• 스마트미디어저널
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• 제11권11호
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• pp.17-24
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• 2022

음성인식 기술과 인공지능 기술을 기반으로 한 스마트스피커의 보급으로 비장애인뿐만 아니라 시각장애인이나 지체장애인들도 홈 네트워크 서비스를 연동하여 주택의 전등이나 TV와 같은 가전제품을 음성을 통해 쉽게 제어할 수 있게 되어 삶의 질이 대폭 향상되었다. 하지만 언어장애인의 경우 조음장애나 구음장애 등으로 부정확한 발음을 하게 됨으로서 스마트스피커의 유용한 서비스를 사용하는 것이 불가능하다. 본 논문에서는 스마트스피커에서 제공되는 기능 중 일부 서비스를 대상으로 언어장애인이 이용할 수 있도록 개인화된 음성분류기법을 제안한다. 본 논문에서는 소량의 데이터와 짧은 학습시간으로도 언어장애인이 구사하는 문장의 인식률과 정확도를 높여 스마트스피커가 제공하는 서비스를 실제로 이용할 수 있도록 하는 것이 목표이다. 본 논문에서는 ResNet18 모델을 fine tuning하고 데이터 증강과 one cycle learning rate 최적화 기법을 추가하여 적용하였으며, 실험을 통하여 30개의 스마트스피커 명령어 별로 10회 녹음한 후 3분 이내로 학습할 경우 음성분류 정확도가 95.2% 정도가 됨을 보였다.

• 한국식생활문화학회지
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• 제6권4호
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• pp.381-391
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• 1991

The following study was done to investigate foodservice management practice. Total subjects were 18 foodservices in social welfare facilities in Seoul. Among studied facilities, nine were the welfare facilities for children, five were the welfare facilities for elderly, two were the welfare facilities for a mentally and physically disabled person and the remaining two were vagabond care facilities. Methods used were mainly questionaires. These questionaires were answered by manager and interviews were also done for a same person. Equipments were evaluated by investigators using the evaluation form. The results of the study were summarized as follows. Number of cooks and assistant cooks among employee in foodservice establishment were about 2-6 persons. One dietitian is stationed in 2 places among 18 places. Food purchasing and menu plannings were mainly practiced by manager, secretary and other personnels, in more than 50% of social welfare facilities. The type of the menu in most facilities was the set menu. The period of turn over for cycle menu was a week in 50% of facilities. Seventy seven point eight percentage of the welfare facilities were used the weekly or monthly cycle. For the food preparation, there was almost no place using standard recipes. Foodstuffs were purchased in local market. Moreover, the preference test of served foods were done for residence of each facilities. But it was not applicated effectively. Conditions of most equipments in the kitchen were defective specially in dishwashing and sterilization step.

• 재활간호학회지
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• 제3권1호
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• pp.80-97
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• 2000

The purpose of this study is to identify and describe a process of sexual adjustment of individuals with spinal cord injury: and to describe and explore positive and negative influences on the adjustment process. This qualitative study was conducted with 10 Korean individuals with spinal cord injury who had been physically disabled for more than one year. Data were collected and analysed at a same time using grounded theory method. Major categories of this study showed a process how the individuals with spinal cord injury adjust to their individual life as sexual beings. The process included and individual responses to the behavioral efforts including and . Initially physical aspects of sexuality seemed to be affected by spinal cord injuries. The changed physical aspects then influenced other aspects of their sexual life. Life satisfaction of each individual as a sexual being revealed as very subjective. It could be defined according to how the individual approved their sexual life no matter what and how much behavioral effort the person had done. In this study 3 types of sexual adjustment aspects were explored: 'Active adjustment' 'Passive adjustment' 'Maladjustment'. There were negative and positive factors influencing the adjustment process of individuals with spinal cord injury. Those factors might come from themselves, from families, or from social situations. Findings of this study suggested that sexual life of individuals with spinal cord injury should not be understood as a physical or behavioral matter. It was a combination of physical, psychological and social aspects of life. Therefore, appropriate rehabilitation programs for the sexual adjustment of individuals with spinal cord injury need to concern heterogeneous life values of them and obtain individualized services for each individual at a different stage of the sexual adjustment process.

