scholarly journals Implementing lateral flow devices in long-term care facilities: experiences from the Liverpool COVID-19 community testing pilot in care homes— a qualitative study

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Patrick Kierkegaard ◽  
Massimo Micocci ◽  
Anna McLister ◽  
John S. P. Tulloch ◽  
Paula Parvulescu ◽  
...  

Abstract Introduction Antigen-based lateral flow devices (LFDs) offer the potential of widespread rapid testing. The scientific literature has primarily focused on mathematical modelling of their use and test performance characteristics. For these tests to be implemented successfully, an understanding of the real-world contextual factors that allow them to be integrated into the workplace is vital. To address this gap in knowledge, we aimed to explore staff’s experiences of integrating LFDs into routine practice for visitors and staff testing with a view to understand implementation facilitators and barriers. Methods Semi-structured interviews and thematic analysis. Results We identified two main themes and five subthemes. The main themes included: visitor-related testing factors and staff-related testing factors. Subthemes included: restoring a sense of normality, visitor-related testing challenges, staff-related testing challenges, and pre-pilot antecedent factors. Conclusion Our study demonstrates that the real-world implementation of LFDs to test visitors and staff faces significant challenges as a result of several contextual factors negatively affecting the work practice and environment. More comprehensive studies are needed to identify and inform effective implementation strategies to ensure that LFDs can be adopted in an agile way that better supports an already exhausted and morally depleted workforce.

2020 ◽  
Author(s):  
Abhishek Pratap ◽  
Daniel Grant ◽  
Ashok Vegesna ◽  
Meghasyam Tummalacherla ◽  
Stanley Cohan ◽  
...  

BACKGROUND Multiple sclerosis (MS) is a chronic neurodegenerative disease. Current monitoring practices predominantly rely on brief and infrequent assessments, which may not be representative of the real-world patient experience. Smartphone technology provides an opportunity to assess people’s daily-lived experience of MS on a frequent, regular basis outside of episodic clinical evaluations. OBJECTIVE The objectives of this study were to evaluate the feasibility and utility of capturing real-world MS-related health data remotely using a smartphone app, “elevateMS,” to investigate the associations between self-reported MS severity and sensor-based active functional tests measurements, and the impact of local weather conditions on disease burden. METHODS This was a 12-week, observational, digital health study involving 3 cohorts: self-referred participants who reported an MS diagnosis, clinic-referred participants with neurologist-confirmed MS, and participants without MS (controls). Participants downloaded the elevateMS app and completed baseline assessments, including self-reported physical ability (Patient-Determined Disease Steps [PDDS]), as well as longitudinal assessments of quality of life (Quality of Life in Neurological Disorders [Neuro-QoL] Cognitive, Upper Extremity, and Lower Extremity Function) and daily health (MS symptoms, triggers, health, mobility, pain). Participants also completed functional tests (finger-tapping, walk and balance, voice-based Digit Symbol Substitution Test [DSST], and finger-to-nose) as an independent assessment of MS-related cognition and motor activity. Local weather data were collected each time participants completed an active task. Associations between self-reported baseline/longitudinal assessments, functional tests, and weather were evaluated using linear (for cross-sectional data) and mixed-effects (for longitudinal data) regression models. RESULTS A total of 660 individuals enrolled in the study; 31 withdrew, 495 had MS (n=359 self-referred, n=136 clinic-referred), and 134 were controls. Participation was highest in clinic-referred versus self-referred participants (median retention: 25.5 vs 7.0 days). The top 5 most common MS symptoms, reported at least once by participants with MS, were fatigue (310/495, 62.6%), weakness (222/495, 44.8%), memory/attention issues (209/495, 42.2%), and difficulty walking (205/495, 41.4%), and the most common triggers were high ambient temperature (259/495, 52.3%), stress (250/495, 50.5%), and late bedtime (221/495, 44.6%). Baseline PDDS was significantly associated with functional test performance in participants with MS (mixed model–based estimate of most significant feature across functional tests [β]: finger-tapping: β=–43.64, <i>P</i>&lt;.001; DSST: β=–5.47, <i>P</i>=.005; walk and balance: β=–.39, <i>P</i>=.001; finger-to-nose: β=.01, <i>P</i>=.01). Longitudinal Neuro-QoL scores were also significantly associated with functional tests (finger-tapping with Upper Extremity Function: β=.40, <i>P</i>&lt;.001; walk and balance with Lower Extremity Function: β=–99.18, <i>P</i>=.02; DSST with Cognitive Function: β=1.60, <i>P</i>=.03). Finally, local temperature was significantly associated with participants’ test performance (finger-tapping: β=–.14, <i>P</i>&lt;.001; DSST: β=–.06, <i>P</i>=.009; finger-to-nose: β=–53.88, <i>P</i>&lt;.001). CONCLUSIONS The elevateMS study app captured the real-world experience of MS, characterized some MS symptoms, and assessed the impact of environmental factors on symptom severity. Our study provides further evidence that supports smartphone app use to monitor MS with both active assessments and patient-reported measures of disease burden. App-based tracking may provide unique and timely real-world data for clinicians and patients, resulting in improved disease insights and management.


