54 résultat(s) recherche sur le mot-clé 'Qualitative research'    

Participants’ experiences of an Education, self-management and upper extremity eXercise Training for people with Rheumatoid Arthritis programme (EXTRA) / Lindsay M. Bearne in Physiotherapy, 2017/4 (2017)  

[article]  inPhysiotherapy > 2017/4 (2017) . - p. 430-438 Titre : Participants’ experiences of an Education, self-management and upper extremity eXercise Training for people with Rheumatoid Arthritis programme (EXTRA) Type de document : Article Auteurs : Lindsay M. Bearne ; Victoria L. Manning ; Ernest Choy Année de publication : 2017 Article en page(s) : p. 430-438 Langues : Anglais (eng) Descripteurs : HE Vinci Polyarthrite rhumatoide ; Recherche qualitative Mots-clés : Arthritis  Rheumatoid  The EXTRA programme  Qualitative Research Résumé : Background The Education, self-management and upper extremity eXercise Training for people with Rheumatoid Arthritis programme (EXTRA) is an individualized, upper limb, home exercise regimen supplemented by four supervised, group sessions, a handbook and exercise dairy which improves upper extremity disability and self-efficacy. Objective and study design This qualitative interview study explored participants’ experience of EXTRA to inform development and implementation of EXTRA into practice. Participants Adults with Rheumatoid Arthritis who completed EXTRA were purposively sampled to include a range of ages, upper extremity disabilities, self-efficacy for arthritis self-management and attendance at EXTRA sessions. Methods Individual, semi-structured interviews were conducted with a single researcher until data saturation of themes was reached. Interviews were audio-recorded, transcribed verbatim and analysed using thematic analysis. Results Twelve participants (10 females; 32 to 87 years) were interviewed. Four overarching themes were identified: (i) empowering self-management; (ii) influence of others and (iii) the challenge of sustaining exercise, which resonate with the Social Cognition Theory, and (iv) refining EXTRA: consistent and personalised. Conclusions EXTRA enhanced participants’ confidence to manage their arthritis independently and was adaptable so it could be integrated with other life commitments. Whilst healthcare professionals, peers and family and friends influenced exercise uptake, sustaining exercise was challenging. Participants desired consistent and continuing contact with a familiar physiotherapist (e.g. via follow-up appointments, digital health technologies) which accommodated individual needs (e.g. different venues, session frequency). Implementation of EXTRA needs to appreciate and address these considerations to facilitate success. Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=134363 [article]

Carers' Experiences, Needs, and Preferences During Inpatient Stroke Rehabilitation: A Systematic Review of Qualitative Studies / Julie Luker in Archives of Physical Medicine and Rehabilitation, 2017/9 (2017)  

[article]  inArchives of Physical Medicine and Rehabilitation > 2017/9 (2017) . - p. 1852–1862 Titre : Carers' Experiences, Needs, and Preferences During Inpatient Stroke Rehabilitation: A Systematic Review of Qualitative Studies Type de document : Article Auteurs : Julie Luker ; Carolyn Murray ; Elizabeth Lynch Année de publication : 2017 Article en page(s) : p. 1852–1862 Langues : Anglais (eng) Descripteurs : HE Vinci Accident vasculaire cérébral (AVC) ; Aidants ; Recherche qualitative ; Rééducation et réadaptation ; Revue de la littérature Mots-clés : Caregivers  Qualitative research  Review  Stroke Résumé : Objective To report and synthesize the experiences, needs, and preferences of carers of stroke survivors undergoing inpatient rehabilitation. Data Sources MEDLINE, CINAHL, Embase, PsycINFO, and Web of Science were searched to March 2016. Reference lists of relevant publications were searched. No language restrictions were applied. Study Selection Eligible qualitative studies reported the experiences of carers of stroke survivors who underwent inpatient rehabilitation. The search yielded 3532 records; 93 full-text publications were assessed for eligibility, and 34 documents (33 studies) were included. Comprehensiveness of reporting was assessed using the Consolidated Criteria for Reporting Qualitative Health Research framework. Data Extraction Data on the characteristics of included studies were independently extracted by 2 authors. Differences in data extraction between authors were resolved through discussion or by a third author. All text in studies' results and discussion sections were extracted for analysis. Data Synthesis Extracted texts were analyzed inductively using thematic synthesis. Seven analytical themes were developed that related to the carers' experiences, needs, and preferences: (1) overwhelmed with emotions; (2) recognition as a stakeholder in recovery; (3) desire to be heard and informed; (4) persisting for action and outcomes; (5) being legitimate clients; (6) navigating an alien culture and environment; and (7) managing the transition home. Conclusions This systematic review provides new insights into the experiences, needs, and preferences of carers of stroke survivors undergoing inpatient rehabilitation. Carers experienced distress as they navigated a foreign culture and environment without adequate communication and processes in place for their inclusion. We recommend deliberate efforts to provide a more inclusive environment that better supports and prepares carers for their new role. Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=118283 [article]

Environmental Barriers and Supports to Everyday Participation: A Qualitative Insider Perspective From People With Disabilities / Joy Hammel in Archives of Physical Medicine and Rehabilitation, 2015/4 (2015)  

