The experience of long-term hospital follow-up for women who have suffered early stage gynecological cancer: a qualitative interview study

1999 ◽  
Vol 9 (6) ◽  
pp. 491-496 ◽  
Author(s):  
E.J. Bradley ◽  
M.K. Pitts ◽  
C.W.E. Redman ◽  
E. Calvert
2019 ◽  
pp. 003022281985614
Author(s):  
Ditte A. Winther-Lindqvist ◽  
Ida O. Larsen

This article explores the relationship between grief and best friendship (BF) dynamics among adolescent girls. Based on a qualitative interview study with 10 Danish girls, findings suggest that bereavement affects friendship dynamics in ways that challenge the by-standing friend in succeeding with being and staying supportive. Through a thematic analysis, we identify 12 themes that cut across the case stories, all of which testify to the difficulties bereavement represent to friendship quality and maintenance. Among other issues, it seems like grief is contagious and the bereaved friend changes her way of responding to the by-standing friend in ways that disturb expectations, values, and virtues of BF among girls in adolescence. The general categories found to be characteristic for long-term BFs, that is, positivity, supportiveness, openness, and interaction are all affected by bereavement in adolescent BFs among girls.


BJGP Open ◽  
2020 ◽  
Vol 4 (5) ◽  
pp. bjgpopen20X101092
Author(s):  
Vincent A van Vugt ◽  
Anja JThCM de Kruif ◽  
Johannes C van der Wouden ◽  
Henriëtte E van der Horst ◽  
Otto R Maarsingh

BackgroundInternet-based vestibular rehabilitation (VR) with physiotherapy support, known as blended VR, was effective in reducing vestibular symptoms in a recent randomised controlled trial. Blended VR is a complex intervention comprised of physiotherapeutic visits, the vertigo training website, and VR exercises. Because of these interacting components, it is important to understand how blended VR works, for whom it works best, and how it should ideally be delivered.AimTo investigate the experiences of both patients and physiotherapists with blended internet-based VR.Design & settingA qualitative interview study was performed with patients who received blended internet-based VR with physiotherapy support, and physiotherapists who provided this support.MethodSemi-structured interviews were conducted with 14 patients and eight physiotherapists after the 6-month follow-up of the randomised trial. All interviews were audio-recorded, transcribed, and thematically analysed.ResultsAccording to both patients and physiotherapists, the physiotherapist visits were useful in providing personal attention, helping patients safely execute exercises, and improving patients’ adherence to therapy. Some patients said they did not need physiotherapist support and, according to physiotherapists, both the necessity and the optimal way to deliver guidance differed greatly between patients. The Vertigo Training website and exercises provided patients with a sense of control over their symptoms. Patients reported that the VR exercises were easy to perform and most patients continued to use them long after the trial ended.ConclusionIn blended VR, physiotherapeutic visits appear to offer benefits above the vertigo training website and VR exercises alone. Physiotherapy support may best be used when individually tailored.


2020 ◽  
Vol 34 (10) ◽  
pp. 1268-1281
Author(s):  
Marion F Walker ◽  
Sheila Birchall ◽  
Christine Cobley ◽  
Laura Condon ◽  
Rebecca Fisher ◽  
...  

Objective: To determine the feasibility of recruiting to and delivering a biopsychosocial intervention for carers of stroke survivors. Design: Feasibility randomised controlled study with nested qualitative interview study. Setting: The intervention was delivered in the community in either a group or one-to-one format. Subjects: Carers and stroke survivors within one year of stroke onset. Interventions: A carer targeted intervention delivered by a research psychologist in six structured two-hour sessions or usual care control. The intervention combined education about the biological, psychological and social effects of stroke with strategies and techniques focussing on adjustment to stroke and caregiving. Stroke survivors in both groups received baseline and follow-up assessment but no intervention. Main Outcome: Recruitment rate, study attrition, fidelity of intervention delivery, acceptability and sensitivity of outcome measures used (health related quality of life, anxiety and depression and carer burden six months after randomisation). Results: Of the 257 carers approached, 41 consented. Six withdrew before randomisation. Eighteen participants were randomised to receive the intervention and 17 to usual care. Attendance at sessions was greater when treated one-to-one. Feedback interviews suggested that participants found the intervention acceptable and peer support particularly helpful in normalising their feelings. Thirty participants were assessed at follow-up with improvements from baseline on all health measures for both groups. Conclusions: Our results suggest that a biopsychosocial intervention was acceptable to carers and can be delivered in group and one-to-one formats. Timing of approach and mode of intervention delivery is critical and requires tailoring to the carers individual needs.


2019 ◽  
Vol 24 (4) ◽  
pp. 659-667 ◽  
Author(s):  
Stephanie A. Chamberlain ◽  
Wendy Duggleby ◽  
Pamela Teaster ◽  
Carole Estabrooks

2021 ◽  
pp. BJGP.2020.1027
Author(s):  
Julian Stephen Treadwell ◽  
Joanna Crocker ◽  
Alexander Rushforth ◽  
Kamal R. Mahtani ◽  
Trish Greenhalgh

Background: To support shared decision making and improve the management of polypharmacy, it is recommended that GPs take into account quantitative information on the benefits and harms of treatments. Quantitative evidence shows GPs’ knowledge of this is low. Aim: To explore GPs’ attitudes to and understanding of the quantitative benefits and harms of treatments for long term conditions. Design and Setting: Qualitative interview study in UK General Practice. Method: Semi-structured interviews with 15 GPs. Audio-recordings were transcribed verbatim and a framework approach used for analysis. Results: Participants described knowing or using quantitative information on benefits and harms for only a few treatments. There was awareness of this knowledge deficit coupled with low confidence in statistical terminology. Some perceived an absence of this information as an important barrier to optimal care, others were content to follow guidelines. In the absence of this knowledge, other strategies were described to individualise treatment decisions. The idea of increasing the use of quantitative information on the benefits and harms of treatment appealed to most, with imagined benefits for patients and themselves. However, potential barriers were described: a need for accessible information that can be understood and integrated into real-world practice, system factors and communication challenges. Conclusion: GPs are aware of their knowledge deficit with regard to an understanding of quantitative benefits and harms of treatments. Most were positive about the idea of increasing their use of this in practice but described important challenges which need to be considered when designing solutions.


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