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  1. AU="Band, Rebecca"
  2. AU=Pablos Isabel AU=Pablos Isabel
  3. AU="O'Flaherty, Vincent"
  4. AU="Jérémie, Riou"
  5. AU="Ma, Yunshu"
  6. AU="Pu, Junyi"
  7. AU="Benlloch, Sara"
  8. AU="Jay D Evans"
  9. AU=Unger Jean-Pierre
  10. AU="Soday, Lior"
  11. AU="Wan, Xuan"
  12. AU="Camille Fritzell"
  13. AU=Wei Huijun
  14. AU="Levine, Morgan E"
  15. AU="Chen, Yalei"
  16. AU="Rogaeva, Ekaterina" AU="Rogaeva, Ekaterina"
  17. AU="Jain, Ishaan"
  18. AU="Chatelier, Josh"
  19. AU="Passarelli, L."
  20. AU="Marques, R"
  21. AU="Restaino, Valeria"
  22. AU="Wang, Haochen"
  23. AU=Shoib Sheikh
  24. AU=Patel Ishan
  25. AU="Mongioì, Laura M"
  26. AU="Fernández-Pacheco, Borja Camacho"
  27. AU=Waghmare Alpana AU=Waghmare Alpana
  28. AU="Peyre, Marion"
  29. AU=Mulazimoglu L
  30. AU=Roy Satyaki
  31. AU="Li Yuanyuan"
  32. AU=Khan Shehryar
  33. AU=Cole Sarah L
  34. AU="Júnior, Raimundo Nonato Colares Camargo"
  35. AU="Feeney, Judith A"

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  1. Artikel ; Online: The experiences of men on active surveillance for prostate cancer and their significant others: A qualitative synthesis.

    Hughes, Stephanie / Everitt, Hazel / Stuart, Beth / Band, Rebecca

    Psycho-oncology

    2024  Band 33, Heft 4, Seite(n) e6324

    Abstract: Background: Active surveillance (AS) for prostate cancer (PCa) is a monitoring pathway for men with low-grade, slow growing PCa and aims to delay or avoid active treatment by treating only in the case of disease progression. Experiences of this pathway ... ...

    Abstract Background: Active surveillance (AS) for prostate cancer (PCa) is a monitoring pathway for men with low-grade, slow growing PCa and aims to delay or avoid active treatment by treating only in the case of disease progression. Experiences of this pathway vary but living with an untreated cancer can have a negative psychological impact on both the patient and their significant other (SO). Literature suggests partners are the primary source of support for men on AS, and therefore it is important to consider SO experiences alongside those of the patient. To the best of our knowledge this is the first UK-based qualitative review looking specifically at experiences of AS for both men with PCa and their SOs.
    Methods: MEDLINE (Ovid), EMBASE, PsychINFO, CINAHL and Cochrane Library were searched for literature reporting qualitative experiences of AS for PCa for either men on AS or SOs (or both). 2769 records were identified and screened, with 28 meeting the eligibility criteria. Qualitative data were synthesised and included men on AS (n = 428), and SOs (n = 51).
    Results: Experiences of the AS pathway vary but reports of uncertainty and anxiety were present in the accounts of both men on AS and SOs. SOs are intertwined throughout every part of the PCa journey, and couples presented as a unit that were on AS together. Both patients and SOs expressed a need for more support, and highly valued peer support. Despite this finding, men expressed a dislike towards 'support groups'.
    Conclusions: Increased recognition in clinical practice of SO involvement in AS is needed. Further research is required to explore the specific types of support that would be most acceptable to this population to address the unmet support needs uncovered in this review.
    Mesh-Begriff(e) Male ; Humans ; Watchful Waiting ; Prostatic Neoplasms/therapy ; Prostatic Neoplasms/psychology ; Qualitative Research
    Sprache Englisch
    Erscheinungsdatum 2024-01-02
    Erscheinungsland England
    Dokumenttyp Journal Article ; Review
    ZDB-ID 1118536-3
    ISSN 1099-1611 ; 1057-9249
    ISSN (online) 1099-1611
    ISSN 1057-9249
    DOI 10.1002/pon.6324
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  2. Artikel ; Online: Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM).

