• 제목/요약/키워드: Cognitive Rigidity

검색결과 8건 처리시간 0.017초

꼰대 척도의 개발 및 타당화 (Development and Validation of the Kkondae Scale)

  • 이지연;고동우;최경찬
    • 한국콘텐츠학회논문지
    • /
    • 제21권9호
    • /
    • pp.164-175
    • /
    • 2021
  • 본 연구의 목적은 꼰대척도를 개발하고, 그에 대한 타당도를 검증하는 것이다. 이를 위해 전문가 면담과 선행연구 및 문헌 분석을 통해 꼰대의 3가지 구성 개념(귀인 오류, 인지적 경직성, 일방적 소통)을 도출하고 15개의 예비 문항을 선정하였다. 그리고 전문가의 내용 타당도 평정을 거치며 각 구성개념에 부합하도록 문항을 수정하거나 추가하여 예비 척도를 개발하였다. 다음으로 성인 250 여명을 대상으로 한 탐색적 요인분석 결과, 3 요인 구조 모델이 도출 되었고, 성인 401 여명을 대상으로 예비 척도에 대한 확인적 요인분석 결과, 3요인 구조의 적합도가 양호하다는 것을 확인하였다. 수렴 및 변별타당도 분석 결과, 개발된 척도가 경청태도, 공감, 타인 수용, 지적겸손과 적절한 상관을 나타내어 꼰대를 측정하는 타당한 도구임을 확인하였다. 마지막으로 본연구 결과를 토대로 연구의 의의, 제한점 및 향후 연구 방향을 논의하였다.

중풍환자의 초발군과 재발군에 관한 임상적 고찰 (A Comparative Study between First Attack and Reattack Groups in C.V.A)

  • 박숙자;권정남;김영균
    • 대한한의학회지
    • /
    • 제23권3호
    • /
    • pp.119-133
    • /
    • 2002
  • Objectives : This study was designed to investigate significant differences between the first attack and reattack groups to form fundamental data for decreasing recurrence and secondary prevention of stroke. Methods : I studied 204 patients admitted within 7 days of onset, after the diagnosis of stroke, in the Oriental Medical Hospital of Dongeui University from February to July in 2001.compared the reattack group with the first attack group for risk factors, clinical symptoms and progress, average mark and degree of improvement in Activity Index. Results : 1. Meaningful risk factors associated with the reattack group were male sex, a past history of hypertension and transient ischemic attack, and a family history of stroke. 2. The reattack group had conscious or cognitive disorder in early stage of onset, dysphagia, constipation, urinary incontinence, visual field defect in acute stage, high blood pressure and tachycardia in abnormalvital sign in acute stage, neuropsychosis, shoulder pain and rigidity, and pneumonia in complications more than the first attack group. 3. In Activity Index, the average mark of reattack group was lower than that of the first stroke group and improvement of the reattack group was delayed compared with the first attack group. Conclusions : The reattack group had more severe symptoms and clinical progress than the first attack group.

  • PDF

Categorization and production in lexical pitch accent contrasts of North Kyungsang Korean

  • Kim, Jungsun
    • 말소리와 음성과학
    • /
    • 제10권1호
    • /
    • pp.1-7
    • /
    • 2018
  • Categorical production in language processing helps speakers to produce phonemic contrasts. This categorization and production is utilized for the production-based and imitation-based approach in the present study. Contrastive signals in speakers' speech reflect the shapes of boundaries with categorical characteristics. Signals that provide information about lexical pitch accent contrasts can introduce categorical distinctions for productive and cognitive selection. This experiment was conducted with nine North Kyungsang speakers for a production task and nine North Kyungsang speakers for an imitation task. The first finding of the present study is the rigidity of categorical production, which controls the boundaries of lexical pitch accent contrasts. The categorization of North Kyungsang speakers' production allows them to classify minimal pitch accent contrasts. The categorical production in imitation appeared in two clusters, representing two meaningful contrasts. The second finding of the present study is that there are individual differences in speakers' production and imitation responses. The distinctive performances of individual speakers showed a variety of curves. For the HL-LH patterns, the categorical production tended to be highly distinctive as compared to the other pitch accent patterns (HH-HL and HH-LH), showing that there are more continuous curves than categorical curves. Finally, the present study shows that, for North Kyungsang speakers, imitative production is the core type of categorical production for determining the existence of the lexical pitch accent system. However, several questions remain for defining that categorical production, which leads to ideas for future research.

