-부모간 돌봄도 그들이 맺어온 관계에 따라 돌봄경험이 달라지는 것으로 나타났다. 또한 딸이 부모를 돌볼 경우에 남성 배우자로부터의 무관심이 더 높고 도움이 수반되지 않아서 딸로서의 돌봄이 며느리로서의 돌봄의 경우보다 부담이 가중되기도 하였다. 결론에서는 이중돌봄의 어려움을 감소시킬 수 있는 사회적 지원방안과 정책이 제안되었다.

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