DOI： 10.1101/2024.04.13.24305766

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担当区分：筆頭著者   掲載種別：研究論文（学術雑誌）  

DOI： 10.5926/arepj.63.144

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

INTRODUCTION: Hyperkalaemia (HK) is a frequent complication in patients with chronic kidney disease (CKD) and/or chronic heart failure (CHF). HK must be managed, both to protect patients from its direct clinical adverse outcomes and to enable treatment with disease-modifying therapies including renin-angiotensin-aldosterone system inhibitors. However, the experiences of patients undergoing treatment of HK are not clearly understood. Optimising treatment decisions and improving long-term patient management requires a better understanding of patients' quality of life (QOL). Thus, the aims of this research are: (1) to describe treatment patterns and the impact of treatment on a patient's QOL, (2) to study the relationships between treatment patterns and the impact of treatment on a patient's QOL and (3) to study the relationships between the control of serum potassium (S-K) and the impact of treatment on a patient's QOL, in patients with HK. METHODS AND ANALYSIS: This is a prospective cohort study with 6 months of follow-up in 30-40 outpatient nephrology and cardiology clinics in Japan. The participants will be 350 patients with CKD or CHF who received their first potassium binders (PB) prescription to treat HK within the previous 6 months. Medical records will be used to obtain information on S-K, on treatment of HK with PBs and with diet, and on the patients' characteristics. To assess the impact of treatment on a patient's QOL, questionnaires will be used to obtain generic health-related QOL, CKD-specific and CHF-specific QOL, and PB-specific QOL. Multivariable regression models will be used to quantify how treatment patterns and S-K control are related to the impact of treatment on a patient's QOL. ETHICS AND DISSEMINATION: Institutional review boards at all participating facilities review the study protocol. Patient consent will be obtained. The results will be published in international journals. TRIAL REGISTRATION NUMBER: NCT05297409.

DOI： 10.1136/bmjopen-2023-074090

PubMed

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

Introduction Establishing a scale that can easily be used to appropriately measure the impact of constipation on the quality of life in Japan is a first step toward addressing this important health issue. We developed a Japanese language version of the Constipation-Related Quality of Life scale, which has 18 items and four subscales, and then subjected it to validation testing. Methods After translation according to a standardized and commonly used procedure, the Japanese version of the Constipation-Related Quality of Life scale was administered to people in an internet-based panel, in March 2023. The participants included 1,276 adults who had constipation (median age: 60 years, 690 {54.1%} males). The outcome measures included the Constipation-Related Quality of Life scale, the Constipation Scoring System (an index of constipation severity), and the Medical Outcomes Study (MOS) eight-item short form (a measure of generic health-related quality of life). Results Confirmatory factor analysis (four-factor model) indicated that all 18 Constipation-Related Quality of Life items had sufficiently high factor loadings (0.686-0.926). Internal consistency reliability was high (Cronbach's alpha: 0.86-0.94). Scores on the social impairment subscale and on the distress subscale of the Constipation-Related Quality of Life scale were significantly worse in the participants who had worse scores on the social functioning and mental health domains, respectively, of the MOS eight-item short form, which indicates good concurrent validity. Regarding criterion-based validity, the four subscale scores differed significantly among the four constipation-severity groups. The four subscale scores were also 1.16-4.53 times more sensitive than the MOS eight-item short form's mental component score to differences among the four constipation-severity groups (relative validity: 1.16-4.53), which indicates good discriminant validity. Conclusion The Japanese version of the Constipation-Related Quality of Life scale can be used with confidence in its factor structure, its concurrent, criterion-based, and discriminant validity, and its internal consistency reliability.