정상압수두증에 의한 보행장애 환자 치험 1례 (A case study of normal pressure hydrocephalus patient with gait disturbance using conservative Korean medical treatment)

  • 정민호;이미림;이유리;조기호;문상관;정우상
    • 대한중풍순환신경학회지
    • /
    • 제17권1호
    • /
    • pp.45-54
    • /
    • 2016
  • A case of a 75-year-old Korean female with gait disturbance due to Normal pressure hydrocephalus (NPH) is presented. She was treated with acupuncture, electroacupuncture and herbal medicine - 柴苓湯(Shirhyung-Tang, Chai-ling-tang, Sairei-to) We used iNPH grading scale, and specified further the grade of gait disturbance category. After Korean medical treatment, there was notable improvement in gait disturbance on our specified scale. Cognitive impairment, tremor and rigidity were improved on each scale alongside. Korean medical treatment may be effective in treating NPH patients.

  • PDF

우울증으로 내원한 진행성 핵상 마비 환자 1례 (A Case of a Depressed Patient With Progressive Supranuclear Palsy)

  • 한서윤 ;장진구 ;이수영
    • 대한불안의학회지
    • /
    • 제19권2호
    • /
    • pp.56-60
    • /
    • 2023
  • Progressive supranuclear palsy (PSP) is rare atypical Parkinsonism accompanied by various psycho-behavioural problems. In this case report, we describe the diagnostic and treatment progress of a 65-year-old PSP patient who visited the psychiatric clinic with a depressed mood and lumbar pain resulting in a suicide attempt. Over the course of 30 months of treatment, typical characteristics of PSP, such as postural instability, dyskinesia, cognitive dysfunction and supranuclear gaze palsy, became prominent, and magnetic resonance imaging and the F-18 FP-CIT positron emission tomography revealed midbrain atrophy and reduced dopamine uptake in the basal ganglia. When treating elderly patients with depression, parkinsonism symptoms such as gait disturbances, frequent falls, tremors, and rigidity should be closely examined.

루이소체 치매로 추정되는 이차성 파킨슨증 환자의 Non-Motor Symptom Scale(NMSS)로 평가한 비운동성 증상을 한약과 침의 복합치료로 호전시킨 증례보고 1례 (A Case Report of Non-Motor Symptoms Evaluated Using the Non-Motor Symptom Scale in a Patient with Secondary Parkinsonism Presumed to be Probable Lewy Body Dementia and Improved with Combined Treatment with Herbal Medicine and Acupuncture)

  • 노민영;이지현;한양희;임정태
    • 대한한방내과학회지
    • /
    • 제42권5호
    • /
    • pp.833-845
    • /
    • 2021
  • Parkinson's syndrome is a degenerative brain disease that presents characteristic motor symptoms of tremor, rigidity, and gait disturbance. In addition to these motor symptoms, Parkinson's syndrome also presents non-motor symptoms (NMSs) such as sleep disturbance and cognitive decline. NMSs reduce patient's quality of life and psychosocial functioning and cause economic burden on the patient, so appropriate evaluation and treatment are required. Lewy body dementia is one of the several diseases belonging to Parkinson's syndrome. Its symptoms such as cognitive function, memory impairment, and hallucinations occur with Parkinsonism. Although drug therapy is being used with drug treatment to treat non-motor symptoms, it has limitations such as side effects, which stimulated interest in other complementary treatment methods such as oriental medicine treatment, dance, and yoga. The patient in this case complained of tremor in the right upper extremity, muscle hypertension and pain, and persistent vision, memory, and cognitive decline. The patient was diagnosed with probable Lewy body dementia. The patient was hospitalized for 4 months and received acupuncture and herbal medicines. After treatment, the patient's NMS scale scores decreased from 90 to 63, and the Unified Parkinson's Disease Rating Scale scores (summed I, II, and III) decreased from 17 points to 8 points. The Beck Depression Inventory score decreased from 22 points to 13 points. In addition, the patient's subjective evaluation revealed improvement. In this case, a patient diagnosed with probable Lewy body dementia who did not respond to the standard treatment and did not want to take medications showed improvement in not only motor symptoms but also NMSs after integrative Korean medicine treatment.