• 한국사회복지학
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• 제65권1호
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• pp.5-31
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• 2013

본 연구는 WHO의 국제건강관련분류체계인 ICF를 적용하여, 한국의 근골격계질환 장애인(척수손상, 근육디스트로피, 왜소증, 류마티즘) 352명의 사회참여 관련요인을 분석하였다. 연구방법은 기술분석, 집단별 평균분석 및 분산분석과 사후검정, 단순상관분석, 다중회귀분석을 사용하였다. 연구결과 근골격계질환 장애인의 정신기능, 신경근육골격 및 운동과 연관된 기능, 비뇨생식기와 생식기능, 피부 및 관련구조, 학습과 지식 적용, 일반적 과제와 요구, 이동의 수준이 높을수록 사회참여의 수준도 높았다. 개인요인에서 소득이 근육디스트로피질환 장애인의 사회참여 관련요인으로 나타났고, 환경요인에서 서비스, 시스템 및 정책이 척수손상 장애인의 사회참여에 영향을 미치는 것으로 나타났다. 본 연구는 장애에 관한 보편주의적 접근을 의미하는 ICF 구성요소로 연구모형을 설정하고, ICF 코어셋을 검토하여 질환관련범주를 측정하였다는 점에 의의가 있다.

• 한국컴퓨터정보학회논문지
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• 제13권5호
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• pp.187-193
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• 2008

웨어러블 환경에서 사용자가 홈오토메이션 시스템을 제어할 수 있는 인터페이스기술들이 최근 많이 개발되고 있다. 본 논문에서는 수족이 불편한 사용자가 웨어러블 환경에서 EOG 감지 회로와 사람이 인지 가능한 마커를 이용하여 홈오토메이션을 직접 제어할 수 있는 인터페이스 방법을 제안한다. 제안된 사용자 인터페이스에서는 지시 장치로 EOG 감지 회로를 사용하고, 사용자가 다루고자 하는 홈오토메이션 기기에 해당되는 마커를 눈의 움직임을 이용해 사용자가 선택하면 선택된 마커를 인식하여 해당 기능을 수행하는 제어 명령을 홈오토메이션 제어장비에 보냄으로써 사용자가 원하는 기능이 수행되도록 한다. EOG 감지 회로와 마커 인식 시스템을 이용함으로써 수족 사용이 불가능한 사용자도 눈동자의 움직임만으로 홈오토메이션 조작을 손쉽게 수행할 수 있다.

• 보건행정학회지
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• 제29권2호
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• pp.184-194
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• 2019

Background: The extent of coverage rate of the public health insurance is still insufficient to meet healthcare needs. Private health insurance (PHI) plays a role to supplement coverage level of national health insurance in Korea. It is expected that reduce unmet need healthcare. This study was aimed to identify relationship between PHI type and the unmet healthcare need and its associated factors. Methods: Data were obtained from the 2014 Korea Health Panel Survey using nationally representative sample was analyzed. Respondents were 8,667 who were adults over 20 years covered by PHI but have not changed their contract. According to the enrollment form, PHI was classified into three types: fixed-benefit, indemnity, and mixed-type. To identify factors associated with unmet needs, multiple logistic regression conducted using the Andersen model factors, which are predisposing factors, enabling factors, and need factors. Results: Our analysis found that subjects who had PHI with mixed-type were less likely to experience unmet health care needs compared than those who did not have it (odds ratio, 0.80; 95% confidence interval, 0.66-0.98). As a result of analyzing what affected their unmet healthcare needs, the significant factors associated with unmet medical need were gender, marital status, residence in a metropolitan area, low household income, economic activity participation, self-employed insured, physically disabled, low subjective health status, and health-risk factors such as current smoking and drinking. Conclusion: The results of this study suggest that having PHI may reduce experience of unmet healthcare needs. Findings unmet healthcare needs factors according to various subjects may be useful in consideration of setting policies for improving accessibility to healthcare in Korea.