    Ballard, Lisa Marie / Band, Rebecca / Lucassen, Anneke M

    European journal of human genetics : EJHG

    2023  Band 31, Heft 9, Seite(n) 988–1002

    Abstract: Whilst the finding of heritable susceptibility to disease was once relatively rare, mainstreaming of genetic testing has resulted in a steady increase. Patients are often encouraged to share their genetic test results with relevant relatives, but ... ...

    Abstract Whilst the finding of heritable susceptibility to disease was once relatively rare, mainstreaming of genetic testing has resulted in a steady increase. Patients are often encouraged to share their genetic test results with relevant relatives, but relatives may not receive this information, leaving them without knowledge of their own risk. Therefore, strategies to help communicate such information are important. This review aimed to explore the efficacy of existing interventions to improve the sharing of genetic test results. A synthesis without meta-analysis design was used. A systematic search of Medline, CINAHL, PsychINFO, and AMED was conducted, and five studies were identified worldwide. Data were extracted for each study regarding study aim, participant characteristics, condition, intervention details, comparison, study duration, outcome measures, theory and behaviour change techniques used. Limited efficacy and application of theory was found. Knowledge, motivation and self-efficacy were not increased in any intervention. No gender differences in communication behaviour were encountered in interventions that recruited men and women. Two studies reported an evaluation of acceptability, which showed that the interventions were well received by patients and health professionals. No study reported the involvement of the target population in any phase of intervention development. Given the lack of health psychology-informed interventions in this area of clinical genetics, we recommend genetic health professionals, health psychologists and patients collaborate on all stages of future interventions that involve the cascading of genetic health information within families. We also provide guidance regarding use of theory and intervention elements for future intervention development.
    Mesh-Begriff(e) Male ; Humans ; Female ; Health Personnel ; Patients ; Genetic Testing
    Sprache Englisch
    Erscheinungsdatum 2023-06-21
    Erscheinungsland England
    Dokumenttyp Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 1141470-4
    ISSN 1476-5438 ; 1018-4813
    ISSN (online) 1476-5438
    ISSN 1018-4813
    DOI 10.1038/s41431-023-01400-1
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 3589: Hefte anzeigen Standort:
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  3. Artikel ; Online: Rural influences on the social network dynamics of district nursing services: A qualitative meta-synthesis.

    Gillham, Jack / Vassilev, Ivaylo / Band, Rebecca

    Health science reports

    2021  Band 4, Heft 3, Seite(n) e336

    Abstract: Background and aims: As demands on healthcare services grow, fiscal restrictions place increased emphasis on services outside of traditional healthcare settings. Previous research into long-term-conditions suggests that social network members (including ...

    Abstract Background and aims: As demands on healthcare services grow, fiscal restrictions place increased emphasis on services outside of traditional healthcare settings. Previous research into long-term-conditions suggests that social network members (including weaker ties such as acquaintances, community groups, and healthcare professionals) play a key role in illness management. There is limited knowledge about the engagement of social networks in supporting people who are receiving medical interventions at home. This qualitative metasynthesis explores the work and the interactions between district nurses (DN) and informal network members supporting people who are receiving medical interventions at home and living in rural areas.
    Methods: A search was undertaken on CINAHL, Medline, and PsychINFO for qualitative research articles from 2009 to 2019. Studies that examined DN in rural locations and/or social network support in rural locations were eligible. Fourteen articles were selected.
    Results: Thematic analysis of results and discussion data from the studies resulted in four themes being developed: the development of both transactional and friend-like nurse-patient ties in rural localities, engagement of the wider network in the delivery of good care, blurring of professional boundaries in close community relationships, and issues accessing and navigating formal and informal support in the context of diminishing resources in rural areas.These findings suggest that DNs in rural localities work beyond professional specialties and experience to provide emotional support, help with daily tasks, and build links to communities. There was also evidence that nurses embedded within rural localities developed friend-like relationships with patients, and negotiated with existing support networks and communities to find support for the patient.
    Conclusions: Findings indicated that developing strong links with patients and members of their networks does not automatically translate into positive outcomes for patients, and can be unsustainable, burdensome, and disruptive. DNs developing weak ties with patients and building awareness of the structure of individual networks and local sources of support offers avenues for sustainable and tailored community-based nursing support.
    Sprache Englisch
    Erscheinungsdatum 2021-08-17
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ISSN 2398-8835
    ISSN (online) 2398-8835
    DOI 10.1002/hsr2.336
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  4. Artikel: Planning and developing a web-based intervention for active surveillance in prostate cancer: an integrated self-care programme for managing psychological distress.

