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  1. AU="Jenkinson, Crispin"
  2. AU="Hernández-Huérfano, Emilio Ernesto"
  3. AU="Conowall, Peter"
  4. AU="Nesan, Daniel"
  5. AU="Ueda, Takashi"
  6. AU="Yuan, Jiacheng"
  7. AU="Kahama, C B"
  8. AU="D’Alessio, Roberto"
  9. AU="Reuhl, Kenneth"
  10. AU="Seeleman, Conny"
  11. AU="Delaquis, Pascal"
  12. AU="Bommineni, Gopal R"
  13. AU="Kuhn, Cynthia M."
  14. AU="Olson, Jason C"
  15. AU="Buchholz, V."
  16. AU="Urquhart, Bradley L"
  17. AU="Ezaki, Kazune"
  18. AU="Choi, Jong Hyun"
  19. AU="Xie, Qiaowei"
  20. AU=Rojas-Marte G AU=Rojas-Marte G
  21. AU="Belli, A"
  22. AU="Moolman, M Charl"
  23. AU="Mazzoni, Stefania"
  24. AU=Stryjewski Martin E
  25. AU=Vallon Volker AU=Vallon Volker
  26. AU="Knowland, K E"
  27. AU="Beker, M. G."

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Treffer 1 - 10 von insgesamt 162

Suchoptionen

  1. Buch: Evolutionary thinking in medicine

    Alvergne, Alexandra / Jenkinson, Crispin / Faurie, Charlotte

    from research to policy and practice

    (Advances in the evolutionary analysis of human behaviour)

    2016  

    Verfasserangabe Alexandra Alvergne, Crispin Jenkinson, Charlotte Faurie, editors
    Serientitel Advances in the evolutionary analysis of human behaviour
    Sprache Englisch
    Umfang xiv, 382 Seiten, Illustrationen, Diagramme
    Verlag Springer
    Erscheinungsort Cham
    Erscheinungsland Schweiz
    Dokumenttyp Buch
    HBZ-ID HT019007817
    ISBN 978-3-319-29714-9 ; 3-319-29714-7 ; 9783319297163 ; 3319297163
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  2. Buch: Assessment and evaluation of health and medical care

    Jenkinson, Crispin

    a methods text

    1997  

    Verfasserangabe ed. by Crispin Jenkinson
    Schlagwörter Outcome Assessment (Health Care) ; Health Services Research / methods ; Epidemiologic Methods
    Sprache Englisch
    Umfang VIII, 189 S.
    Verlag Open University Press
    Erscheinungsort Buckingham u.a.
    Erscheinungsland Vereinigtes Königreich
    Dokumenttyp Buch
    HBZ-ID HT007922181
    ISBN 0-335-19706-x ; 0-335-19705-1 ; 978-0-335-19706-x4 ; 978-0-335-19705-7
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  3. Buch: The UK SF-36

    Jenkinson, Crispin

    an analysis and interpretation manual ; a guide to health status measurement with particular reference to the short form 36 health survey

    1996  

    Titelvarianten The UK SF 36
    Verfasserangabe Crispin Jenkinson
    Sprache Englisch
    Umfang 65 S.
    Verlag Health Services Research Unit, Dep. of Public Health and Primary Care, Univ. of Oxford
    Erscheinungsort Oxford
    Erscheinungsland Vereinigtes Königreich
    Dokumenttyp Buch
    HBZ-ID HT013028424
    ISBN 1-874551-05-7 ; 978-1-874551-05-8
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  4. Buch: Measuring health and medical outcomes

    Jenkinson, Crispin

    (SRT ; 3)

    1994  

    Verfasserangabe ed. by Crispin Jenkinson
    Serientitel SRT ; 3
    Social research today
    Überordnung Social research today
    Schlagwörter Health Surveys ; Therapieerfolg ; Lebensqualität ; Bewertung ; Gesundheitsstörung
    Schlagwörter Wertansatz ; Wertung ; Wertermittlung ; Leben ; Gesundheit ; Körperliche Beschwerden ; Beschwerden ; Bagatellkrankheit ; Gesundheitsbeeinträchtigung ; Geringfügige Gesundheitsstörung ; Therapie ; Behandlungserfolg ; Heilungserfolg ; Heilerfolg
    Sprache Englisch
    Umfang VIII, 215 S. : Ill., graph. Darst.
    Verlag UCL Press
    Erscheinungsort London
    Erscheinungsland Vereinigtes Königreich
    Dokumenttyp Buch
    HBZ-ID HT006503116
    ISBN 1-85728-083-0 ; 1-85728-084-9 ; 978-1-85728-083-8 ; 978-1-85728-084-5
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  5. Buch: Quality of life measurement in neurodegenerative and related conditions

    Jenkinson, Crispin / Peters, Michele / Bromberg, Mark B.