• 한국엔터테인먼트산업학회논문지
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• 제14권3호
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• pp.443-454
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• 2020

본 연구는 ALS(루게릭)장애인의 병진행 단계에 따른 원스탑지원서비스 개발을 목적으로 하였다. 목적 달성을 위해 한국과 일본의 사례를 다중사례연구로 분석하였다. 연구분석에 사용된 자료는 한국과 일본의 루게릭장애인의 일기, 블로그, SNS, 유트브, 그리고 인터뷰 등을 통해 양국의 지원서비스를 분석하였다. 연구결과 루게릭병 발병단계에는 한국루게릭협회와 같은 당사자 조직에 루게릭질환을 경험한 사람이나 가족에 의한 동료상담가를 배치하여야 한다. 연화장애단계에서는 위루술시술 후 소독과 경관식투여와 같은 의료적 처치를 위해 방문간호사의 재택방문횟수가 늘어야 하며, OT,PT에 의한 재택서비스가 필요하다. 호흡장애의 단계에서는 인공호흡기의 착용과 거부를 스스로 결정할 수 있는 다양한 방법을 강구해야 한다. 호홉기착용단계에서는 루게릭전용활동지원인의 양성과 파견이 필요하다. 또한 주 부양자를 위한 가족쉼터나 루게릭장애인 당사자가 이용할 수 있는 단기보호센터의 설치가 필요하다. 무엇보다 이러한 서비스는 단계별로 연계성 있는 원스탑지원서비스가 되어야 한다.

• 여성건강간호학회지
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• 제30권1호
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• pp.56-66
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• 2024

Purpose: This study explored the factors influencing the health-related life satisfaction of people with disabilities who engaged in physical activity, by age and gender. Methods: A secondary analysis was conducted of the 2020 Third Disability and Life Dynamics Panel (2021). The participants were 2,796 people who performed regular physical activity at least once a week. The variables selected were disability-related factors (degree of disability, multiple disabilities, and type of disability), sociodemographic factors (age, gender, living alone, and mean monthly family income), and health-related factors (amount of physical activity, self-esteem, depression, chronic disease, subjective health, and health-related life satisfaction). Descriptive statistics, the chi-square test, the t-test, two-way analysis of variance, and multiple regression analysis were conducted. Results: In total, 58.0% of participants were male, and 42.0% were female. For age groups, 14.4% were children/adolescents (0-19 years), 42.6% were adults (20-59 years), and 43.0% were seniors (≥60 years). The mean score for health-related life satisfaction was 5.0±2.15 out of 10. Adults and seniors whose level of physical activity met or exceeded recommendations had higher subjective health. Moreover, men had better subjective health than women in seniors. Health-related life satisfaction was higher among those who had higher self-esteem, were not depressed, did not have chronic diseases, and had better subjective health. Conclusion: Gender significantly influenced health-related life satisfaction in children/ adolescents and seniors. Disability-related factors were significant in adults, and health-related factors were significant in all age groups. Therefore, these factors should be considered when designing interventions to promote subjective health and health-related life satisfaction of people with disabilities.

• 한국사회복지학
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• 제62권4호
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• pp.193-222
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• 2010

