16 research outputs found

    One Wedding, Two Cultures, Four Outfits: The Phenomenological Exploration of Fashion and Textiles

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    Textiles can evoke an emotional response that is induced by the smell, texture, memory, and embodied experiences that are released through wearing, touching, and talking about textiles. The textile artifact is our most universal designed object, with the capacity for us to experience it simultaneously with all our senses and emotions. The personal textile archive is a term created for this study to describe textiles that have been taken out of practical use, and have been informally, yet purposefully, gathered together. Textile artifacts within the personal textile archive function as both a treasury of personal, social, and family memories, and as a treasury of design details. A series of interviews were conducted in which participants were asked to discuss their own personal textile archives, in order to uncover the embodied experience that arises through interactions with these sentimental textiles. This rich experience of textiles was explored through the use of qualitative research methods developed from a phenomenological research methodology, Interpretative Phenomenological Analysis. Through a case study in which a couple of English and Punjabi heritage describe their wedding outfits, interviews set and analyzed within a phenomenological paradigm demonstrate this method's facility to explore the interplay between design and experience

    Drawn Threads: Drawing as a visual methodology to enhance qualitative studies

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    The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the URI link.This paper is an analysis of the value that drawing can bring to a formal research methodology. It is based on a series of drawings that were produced to extend and develop a form of qualitative enquiry, an Interpretative Phenomenological Analysis (IPA). This analysis was conducted as part of a study of personal textiles that individuals retain and value beyond their practice use, solely for their sentimental or family historical value, termed, the personal textile archive. Interpretative Phenomenological Analysis was used for analysing the individual experience of these textiles, and was found to be a methodologically sound, yet flexible and creative method of uncovering the data. Phenomenological research methods are established as valid means to investigate subjective human experience, across a range of different subject disciplines (Smith, Flowers & Larkin, 2009). Such an interpretative approach was found to be an effective method to discern and illustrate the themes that arise through the individual’s engagement with their own archived personal textiles. However, a visual rather than a text-based method is investigated for the supplementary value and illumination such an approach could bring to a qualitative study. In this respect, drawing is explored as a practice-based method of visual inquiry to supplement and support the initial research analysis. Within this model of thinking, drawing is a means of embodied, visual enquiry, which can be used to produce an analytical and evaluative practice that offers further insights to the text-based analysis. Drawing from the final and completed artefacts is a method for making implicit aspects of the experience of their making explicit. The drawn exploration of the material qualities of a textile design enabled an increased understanding of the tacit expertise of the designer or crafts-person, through applied drawing expertise

    The Textile Archive: curating personal histories and family narratives

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    Textiles are a ubiquitous facet of global culture, with the potential to become records of significant relationships, events, and stories over their lifetime. This research project investigates textiles which have been informally gathered together, and kept within the home, for their emotional or symbolic resonance. No longer used for their designed function, these textiles are saved from disposal for their ability to prompt personal and family histories and stories, in a phenomenon identified within the study as the personal textile archive. Textile design research is increasingly concerned with incorporating interdisciplinary social and cultural frameworks within its traditional research fields of technology, innovation and creativity, to frame a textile's socio-cultural relevance. This shift in the field requires the development of specific textile design research tools which are capable of producing purposeful research which analyses the material and designed properties of textiles in relation to their symbolic or affective experience, in order to understand the user-experience of a textile. Phenomenological research methods are established as tools for investigating phenomena and lived experience from a first-person perspective, which the investigation of the personally significant textiles within this study requires. A particular method, interpretative phenomenological analysis, has been specifically adapted for textile design research, and it is demonstrated within this research project that is is able to investigate and analyse the personal textile archive, producing original insights into this phenomenon. Through this application of this adaptation of interpretative phenomenological analysis, the design, affordances and craftsmanship of a textile are revealed as interweaving with its emotional, sentimental, biographical orfamily historical meaning. This is a useful and important original contribution to textile design research, and the recommendation is made that other researchers in the field will be able to utilise and further test this tool within future textile design research studies

    The future of heuristic fossils

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    The authors propose that while many fields of design are involved in reflexive interactions with design research tools, others are strongly heuristic in both their application of historic knowledge bases and in the ways in which they allow themselves tomove forward, toconstructnewknowledgeasanextensionofcraft thinkingwithuser-centredevidence.Thesehistoricalframesbecomealimitingfactor inboththewaysthatpracticecandevelopbutalso,moreworryingly,inthewaysin whichthesefieldscandeveloptheirownresearchtools