DOI： 10.7759/cureus.48661

PubMed

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DOI： 10.32286/00028003

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: The burden of COVID-19 on healthcare workers (HCWs) is reported to be increasing, yet the psychometric scales now in use evaluate only single aspects; few measure the pandemic-specific burden on HCWs comprehensively. OBJECTIVE: To develop a scale to quantify the physical, mental, and socioeconomic burden of the COVID-19 pandemic on HCWs. DESIGN: Scale development and cross-sectional survey. PARTICIPANTS: Consenting HCWs aged ≥20. MAIN MEASURES: Development of an item-list based on literature reviews and HCW panel input, evaluation of content validity and item selection using the Delphi method, psychometric testing conducted on HCWs, validity assessment by factor analyses and hypothesis verification, internal consistency evaluation by Cronbach's alpha, test-retest analysis, and interpretability assessment. KEY RESULTS: Through the Delphi process, a 29-item pilot scale was generated. In psychometric testing, data from 863 HCWs contributed to the development of the final version of this scale, called Pandemic Burden Index twenty for HCWs (PBI-20), a 20-item scale to measure six domains: fatigue, fear of infection, inadequacy as a medical professional, mental health concerns, prejudice or discrimination, and anxiety about one's livelihood and daily life. Factor analysis showed each factor corresponded to the six domains of this scale. Hypothesis verification showed the PBI-20 total score to be moderately to highly correlated with the Short Form 36 vitality score and mental health score and with intention of turnover. The PBI-20 had good internal consistency (Cronbach's alpha 0.92). Test-retest analysis showed the intraclass correlation coefficient to be 0.70 and the minimal important change to be -7.0. CONCLUSIONS: The psychometrically sound questionnaire we developed to measure pandemic-specific burdens for HCWs provides an understanding of comprehensive burdens on HCWs and may serve to evaluate interventions to reduce the burdens.

DOI： 10.1007/s11606-023-08028-3

PubMed

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出版者・発行元：Cold Spring Harbor Laboratory  

Rationale & Objective In chronic kidney disease (CKD), the durability of patient adherence to fluid and dietary restrictions may depend on the degree to which they have hope that they will enjoy life. However, few studies have examined the long-term role of health-related hope (HR-Hope) on distress from fluid and dietary restrictions. Study Design Prospective cohort study. Setting & Participants A total of 444 non-dialysis stage 3-5 patients and stage 5D patients attending one of five Japanese nephrology centers. Exposure An 18-item HR-Hope scale with a score ranging from 0 to 100. Outcomes Two-item measures of restrictions on fluid and dietary intake from the Japanese version of the Kidney Disease Quality of Life Short Form, Version 1.3, with each score ranging from 0 to 100. Analytical Approach Multivariate linear mixed models were used to estimate the association of baseline HR-Hope with distress from fluid and dietary restrictions at baseline and follow-up. Results The mean age of participants was 67 years, 31.1% were female, and 124, 98, and 222 had non-dialysis CKD, peritoneal dialysis, and hemodialysis, respectively. Baseline HR-Hope buffered the growing distress from fluid restriction after one year (-18.01 pts [95% CI, -28.24 to -7.79]) per 10-pt increase, 2.59 pts [95% CI, 1.05 to 4.13]. The distress from fluid restriction at 2 years did not differ from baseline. Baseline HR-Hope buffered the growing distress from dietary restriction after one year (-12.4 pts [95% CI, -22.68 to -2.12]) per 10-pt increase, 1.96 pts (95% CI, 0.34 to 3.57). The distress from dietary restriction at 2 years did not differ from baseline. Limitations Use of self-reported measures as proxies for adherence. Conclusions Our study shows that HR-Hope, regardless of depression, can potentially mitigate the long-term distress from fluid and dietary restrictions in patients with a wide range of CKD severities.

DOI： 10.1101/2023.01.14.23284563

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記述言語：日本語  

CiNii Books

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記述言語：日本語   出版者・発行元：(一社)日本腎臓学会  

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記述言語：日本語   出版者・発行元：厚生労働統計協会  

CiNii Books

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その他リンク： https://search.jamas.or.jp/link/ui/2022089442

記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: To elucidate the experience of patients with cancer from diagnosis to early survivorship in Japan using a nationwide questionnaire survey, and to inform the current progress of the cancer control programs. METHODS: The survey was sent to a representative sample of adult patients with cancer identified from the national database of hospital-based cancer registries. The patients' responses were compared across three groups: patients with rare cancers, patients aged < 40 years, and patients with non-rare cancers aged ≥40 years. RESULTS: Of 20,488 patients invited to participate in the survey, 8935 (43.6%) responded. Respondents reported an average score of 7.9 out of 10 on global ratings of care. Patients with rare cancers experienced a longer time to diagnosis but the shortest time from diagnosis to first treatment (p < 0.05). Patients aged < 40 years rated worse for the majority of the survey items, especially on items that related to communication with medical staff and items referring to early survivorship. CONCLUSION: The care experienced by patients with cancer in Japan varies on the basis of age group and cancer type. Efforts should be directed to ensuring prompt access to diagnostic facilities for patients with rare cancers and providing sufficient support to younger patients.

