• Journal of Hospice and Palliative Care
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• 제11권2호
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• pp.91-98
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• 2008

목적: 본 연구는 암환자와 건강한 성인을 대상으로 각 군에서 스트레스 지각, 대응양상 및 우울을 조사하고 스트레스 지각과 대응양상이 우울에 미치는 영향을 비교하기 위함이다. 방법: 연구대상은 W시에 위치한 3차 병원에 내원하는 외래 암환자 139명과 지역사회에 거주하는 건강한 성인 139명의 종 278명을 편의표집 하였다. 자료수집은 스트레스 측정을 위한 스트레스 VAS (Visual Analog Scale), 대응양상 측정을 위한 W.C.C.L (Ways of Coping Check List), 우울 측정을 위한 Depression Index 및 일반적 특성과 질병특성을 포함하는 구조화된 질문지를 이용하여 설문조사를 실시한 후 자료를 분석하였다. 결과: 암환자와 건강한 성인간의 스트레스 지각, 대응 양상 및 우울에 대한 비교는 교육수준과 평균수입을 통제한 ANCOVA 분석을 실시한 결과, 암환자가 건강한 성인보다 스트레스 지각이 높았고 소망적 사고 대응이 낮았으며 우울이 더 높았다. 스트레스 지각과 우울과의 관계에 영향을 미치는 대응양상은 암환자에서는 조력추구 대응, 스트레스 지각, 그리고 교육정도의 순으로 우울을 유의하게 설명하였고 설명력은 20.2%였다. 건강한 성인에서는 스트레스 지각, 문제해결 대응, 그리고 조력추구 대응양상 순으로 우울을 유의하게 설명하였으며 설명력은 30.7%였다. 결론: 본 연구결과 암환자의 우울 감소를 위해서는 전체적으로 대응 전략 사용을 증진시키되 우울 감소에 효과적인 대응양상의 선택과 사용을 위한 훈련 프로그램 및 지원체계, 그리고 스트레스 감소를 위한 중재의 개발과 적용이 필요하다.

• 재활복지
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• 제22권4호
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• pp.1-22
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• 2018

본 연구는 일상생활에서 스스로 자신의 통증을 관리할 수 있도록 키네시오 테이핑 자가적용 교육을 적용하여 만성요통 여성들을 대상으로 통증과 만족도 및 보행에 미치는 영향을 분석하고자 하였으며, 키네시오 테이핑 자가적용에 대한 기초자료를 제공하고자 수행되었다. 연구대상자는 만성요통 여성 30명이며, 키네시오 테이핑 적용을 2주간 실시한 후 자가적용 교육에 따른 자가적용을 4주간 실시하였다. 대상자들의 통증 평가는 Visual Analog Scale (VAS)을 활용하였으며, 만족도의 분석은 Canadian Occupational Performance Measure (COPM)를 활용하였다. 또한, 보행의 분석은 Walkway MG-1000 보행분석기를 활용하여 Stride length, Step length, Step width and Gait time을 분석하였다. 그 결과 테이핑 적용에 따라 통계적으로 유의미한 통증의 감소와 만족도의 증가, 보행 능력의 증가가 지속적으로 나타남을 확인할 수 있었다. 또한, 대비검정 분석결과 처치 내 효과검증에서 통증, 만족도 및 보행 분석결과 에서 (처치 전과 테이핑 적용 2주 후) 통계적인 유의미한 차이가 나타났으며, Step width와 만족도 분석결과에서 (처치 전과 테이핑 적용 2주 후)와 (자가적용교육에 따른 자가적용 4주 후) 통계적으로 유의미한 차이가 나타났다. 자기관리능력의 향상은 만성통증 환자들에게 필수적이며, 일상생활에서 스스로 관리하여 적용할 수 있어야 한다. 따라서, 적극적이고 지속적인 통증관리를 위한 자기관리능력의 향상을 위해 키네시오 테이핑 자가적용 교육의 적용을 고려해야 할 것이다.

• 대한한방내과학회지
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• 제40권3호
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• pp.390-408
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• 2019