    Peroxidase-catalysed coloration of wool fabrics

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    The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link.An enzyme-based textile coloration process using peroxidase (EC1.11.1.7) was investigated for its potential as an alternative to conventional textile dyeing processes, with the benefits of being low in energy use and non-damaging to fibres. The current study presents a process for the coloration of wool fabric using peroxidase oxidation of a range of different aromatic compounds in the presence of hydrogen peroxide. The results revealed that wool can be successfully dyed by peroxidase-catalysed coloration at temperatures as low as 30°C. By controlling the pH values and buffer systems during processing, a diverse colour palette was produced, depending on the small molecular aromatic compound used as the precursor. Colour fastness testing found that fastness to washing, rubbing and light properties achieved good to excellent ratings, with further improvement to wash fastness provided by a post-soaping wash. No fibre damage occurred due to peroxidase-catalysed coloration. This enzyme coloration process is a promising alternative to conventional wool dyeing processes with the advantage of effective dyeing at low temperatures, therefore having the potential of reducing energy consumption and preventing fibre damage

    Effects of antiplatelet therapy on stroke risk by brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases: subgroup analyses of the RESTART randomised, open-label trial

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    Background Findings from the RESTART trial suggest that starting antiplatelet therapy might reduce the risk of recurrent symptomatic intracerebral haemorrhage compared with avoiding antiplatelet therapy. Brain imaging features of intracerebral haemorrhage and cerebral small vessel diseases (such as cerebral microbleeds) are associated with greater risks of recurrent intracerebral haemorrhage. We did subgroup analyses of the RESTART trial to explore whether these brain imaging features modify the effects of antiplatelet therapy

    Effects of antiplatelet therapy after stroke due to intracerebral haemorrhage (RESTART): a randomised, open-label trial

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    Background: Antiplatelet therapy reduces the risk of major vascular events for people with occlusive vascular disease, although it might increase the risk of intracranial haemorrhage. Patients surviving the commonest subtype of intracranial haemorrhage, intracerebral haemorrhage, are at risk of both haemorrhagic and occlusive vascular events, but whether antiplatelet therapy can be used safely is unclear. We aimed to estimate the relative and absolute effects of antiplatelet therapy on recurrent intracerebral haemorrhage and whether this risk might exceed any reduction of occlusive vascular events. Methods: The REstart or STop Antithrombotics Randomised Trial (RESTART) was a prospective, randomised, open-label, blinded endpoint, parallel-group trial at 122 hospitals in the UK. We recruited adults (≥18 years) who were taking antithrombotic (antiplatelet or anticoagulant) therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage, discontinued antithrombotic therapy, and survived for 24 h. Computerised randomisation incorporating minimisation allocated participants (1:1) to start or avoid antiplatelet therapy. We followed participants for the primary outcome (recurrent symptomatic intracerebral haemorrhage) for up to 5 years. We analysed data from all randomised participants using Cox proportional hazards regression, adjusted for minimisation covariates. This trial is registered with ISRCTN (number ISRCTN71907627). Findings: Between May 22, 2013, and May 31, 2018, 537 participants were recruited a median of 76 days (IQR 29–146) after intracerebral haemorrhage onset: 268 were assigned to start and 269 (one withdrew) to avoid antiplatelet therapy. Participants were followed for a median of 2·0 years (IQR [1·0– 3·0]; completeness 99·3%). 12 (4%) of 268 participants allocated to antiplatelet therapy had recurrence of intracerebral haemorrhage compared with 23 (9%) of 268 participants allocated to avoid antiplatelet therapy (adjusted hazard ratio 0·51 [95% CI 0·25–1·03]; p=0·060). 18 (7%) participants allocated to antiplatelet therapy experienced major haemorrhagic events compared with 25 (9%) participants allocated to avoid antiplatelet therapy (0·71 [0·39–1·30]; p=0·27), and 39 [15%] participants allocated to antiplatelet therapy had major occlusive vascular events compared with 38 [14%] allocated to avoid antiplatelet therapy (1·02 [0·65–1·60]; p=0·92). Interpretation: These results exclude all but a very modest increase in the risk of recurrent intracerebral haemorrhage with antiplatelet therapy for patients on antithrombotic therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage. The risk of recurrent intracerebral haemorrhage is probably too small to exceed the established benefits of antiplatelet therapy for secondary prevention

    Effects of antiplatelet therapy after stroke due to intracerebral haemorrhage (RESTART): a randomised, open-label trial