DOI： 10.1186/s12913-021-07184-8

PubMed

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: A family member's negative experiences with medical care have long-term effects on a patient's attitudes and emotions. However, the impact of family members' experiences on patients' trust in their own physicians and in physicians generally is poorly understood. This study aims to quantify these associations. METHODS: A cross-sectional online survey involving adults with non-communicable diseases (cardiac disease, diabetes, cancer, depression, and rheumatic disease) was conducted in Japan during April 2020. The main exposure variable was dissatisfaction with the medical care that family members had received. The main outcomes were patients' (N = 661) own trust in their personal physicians and in physicians generally. The study adopted the Japanese version of the Abbreviated Wake Forest Physician Trust Scales. Both 5-item scales (general and individual physician trust) were translated and validated for the study. The total scores were transformed into a scale of 0-100 points. A series of linear mixed-effects models with consideration for clustering effect by prefectures were fit. RESULTS: The results showed a lower rating for trust in physicians generally as compared to trust in the respondent's personal physician (mean 57.0 vs. 66.4 points; p < 0.001). Furthermore, dissatisfaction with a family member's medical care was associated with lower trust in physicians generally (mean difference - 9.58, 95 %CI -12.4 to -6.76). Interestingly, dissatisfaction with a family member's care was also associated with lower trust in the respondent's personal physician (mean difference - 3.19, 95 %CI -6.02 to -0.36), but the magnitude of this association was weaker. The lower trust in personal physicians may be mediated by reduced trust in physicians generally. CONCLUSIONS: We suggest that physicians enquire about past patients' negative experiences, including dissatisfaction with family members' medical care, to repair hidden loss of trust, when they sense that patients doubt them or physicians generally.

DOI： 10.1186/s12913-021-07172-y

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: Previous qualitative research has described that previous misdiagnoses may reduce patient and their families' trust in healthcare. OBJECTIVE: To quantify the associations between patients or family members' misdiagnosis experiences and trust in their physician. DESIGN: Cross-sectional study. PARTICIPANTS: Adult Japanese people with non-communicable diseases (cancer, diabetes, depression, heart disease, and connective tissue disease), recruited using a web-based panel survey. MAIN MEASURES: Surveys assessed the patient and the patient's family's experience with misdiagnosis. Trust in the respondent's current physician was measured using the Japanese version of the 11-item Trust in Physician Scale. KEY RESULTS: Among 661 patients (response rate 30.1%), 23.2% had a personal history of misdiagnosis and 20.4% had a family history of misdiagnosis. In a multivariable-adjusted general linear model, patients or a family members' misdiagnosis experiences were associated with lower confidence in their current physician (mean difference -4.3, 95%CI -8.1 to -0.49 and -3.2, 95%CI -6.3 to -0.05, respectively). The impact of having a personal and a family member's experience of misdiagnosis on trust was additive, with no evidence of interaction (P for interaction = 0.494). CONCLUSIONS: The patient's or family members' misdiagnosis experiences reduced trust in the patient's current physicians. Interventions specifically targeting misdiagnosed patients are needed to restore trust.

DOI： 10.1007/s11606-021-06950-y

PubMed

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掲載種別：研究論文（学術雑誌）   出版者・発行元：Springer Science and Business Media LLC  

DOI： 10.1007/s12603-020-1556-4

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その他リンク： https://link.springer.com/article/10.1007/s12603-020-1556-4/fulltext.html

記述言語：日本語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1101/2021.04.21.21255773

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出版者・発行元：Cold Spring Harbor Laboratory  

Background
Previous qualitative research has described that past misdiagnosis experiences may reduce patients' own and their families' trust in healthcare.
Objective
To quantify the associations between patients' or family member' misdiagnosis experiences and the former's trust in their current physicians.
Design
A cross-sectional online survey.
Participants
Adult Japanese people with non-communicable diseases (cancer, diabetes, depression, heart disease, and connective tissue disease), recruited using a web-based panel survey.
Main Measures
The misdiagnosis experiences of patients and their family members were measured as exposures. The former's trust in their current physicians was measured using the Japanese version of the 11-item Trust in Physicians Scale modified by Thom, which was translated and validated by us for this study.
Key Results
A total of 661 patients with a mean age of 62.7 years were analyzed. Overall, 23.2% had a history of misdiagnosis and 20.4% had a family member who had been misdiagnosed. The internal consistency (Cronbach's α) was 0.91. The factor analysis suggested unidimensionality with all 11 loadings being higher than 0.40. In a multivariable-adjusted general linear model, patients' and family members' misdiagnosis experiences were associated with lower confidence in their current physicians (mean difference -4.30, 95%CI -8.12 to -0.49 and -3.20, 95%CI -6.34 to -0.05, respectively). An additive effect was suggested for the associations of patients' and family's experience of misdiagnosis on trust (P for interaction = 0.494).
Conclusions
The individuals' and family members' misdiagnosis experiences were associated with reduced trust in their current physicians. Interventions specifically targeting misdiagnosed patients are needed to restore patients' confidence in their current physicians.