Sensors ◽  
2018 ◽  
Vol 18 (7) ◽  
pp. 2365 ◽  
Author(s):  
Emma Tonkin ◽  
Alison Burrows ◽  
Przemysław Woznowski ◽  
Pawel Laskowski ◽  
Kristina Yordanova ◽  
...  

Delivering effortless interactions and appropriate interventions through pervasive systems requires making sense of multiple streams of sensor data. This is particularly challenging when these concern people’s natural behaviours in the real world. This paper takes a multidisciplinary perspective of annotation and draws on an exploratory study of 12 people, who were encouraged to use a multi-modal annotation app while living in a prototype smart home. Analysis of the app usage data and of semi-structured interviews with the participants revealed strengths and limitations regarding self-annotation in a naturalistic context. Handing control of the annotation process to research participants enabled them to reason about their own data, while generating accounts that were appropriate and acceptable to them. Self-annotation provided participants an opportunity to reflect on themselves and their routines, but it was also a means to express themselves freely and sometimes even a backchannel to communicate playfully with the researchers. However, self-annotation may not be an effective way to capture accurate start and finish times for activities, or location associated with activity information. This paper offers new insights and recommendations for the design of self-annotation tools for deployment in the real world.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Brian P. Jenssen ◽  
Robert Schnoll ◽  
Rinad Beidas ◽  
Justin Bekelman ◽  
Anna-Marika Bauer ◽  
...  

Abstract Background Routine evidence-based tobacco use treatment minimizes cancer-specific and all-cause mortality, reduces treatment-related toxicity, and improves quality of life among patients receiving cancer care. Few cancer centers employ mechanisms to systematically refer patients to evidence-based tobacco cessation services. Implementation strategies informed by behavioral economics can increase tobacco use treatment engagement within oncology care. Methods A four-arm cluster-randomized pragmatic trial will be conducted across nine clinical sites within the Implementation Science Center in Cancer Control Implementation Lab to compare the effect of behavioral economic implementation strategies delivered through embedded messages (or “nudges”) promoting patient engagement with the Tobacco Use Treatment Service (TUTS). Nudges are electronic medical record (EMR)-based messages delivered to patients, clinicians, or both, designed to counteract known patient and clinician biases that reduce treatment engagement. We used rapid cycle approaches (RCA) informed by relevant stakeholder experiences to refine and optimize our implementation strategies and methods prior to trial initiation. Data will be obtained via the EMR, clinician survey, and semi-structured interviews with a subset of clinicians and patients. The primary measure of implementation is penetration, defined as the TUTS referral rate. Secondary outcome measures of implementation include patient treatment engagement (defined as the number of patients who receive FDA-approved medication or behavioral counseling), quit attempts, and abstinence rates. The semi-structured interviews, guided by the Consolidated Framework for Implementation Research, will assess contextual factors and patient and clinician experiences with the nudges. Discussion This study will be the first in the oncology setting to compare the effectiveness of nudges to clinicians and patients, both head-to-head and in combination, as implementation strategies to improve TUTS referral and engagement. We expect the study to (1) yield insights into the effectiveness of nudges as an implementation strategy to improve uptake of evidence-based tobacco use treatment within cancer care, and (2) advance our understanding of the multilevel contextual factors that drive response to these strategies. These results will lay the foundation for how patients with cancer who smoke are best engaged in tobacco use treatment and may lead to future research focused on scaling this approach across diverse centers. Trial registration Clinicaltrials.gov, NCT04737031. Registered 3 February 2021.