Objectives: Several pattern diagnosis questionnaires have been developed to objectify the process of pattern diagnosis in Korean medicine. In this context, this study aimed to develop a food retention questionnaire for functional dyspepsia (FRQ-FD) by modifying the previously developed food retention questionnaire (FRQ) and to verify its reliability and validity. Furthermore, this study aimed to identify the optimal cut-off value of the FRQ-FD for standardization and use in clinical situations. Methods: To develop the FRQ-FD, we extracted the major symptoms of food retention pattern for functional dyspepsia from Chinese/Korean medicine textbooks and requested an importance survey from experts using the Delphi method. The first draft of the FRQ-FD was composed of 25 questions comprising 8 questions from the textbooks and the Delphi method and 17 questions from the FRQ already developed in 2013. To analyze its reliability, validity, and optimal cut-off value, 60 subjects were enrolled in this study from June 25 to August 13, 2018. Thirty patients were diagnosed as both functional dyspepsia and food retention pattern, and 30 healthy participants were not. All participants were requested to fill up the FRQ-FD, Stomach Qi Deficiency Questionnaire (SQDQ), Scale for Stomach Qi Deficiency pattern (SSQD), visual analog scale (VAS) for dyspepsia, Nepean Dyspepsia Index-Korean version (NDI-K), and functional dyspepsia-related quality of life (FD-QoL). Results: No statistically significant differences were found in sex distribution, age, and body mass index between the patient group and the control group. As five questions affected the reliability negatively and three questions affected the clinical validity negatively, we decided to exclude the eight questions upon further investigation. The Cronbach's ${\alpha}$ coefficient of the revised FRQ-FD (17 items) was 0.899, and its clinical validity was verified. Construct validity was analyzed by factor analysis and produced five factors. Statistically significant positive correlations were found between the revised FRQ-FD and the other dyspepsia scales, namely, SQDQ, SSQD, VAS, NDI-K, and FD-QoL. VAS and NDI-K especially had strong positive correlations with FRQ-FD. Conclusions: The FRQ-FD developed in this study can provide fundamental reliability and validity for a pattern diagnosis questionnaire. FRQ-FD can help to diagnose food retention pattern in functional dyspepsia patients. Further studies are required to inspect several statistical factors.

• 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.

• Journal of Acupuncture Research
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• 제28권1호
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• pp.65-75
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• 2011

Objectives : The purpose of this study was to evaluate the clinical effect of indirect moxibustion treatment for HIVD patients. Methods : From March 2010 to December 2010, 32 HIVD patients who admitted to Semyung oriental medical hospital were divided into two groups. Group I was treated by indirect moxibustion and general acupuncture, group II by general acupuncture. We evaluated the treatment effect of each group with the visual analog scale(VAS) and Oswestry disability index(ODI) by dividing three period(from admission day to third day after admission, from third day to sixth day after admission and from sixth day to ninth day after admission). Results : 1. Group I was more effective than group II in VAS score reducing rate at sixth day after admission and ninth day after admission but there was no statistical significance between two groups at third day after admission 2. Group I was more effective than group II in VAS improvement rate from third day to sixth day after admission but there was no statistical significance between two groups from admission day to third day after admission and sixth day to ninth day after admission. 3. Group I was more effective than group II in ODI score reducing rate at sixth day after admission and ninth day after admission but there was no statistical significance between two groups at third day after admission. 4. In ODI improvement rate group I was higher than group II, but there was no statistical significance. Conclusions : Through this research, Indirect moxibustion treatment is considered to be effective reducing pain for HIVD(Herniated intervertebral disc) patients.

• Clinics in Shoulder and Elbow
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• 제13권1호
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• pp.7-13
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• 2010

목적: 상완 이두근 장두의 고정술을 시행하는데 있어 흉근하 (subpectoral) 간섭 나사못 고정술의 임상적 결과에 대해 후향적으로 분석하고자 하였다. 대상 및 방법: 2008년 1월부터 2009년 1월까지 상완 이두근 장두의 건 고정술을 시행한 환자를 대상으로 하였으며, 최소 1년 이상 추시가 가능하였던 23예를 대상으로 하였다. 그 중 회전근개 파열을 동반한 경우는 16예였다. 결과는 VAS, ASES, 상완 이두건 구의 통증, 고정실패 및 변형의 정도로 판단하였다 (BAD). 결과: 최종 추시 시 모든 환자에서 수술 전에 비해서 VAS, ASES점수는 의미 있게 호전되었으며 고정의 실패나 합병증은 없었다. 회전근개 파열을 동반한 군과 그렇지 않는 군에서는 최종 추시시 회전근개 파열이 없는 군에서 좋은 결과를 얻을 수 있었으나 통계학적인 의미는 없었다(p>0.05). 결론: 상완 이두건 근위부 병변에 의한 통증이 있는 환자에서 흉근하 건 고정술은 최종 추시시 통증의 경감이나 기능적인 이두근 근력의 유지, 미용상으로 좋은 결과를 얻을 수 있을 것으로 사료된다.

• Annals of Rehabilitation Medicine
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• 제39권6호
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• pp.957-963
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• 2015

Objective To compare the pain-reducing effect of forest bathing alone versus forest bathing in combination with stretching and strengthening exercises in patients with chronic posterior neck pain. Methods Sixty-four subjects with posterior neck pain that had lasted more than 3 months were enrolled. They were randomly divided into a forest bathing alone (FBA) group and a forest bathing with exercise (FBE) group; each group included 32 subjects. All subjects from both groups walked every morning in the forest for about 2 hours for 5 days. In the afternoon, the FBE group did a stretching and strengthening exercise for about 4 hours; the FBA group had free time in the woods. Visual analog scale (VAS) on one day, VAS over the previous week, neck disability index (NDI), EuroQol 5D-3L VAS (EQ VAS) and index (EQ index), McGill pain questionnaire (MPQ), the number of trigger points in the posterior neck region (TRPs), and the range of motion of the cervical spine were evaluated on the first and last day of the program and compared between the two groups. Results The number of TRPs were significantly reduced in the FBE group compared with the FBA group (p=0.013). However, the other scales showed no significant difference between the two groups. Conclusion When patients with chronic posterior neck pain underwent a short-term forest bathing (less than 7 days) program, FBE was more effective in the reduction of the number of TRPs than FBA. However, all other pain measurement scales we evaluated showed no statistically significant difference between the two protocols.