DOI： 10.1101/2021.01.25.21250300

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: Understanding patient journey and burden of disease in patients with chronic thromboembolic pulmonary hypertension (CTEPH) helps improve diagnostic and treatment processes. OBJECTIVES: This study aimed to explore patient journey from time of disease onset to a definitive diagnosis and disease burden in Japanese patients with CTEPH. METHODS: A mixed-methods study exploring patient journey and disease burden of 33 Japanese patients with a definitive diagnosis of CTEPH. The patients from 2 university hospitals underwent semistructured interviews. Data were transcribed into verbatim records, and 2 independent researchers conducted thematic analyses. Data concerning patient journey were also analyzed quantitatively with supplementary use of medical records. RESULTS: Median times from initial onset of symptoms to a confirmed diagnosis and first visitation to a medical institution to a definitive diagnosis of CTEPH were 32 and 20 months, respectively. Thematic analyses found that, for patients, reasons for delay in seeking initial consultations included misattribution of symptoms to aging or lack of physical strength. For healthcare providers, reasons for delays in diagnosis included poor recognition of CTEPH and difficulty in recalling the disease as a differential diagnosis. Burdens of CTEPH were caused by physical symptoms, and mental and social issues, including restriction of daily activities owing to oxygen therapy, disappointment with the intractable nature of the disease, poor understanding of the disease by other people, and lack of social networks. CONCLUSIONS: This study highlighted physical, mental, and social burdens in patients with CTEPH and possible missed opportunities in making the diagnosis of CTEPH during the patient journey. Increasing disease awareness in healthcare providers and networking among patients may contribute to better patient care.

DOI： 10.1016/j.vhri.2020.06.005

PubMed

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

We aimed to develop and validate a new simple decision support tool (U-TEST) for diagnosis of sarcopenia in orthopaedic patients. We created seventeen candidate original questions to detect sarcopenia in orthopaedic patients with sarcopenia through expert opinions and a semi-structured interview. To derive a decision support tool, a logistic regression model with backward elimination was applied to select variables from the seventeen questions, age and underweight (BMI < 18·5 kg/m2). Sarcopenia was defined by Asian Working Group for Sarcopenia 2019 criteria. After assigning a score to each selected variable, the sum of scores was calculated. We evaluated the diagnostic performance of the new tool using a logistic regression model. A bootstrap technique was used for internal validation. Among a total of 1334 orthopaedic patients, sixty-five (4·9 %) patients were diagnosed with sarcopenia. We succeeded in developing a 'U-TEST' with scores ranging from 0 to 11 consisting of values for BMI (Underweight), age (Elderly) and two original questions ('I can't stand up from a chair without supporting myself with my arms' (Strength) and 'I feel that my arms and legs are thinner than they were in the past' (Thin)). The AUC was 0·77 (95 % CI 0·71, 0·83). With the optimal cut-off set at 3 or greater based on Youden's index, the sensitivity and the specificity were 76·1 and 63·6 %, respectively. In orthopaedic patients, our U-TEST scoring with two questions and two simple clinical variables can help to screen for sarcopenia.

