• 가정∙방문간호학회지
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• 제8권1호
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• pp.5-24
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• 2001

The purpose of this study was to develop a parenting intervention program and determine the efficacy of the program with low-birth weight infants and their mothers. Nine dyads for the experimental group and twelve dyads for the control group discharged from the Neonatal Intensive Care Unit of a University Hospital in Seoul were recruited for the study. For the intervention group, programmed education and support which focused on the maternal sensitivity of the infant's behavior. rearing environment. motherinfant interaction and infant care were given to each subject. Individual counseling and home visits were provided at discharge, one week after discharge. and one and three months of corrected age in every infant. Structured questionaires were administered and feeding interactions were videotaped and coded by a blinded certified observer. A Quasi-experimental design was conducted for this study. Postpartum depression, maternal self esteem. infant care burden, HOME. mother-infant interaction, and infant development were measured. Results were in favor of the intervention versus the control group. On the Beck depression inventory, intervention mothers showed decreasing trends in depressive symptom vs control mothers although, there were statistically no significant differences between the two groups at each time. The mean score of experimental group was 11.55(mild depression state) at discharge and became 8,6(normal state) at 1 month of corrected age. On the other hand, the mean score of the control group was 13.92(mild depression state) at discharge and became 14.0. Maternal self esteem in both groups improved over time. Infant care burden in both groups was also shown to increase over time. There was a significant difference between the two groups in HOME(p=.0340) at 3 months of corrected age. HOME scores of the experimental group and the control's were 31.10 and 25.58, respectively. Mothers' emotional and language responses were significantly high in the intervention group compared with the control group(p=.0155). Intervention group (53.33) showed a significantly high quality of motherinfant interaction compared with the in control group (42.80)(p =.0340). Intervention group mothers appeared have a better quality of mother-infant interaction behaviors. On the other hand, there was no statistical difference in the infant part between groups. Intervention group infants had higher trends in a general developmental quotient: although, there was no statistical difference between groups. The general developmental quotient of intervention infants was 102.56 and control's was 91.28. However, the developmental quotient of the domain of 'individuality-sociality' was higher in the intervention group infants compared with the control's(p=.0155). The concerns identified by parents revealed two domains of an infants' health management -knowledge and skills in caregiving of lowbirthweight-infants, characteristics of lowbirthweight infants, identifying a developmental milestone, coping with emergency situations and relaxation strategies of mothers from the infant care burden. Interview data with the mothers of low-birth weight infants can be used to develop intervention program contents. Limited intervention time and frequency due to time and cost limitations of this study should be modified. The intervention should be continuously implemented when low-birth weight infants become three years old. An NNNS demonstration appeared to be a very effective intervention for the mothers to improve the quality of mother-infant interactions. Therefore intervening in the mothers of low-birth weight infants as early after delivery as possible is desirable. This study has shown that home visit interventions are worthwhile for mothers only beyond the approach as an essential factor in ability of facilitating a growth fostering environment. In conclusion. the intervention program of this study was very effective in enhancing the parenting for the mothers of low-birth weight infants, resulting in health promotion of low-birth weight infants. The home-visit outreach intervention program of this study will contribute to the health delivery system in this country where there is a lack of continuous follow-up programs for low-birth weight infants after discharge from NICU, if it is activated as part of the home visit programs in community health systems.

• 정신신체의학
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• 제20권2호
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• pp.127-134
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• 2012