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    Background: Antiplatelet therapy reduces the risk of major vascular events for people with occlusive vascular disease, although it might increase the risk of intracranial haemorrhage. Patients surviving the commonest subtype of intracranial haemorrhage, intracerebral haemorrhage, are at risk of both haemorrhagic and occlusive vascular events, but whether antiplatelet therapy can be used safely is unclear. We aimed to estimate the relative and absolute effects of antiplatelet therapy on recurrent intracerebral haemorrhage and whether this risk might exceed any reduction of occlusive vascular events. Methods: The REstart or STop Antithrombotics Randomised Trial (RESTART) was a prospective, randomised, open-label, blinded endpoint, parallel-group trial at 122 hospitals in the UK. We recruited adults (≥18 years) who were taking antithrombotic (antiplatelet or anticoagulant) therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage, discontinued antithrombotic therapy, and survived for 24 h. Computerised randomisation incorporating minimisation allocated participants (1:1) to start or avoid antiplatelet therapy. We followed participants for the primary outcome (recurrent symptomatic intracerebral haemorrhage) for up to 5 years. We analysed data from all randomised participants using Cox proportional hazards regression, adjusted for minimisation covariates. This trial is registered with ISRCTN (number ISRCTN71907627). Findings: Between May 22, 2013, and May 31, 2018, 537 participants were recruited a median of 76 days (IQR 29–146) after intracerebral haemorrhage onset: 268 were assigned to start and 269 (one withdrew) to avoid antiplatelet therapy. Participants were followed for a median of 2·0 years (IQR [1·0– 3·0]; completeness 99·3%). 12 (4%) of 268 participants allocated to antiplatelet therapy had recurrence of intracerebral haemorrhage compared with 23 (9%) of 268 participants allocated to avoid antiplatelet therapy (adjusted hazard ratio 0·51 [95% CI 0·25–1·03]; p=0·060). 18 (7%) participants allocated to antiplatelet therapy experienced major haemorrhagic events compared with 25 (9%) participants allocated to avoid antiplatelet therapy (0·71 [0·39–1·30]; p=0·27), and 39 [15%] participants allocated to antiplatelet therapy had major occlusive vascular events compared with 38 [14%] allocated to avoid antiplatelet therapy (1·02 [0·65–1·60]; p=0·92). Interpretation: These results exclude all but a very modest increase in the risk of recurrent intracerebral haemorrhage with antiplatelet therapy for patients on antithrombotic therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage. The risk of recurrent intracerebral haemorrhage is probably too small to exceed the established benefits of antiplatelet therapy for secondary prevention

    Effects of antiplatelet therapy after stroke due to intracerebral haemorrhage (RESTART): a randomised, open-label trial

    Get PDF
    BACKGROUND: Antiplatelet therapy reduces the risk of major vascular events for people with occlusive vascular disease, although it might increase the risk of intracranial haemorrhage. Patients surviving the commonest subtype of intracranial haemorrhage, intracerebral haemorrhage, are at risk of both haemorrhagic and occlusive vascular events, but whether antiplatelet therapy can be used safely is unclear. We aimed to estimate the relative and absolute effects of antiplatelet therapy on recurrent intracerebral haemorrhage and whether this risk might exceed any reduction of occlusive vascular events. METHODS: The REstart or STop Antithrombotics Randomised Trial (RESTART) was a prospective, randomised, open-label, blinded endpoint, parallel-group trial at 122 hospitals in the UK. We recruited adults (≥18 years) who were taking antithrombotic (antiplatelet or anticoagulant) therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage, discontinued antithrombotic therapy, and survived for 24 h. Computerised randomisation incorporating minimisation allocated participants (1:1) to start or avoid antiplatelet therapy. We followed participants for the primary outcome (recurrent symptomatic intracerebral haemorrhage) for up to 5 years. We analysed data from all randomised participants using Cox proportional hazards regression, adjusted for minimisation covariates. This trial is registered with ISRCTN (number ISRCTN71907627). FINDINGS: Between May 22, 2013, and May 31, 2018, 537 participants were recruited a median of 76 days (IQR 29-146) after intracerebral haemorrhage onset: 268 were assigned to start and 269 (one withdrew) to avoid antiplatelet therapy. Participants were followed for a median of 2·0 years (IQR [1·0- 3·0]; completeness 99·3%). 12 (4%) of 268 participants allocated to antiplatelet therapy had recurrence of intracerebral haemorrhage compared with 23 (9%) of 268 participants allocated to avoid antiplatelet therapy (adjusted hazard ratio 0·51 [95% CI 0·25-1·03]; p=0·060). 18 (7%) participants allocated to antiplatelet therapy experienced major haemorrhagic events compared with 25 (9%) participants allocated to avoid antiplatelet therapy (0·71 [0·39-1·30]; p=0·27), and 39 [15%] participants allocated to antiplatelet therapy had major occlusive vascular events compared with 38 [14%] allocated to avoid antiplatelet therapy (1·02 [0·65-1·60]; p=0·92). INTERPRETATION: These results exclude all but a very modest increase in the risk of recurrent intracerebral haemorrhage with antiplatelet therapy for patients on antithrombotic therapy for the prevention of occlusive vascular disease when they developed intracerebral haemorrhage. The risk of recurrent intracerebral haemorrhage is probably too small to exceed the established benefits of antiplatelet therapy for secondary prevention. FUNDING: British Heart Foundation
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