DOI： 10.1017/S0007114521000106

PubMed

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

BACKGROUND: In chronic kidney disease (CKD), patients' adherence to prescriptions for diet and for medications might depend on the degree to which they have hope that they will enjoy life, and that hope could vary with the stage of CKD. The aims of this study were to quantify both the association of CKD stage with health-related hope (HR-Hope), and the association of that hope with psychological and physiological manifestations of adherence. METHODS: This was a cross-sectional study involving 461 adult CKD patients, some of whom were receiving dialysis. The main exposure was HR-Hope, measured using a recently-developed 18-item scale. The outcomes were perceived burden of fluid restriction and of diet restriction, measured using the KDQOL, and physiological manifestations of adherence (systolic and diastolic blood pressure [BP], and serum phosphorus and potassium levels). General linear models and generalized ordered logit models were fit. RESULTS: Participants at non-dialysis stage 4 and those at stage 5 had lower HR-Hope scores than did those at stage 2 or 3 (combined). Those at non-dialysis stage 5 had the lowest scores. HR-Hope scores of participants at stage 5D were similar to those of participants at stage 4, but they were lower than the scores of participants at stage 2 or 3 (combined). Higher HR-Hope scores were associated with lower perceived burdens of fluid restriction and of diet restriction (adjusted ORs per ten-point difference were 0.82 and 0.84, respectively). Higher HR-Hope scores were associated with lower systolic BP (adjusted mean difference in systolic BP per ten-point difference in HR-Hope scores was - 1.87 mmHg). In contrast, HR-Hope scores were not associated with diastolic BP, serum phosphorus levels, or serum potassium levels. CONCLUSIONS: Among CKD patients, HR-Hope is associated with disease stage, with psychological burden, and with some physiological manifestations of adherence.

DOI： 10.1186/s12882-020-02120-0

PubMed

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掲載種別：研究論文（学術雑誌）   出版者・発行元：Elsevier BV  

DOI： 10.1016/j.xkme.2020.07.004

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記述言語：日本語   掲載種別：研究論文（大学，研究機関等紀要）   出版者・発行元：関西大学社会学部  

本研究では、Likert法における社会的望ましさなどの影響による回答分布の偏りを解決する方法として、回答選択肢の評定尺度表現を変化させる適応型選択肢の考え方を提案した。また、その実現に向けて、同じ尺度に対して異なる2種類の評定尺度表現を用いることで回答分布等がどのように変化するかを検討した。その結果、評定尺度表現を変化させることにより、回答分布が変わることが確認された。本研究はJSPS科研費17K13926の助成を受けたものである。

CiNii Books

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その他リンク： http://hdl.handle.net/10112/00020016

記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.62.0_324

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s12603-019-1222-x

PubMed

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記述言語：日本語   出版者・発行元：関西大学大学院心理学研究科  

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s12603-019-1222-x

PubMed

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：Society for Clinical Epidemiology  

DOI： 10.37737/ace.1.3_102

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掲載種別：研究論文（学術雑誌）  

DOI： 10.1027/1015-5759/a000371

Scopus

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記述言語：日本語   出版者・発行元：(公社)日本心理学会  

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.60.0_358

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記述言語：日本語   出版者・発行元：(一社)日本透析医学会  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2017&ichushi_jid=J02822&link_issn=&doc_id=20170413360002&doc_link_id=10.4009%2Fjsdt.50.180&url=https%3A%2F%2Fdoi.org%2F10.4009%2Fjsdt.50.180&type=J-STAGE&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00007_3.gif

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.2147/JPR.S129957

Web of Science

PubMed

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その他リンク： http://orcid.org/0000-0003-2293-5918

記述言語：日本語   出版者・発行元：(一社)日本発達心理学会  

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記述言語：日本語   出版者・発行元：関西大学大学院心理学研究科  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2016&ichushi_jid=J06738&link_issn=&doc_id=20160427050002&doc_link_id=http%3A%2F%2Fhdl.handle.net%2F10112%2F10472&url=http%3A%2F%2Fhdl.handle.net%2F10112%2F10472&type=%8A%D6%90%BC%91%E5%8Aw%81F%8A%D6%90%BC%91%E5%8Aw%8Aw%8Fp%83%8A%83%7C%83W%83g%83%8A_KU%83%8A%83%7C%83W%83g%83%8A&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F80199_3.gif

記述言語：日本語   出版者・発行元：日本パーソナリティ心理学会  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2015&ichushi_jid=J04150&link_issn=&doc_id=20150918060004&doc_link_id=%2Fdm3perso%2F2015%2F002401%2F005%2F0049-0060%26dl%3D0&url=http%3A%2F%2Fwww.medicalonline.jp%2Fjamas.php%3FGoodsID%3D%2Fdm3perso%2F2015%2F002401%2F005%2F0049-0060%26dl%3D0&type=MedicalOnline&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00004_2.gif