2021 ◽  
Author(s):  
Dylan A Mistry ◽  
Jenny Y Wang ◽  
Mika-Erik Moeser ◽  
Thomas Starkey ◽  
Lennard YW Lee

Abstract Background: Lateral flow devices (LFDs) are viral antigen tests for the detection of SARS-CoV-2 that produce a rapid result, are inexpensive and easy to operate. They have been advocated for use by the World Health Organisation to help control outbreaks and break the chain of transmission of COVID-19 infections. There are now several studies assessing their accuracy but as yet no systematic review. Our aims were to assess the sensitivity and specificity of LFDs in a systematic review and summarise the sensitivity and specificity of these tests. Methods: A targeted search of Pubmed and Medxriv, using PRISMA principles, was conducted identifying clinical studies assessing the sensitivity and specificity of LFDs as their primary outcome compared to reverse transcriptase polymerase chain reaction (RT-PCR) for the detection of SARS-CoV-2. Based on extracted data sensitivity and specificity was calculated for each study. Data was pooled based on manufacturer of LFD and split based on operator (self-swab or by trained professional) and sensitivity and specificity data were calculated. Results: Twenty-four papers were identified involving over 26,000 test results. Sensitivity from individual studies ranged from 37.7% (95% CI 30.6-45.5) to 99.2% (95% CI 95.5-99.9) and specificity from 92.4% (95% CI 87.5-95.5) to 100.0% (99.7-100.0). BD Veritor was the best performing manufacturer of LFD with a sensitivity of 99.2% (95% CI 95.5-99.9) and specificity of 100.0% (98.9-100.0). Operation of the test by a trained professional or by the test subject with self-swabbing produced comparable results. Conclusions: This systematic review identified that the performance of lateral flow devices is heterogeneous and dependent on the manufacturer. Some perform with high specificity with reasonable sensitivity. Test performance does appear dependent on the operator. Potentially, LFDs could support the scaling up of mass testing to aid track and trace methodology and break the chain of transmission of COVID-19 with the additional benefit of providing individuals with the results in a much shorter time frame.


2019 ◽  
Vol 9 (2) ◽  
pp. 80-91 ◽  
Author(s):  
Rosie Whitehead ◽  
Frances O'Callaghan ◽  
Jenny Gamble ◽  
Natasha Reid

PURPOSETo understand the experiences and contextual factors that influence the ability of midwives to provide appropriate support to women regarding alcohol and other drug (AOD)e use during pregnancy, in the Queensland context.DESIGNUsing a qualitative approach underpinned by critical realism, we explored the experiences of eleven midwives using semi-structured interviews. Thematic analysis was utilized, which was inductive and deductive, as it aimed to explicate different contextual factors at play, based on the experiences of the current sample of midwives.MAJOR FINDINGSExperiences of midwives in the current study were influenced by five overarching contextual factors: (a) patient-level factors (complexities experienced by women and lack of knowledge regarding maternity care options); (b) provider/patient-level factors (importance of midwives building relationships with women and importance of continuity of care); (c) provider-level factors (importance of taking a supportive approach, midwife confidence, engagement in AOD screening, variable attitudes and knowledge); (d) organizational-level factors (lack of support and training, concerns regarding communication, time constraints and organizations that limited midwife involvement); (e) broader system-level factors (lack of effective services and inconsistent messages regarding AOD use during pregnancy).CONCLUSIONSThe current study has highlighted a range of practice areas and potential implementation strategies across a number of contextual levels that could be beneficial in the Queensland context to improve maternity care provision for women who are experiencing AOD use challenges during pregnancy.