성인기에 발생하는 중도장애나 이혼과 같은 생애위기는 당사자의 독립성이나 상호의존성에 대한 도전을 수반하여 그러한 자기인식과 해석에 변화를 초래할 수 있다. 이 연구는 생애위기 경험자의 그와 같은 자기해석이 복합적일수록 긍정적인 자기특성이 양성되어 심리적 안녕이 높을 것으로 보고, 자기해석의 복합성과 심리적 안녕 간의 관계가 자기긍정성을 구성하는 세 요인, 즉 관점의 다각화, 자기수용, 자기조절에 의해 매개되는 경로를 조사하였다. 편의표집에 의해 서울과 수도권 지역에 거주하는 중도장애인, 이혼인, 일반인 비교집단 총 359명을 조사한 결과, 생애위기 경험집단이 평균적으로 일반인 비교집단에 비해 독립적 자기해석이 높았고, 상호의존적 자기해석이 낮았다. 복합적인 자기해석은 예측대로 의미 발견과 의미 부여를 돕는 관점의 다각화와 밀접하게 연관되었고 이를 통해 자기수용, 자기조절과 같은 긍정적 태도에 기여하였으며, 이 중 관점의 다각화와 자기수용을 통한 경로로 생애위기의 경험여부와 상관없이 응답자들의 심리적 안녕, 즉 긍정적 정서의 경험과 우울과 같은 부정적 정서의 감소를 도왔다. 관점의 다각화가 우울을 직접 낮추는 효과는 예측대로 생애위기 경험집단에서만 나타났고, 긍정적 정서를 양성하는 직접효과는 모든 집단에서 발견되었다. 따라서 관점의 다각화가 생애위기의 경험자들 사이에서는 의미 발견과 긍정적 태도 양쪽에 탄력을 주어 적응과 심리적 안녕을 돕는 반면 일반인들 사이에서는 우선적으로 긍정적 태도, 긍정적 정서 등 긍정성을 키워 심리적 안녕에 기여함을 추론할 수 있었다. 이 연구는 관점의 다각화와 복합적인 자기해석이 역경극복에 동력이 되는 의미 찾기를 도우며 긍정적 태도를 양성하여 생애위기 경험자의 심리적 안녕에 기여하는 기제와 심리적 자원으로 각각 기능할 수 있음을 시사하여, 이를 토대로 사회복지실천을 위한 함의를 논의하였다.

• Child Health Nursing Research
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• 제7권4호
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• pp.434-450
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• 2001

This study is designed to understand the meaning and nature of raising children with cerebral palsy. It researches the experience of mothers of schoolchildren with cerebral palsy by the research method of hermeneutic phenomenology. The study was conducted from November 10, 1999 to December 20, 2000. When children with cerebral palsy usually show symptoms in the early stage of cerebral palsy, mothers do not take children to a doctor for diagnosis. And, most of mothers have a difficult time to accept the reality; they usually respond to the initial diagnosis with shock, reproach, and deny. When mothers start recognizing the reality, they consider that their children have cerebral palsy due to the their mismanagement during pregnancy, delivery, nursing, and initial treatment. They shelter their children from view and feel guilty that they cannot afford to try folk remedies for their children. As time passes, mothers face conflicts between families in diverse ways. Families put the blame on genetic effects. Mothers-in-law give their daughters-in-law a hard time, husbands shift the responsibility of raising children onto their wives, and trouble arises between families-in-law and mothers native families. When children grow up, it is physically difficult for mothers to take care their children. In addition, they suffer from all the troubles in family due to childrens handicap. Mothers try the diverse methods of bringing up children. However, they start getting tired of raising children as they experience failures and financial difficulties. Mothers feel collapsed recalling the ways of raising children. They feel anxiety, miserable, lonely, and worrying when they think how children would attend school, make friends, and live in the future. In this stage, mothers do their best to raise their children with hope. They tend to compare their children with others without handicap and spend money and time in attempting all the treatments. When mothers and children join the society at school, they find that the society does not understand disabled people, teachers show inconsiderate attitude, friends avoid them, and children hardly follow classes. Such experiences make mothers feel angry and frustrated. However, when children adapt to school, mothers see the possibility that children could accomplish schoolwork. They appreciate teachers help and others consideration. Mothers place appropriate expectations on their children and help them to prepare for the future. I would make following suggestions based on the results. 1. As a primary basic course of rehabilitation nursing intervention, solution-centered nursing intervention system should be developed. The intervention needs to be based on the understanding of mothers, who raise children with cerebral palsy, through in-depth interview. 2. Advance researches on the development of individual nursing intervention should be conducted. Individual nursing intervention needs to prevent and release actual pain focusing on mothers raising children with cerebral palsy. 3. Integrated curriculum that help children with cerebral palsy lead a normal school life with ordinary children should be developed. 4. Basic research on using of facilities and effective application of service volunteer to help children with cerebral palsy in school needs to be conducted.