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s00776-015-0694-8

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1371/journal.pone.0116677

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PubMed

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.57.0_462

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.57.0_28

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

本研究では, 日本で測定されたRosenberg（1965）の自尊感情尺度の平均値に与える調査対象者の年齢段階や調査年の要因を検討するために, 時間横断的メタ分析を試みた。1980年から2013年までに日本で刊行された査読誌に掲載された論文のうち256研究を分析の対象とした。全サンプルサイズは48,927名であった。重回帰分析の結果, 調査対象者の年齢段階と調査年がともに, 自尊感情の平均値に影響を及ぼすことが明らかにされた。年齢段階に関しては, 大学生を基準として, 調査対象者が中高生であることが自尊感情の平均値を低下させ, 成人以降であることが自尊感情の平均値を上昇させていた。また調査年に関しては年齢層によって効果が異なっていた。中高生や成人においては最近の調査であるほど直線的に自尊感情の平均値が低下しており, 大学生では曲線的に変化し, 近年は低下していた。また件法が自尊感情得点の平均値に影響を及ぼすことも明らかにされた。

DOI： 10.5926/jjep.62.273

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記述言語：日本語   出版者・発行元：日本自閉症スペクトラム学会  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2014&ichushi_jid=J05573&link_issn=&doc_id=20150127520002&doc_link_id=10.32220%2Fjapanacademyofas.12.1_19&url=https%3A%2F%2Fdoi.org%2F10.32220%2Fjapanacademyofas.12.1_19&type=J-STAGE&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00007_3.gif

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1097/BRS.0000000000000583

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記述言語：日本語   出版者・発行元：(一社)日本消化器外科学会  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2014&ichushi_jid=J01117&link_issn=&doc_id=20140826330001&doc_link_id=10.5833%2Fjjgs.2013.0186&url=https%3A%2F%2Fdoi.org%2F10.5833%2Fjjgs.2013.0186&type=J-STAGE&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00007_3.gif

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1186/1471-2296-15-134

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.jamcollsurg.2014.05.017

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1038/ctg.2013.20

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記述言語：日本語   出版者・発行元：一般社団法人 日本消化器外科学会  

<b>目的：</b>上部消化管術後のQOLを測定する尺度としてGastrointestinal Symptom Rating Scale（以下，GSRSと略記）がしばしば用いられている．今回，術後患者の評価尺度としてのGSRSの妥当性を検証した．<b>対象と方法</b>：2012年6月から12月の期間，胃・食道術後患者を対象に横断的調査を行い，GSRSの各下位尺度得点（酸逆流，腹痛，消化不良，下痢，便秘）を評価した．併存的妥当性としてSF-12，known-groups妥当性として，術式，栄養学的指標，および上部消化管内視鏡検査との関連を評価した．<b>結果：</b>対象は325例，年齢中央値66歳，施行術式は食道切除109，胃全摘89，胃切除124，胃部分切除5例であった（重複あり）．GSRSの得点は全項目で分布が偏っており，強い床効果を認めた．SF-12のサマリースコアとGSRSの相関係数は，腹痛と精神的側面のQOLスコアにおいて0.314であったが，その他の組み合わせは0.3以下であり，相関関係が強いとはいえなかった．BMI 18未満の群では腹痛のスコアが有意に高値であったが，その他の指標（術式，血清アルブミン値，内視鏡所見）のいずれにおいても有意な関連は認めなかった．<b>まとめ：</b>GSRSは上部消化管術後患者に対するQOL尺度としては計量心理学的妥当性が低く，臨床研究のアウトカムとしては不適切である．

DOI： 10.5833/jjgs.2013.0186

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その他リンク： https://search.jamas.or.jp/link/ui/2014356407

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1371/journal.pone.0073084

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記述言語：日本語   出版者・発行元：(一財)日本消化器病学会  

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s00776-013-0455-5

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記述言語：日本語   出版者・発行元：(一社)日本脊椎脊髄病学会  