    Hughes, Stephanie / Kassianos, Angelos P / Everitt, Hazel A / Stuart, Beth / Band, Rebecca

    Pilot and feasibility studies

    2022  Band 8, Heft 1, Seite(n) 175

    Abstract: Objectives: To outline the planning, development and optimisation of a psycho-educational behavioural intervention for patients on active surveillance for prostate cancer. The intervention aimed to support men manage active surveillance-related ... ...

    Abstract Objectives: To outline the planning, development and optimisation of a psycho-educational behavioural intervention for patients on active surveillance for prostate cancer. The intervention aimed to support men manage active surveillance-related psychological distress.
    Methods: The person-based approach (PBA) was used as the overarching guiding methodological framework for intervention development. Evidence-based methods were incorporated to improve robustness. The process commenced with data gathering activities comprising the following four components: • A systematic review and meta-analysis of depression and anxiety in prostate cancer • A cross-sectional survey on depression and anxiety in active surveillance • A review of existing interventions in the field • A qualitative study with the target audience The purpose of this paper is to bring these components together and describe how they facilitated the establishment of key guiding principles and a logic model, which underpinned the first draft of the intervention.
    Results: The prototype intervention, named PROACTIVE, consists of six Internet-based sessions run concurrently with three group support sessions. The sessions cover the following topics: lifestyle (diet and exercise), relaxation and resilience techniques, talking to friends and family, thoughts and feelings, daily life (money and work) and information about prostate cancer and active surveillance. The resulting intervention has been trialled in a feasibility study, the results of which are published elsewhere.
    Conclusions: The planning and development process is key to successful delivery of an appropriate, accessible and acceptable intervention. The PBA strengthened the intervention by drawing on target-user experiences to maximise acceptability and user engagement. This meticulous description in a clinical setting using this rigorous but flexible method is a useful demonstration for others developing similar interventions. TRIAL REGISTRATION AND ETHICAL APPROVAL: ISRCTN registered: ISRCTN38893965 . NRES Committee South Central - Oxford A. REC reference: 11/SC/0355.
    Sprache Englisch
    Erscheinungsdatum 2022-08-09
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2809935-7
    ISSN 2055-5784
    ISSN 2055-5784
    DOI 10.1186/s40814-022-01124-x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Examining the optimal factors that promote implementation and sustainability of a network intervention to alleviate loneliness in community contexts.

    Ellis, Jaimie / Kinsella, Karina / James, Elizabeth / Cheetham-Blake, Tara / Lambrou, Madeleine / Ciccognani, Alexandra / Rogers, Anne / Band, Rebecca

    Health & social care in the community

    2022  Band 30, Heft 6, Seite(n) e4144–e4154

    Abstract: Community environments have the potential to alleviate loneliness and social isolation as they offer opportunity for sociality and to expand personal social network connections. Implementing a social network intervention in community environments to ... ...