    2011  

    Verfasserangabe ed. by Crispin Jenkinson ; Michele Peters ; Mark B. Bromberg
    Schlagwörter Nervous System Diseases ; Outcome Assessment (Health Care) ; Quality of Life
    Sprache Englisch
    Umfang XII, 194 S. : Ill.
    Verlag Cambridge Univ. Press
    Erscheinungsort Cambridge u.a.
    Erscheinungsland Vereinigtes Königreich
    Dokumenttyp Buch
    HBZ-ID HT016722358
    ISBN 978-0-521-82901-4 ; 0-521-82901-1
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  6. Artikel ; Online: Carers using assistive technology in dementia care at home: a mixed methods study.

    Sriram, Vimal / Jenkinson, Crispin / Peters, Michele

    BMC geriatrics

    2022  Band 22, Heft 1, Seite(n) 490

    Abstract: Introduction: Informal carers support persons with dementia to live at home, even with deteriorating physical, social and cognitive issues. This study aims to examine the experiences and impact of Assistive Technology (AT) on carers, providing care for ... ...

    Abstract Introduction: Informal carers support persons with dementia to live at home, even with deteriorating physical, social and cognitive issues. This study aims to examine the experiences and impact of Assistive Technology (AT) on carers, providing care for a person with dementia.
    Methods: This is an explanatory sequential mixed methods study. The quantitative phase was an online and postal survey using the Carers Assistive Technology Experience Questionnaire and Short Form-12 (SF-12) questionnaire, with carers of persons with dementia in the UK, who used AT. The qualitative phase involved in-depth telephone interviews with a purposive sample of survey respondents and was analysed using hermeneutic phenomenology to develop, compare and explain the findings of the survey.
    Results: The survey included data from 201 carers. Smartphones (45.5%) and tablet computers (45.0%) were the most frequently used AT. Multiple AT were used in the care of persons with dementia predominantly for safety (78.5%), communication (66.0%), and reminders (62.5%). The SF-12 indicated that carers in the 46-65 age group and carers who were not extremely satisfied with AT had lower mental component scores whilst carers who lived with the person with dementia and older carers had lower physical component scores. Twenty-three carers participated in the interviews, and 5 themes with 14 sub-themes were identified. The interviews helped confirm data from the survey on the impact of AT on the physical, mental and social wellbeing of the carers. It helped describe reasons for satisfaction with AT; how AT was used in daily life and strengthened caring relationships and how wider support systems enhanced the care of a person with dementia using AT.
    Conclusions: This study describes the use of AT in the real-world context. AT supplements the care provided to people with dementia in the community. Appropriate use, access to AT and abilities of the carer can enhance the support provided through AT to both carers and the person with dementia.
    Mesh-Begriff(e) Caregivers/psychology ; Communication ; Dementia/psychology ; Dementia/therapy ; Humans ; Self-Help Devices ; Surveys and Questionnaires
    Sprache Englisch
    Erscheinungsdatum 2022-06-08
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2059865-8
    ISSN 1471-2318 ; 1471-2318
    ISSN (online) 1471-2318
    ISSN 1471-2318
    DOI 10.1186/s12877-022-03167-4
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Commentary on Long-term Effectiveness of Adjuvant Treatment in Parkinson Disease-Reply.

    Gray, Richard / Jenkinson, Crispin / Clarke, Carl E

    JAMA neurology

    2022  Band 79, Heft 7, Seite(n) 726–727

    Mesh-Begriff(e) Chemotherapy, Adjuvant ; Humans ; Parkinson Disease/drug therapy
    Sprache Englisch
    Erscheinungsdatum 2022-06-27
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Comment
    ZDB-ID 2702023-X
    ISSN 2168-6157 ; 2168-6149
    ISSN (online) 2168-6157
    ISSN 2168-6149
    DOI 10.1001/jamaneurol.2022.1604
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: The development of a patient reported outcome measure for fatigue and breathlessness for patients with chronic heart failure (OxFAB).

    Walthall, Helen / Strickland, Louise H / Jenkinson, Crispin

    Heart & lung : the journal of critical care

    2022  Band 58, Seite(n) 116–124

    Abstract: Background: Fatigue and breathlessness are the two most common and distressing symptoms for patients with chronic heart failure. They affect a patient's quality of life and ability to undertake activities of daily living. Currently there are no symptom ... ...