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記述言語：日本語   出版者・発行元：関西大学社会学部  

With the social perception of manga drastically changing in Japan, studies on manga have proliferated in recent years. However, few of these studies have adopted a psychological approach. This study aimed to develop scales to measure the perception that people have of manga (Manga Image Scale), and how readers actually read manga (Manga Reading Behavior Scale). We conducted a questionnaire survey with 419 visitors to the Kyoto International Manga Museum and analyzed the results using psychometrical methods such as factor analysis. On the basis of the results, we developed three factors ("Soft Power," "Attractive Media," and "Educational") for the Manga Image Scale and two factors ("Pleasure Oriented" and "Manga Capital Oriented") for the Manga Reading Behavior Scale. Each scale score was relevant with factors such as age and the frequency of manga reading and thus proved valid. While the results suggest that further refinement of the scales is required, they may be helpful in further developing this field of study. 近年，日本社会におけるマンガに対する認識は変わりつつある。それに応じて，マンガ研究も増えてきたが，心理学的アプローチを用いた研究はほとんど見られない。本研究では人々がマンガに対してどのようなイメージを持ち（マンガイメージ尺度），実際にどのようにマンガを読んでいるのか（マンガ読書行動尺度）を測定する尺度を開発することを目的とする。京都国際マンガミュージアムを訪れた419名にアンケートへの回答を求め，因子分析等心理計量学的な手法を用いて検討を行った。その結果，マンガイメージ尺度では，「ソフトパワー」「魅力的なメディア」「学習効果」の3因子が，マンガ読書行動尺度では「快楽志向」「マンガ資本志向」の2因子が見いだされた。各尺度得点は，年齢やマンガを読んでいる日数等と関連が認められ，尺度の妥当性が示された。

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その他リンク： http://hdl.handle.net/10112/7741

記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.55.0_216

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記述言語：日本語   出版者・発行元：(公社)日本心理学会  

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その他リンク： https://search.jamas.or.jp/index.php?module=Default&action=Link&pub_year=2012&ichushi_jid=J00682&link_issn=&doc_id=20120626100003&doc_link_id=40019313290&url=http%3A%2F%2Fci.nii.ac.jp%2Fnaid%2F40019313290&type=CiNii&icon=https%3A%2F%2Fjk04.jamas.or.jp%2Ficon%2F00003_3.gif

記述言語：日本語   出版者・発行元：(一社)日本脊椎脊髄病学会  

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記述言語：日本語   出版者・発行元：関西大学社会学部  

心理測定場面で用いられるLikert 法では、選択枝に数直線や数値などさまざまな形式のレイアウトが用いられている。本研究では、選択枝のレイアウトが、回答者の回答行動にどのような影響を与えるかを、選択枝間の心理的距離の観点から検討することを目的とした。本研究では、同一尺度、同一内容でレイアウトのみが異なる4 つのバージョンを940名の大学生にランダムに配布した。Wakita et al.（2012）の方法を用いて、選択枝間の心理的距離を検討した結果、レイアウトによって違いは見られなかった。In applying Likert scale to psychological measurement, various layouts are used in rating scales such as number line or numerical number formats. The present study examined whether the layout of options in the Likert Scale influences the responses. In this study, we focused on the psychological distance between options and considered what effect the difference of rating scale format has. For this aim, we used 4 formats of rating scale, and provided 940 undergraduate students with 4 types of questionnaires that were composed of the same items but with different layouts of options to assess these items, asking them to fill them in. We used the method suggested by Wakita et al. in Educational and Psychological Measurement (2012) for an evaluation of psychological distance. It was concluded that layouts did not make a difference in responses.

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その他リンク： http://hdl.handle.net/10112/6794

記述言語：日本語   出版者・発行元：(公社)日本整形外科学会  

DOI： 10.1007/s00776-013-0482-2

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1097/brs.0b013e318216afb4

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.54.0_478

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記述言語：日本語   出版者・発行元：埼玉大学教育学部  

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1111/j.1365-2753.2011.01808.x

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1097/brs.0b013e31821fd4b1

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s00540-011-1151-2

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記述言語：日本語   出版者・発行元：医学書院  

DOI： 10.11477/mf.1405101871

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記述言語：日本語   掲載種別：研究論文（その他学術会議資料等）  

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記述言語：日本語   掲載種別：研究論文（その他学術会議資料等）  

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1007/s00776-010-0012-4

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1016/j.diabres.2010.07.007

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記述言語：英語   掲載種別：研究論文（国際会議プロシーディングス）  

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記述言語：英語   掲載種別：研究論文（国際会議プロシーディングス）  

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記述言語：英語   掲載種別：研究論文（国際会議プロシーディングス）  

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1159/000232601

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1053/j.ajkd.2009.05.011

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ELSEVIER SCIENCE BV  

Background: Various Japanese versions of the Epworth Sleepiness Scale (ESS) have been used, but none was developed via standard procedures. Here we report on the construction and testing of the developer-authorized Japanese version of the ESS (JESS).
Methods: Developing the JESS involved translations, back translations, a pilot study, and psychometric testing. We identified questions in the ESS that were difficult to answer or were inappropriate in Japan, proposed possible replacements for those questions, and tested them with analyses based on item response theory (IRT) and classical test theory. The subjects were healthy people and patients with narcolepsy, idiopathic hypersomnia, or obstructive sleep apnea syndrome.
Results: We identified two of our proposed questions as appropriate replacements for two problematic questions in the ESS. The JESS had very few missing data. Internal consistency reliability and test-retest reliability were high. The patients had significantly higher JESS scores than did the healthy people, and higher JESS scores were associated with worse daytime function, as measured with the Pittsburgh Sleep Quality Index.
Conclusions.-In Japan, the JESS provides reliable and valid information on daytime sleepiness. Researchers who use the ESS with other populations should combine their knowledge of local conditions with the results of psychometric tests. (C) 2008 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.sleep.2008.04.015