    Abstract Community environments have the potential to alleviate loneliness and social isolation as they offer opportunity for sociality and to expand personal social network connections. Implementing a social network intervention in community environments to connect people to who are at risk of loneliness or social isolation could help alleviate these concerns. However, implementing interventions in community environments is made difficult by the interplay between the community context and intervention. Thus, to support implementation a detailed understanding of the types of community contexts is required. To examine the optimal factors that promote the implementation of a social network designed to alleviate loneliness and social isolation intervention in the community observations, interviews and documentary analysis were conducted. The Consolidated Framework for Implementation Research and a typology of community contexts were used to inform the data analysis and interpret the findings. Key factors were found to affect the implementation of the intervention in the different community contexts. These inter-related factors operated across three domains. Service User Needs affected intervention take up as its suitability varied. The stability of the workforce and nature of everyday work also impacted on implementation. Finally, the fluctuating capacity of organisations and the organisational culture were also influential. No single community environment was found to have all of the optimal factors required for implementation and sustainably. The UK policy agenda of austerity had negatively affected community environments' capacity to deliver such intervention through increasing service user needs and reducing available resources. Trial registration: ISRCTN19193075.
    Mesh-Begriff(e) Humans ; Loneliness ; Social Isolation ; Social Environment
    Sprache Englisch
    Erscheinungsdatum 2022-04-26
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1155902-0
    ISSN 1365-2524 ; 0966-0410
    ISSN (online) 1365-2524
    ISSN 0966-0410
    DOI 10.1111/hsc.13808
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: The role of collective efficacy in long-term condition management: A metasynthesis.

    Vassilev, Ivaylo / Band, Rebecca / Kennedy, Anne / James, Elizabeth / Rogers, Anne

    Health & social care in the community

    2019  Band 27, Heft 5, Seite(n) e588–e603

    Abstract: Social networks have been found to have a valuable role in supporting the management of long-term conditions. However, the focus on the quality and how well self-management interventions work focus on individualised behavioural outcomes such as self- ... ...

    Abstract Social networks have been found to have a valuable role in supporting the management of long-term conditions. However, the focus on the quality and how well self-management interventions work focus on individualised behavioural outcomes such as self-efficacy and there is a need for understanding that focuses on the role of wider collective processes in self-management support. Collective efficacy presents a potentially useful candidate concept in the development and understanding of self-management support interventions. To date it has mainly been utilised in the context of organisations and neighbourhoods related to social phenomena such as community cohesion. Drawing on Bandura's original theorisation this meta-synthesis explores how studies of collective efficacy might illuminate collective elements operating within the personal communities of people with long-term conditions. A qualitative meta-synthesis was undertaken. Studies published between 1998 and 2018 that examined collective efficacy in relation to health and well-being using qualitative and mixed methods was eligible for inclusion. Timing of engagement with others, building trust in the group, and legitimising ongoing engagement with the group arised as central elements of collective efficacy. The two themes forming third order constructs were related to the presence of continuous interaction and ongoing relational work between members of the group. Collective efficacy can develop and be sustained over time in a range of situations where individuals may not have intense relationships with one another and have limited commitment and contact with one another. Extending this to the personal communities of people with long-term conditions it may be the case that collective efficacy enables a number of engagement opportunities which can be oriented towards assisting with support from networks over a sustained length of time. This may include negotiating acceptable connections to resources and activities which in turn may help change existing practice in ways that improve long-term condition management.
    Mesh-Begriff(e) Chronic Disease/psychology ; Chronic Disease/therapy ; Disease Management ; Humans ; Longitudinal Studies ; Self Care/methods ; Self Efficacy ; Self-Management/methods ; Social Networking ; Social Support ; Trust
    Sprache Englisch
    Erscheinungsdatum 2019-06-24
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1155902-0
    ISSN 1365-2524 ; 0966-0410
    ISSN (online) 1365-2524
    ISSN 0966-0410
    DOI 10.1111/hsc.12779
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  7. Artikel ; Online: Development of a measure of collective efficacy within personal networks: A complement to self-efficacy in self-management support?

    Band, Rebecca / James, Elizabeth / Culliford, David / Dimitrov, Borislav / Kennedy, Anne / Rogers, Anne / Vassilev, Ivaylo

    Patient education and counseling

    2019  Band 102, Heft 7, Seite(n) 1389–1396

    Abstract: Objective: To develop and evaluate the Collective Efficacy of Networks (CENS) questionnaire to measure perceived collective efficacy within personal social networks.: Methods: A mixed methods approach was used, guided by theory and with extensive ... ...