    Abstract Background: Fatigue and breathlessness are the two most common and distressing symptoms for patients with chronic heart failure. They affect a patient's quality of life and ability to undertake activities of daily living. Currently there are no symptom specific measures for fatigue and breathlessness available or developed and validated for use with this patient group and no questionnaire that incorporates both symptoms into one measure.
    Objective: To develop a patient-reported outcome measure for patients with chronic heart failure for their fatigue and breathlessness symptoms.
    Methods: A three-staged, approach was used. In stage One in-depth qualitative patient-interviews on factors of fatigue and breathlessness in chronic heart failure were undertaken to provide question themes. Items from these interviews were generated and pilot questionnaires developed and tested. In Stage Two, exploratory factor analysis with item reduction and final testing of the questionnaire was performed. Stage Three involved validation testing.
    Results: In Stage One, issues raised in interviews (n = 25) were used to generate items. Pilot questionnaires were developed and tested. Items were refined in the context of cognitive debrief interviews (n = 7) for possible inclusion in the final measure. Final testing of questionnaire properties with item reduction was carried out in Stage Two (n = 112). Validity and reliability were assessed in Stage Three (n = 96). Psychometric testing showed positive results, in internal consistency (Cronbach's alpha ranging from 0.8 to 0.94) and test-retest (no difference in means), content validity and relevance to patients.
    Conclusions: This questionnaire could be useful in the assessment of fatigue and breathlessness in patients living with chronic heart failure.
    Mesh-Begriff(e) Humans ; Quality of Life ; Activities of Daily Living ; Reproducibility of Results ; Chronic Disease ; Dyspnea ; Surveys and Questionnaires ; Fatigue ; Patient Reported Outcome Measures ; Heart Failure/psychology ; Psychometrics/methods
    Sprache Englisch
    Erscheinungsdatum 2022-12-06
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 193129-5
    ISSN 1527-3288 ; 0147-9563
    ISSN (online) 1527-3288
    ISSN 0147-9563
    DOI 10.1016/j.hrtlng.2022.11.018
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Test-retest reliability of the PDQ-Carer.

    Morley, David / Dummett, Sarah / Kelly, Laura / Jenkinson, Crispin

    Parkinsonism & related disorders

    2022  Band 102, Seite(n) 16–18

    Abstract: Introduction: The PDQ-Carer is a 29-item measure of health-related quality of life (QoL) for use with carers of people with Parkinson's (PwP). The measure produces a profile of scores across four domains. Previous validation data indicates that the ... ...

    Abstract Introduction: The PDQ-Carer is a 29-item measure of health-related quality of life (QoL) for use with carers of people with Parkinson's (PwP). The measure produces a profile of scores across four domains. Previous validation data indicates that the measure possesses sound psychometric properties in terms of validity and internal consistency. An additional important attribute of any measure is test-retest reliability, i.e. the ability to provide stable results over time, presuming that there has been no change in the status of the construct being measured. To date, no assessment of the test-retest reliability of the PDQ-Carer has been undertaken.
    Methods: Carers of PwP were recruited via Parkinson's UK. Participants completed the PDQ-Carer online on two occasions, two weeks apart. On second administration participants answered an additional question asking how much, if at all, their QoL had changed over the two week period. Subsequent analyses focused on those carers who reported no change in their QoL.
    Results: At first administration 142 carers fully completed the PDQ-Carer and at second administration 104 participants with no missing data responded. Seventy four of these participants (71.2%) reported no change in QoL and thus went forward to the final analysis. Intraclass correlation coefficients for each domain were calculated as follows: Social and Personal Activities .97; Anxiety and Depression .95; Self-Care .96; Stress .95 CONCLUSION: Results indicate that the PDQ-Carer demonstrates sound test-retest reliability and can be confidently used by researchers who wish to incorporate it in studies of carers of PwP.
    Mesh-Begriff(e) Caregivers ; Humans ; Parkinson Disease ; Psychometrics ; Quality of Life ; Reproducibility of Results ; Surveys and Questionnaires
    Sprache Englisch
    Erscheinungsdatum 2022-07-22
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1311489-x
    ISSN 1873-5126 ; 1353-8020
    ISSN (online) 1873-5126
    ISSN 1353-8020
    DOI 10.1016/j.parkreldis.2022.07.010
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Buch: Health status measurement

    Jenkinson, Crispin / Mcgee, Hannah M.

    a brief but critical introduction

    1998  

    Verfasserangabe Crispin Jenkinson and Hannah McGee
    Sprache Englisch
    Umfang 98 S.
    Verlag Radcliffe Med. Press
    Erscheinungsort Abingdon, Oxon
    Erscheinungsland Vereinigtes Königreich
    Dokumenttyp Buch
    Anmerkung Includes bibliographies and index
    HBZ-ID HT009855330
    ISBN 1-85775-228-7 ; 978-1-85775-228-1
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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