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  • 1
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Vox Sanguinis Vol. 114, No. 2 ( 2019-02), p. 154-161
    In: Vox Sanguinis, Wiley, Vol. 114, No. 2 ( 2019-02), p. 154-161
    Abstract: Previous studies observed a transient increase in well‐being in about one‐third of regular donors after blood donation. In addition, personal contact with donors after donation seems to increase return rates. We were interested whether changes in well‐being and/or personal contact after the first donation impact return rates of first‐time donors ( FTD s). Materials and methods First‐time donors were randomized to a questionnaire group ( QG ), in which questionnaires assessing the well‐being had to be filled in, or a control group ( CG ), which was not contacted with a questionnaire. The QG had to complete the same questionnaire three times at the day of the first donation and then four times over an 8‐week period with reminding calls by the study coordinator. Return rates of participants were followed for 12 months. Results A total of 102 FTD s participated in the QG and 115 in the CG . Changes in well‐being after the first donation had minimal impact on the return rates. In contrast, contacting FTD s after their first donation had a significant impact on the return rate of male donors (89·2% in the QG vs. 58·3% in the CG ; P  = 0·001). Females showed no significant difference in return rates between both groups ( P  = 0·32). Conclusion The well‐being of FTD s had no influence on their return rate. The intervention of regular contacts during a research project follow‐up resulted in an increased return rate of male but not of female FTD s. The pronounced difference of the impact of this intervention between male and female donors requires further studies.
    Type of Medium: Online Resource
    ISSN: 0042-9007 , 1423-0410
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 1483587-3
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  • 2
    In: International Journal of Environmental Research and Public Health, MDPI AG, Vol. 18, No. 19 ( 2021-10-05), p. 10454-
    Abstract: Quality of life (QoL) is a core patient-reported outcome in healthcare research, alongside primary clinical outcomes. A conceptual, operational, and psychometric elaboration of QoL in the context of TM is needed, because standardized instruments to assess QoL do not sufficiently represent essential aspects of intended outcomes of telemedical applications (TM). The overall aim is to develop an instrument that can adequately capture QoL in TM. For that purpose, an extended working model of QoL will be derived. Subsequently, an instrument will be developed and validated that captures those aspects of QoL that are influenced by TM. The initial exploratory study section includes (a) a systematic literature review, (b) a qualitative survey for concept elicitation, and (c) pre-testings using cognitive debriefings with patients and an expert workshop. The second quantitative section consists of an online expert survey and two patient surveys for piloting and validation of the newly developed instrument. The resulting questionnaire will assess central experiences of patients regarding telemedical applications and its impact on QoL more sensitively. Its use as adjunct instrument will lead to a more appropriate evaluation of TM and contribute to the improvement of care tailored to patients’ individual needs.
    Type of Medium: Online Resource
    ISSN: 1660-4601
    Language: English
    Publisher: MDPI AG
    Publication Date: 2021
    detail.hit.zdb_id: 2175195-X
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  • 3
    In: Health and Quality of Life Outcomes, Springer Science and Business Media LLC, Vol. 19, No. 1 ( 2021-07-05)
    Abstract: Although telemedical applications are increasingly used in the area of both mental and physical illness, there is no quality of life (QoL) instrument that takes into account the specific context of the healthcare setting. Therefore, the aim of this study was to determine a concept of quality of life in telemedical care to inform the development of a setting-sensitive patient-reported outcome measure. Methods Overall, 63 semi-structured single interviews and 15 focus groups with 68 participants have been conducted to determine the impact of telemedical care on QoL. Participants were patients with chronic physical or mental illnesses, with or without telemedicine supported healthcare as well as telemedical professionals. Mayring's content analysis approach was used to encode the qualitative data using MAXQDA software. Results The majority of aspects that influence the QoL of patients dealing with chronic conditions or mental illnesses could be assigned to an established working model of QoL. However, some aspects that were considered important (e. g. perceived safety) were not covered by the pre-existing domains. For that reason, we re-conceptualized the working model of QoL and added a sixth domain, referred to as healthcare-related domain . Conclusion Interviewing patients and healthcare professionals brought forth specific aspects of QoL evolving in telemedical contexts. These results reinforce the assumption that existing QoL measurements lack sensitivity to assess the intended outcomes of telemedical applications. We will address this deficiency by a telemedicine-related re-conceptualization of the assessment of QoL and the development of a suitable add-on instrument based on the resulting category system of this study.