    Abstract Objective: To develop and evaluate the Collective Efficacy of Networks (CENS) questionnaire to measure perceived collective efficacy within personal social networks.
    Methods: A mixed methods approach was used, guided by theory and with extensive input from adults with long-term conditions who completed the initial questionnaire (n = 78) with test-retest assessed at 2 weeks (n = 68). A second sample (n = 85) completed a postal questionnaire including CENS, theoretically linked constructs (self-efficacy, social support) and health outcomes (loneliness, mental and physical health).
    Results: Principal components analysis demonstrated a two-factor structure with 12-items selected to represent Network responsiveness (8 items, Cronbach's alpha = 0.896) and Access to collective efficacy (4 items, Cronbach's alpha = .773). Good test-retest reliability was established for both subscales (r
    Conclusion: The CENS is an acceptable and psychometrically robust measure of collective efficacy in personal social networks.
    Practice implications: Measuring collective efficacy with self-efficacy will provide useful information for researchers and policymakers interested in capacity for self-management and social determinants of behaviour change.
    Mesh-Begriff(e) Adult ; Aged ; Female ; Humans ; Male ; Middle Aged ; Principal Component Analysis ; Psychometrics ; Self Efficacy ; Self-Management ; Social Networking ; Surveys and Questionnaires
    Sprache Englisch
    Erscheinungsdatum 2019-03-02
    Erscheinungsland Ireland
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Validation Study
    ZDB-ID 605590-4
    ISSN 1873-5134 ; 0738-3991
    ISSN (online) 1873-5134
    ISSN 0738-3991
    DOI 10.1016/j.pec.2019.02.026
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    Zs.A 1465: Hefte anzeigen Standort:
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  8. Artikel ; Online: Exploring the lived experience of Long Covid in black and minority ethnic groups in the UK: Protocol for qualitative interviews and art-based methods.

    Smyth, Nina / Alwan, Nisreen A / Band, Rebecca / Chaudhry, Ashish / Chew-Graham, Carolyn A / Gopal, Dipesh / Jackson, Monique / Kingstone, Tom / Wright, Alexa / Ridge, Damien

    PloS one

    2022  Band 17, Heft 10, Seite(n) e0275166

    Abstract: Some people experience prolonged symptoms following an acute COVID-19 infection including fatigue, chest pain and breathlessness, headache and cognitive impairment. When symptoms persist for over 12 weeks following the initial infection, and are not ... ...

    Abstract Some people experience prolonged symptoms following an acute COVID-19 infection including fatigue, chest pain and breathlessness, headache and cognitive impairment. When symptoms persist for over 12 weeks following the initial infection, and are not explained by an alternative diagnosis, the term post-COVID-19 syndrome is used, or the patient-defined term of Long Covid. Understanding the lived experiences of Long Covid is crucial to supporting its management. However, research on patient experiences of Long Covid is currently not ethnically diverse enough. The study aim is to explore the lived experience of Long Covid, using qualitative interviews and art-based methods, among people from ethnically diverse backgrounds (in the UK), to better understand wider systems of support and healthcare support needs. Co-created artwork will be used to build on the interview findings. A purposive sampling strategy will be used to gain diverse experiences of Long Covid, sampling by demographics, geographic locations and experiences of Long Covid. Individuals (aged >18 years) from Black and ethnic minority backgrounds, who self-report Long Covid symptoms, will be invited to take part in a semi-structured interview. Interviews will be analysed thematically. A sub-sample of participants will be invited to co-create visual artwork to further explore shared narratives of Long Covid, enhance storytelling and increase understanding about the condition. A patient advisory group, representing diversity in ethnicity and experiences of Long Covid, will inform all research stages. Stakeholder workshops with healthcare professionals and persons, systems or networks important to people's management of Long Covid, will advise on the integration of findings to inform management of Long Covid. The study will use patient narratives from people from diverse ethnic backgrounds, to raise awareness of Long Covid and help inform management of Long Covid and how wider social systems and networks may inform better healthcare service access and experiences.
    Mesh-Begriff(e) COVID-19/complications ; COVID-19/epidemiology ; Ethnicity ; Humans ; Minority Groups ; Qualitative Research ; United Kingdom/epidemiology
    Sprache Englisch
    Erscheinungsdatum 2022-10-03
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0275166
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Patient Outcomes in Association With Significant Other Responses to Chronic Fatigue Syndrome: A Systematic Review of the Literature.