[article]  inArchives of Physical Medicine and Rehabilitation > 2015/4 (2015) . - p. 578-588 Titre : Environmental Barriers and Supports to Everyday Participation: A Qualitative Insider Perspective From People With Disabilities Type de document : Article Auteurs : Joy Hammel ; Susan Magasi ; Allen Heinemann Année de publication : 2015 Article en page(s) : p. 578-588 Langues : Anglais (eng) Descripteurs : HE Vinci Déterminants sociaux de la santé ; Environnement ; Groupes focalisés ; Participation sociale ; Recherche qualitative ; Rééducation et réadaptation Mots-clés : Environment  Focus groups  Qualitative research  Social determinants of health  Social participation Résumé : Objective To describe environmental factors that influence participation of people with disabilities. Design Constant comparative, qualitative analyses of transcripts from 36 focus groups across 5 research projects. Setting Home, community, work, and social participation settings. Participants Community-dwelling people (N=201) with diverse disabilities (primarily spinal cord injury, traumatic brain injury, and stroke) from 8 states. Interventions None. Main Outcome Measures Environmental barriers and supports to participation. Results We developed a conceptual framework to describe how environmental factors influence the participation of people with disabilities, highlighting 8 domains of environmental facilitators and barriers (built, natural, assistive technology, transportation, information and technology access, social support and attitudes, systems and policies, economics) and a transactional model showing the influence of environmental factors on participation at the micro (individual), mesa (community), and macro (societal) levels. Focus group data validated some International Classification of Functioning, Disability and Health environmental categories while also bringing unique factors (eg, information and technology access, economic quality of life) to the fore. Data were used to construct items to enable people with disabilities to assess the impact of environmental factors on everyday participation from their firsthand experience. Conclusions Participants with disabilities voiced the need to evaluate the impact of the environment on their participation at the immediate, community, and societal levels. The results have implications for assessing environmental facilitators and barriers to participation within rehabilitation and community settings, evaluating outcomes of environmental interventions, and effecting system and policy changes to target environmental barriers that may result in societal participation disparities versus opportunities. Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=118452 [article]

Environmental Factors Item Development for Persons With Stroke, Traumatic Brain Injury, and Spinal Cord Injury / Allen W. Heinemann in Archives of Physical Medicine and Rehabilitation, 2015/4 (2015)  

[article]  inArchives of Physical Medicine and Rehabilitation > 2015/4 (2015) . - p. 589-595 Titre : Environmental Factors Item Development for Persons With Stroke, Traumatic Brain Injury, and Spinal Cord Injury Type de document : Article Auteurs : Allen W. Heinemann ; Susan Magasi ; Joy Hammel Année de publication : 2015 Article en page(s) : p. 589-595 Langues : Anglais (eng) Descripteurs : HE Vinci Environnement ; Recherche qualitative ; Rééducation et réadaptation Mots-clés : Environment  Qualitative research  Surveys and Questionnaires  Enquêtes et questionnaires Résumé : Objectives To describe methods used in operationalizing environmental factors; to describe the results of a research project to develop measures of environmental factors that affect participation; and to define an initial item set of facilitators and barriers to participation after stroke, traumatic brain injury, and spinal cord injury. Design Instrument development included an extensive literature review, item classification and selection, item writing, and cognitive testing following the approach of the Patient-Reported Outcomes Measurement Information System. Setting Community. Participants Content area and outcome measurement experts (n=10) contributed to instrument development; individuals (n=200) with the target conditions participated in focus groups and in cognitive testing (n=15). Interventions None. Main Outcome Measures Environmental factor items were categorized in 6 domains: assistive technology; built and natural environment; social environment; services, systems, and policies; access to information and technology; and economic quality of life. Results We binned 2273 items across the 6 domains, winnowed this pool to 291 items for cognitive testing, and recommended 274 items for pilot data collection. Conclusions Five of the 6 domains correspond closely to the International Classification of Functioning, Disability and Health taxonomy of environmental factors; the sixth domain, economic quality of life, reflects an important construct that reflects financial resources that affect participation. Testing with a new and larger sample is underway to evaluate reliability, validity, and sensitivity. Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=118453 [article]

Exploring experiences of physical activity among people with Alzheimer's disease and their spouse carers: a qualitative study / R. Malthouse in Physiotherapy, 2014/2 (2014)  