연구목적 : 스트레스 자각척도는 일상 생활에서 주관적으로 느끼는 스트레스의 정도를 평가하는 척도이다. 본 연구는 한글판 스트레스 자각척도의 신뢰도와 타당도를 평가하고 척도를 이용하여 종합병원에서 근무하는 여성들의 스트레스 정도를 측정하고자 하였다. 방 법 : 종합병원 근무 여성들을 대상으로 주사바늘 자상을 입은 전후로 한글판 스트레스 자각척도, 해밀턴 불안 척도, 벡 우울 척도를 실시하여 스트레스 및 불안, 우울 정도를 평가하였다. 내적 일치도와 검사-재검사 신뢰도를 통해 척도의 신뢰도를 평가하였으며, 타 척도와의 상관관계분석을 통해 공존 타당도를 평가하였다. 척도의 요인구조는 탐색적 요인분석을 시행하여 확인하였다. 결 과 : 연구 참여자 중 총 154명이 연구 절차를 완료하여 최종 분석에 포함되었으며, 이들의 스트레스 자각척도의 평균 점수는 20.69(${\pm}4.56$)점이었다. 한글판 스트레스 자각척도의 Cronbach's alpha는 0.819이었으며 검사-재검사 신뢰도는 0.66(p<0.01)이었다. 해밀턴 불안 척도 및 벡 우울 척도와 상관계수는 각각 0.49(p<0.01), 0.55(p<0.01)로 나타났다. 요인 분석 결과 한글판 스트레스 자각척도는 2가지 요인으로 이루어져 이었으며 각각 '스트레스와 관련된 요인', '스트레스의 조절과 관련된 요인'으로 명명하였다. 결 론 : 본 연구를 통해 한글판 스트레스 자각척도가 주관적으로 지각하는 스트레스 정도를 평가하는데 신뢰할 만하고 타당한 도구임을 확인할 수 있었다. 지각된 스트레스는 정신적, 신체적인 건강 상태 모두에 영향을 끼치는 것으로 알려져 있어 향후 스트레스 자각척도를 이용한 스트레스 평가 및 관리가 유용할 것으로 생각된다.

• Korean Journal of Acupuncture
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• 제28권4호
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• pp.1-15
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• 2011

Objectives : The purpose of this study is to evaluate the feasibility of massive clinical research and to make a basic analysis on the effectiveness and safety of moxibustion treatment on knee osteoarthritis compared to usual care. Methods and Results : This study is a protocol for a pilot randomized controlled trial. Forty participants are assigned to the moxibustion group (n=20) and usual care group (n=20). Participants assigned to the moxibustion group receive moxibustion treatment on the affected knee(s) at six standard acupuncture points (ST36, ST35, ST34, SP9, Ex-LE04 and SP10) three times per week for four weeks (total of 12 sessions). Participants in the usual care group don't receive moxibustion treatment during the study period and follow-up are made on the 5th, 9th and 13th weeks after random allocation. Both groups are allowed to use any kind of treatment, including surgery, conventional medication, physical treatment, acupuncture, herbal medicine, over-the-counter drugs and other active treatments. Education material that explains knee osteoarthritis and current management options and self-exercise is provided for each group. The pain scale of the Korean Western Ontario and McMaster Universities Questionnaire (K-WOMAC) is the primary outcome measurement used in this study. Other subscales of the K-WOMAC, the Short-Form 36 Health Survey (SF-36), Beck Depression Inventory (BDI), Physical Function test, Patient Global Assessment, and Pain Numeric Rating Scale (NRS) are used as outcome variables to evaluate the effectiveness of acupuncture. Safety is assessed at every visit. Conclusions : The result of this trial will provide a basis for the effectiveness and safety of acupuncture treatment for knee osteoarthritis.

• Journal of Magnetics
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• 제19권2호
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• pp.161-169
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• 2014

The aim of this study is to investigate the efficacy of pulsed electromagnetic field (PEMF) on the alleviation of lumbar myalgia. This is a randomized, real-sham, double blind pilot study. 38 patients were divided into the PEMF group and the Sham group, each of which was composed of 19 patients (1 patient dropped out in the Sham group) of randomized allocation. The PEMF group was treated by using the PEMF device and the Sham group by using a sham device on the lumbar muscle and acupuncture points, three times a week for a total of two weeks. Evaluations of Visual Analogue Scale for bothersomeness (VASB), Visual Analogue Scale for pain intensity (VASP), Oswestry Disability Index (ODI), 36-Item Short Form Health Survey Instrument (SF-36), EuroQol-5Dimension (EQ-5D), Beck's Depression Inventory (BDI) and Roland-Morris Disability Questionnaire (RMDQ), etc. before and 1 week after treatment were carried out. The primary outcome measure was the VASB, measured 1 week after the end of the pulsed electromagnetic therapy. VASB scores for the PEMF group changed by $-2.06{\pm}2.12$ from the baseline, and that for the Sham group changed by $-0.52{\pm}0.82$ (p < 0.05). VASP scores for the PEMF group were reduced by $-2.10{\pm}2.12$ from the base line, and that for the Sham group was reduced by $-0.53{\pm}1.50$ (p < 0.05). PEMF group showed significant improvements in all VASB, VASP, ODI, SF-36, EQ-5D, BDI and RMDQ scores, while the Sham group showed significant improvements in all scores, except the VASP score. However, the VASB, VASP and RMDQ scores of the PEMF group were much lower than those of the Sham group. The two groups showed no significant difference in ODI, SF-36, EQ-5D and BDI. This study demonstrates the effectiveness of PEMF treatment for alleviating lumbar myalgia.