    Type of Medium: Online Resource
    ISSN: 1477-7525
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2098765-1
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  • 4
    In: Quality of Life Research, Springer Science and Business Media LLC, Vol. 32, No. 11 ( 2023-11), p. 3223-3234
    Abstract: A setting-sensitive instrument for assessing Quality of Life (QoL) in Telemedicine (TM) was unavailable. To close this gap, a content-valid “add-on” measure was developed. In parallel, a brief index was derived featuring six items that summarise the main content of the multidimensional assessment. After pre- and pilot-testing, the psychometric performance of the final measures was investigated in an independent validation study. Methods The questionnaires were applied along with other standardised instruments of similar concepts as well as associated, yet disparate concepts for validation purposes. The sample consisted of patients with depression or heart failure, with or without TM ( n  = 200). Data analyses were aimed at calculating descriptive statistics and testing the psychometric performance on item, scale, and instrument level, including different types of validity and reliability. Results The proposed factor structure of the multidimensional Tele-QoL measure has been confirmed. Reliability coefficients for internal consistency, split-half, and test-retest reliability of the subscales and index reached sufficient values. The Tele-QoL subscales and the index demonstrated Rasch scalability. Validity of both instruments can be assumed. Evidence for discriminant construct validity was provided. Known-groups validity was indicated by respective score differences for various classes of disease severity. Conclusion Both measures show convincing psychometric properties. The final multidimensional Tele-QoL assessment consists of six outcome scales and two impact scales assessing (un-)intended effects of TM on QoL. In addition, the Tele-QoL index provides a short alternative for outcome assessment. The Tele-QoL measures can be used as complementary modules to existing QoL instruments capturing healthcare-related aspects of QoL from the patients’ perspective.
    Type of Medium: Online Resource
    ISSN: 0962-9343 , 1573-2649
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2023
    detail.hit.zdb_id: 2008960-0
    SSG: 5,1
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  • 5
    Online Resource
    Online Resource
    FapUNIFESP (SciELO) ; 2017
    In:  Estudos de Psicologia (Campinas) Vol. 34, No. 3 ( 2017-09), p. 331-344
    In: Estudos de Psicologia (Campinas), FapUNIFESP (SciELO), Vol. 34, No. 3 ( 2017-09), p. 331-344
    Abstract: Resumo Intervenções de eSaúde foram propostas para superar obstáculos relacionados com baixas taxas de adesão, baixa acessibilidade e custos elevados. Devido à diversidade de intervenções existentes, este estudo objetivou conduzir uma revisão abrangente das intervenções parentais para apoiar os pais nas tarefas relacionadas com a saúde e a doença dos filhos. A revisão abrangente encontrou 119 programas baseados em tecnologia, tanto direcionados para objetivos universais e preventivos, quanto para a gestão e adaptação a condições de saúde graves, crônicas ou agudas. Uma diversidade de aplicações foi utilizada de forma criativa em intervenções parentais. A maioria dos programas utiliza metodologias psicológicas baseadas em evidências para promover a autogestão, treinar habilidades parentais específicas e oferecer feedback personalizado e apoio social. São necessárias mais investigações para avaliar a contribuição da Internet e das aplicações móveis para aumentar a eficácia das intervenções parentais relacionadas com a saúde e a divulgação de programas empiricamente validados.
    Type of Medium: Online Resource
    ISSN: 0103-166X
    Language: Unknown
    Publisher: FapUNIFESP (SciELO)
    Publication Date: 2017
    detail.hit.zdb_id: 2840625-4
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  • 6
    Online Resource
    Online Resource
    MDPI AG ; 2021
    In:  International Journal of Environmental Research and Public Health Vol. 18, No. 8 ( 2021-04-16), p. 4238-
    In: International Journal of Environmental Research and Public Health, MDPI AG, Vol. 18, No. 8 ( 2021-04-16), p. 4238-
    Abstract: It is crucial to provide updated knowledge about blood (non-)donors, as it is necessary to design targeted interventions with the aim of retaining blood donors and thus contributing to a functioning health system. This study investigates the prevalence and socio-demographic patterning of lifetime blood donation, assessing blood donation intention within the next 12 months and exploring personal motives and deterrents of blood donation qualitatively in the German population. A face-to-face cross-sectional survey with 2531 respondents was conducted, representative of the German population in terms of age, gender, and residency. Closed as well as open questions were asked. Qualitative content analysis was used for coding the qualitative material. Basic descriptive statistics were conducted to address our research questions. More than one-third of the participants reported that they have donated blood at least once in their lifetime. Motives and deterrents were assigned to 10 domains with 50 main categories and 65 sub-categories. The most frequently stated motives for blood donation were “altruism”, “social responsibility”, and “charity”, whereas the most frequently stated deterrents were “health status”, “age”, and “lack of time”. This study provides information to tailor recruitment and reactivation strategies to address donors at different career steps—from non-donor to loyal donor.