베트남 참전 고엽제 환자와 한국전쟁 참전 상이군인의 심리적 특성에 관한 예비 연구 -로샤 반응을 중심으로- (A Preliminary Study on the Psychopathological protocols of the Vietnam War Agent Orange Patients and Korean Civil War Wound Soldier -Focus on Rorschach Tests-)

  • 장문선;김태열
    • 한국산학기술학회논문지
    • /
    • 제10권9호
    • /
    • pp.2492-2500
    • /
    • 2009
  • 본 연구에서는 베트남전 참전 군인 중 고엽제 후유(의)증 환자와 한국전쟁 참전 상이군인을 대상으로 전반적인 심리적 특성을 파악하기 위해 로샤 검사를 실시하고 반응결과를 한국전 참전 재향 군인 집단과 비교분석하였다. 이를 위해 베트남 참전 군인 중 고엽제 후유의증 환자 20명과 한국전쟁 참전 재향군인 21명을 대상으로 개별적으로 로샤 검사를 실시했다. 각각의 변인들을 Exner 종합체계(2006)의 구조적 요약의 대표적 군집들을 중심으로 비교분석하였다. 즉 핵심영역, 반응결정인, 결정적 특수지표에서의 차이를 비교분석하였다. 그 결과 베트남 참전 집단은 6.25 참전집단에 비해 (1)인지적 경직성 (2) 문제해결에 있어서의 비효율성, (3)정서억압 (4)과잉경계 (5)불안 (6)우울 등의 가능성이 더 높은 것으로 나타내었다. 이러한 결과들은 베트남전쟁 참전 재향군인에서 과거 전쟁 경험에서의 정신적 외상과 관련된 후유증이 지속되고 있을 가능성을 보여주는 것이다. 마지막으로 본 연구의 제한점과 시사점에 대해 논의하였다.

Co-occurrence of both maternally inherited neurofibromatosis type 1 and Lesch-Nyhan disease in a child with severe neurodevelopmental impairment

  • Jae Hun Yun;Yong Hee Hong;Go Hun Seo;Young-Lim Shin
    • Journal of Genetic Medicine
    • /
    • 제19권2호
    • /
    • pp.94-99
    • /
    • 2022
  • Lesch-Nyhan disease (LND) is a rare X-linked recessive inherited purine metabolic disorder that accompanies neurodevelopmental problems. Neurofibromatosis type 1 (NF1) is a relatively common autosomal dominant inherited genetic disorder characterized by tumors in various systems. Some children with NF1 also accompanies neurodevelopmental problems. Here, we describe a 5-year-old boy with a maternally inherited pathogenic variant in NF1 and hypoxanthine-guanine phosphoribosyltransferase (HPRT). He was referred for severe neurodevelopmental impairment and hyperuricemia. His mother was diagnosed with NF1 and the patient was also suspected of having NF1 because of cafe au lait macules. He had dystonia, rigidity, cognitive deficit, and speech/language impairment. Serum and urine uric acid concentrations were elevated. He had more severe neurodevelopmental delay than patients with only NF1, so his clinical symptoms could not be fully understood by the disease alone. To find the cause of his neurologic symptoms and hyperuricemia, the patient and his mother underwent a whole-exome sequencing test. As a result, the pathogenic variant c.151C>T (p.Arg51Ter) in HPRT1 was identified as hemizygote in the patient and heterozygote in his mother. The pathogenic variant c.7682C>G (p.Ser2561Ter) in NF-1 was identified as heterozygotes in both of them. Although the clinical symptoms of both diseases were overlapping and complicated, genetic testing was helpful for accurate diagnosis and treatment. Therefore, we suggest to consider preemptive genetic evaluation if there are symptoms not sufficiently explained by known existing diseases. And it is considered valuable to review this rare case to understand the clinical course and possible synergic effects of these diseases.