• 한방재활의학과학회지
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• 제30권4호
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• pp.155-164
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• 2020

Objectives This study is aimed to evaluate the feasibility of further clinical research of warm needle acupuncture as an effective and safe treatment for chronic low back pain. Methods Thirty participants will be randomly assigned to the Warm needle acupuncture group (n=15) and Dry needle acupuncture group (n=15). All patients will receive acupuncture therapy twice a week for 6 weeks, but only the experimental group will receive thermal stimulation. The primary outcome will be measured using the visual analogue scale for bothersomeness of low back pain, and the secondary outcome will be measured using the VAS for pain intensity, Oswestry disability index, 36-Item Short Form Health Survey, Beck's depression inventory, and amount of analgesics used. Conclusions The results of this study will be used to determine the feasibility of a future large-scale randomized controlled trial that provides clinical evidence for the efficacy and safety of warm needle acupuncture in the treatment of patients with chronic low back pain.

• 수면정신생리
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• 제6권1호
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• pp.32-37
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• 1999

목 적 : 본(本) 연구(硏究)는 신경성(神經性) 거식증(拒食症)을 가지고 있는 여대생(女大生)의 DSM-III-R상(上)에 근거한 인격장애(人格障碍)의 빈도(頻度)를 정상대조군(正常對照群)과 비교(比較) 조사하는 것을 목적(目的)으로 한다. 방 법 : Structured Clinical Interview for DSM-III-R을 사용(使用)하여 신경성 거식증을 가지며, 동시에 다른 I 축(軸) 정신장애(精神障碍)를 가지고 있지 않은 62명의 식이장애(食餌障碍) 연구대상군을 모집(募集)하였으며, 같은 도구(道具)를 사용하여 어떠한 I 축(軸) 정신장애(精神障碍)를 가지고 있지 않은, 동수(同數)의 연령(年齡), 성별(性別) 대조군을 모집(募集)하였다. 인격장애(人格障碍)의 빈도(頻度)의 조사를 위해서는, 면접도구(面接道具)인 '인격장애(人格障碍) 진단면접검사(診斷面接檢査)'(Revised Diagnostic Interview for Personality Disorders)와 설문검사(設問檢査)인 '인격장애(人格障碍) 설문검사(設問檢査)'(Personality Disorder Questionnaire-Revised)를 동시에 사용하여 진단적(診斷的) 신뢰도(信賴度)를 높였으며, 특히 경계선(境界線) 인격장애(人格障碍)의 진단(診斷)을 위해서는 '경계선(境界線) 인격(人格) 진단면접검사(診斷面接檢査)'(Diagnostic Interview for Borderlines)를 추가(追加)로 사용하였다. 또한 일반적인 인구역학적 변수(變數)의 조사와 함께 신경성 거식증환자에서 흔히 관찰되는 우울증상(憂鬱症狀)의 평가를 위하여 Beck 우울평가도구(憂鬱評價道具)(Beck Depression Inventory)를 사용하여 우울증(憂鬱症)의 정도를 평가하였다. 결 과 : 신경성 거식증군은 정상대조군과 적 : 본(本) 연구(硏究)는 신경성(神經性) 비교(比較)하여 유의(有意)하게 높은 경계선(境界線) 인격장애(人格障碍), Cluster B 인격장애(人格障碍) 및 전체 인격장애(人格障碍)의 빈도(頻度)를 보였다(Fisher's exact test, p=0.044, p=0.020, p=0.024, respectively, by the Revised Diagnostic Interview for Personality Disorders;p=0.034, p=0.015, p=0.007, respectively, by the Personality Disorder Questionnaire-Revised). 결 론 : 본(本) 연구(硏究)는 한국인(韓國人) 여대생(女大生)집단에서의 신경성(神經性) 거식증군(拒食症群)은 정상대조군(正常對照群)과 비교(比較)하여 통계적(統計的)으로 유의하게 높은 인격장애(人格障碍)를, 특히 경계선(境界線) 인격장애(人格障碍)를 가지고 있음을 보고(報告)하고, 이 결과(結果)의 이론적(理論的), 임상적(臨床的) 의의(意義)에 관하여 논의(論議)한다.