    Band, Rebecca / Wearden, Alison / Barrowclough, Christine

    Clinical psychology : a publication of the Division of Clinical Psychology of the American Psychological Association

    2015  Band 22, Heft 1, Seite(n) 29–46

    Abstract: Social processes have been suggested as important in the maintenance of chronic fatigue syndrome (also known as myalgic encephalomyelitis; CFS/ME), but the specific role of close interpersonal relationships remains unclear. We reviewed 14 articles ... ...

    Abstract Social processes have been suggested as important in the maintenance of chronic fatigue syndrome (also known as myalgic encephalomyelitis; CFS/ME), but the specific role of close interpersonal relationships remains unclear. We reviewed 14 articles investigating significant other responses to close others with CFS/ME and the relationships between these responses and patient outcomes. Significant other beliefs attributing patient responsibility for the onset and ongoing symptoms of CFS/ME were associated with increased patient distress. Increased symptom severity, disability, and distress were also associated with both solicitous and negative significant other responses. Specific aspects of dyadic relationship quality, including high Expressed Emotion, were identified as important. We propose extending current theoretical models of CFS/ME to include two potential perpetuating interpersonal processes; the evidence reviewed suggests that the development of significant other-focused interventions may also be beneficial.
    Sprache Englisch
    Erscheinungsdatum 2015-03-14
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1484850-8
    ISSN 1468-2850 ; 0969-5893
    ISSN (online) 1468-2850
    ISSN 0969-5893
    DOI 10.1111/cpsp.12093
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Assessing the reliability of the five minute speech sample against the Camberwell family interview in a chronic fatigue syndrome sample.

    Band, Rebecca / Chadwick, Ella / Hickman, Hannah / Barrowclough, Christine / Wearden, Alison

    Comprehensive psychiatry

    2016  Band 67, Seite(n) 9–12

    Abstract: Purpose: The current study aimed to examine the reliability of the Five Minute Speech Sample (FMSS) for assessing relative Expressed Emotion (EE) compared with the Camberwell Family Interview (CFI) in a sample of relatives of adult patients with Chronic ...

    Abstract Purpose: The current study aimed to examine the reliability of the Five Minute Speech Sample (FMSS) for assessing relative Expressed Emotion (EE) compared with the Camberwell Family Interview (CFI) in a sample of relatives of adult patients with Chronic Fatigue Syndrome (CFS).
    Method: 21 relatives were recruited and completed both assessments. The CFI was conducted first for all participants, with the FMSS conducted approximately one month later. Trained raters independently coded both EE measures; high levels of rating reliability were established for both measures. Comparisons were conducted for overall EE status, emotional over-involvement (EOI) and criticism.
    Findings: The distribution of high and low-EE was equivalent across the two measures, with the FMSS correctly classifying EE is 71% of cases (n=15). The correspondence between the FMSS and CFI ratings was found to be non-significant for all categorical variables. However, the number of critical comments made by relatives during the FMSS significantly correlated with the number of critical comments made during the CFI. The poorest correspondence between the measures was observed for the EOI dimension.
    Conclusion: The findings suggest that the FMSS may be a useful screening tool for identifying high-EE, particularly criticism, within a sample of relatives of patients with CFS. However, the two measures should not be assumed equivalent, and the CFI should be used where possible, particularly with respect to understanding EOI.
    Mesh-Begriff(e) Adult ; Expressed Emotion ; Family/psychology ; Fatigue Syndrome, Chronic/diagnosis ; Fatigue Syndrome, Chronic/psychology ; Female ; Humans ; Interviews as Topic ; Male ; Middle Aged ; Personality Assessment/statistics & numerical data ; Psychometrics ; Reproducibility of Results ; Speech
    Sprache Englisch
    Erscheinungsdatum 2016-05
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 127556-2
    ISSN 1532-8384 ; 0010-440X
    ISSN (online) 1532-8384
    ISSN 0010-440X
    DOI 10.1016/j.comppsych.2016.02.006
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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