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記述言語：英語   掲載種別：研究論文（学術雑誌）   出版者・発行元：ELSEVIER SCIENCE BV  

Background: Various Japanese versions of the Epworth Sleepiness Scale (ESS) have been used, but none was developed via standard procedures. Here we report on the construction and testing of the developer-authorized Japanese version of the ESS (JESS).
Methods: Developing the JESS involved translations, back translations, a pilot study, and psychometric testing. We identified questions in the ESS that were difficult to answer or were inappropriate in Japan, proposed possible replacements for those questions, and tested them with analyses based on item response theory (IRT) and classical test theory. The subjects were healthy people and patients with narcolepsy, idiopathic hypersomnia, or obstructive sleep apnea syndrome.
Results: We identified two of our proposed questions as appropriate replacements for two problematic questions in the ESS. The JESS had very few missing data. Internal consistency reliability and test-retest reliability were high. The patients had significantly higher JESS scores than did the healthy people, and higher JESS scores were associated with worse daytime function, as measured with the Pittsburgh Sleep Quality Index.
Conclusions.-In Japan, the JESS provides reliable and valid information on daytime sleepiness. Researchers who use the ESS with other populations should combine their knowledge of local conditions with the results of psychometric tests. (C) 2008 Elsevier B.V. All rights reserved.

DOI： 10.1016/j.sleep.2008.04.015

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その他リンク： http://orcid.org/0000-0003-2293-5918

記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1080/10705500801929718

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記述言語：日本語   出版者・発行元：日本テスト学会  

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記述言語：日本語   出版者・発行元：中部大学  

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.48.0_406

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記述言語：英語   掲載種別：研究論文（学術雑誌）  

DOI： 10.1111/j.1751-9861.2007.00007.x

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.48.0_410

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.48.0_416

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記述言語：日本語   出版者・発行元：名古屋大学大学院教育発達科学研究科心理発達科学専攻「心理発達科学論集」編集委員会  

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総ページ数：402   記述言語：日本語  

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総ページ数：ix, 191p   記述言語：日本語  

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総ページ数：xiii, 344p   記述言語：日本語  

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総ページ数：v, 131p   記述言語：日本語  

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総ページ数：xii, 386p   記述言語：日本語  

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.53.0_533

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.53.0_449

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.53.0_379

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記述言語：英語   掲載種別：研究発表ペーパー・要旨（国際会議）  

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記述言語：英語  

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_1PM113

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_WS080

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_1PM116

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_1PM115

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_1PM112

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

DOI： 10.4992/pacjpa.74.0_1PM114

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記述言語：日本語   出版者・発行元：日本腎臓学会  

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

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記述言語：日本語  

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記述言語：英語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.48.0_96

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記述言語：日本語   出版者・発行元：公益社団法人 日本心理学会  

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記述言語：日本語   出版者・発行元：日本教育心理学会  

DOI： 10.20587/pamjaep.47.0_594

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   出版者・発行元：一般社団法人 日本教育心理学会  

DOI： 10.20587/pamjaep.47.0_572

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   出版者・発行元：The Japanese Psychological Association  

DOI： 10.4992/jjpsy.75.331

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   掲載種別：研究発表ペーパー・要旨（全国大会，その他学術会議）  

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記述言語：日本語   出版者・発行元：名古屋大学  

国立情報学研究所で電子化したコンテンツを使用している。

DOI： 10.18999/nupsych.50.366

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記述言語：日本語   出版者・発行元：名古屋大学大学院教育発達科学研究科  

国立情報学研究所で電子化したコンテンツを使用している。

DOI： 10.18999/nupsych.50.83

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その他リンク： http://hdl.handle.net/2237/3175

記述言語：日本語   出版者・発行元：名古屋大学大学院教育発達科学研究科心理発達科学専攻「心理発達科学論集」編集委員会  

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