• 동의신경정신과학회지
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• 제31권1호
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• pp.1-12
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• 2020

Objectives: The purpose of this study was to evaluate the reliability and validity of the instrument on pattern identification for insomnia (PIT-Insomnia) and verify the correlation between PIT-Insomnia and psychological tests. Methods: Two evaluators examined the pattern identification of the participants who met insomnia disorder diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorder, Fifth Edition (DSM-5) and took the Insomnia Severity Index (ISI) score over 15 once manually and twice using the PIT-Insomnia to measure the inter-rater and test-retest reliability. We also conducted the following surveys: the Pittsburgh Sleep Quality Index (PSQI), the Korean version of Beck's depression inventory (K-BDI), the Korean version of the State-Trait Anxiety Inventory (STAI-K), the Korean Symptom checklist-95 (KSCL-95), and the EuroQol-5 dimension (EQ-5D), to measure concurrent validity and correlation between the PTI-Insomnia and psychological tests. Results: 1. The test-retest reliability analysis of the pattern identification results showed moderate agreement, and test-retest reliability analysis of each pattern identification score showed agreements from poor to moderate. 2. The inter-rater reliability analysis of the pattern identification results via manual showed slight agreement, when analysis was performed with calibration, the inter-rater reliability analysis of the pattern identification results via manual showed fair agreement. 3. The concordance analysis between results via manual and the PIT-Insomnia showed poor agreement, when the analysis was performed with calibration, concordance analysis showed fair agreement. 4. The concordance analysis between the PIT-Insomnia and the PSQI showed positive linear correlation. 5. The concordance analysis between the PIT-Insomnia and the PSQI, K-BDI, STAI-K, KSCL-95, and EQ-5D showed that non-interaction between the heart and kidney have positive linear correlation with the K-BDI, anxiety item of KSCL-95, dual deficiency of the heart-spleen have positive linear correlation with somatization item of KSCL-95, paranoia item of KSCL-95, heart deficiency with timidity have positive linear correlation with stress vulnerability item of KSCL-95, parania item of KSCL-95, phlegm-fire harassing the heart have positive linear correlation with K-BDI, paranoia item of KSCL-95, depressed liver qi transforming into fire have positive linear correlation with the anxiety item of KSCL-95, parania item of KSCL-95, all pattern identification have negative linear correlation with EQ-5D. Conclusions: The PIT-Insomnia has moderate agreement of reliability and reflects the severity of insomnia since it has some concurrent validity with the PSQI. There are some correlations between the PTI-Insomnia with specific psychological tests, so we could suggest it can be used appropriately in the clinical situation.