[article]  inPhysiotherapy > 2014/2 (2014) . - pp. 169-175 Titre : Exploring experiences of physical activity among people with Alzheimer's disease and their spouse carers: a qualitative study Type de document : Article Auteurs : R. Malthouse ; F. Fox Année de publication : 2014 Article en page(s) : pp. 169-175 Langues : Anglais (eng) Descripteurs : HE Vinci Exercice physique ; Maladie d'Alzheimer ; Recherche qualitative Mots-clés : Exercise  Alzheimer Disease  Qualitative Research Résumé : Objectives To improve understanding about the barriers and facilitators to physical activity for people with Alzheimer's disease and their spouse carers, and to consider the development of activity interventions that would be acceptable, sustainable and feasible for both groups. Design A qualitative approach, using semi-structured interviews, facilitated exploration of physical activity in a small group of people with Alzheimer's disease and their spouse carers. Setting Participants were recruited from one memory clinic in South West England. Participants Potential participants were identified by clinical psychologists at the memory clinic and were given information about participating in the research. Five people with Alzheimer's disease and their spouse carers were subsequently recruited for semi-structured interviews, which took place at the memory clinic. Interviews were audio-recorded and transcribed verbatim. Main outcome measures Qualitative data were analysed using thematic analysis. Three major themes have been presented. Results The findings illustrate the complex interplay between the overarching themes ‘self’, ‘others’ and ‘couple’ that affect physical activity for both people with Alzheimer's disease and their spouse carers, and which are linked to the progression of dementia. Conclusions An individually tailored approach for couples, which values the role of the carer and accounts for the progressive and changing nature of dementia, should be a guiding principle for intervention design. Disponible en ligne : Oui En ligne : https://login.ezproxy.vinci.be/login?url=https://www.sciencedirect.com/science/a [...] Permalink : https://bib.vinci.be/opac_css/index.php?lvl=notice_display&id=134176 [article]

How the Rehabilitation Environment Influences Patient Perception of Service Quality: A Qualitative Study / Francesc Medina-Mirapeix in Archives of Physical Medicine and Rehabilitation, 2013/6 (2013)  

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‘If you can’t help me, so help me God I will cut it off myself…’ The experience of living with knee pain: a qualitative meta-synthesis / James M. Wride in Physiotherapy, Vol. 104, n° 3 (2018)  

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‘Isn’t it all Whites?’ Ethnic diversity and the physiotherapy profession / Gillian Yeowell in Physiotherapy, 2013/4 (2013)  

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Living With Chronic Pain After Spinal Cord Injury: A Mixed-Methods Study / Eva Widerström-Noga in Archives of Physical Medicine and Rehabilitation, 2017/5 (2017)  

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Musculoskeletal services in primary care in the Republic of Ireland: an insight into the perspective of physiotherapists / H.P. French in Physiotherapy, 2017/2 (2017)  

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‘Oh my gosh I’m going to have to undress’: potential barriers to greater ethnic diversity in the physiotherapy profession in the United Kingdom / Gillian Yeowell in Physiotherapy, 2013/4 (2013)  

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Patients' Views on the Impact of Stroke on Their Roles and Self: A Thematic Synthesis of Qualitative Studies / Ton Satink in Archives of Physical Medicine and Rehabilitation, 2013/6 (2013)  

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Patients with rotator cuff tendinopathy can successfully self-manage, but with certain caveats: a qualitative study / Chris Littlewood in Physiotherapy, 2014/1 (2014)  

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Relevant patient perceptions and experiences for evaluating quality of interaction with physiotherapists during outpatient rehabilitation: a qualitative study / Elena Del Bano-Aledo in Physiotherapy, 2014/1 (2014)  

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“Six sessions is a drop in the ocean”: an exploratory study of neurological physiotherapy in idiopathic and inherited ataxias / Gavin Daker-White in Physiotherapy, 2013/4 (2013)  

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Therapeutic Alliances in Stroke Rehabilitation: A Meta-Ethnography / Michelle Lawton in Archives of Physical Medicine and Rehabilitation, 2016/11 (2016)  

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Understanding hope in patients with Multiple Sclerosis / Andy Soundy in Physiotherapy, 2012/4 (2012)  

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Understanding the barriers and enablers to implementation of a self-managed exercise intervention: a qualitative study / Chris Littlewood in Physiotherapy, 2015/3 (2015)  

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Acceptance of Tele-Rehabilitation by Stroke Patients: Perceived Barriers and Facilitators / Shilpa Tyagi in Archives of Physical Medicine and Rehabilitation, Vol. 99, n° 12 (2018)  

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Adherence of Individuals in Upper Extremity Rehabilitation: A Qualitative Study / Enrique V. Smith-Forbes in Archives of Physical Medicine and Rehabilitation, 2016/8 (2016)  

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An exploration of the professional identity embedded within UK cardiorespiratory physiotherapy curricula / Carolyn Roskell in Physiotherapy, 2013/2 (2013)  

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Considering how athletic identity assists adjustment to spinal cord injury: a qualitative study / C. Hawkins in Physiotherapy, 2014/3 (2014)  

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Development of Self-Report Measures of Social Attitudes That Act As Environmental Barriers and Facilitators for People With Disabilities / Sofia F. Garcia in Archives of Physical Medicine and Rehabilitation, 2015/4 (2015)  

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Electronic Screening and Decision Support for Poststroke Depression: An Exploration of Doctors' and Patients' Perceptions of Acceptability / Jennifer H. White in Archives of Physical Medicine and Rehabilitation, 2013/4 (2013)  

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Exploring patients’ opinions of activity pacing and a new activity pacing questionnaire for chronic pain and/or fatigue: a qualitative study / Deborah Antcliff in Physiotherapy, 2016/3 (2016)  

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