    Type of Medium: Online Resource
    ISSN: 1660-4601
    Language: English
    Publisher: MDPI AG
    Publication Date: 2021
    detail.hit.zdb_id: 2175195-X
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  • 7
    In: Transfusion Medicine and Hemotherapy, S. Karger AG, Vol. 48, No. 4 ( 2021), p. 220-227
    Abstract: 〈 b 〉 〈 i 〉 Introduction: 〈 /i 〉 〈 /b 〉 To maintain a sufficient donor pool, deferred first-time donors (FTD) should be motivated to return for blood donation. This pilot study investigates how deferral affects momentary mood, satisfaction with the donation process, and subsequent return behavior to examine their potential for motivating (deferred) FTD. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 All of the subjects ( 〈 i 〉 n 〈 /i 〉 = 96) completed a first questionnaire (A1) before pre-donation assessment. Deferred FTD ( 〈 i 〉 n 〈 /i 〉 = 22) were asked to complete a second questionnaire (A2) immediately after deferral, while non-deferred FTD ( 〈 i 〉 n 〈 /i 〉 = 74) filled in the second questionnaire (A3) after blood donation. The impact of deferral, momentary mood, and satisfaction with the donation process on return behavior within 12 months was tested by calculating two path analyses, controlling for sex and age. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Mood ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.001) and satisfaction with social aspects of the donation process ( 〈 i 〉 p 〈 /i 〉 = 0.01) were decreased after deferral. Deferred FTD were less likely than non-deferred FTD to return to the blood donation center within 12 months (60.8 vs. 36.4%; 〈 i 〉 p 〈 /i 〉 = 0.043). However, path analyses revealed that deferral effects on mood and satisfaction were not connected to return behavior. Instead, age had a significant influence on return behavior ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.05) such that, overall, non-returning FTD were older than returning FTD, regardless of their deferral status. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Our findings suggest that mood and satisfaction with the donation process are directly affected by deferral but not clearly responsible for low return rates. It seems promising to embed these variables in established health behavior models in further studies to increase the return rates of deferred FTD.
    Type of Medium: Online Resource
    ISSN: 1660-3796 , 1660-3818
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2021
    detail.hit.zdb_id: 2100533-3
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  • 8
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 2018
    In:  Transfusionsmedizin - Immunhämatologie, Hämotherapie, Immungenetik, Zelltherapie Vol. 8, No. 01 ( 2018-02), p. 24-32
    In: Transfusionsmedizin - Immunhämatologie, Hämotherapie, Immungenetik, Zelltherapie, Georg Thieme Verlag KG, Vol. 8, No. 01 ( 2018-02), p. 24-32
    Abstract: Das derzeitige Verhältnis von Vollblutspendern und -empfängern 1 wird in Zukunft weiter aus dem Gleichgewicht geraten: Der demografische Wandel und die Zunahme von Spenderausschlusskriterien führen zu einer Reduktion potenzieller Vollblutspender, während der Bedarf an Blutprodukten weiterhin steigt. Aus diesem Grund wird die Rekrutierung von Neuspendern allein nicht ausreichend sein, um einen stabilen Spenderpool zu erhalten. Um die Versorgung mit Blutprodukten zukünftig trotzdem gewährleisten zu können, rücken alternative Interventionsoptionen zunehmend in den Vordergrund. Der vorliegende Artikel zeigt psychologische Optionen auf, die auf die Begrenzung des drohenden Blutkonservenmangels abzielen, und richtet dabei den Fokus auf die wichtigste Ressource 2 – den Blutspender. Dafür sollen ergänzende Reaktivierungsmaßnahmen, die der Initiierung eines erneuten Blutspendeversuchs dienen, erläutert und diskutiert werden. Anschließend wird das Konstrukt der Spenderloyalität als eine aussichtsreiche Möglichkeit der langfristigen Spenderbindung vorgestellt.
    Type of Medium: Online Resource
    ISSN: 2191-8805 , 2191-8813
    Language: German
    Publisher: Georg Thieme Verlag KG
    Publication Date: 2018
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