• Journal of Dental Anesthesia and Pain Medicine
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• 제22권5호
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• pp.323-338
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• 2022

Burning mouth syndrome (BMS) is a chronic oral disorder of unknown etiology which presents therapeutic challenges. Alpha-lipoic acid (ALA) has been studied as a potential treatment for BMS. The objective of this systematic review and meta-analysis was to evaluate the effectiveness of ALA compared to that of placebo or other interventions in individuals with BMS. Randomized controlled trials (RCT) using ALA to treat BMS were identified from MEDLINE, Cochrane Library, EMBASE, and Web of Science up to February 3, 2021. The assessment of the risk of bias in the included studies was based on the Cochrane guidelines. The primary outcome evaluated was the visual analog scale (VAS) pain intensity. ALA was compared with placebo, clonazepam, gabapentin, pregabalin, ALA plus gabapentin, capsaicin, Biotène^®, and laser therapy. Altogether, 137 records were scanned for inclusion/exclusion, and nine RCTs (two unclear and seven at high risk of bias) were included in the qualitative and quantitative analyses, with a total of 594 patients with BMS included in this review. All studies reported an improvement in VAS pain scores ranging from -0.72 to -2.77. Meta-analysis results showed a non-significant reduction in pain intensity for ALA (P = 0.616) compared to that of placebo on a VAS of 0-10. Patients taking ALA were 1.923 times more likely to show an improvement in self-reported BMS symptoms (P = 0.031) than those in the placebo group. Clonazepam and pregabalin showed a significant VAS pain reduction of 4.08 and 4.68 (P < 0.001), respectively, compared to that with ALA. Although ALA intervention provided a non-significant improvement in the pain score and was more likely to produce a reduction in BMS symptoms, the evidence was of low quality. Further research is needed to establish clear guidelines for the use of ALA for BMS treatment.

• 한방재활의학과학회지
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• 제33권4호
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• pp.45-59
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• 2023

Objectives The aim of this study was to analyze the trends of researches on oriental medicine treatments for supraspinatus tendinopathy. Methods We used five databases for searching researches; Korean studies Information Service System, Oriental Medicine Advanced Searching Integrated System, Research Information Sharing Service, PubMed, and China National Knowledge Infrastructure. Only randomized controlled trials suitable for the subject were selected. The methodological quality of included randomized controlled trials (RCTs) was assessed by the Cochrane risk of bias tool. Results Twenty randomized controlled trials were analyzed. There were 9 types of treatment interventions; acupuncture, acupotomy, pharmacopuncture, electroacupuncture, fire needling, warming needle, catgut-embedding therapy, herbal medicine, cupping. The most frequently used treatment intervention was acupuncture and acupotomy. There were 9 outcome measurements including visual analog scale (VAS), Constant-Murley Score (CMS), and range of motion. The most used measurement was VAS. As a result of meta-analysis, acupuncture was more effective than control group in VAS. Additionally, acupotomy was clinically significant compared to control groups in VAS and CMS. Conclusions In this review, we analyzed researches on effectiveness of oriental medicine for supraspinatus tendinopathy. A provisional conclusion can be produced that acupuncture and acupotomy showed beneficial effect to supraspinatus tendinopathy. Although there were some RCT studies, many of them had a high risk of bias, so it is hard to conclude that our study can include overall clinical status. Further well-designed trials are needed.

• The Korean Journal of Pain
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• 제25권3호
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• pp.173-182
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• 2012

Background: Fibromyalgia (FM) is characterized by chronic widespread pain with a low pain threshold. The aim of this study was to compare two criteria for the diagnosis and assessment of FM and to analyze the correlation and agreement between the 1990 and 2010 American College of Rheumatology (ACR) preliminary diagnostic criteria for FM. Methods: We studied 98 patients who had already been diagnosed as having FM using the 1990 criteria or 2010 preliminary criteria. Tender point examination, FM impact questionnaire (FIQ) and pain visual analog scale (VAS) were obtained. According to the preliminary criteria, FM was quantified as WPI (widespread pain index) and the SS scale (symptom severity) and the two criteria were compared. Results: Among 98 patients, 78.6% of the patients were diagnosed with the 1990 ACR criteria and 93.9% of the patients were diagnosed with the ACR preliminary diagnostic criteria, and there was also significant agreement between the two criteria (P < 0.01). There was a correlation with the WPI and the tender point, with the SS and the FIQ, and with the sum of the WPI and SS and the FIQ. Conclusions: The ACR preliminary diagnostic criteria for FM were in agreement with the 1990 ACR criteria during the disease course. The preliminary criteria were the more sensitive method than the 1990 criteria. In addition, the 2010 criteria might have advantages since it is easy to assess the physical and psychological symptoms and can be quantified. Therefore, the ACR preliminary diagnostic criteria for FM could be used more conveniently for clinical diagnosis and follow up evaluation after starting management of FM.