• 수면정신생리
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• 제6권2호
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• pp.126-132
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• 1999

목 적: 저자들은 본 연구에서 혈액투석 중인 환자들을 대상으로 불면증의 빈도, 불면증 환자들의 특성, 신체적 그리고 심인적인 증상들과의 상관관계, 수면에 대한 믿음과 태도 등을 조사하여 향후 진료에 도움을 주고자 하였다. 방 법: 부산시내 소재 4개의 혈액투석실에서 혈액투석을 받고 있는 만성 신부전증 환자 153명(남 87명, 여 66명)을 대상으로 저자들이 본 연구에 알맞게 개발한 수면관련 설문지, 벡 우울증 척도, 스필버거 상태-특성 불안 척도를 이용하여 환자들의 증상을 조사하였다. 결 과: 전체 153명의 혈액투석 환자 중 65.4%인 100명이 불면증을 호소하였다. 연령, 남녀비, 교육정도, 결혼상태, 평균 혈액투석 기간, 그리고 혈청 알부민을 제외한 조사된 혈액화학검사 소견들은 불면증군과 비불면증군 사이에 차이가 없었다. 불면증군은 비불면증군에 비해 유의하게 BDI 점수와 투석전 수축기 혈압이 높았고 혈청 알부민치는 더 낮았다. 또, 시각유도척도법을 이용한 두 군간의 주관적인 고통에 대한 조사에서 불면증군은 슬픔, 불안, 걱정, 피부 소양증, 그리고 일상생활에서의 기능장애 등의 주관적인 고통을 비불면증군보다 유의하게 더 많이 호소하고 있었다. 불면증의 심한 정도가 불량한 신체적 건강상태, 피부 소양증, 그리고 골관절 통증 등의 신체적 증상, 슬픔, 불안, 걱정 등의 심인적인 증상, 그리고 낮 동안의 졸음과 일상생활에서의 기능장애와 유의한 혈액투석 중인 만성 신부전증 환자에서의 불면증 132 상관관계가 있었다. 또, 불면증군은 비불면증군에 비해 수면에 대한 비기능적인 믿음이 더 많았다. 결 론: 혈액투석을 받고 있는 말기 신부전증 환자들은 일반 인구에 비해 불면증이 흔하였고, 이들 중 불면을 호소하는 환자들은 대조군에 비해 심인적인 증상과 신체증상 그리고 일상생활에서의 기능저하를 더 호소하였고, 수면에 대한 비기능적인 믿음이 많았다. 그리고 불면증의 심한 정도는 이러한 요인들과 밀접한 관계가 있었다. 이상의 요인들을 고려하여 수면장애를 개선한다면 이들 환자들의 진료에 도움을 주어 치료 순응도와 삶의 질을 높일 수 있으리라고 생각한다.

• 한방재활의학과학회지
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• 제23권4호
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• pp.95-115
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• 2013

Objectives The aim of this review is to provide fundamental data for low back pain scales which can be used in clinical trial. Methods We investigated the latest studies on chronic low back pain via PubMed. And we also investigated domestic studies through "http://oasis.kiom.re.kr". 95 research papers were analyzed. Scales were classified into pain scale, function scale, generic health status scale and psychological scale. Results 1) According to foreign clinical studies, Visual Analog Scale (VAS) and Numerical Rating Scale (NRS) were used 18 times as pain scale. Oswestry Disability Index (ODI) was used 20 times as function scale, Roland-Morris Disability Questionnaire (RMDQ) was 17, and Hannover Functional Ability Questionnaire (HFAQ) was used 3 times. 36-item Short Form Health Survey (SF-36) was used 13 times as generic health status scale, Euroqol-5 Dimentions Questionnaire (EQ-5D) was 11, and 12-item Short Form Health Survey (SF-12) was used 3 times. Fear-Avoidance Beliefs Questionnaire (FABQ) was used 9 times as psychological scale, Pain Catastrophizing Scale (PCS) and Tampa Scale for Kinesiophobia (TSK-R) both were used 3 times. 2) According to domestic clinical studies, VAS was used 37 times as pain scale, NRS was 11, and Short Form McGill Pain Questionnaire (SF-MPQ) was used 6 times. ODI was used 30 times as function scale, RMDQ was 2 times only. SF-36 was used once as generic health status scale and Beck's Depression Inventory (BDI) was used 3 times as psychological scale. Conclusions We recommend VAS or NRS as a measure to evaluate pain, and ODI as a measure to evaluate functional disability. And we also recommend SF-36 or SF-12 and EQ-5D as a measure to evaluate generic health status. Finally, we recommend FABQ for use in measuring psychological scale.