2021 ◽  
Author(s):  
◽  
Antony Zogg

<p>In spite of the risks, people often share large quantities of personal information online. The objective of this research was to gain an understanding as to why people take such risks when engaging with others on social networking sites like Facebook. Initially the existence of online communities had to be established, and consideration given to the possibility that these online communities reflected groups found in the real world. The following hypotheses were then tested using an online survey with Likert Scale questions and freeform questions. This data was then triangulated by and supplemented with data received as a result of semi-structured interviews. Interview and survey questions were informed by a full literature review undertaken on the topic. H1: Humans mimic online behaviours including risky behaviours to gain acceptance in online communities. There was insufficient support for this hypothesis. This may be due to the fact that online and real world groups differ in terms of the way in which they communicate. The five senses are not fully engaged in online communication and there is an absence of body language and other non-verbal communication. This difference may determine that there is less need for social affiliation online than in the real world. H2: The need for personal safety online is secondary to the need for social affiliation. Again there was insufficient support for this hypothesis, and even those with online communities of trusted friends drawn from the real world were concerned for their personal safety and configured their privacy settings. However these people were comfortable sharing personal information online with trusted friends, demonstrating that they were under the illusion that their information was private. H3: Humans reflect the values of their friends on social networks to gain their approval. This hypothesis was well supported and indications were that people were more prepared to share personal information online with those who shared their values. They are also unlikely to share controversial information that violated their personal values. The results of this research were viewed through the lens of "The Online Disinhibition Effect" (Suler, 2004), and recommendations made to companies planning online business.</p>


2021 ◽  
Author(s):  
◽  
Antony Zogg

<p>In spite of the risks, people often share large quantities of personal information online. The objective of this research was to gain an understanding as to why people take such risks when engaging with others on social networking sites like Facebook. Initially the existence of online communities had to be established, and consideration given to the possibility that these online communities reflected groups found in the real world. The following hypotheses were then tested using an online survey with Likert Scale questions and freeform questions. This data was then triangulated by and supplemented with data received as a result of semi-structured interviews. Interview and survey questions were informed by a full literature review undertaken on the topic. H1: Humans mimic online behaviours including risky behaviours to gain acceptance in online communities. There was insufficient support for this hypothesis. This may be due to the fact that online and real world groups differ in terms of the way in which they communicate. The five senses are not fully engaged in online communication and there is an absence of body language and other non-verbal communication. This difference may determine that there is less need for social affiliation online than in the real world. H2: The need for personal safety online is secondary to the need for social affiliation. Again there was insufficient support for this hypothesis, and even those with online communities of trusted friends drawn from the real world were concerned for their personal safety and configured their privacy settings. However these people were comfortable sharing personal information online with trusted friends, demonstrating that they were under the illusion that their information was private. H3: Humans reflect the values of their friends on social networks to gain their approval. This hypothesis was well supported and indications were that people were more prepared to share personal information online with those who shared their values. They are also unlikely to share controversial information that violated their personal values. The results of this research were viewed through the lens of "The Online Disinhibition Effect" (Suler, 2004), and recommendations made to companies planning online business.</p>


2021 ◽  
Author(s):  
Samuel U. Takvorian ◽  
Justin Bekelman ◽  
Rinad S. Beidas ◽  
Robert Schnoll ◽  
Alicia B.W. Clifton ◽  
...  

Abstract BackgroundSerious illness conversations (SICs) are an evidence-based approach to eliciting patients’ values, goals, and care preferences that improve patient outcomes. However, most patients with cancer die without a documented SIC. Clinician-directed implementation strategies informed by behavioral economics (“nudges”) that identify high-risk patients have shown promise in increasing SIC documentation among clinicians. It is unknown whether patient-directed nudges that normalize and prime patients towards SIC completion—either alone or in combination with clinician nudges that additionally compare performance relative to peers—may improve on this approach. Our objective is to test the effect of clinician- and patient-directed nudges as implementation strategies for increasing SIC completion among patients with cancer. MethodsWe will conduct a 2x2 factorial, cluster randomized pragmatic trial to test the effect of nudges to clinicians, patients, or both, compared to usual care, on SIC completion. Participants will include 166 medical and gynecologic oncology clinicians practicing at ten sites within a large academic health system, and their approximately 5,500 patients at high risk of predicted 6-month mortality based on a validated machine-learning prognostic algorithm. Data will be obtained via the electronic medical record, clinician survey, and semi-structured interviews with clinicians and patients. The primary outcome will be time to SIC documentation among high-risk patients. Secondary outcomes will include time to SIC documentation among all patients (assessing spillover effects); palliative care referral among high-risk patients; and aggressive end-of-life care utilization (composite of chemotherapy within 14 days before death, hospitalization within 30 days before death, or admission to hospice within 3 days before death) among high-risk decedents. We will assess moderators of the effect of implementation strategies, and conduct semi-structured interviews with a subset of clinicians and patients to assess contextual factors that shape effectiveness of nudges with an eye towards health equity.DiscussionThis will be the first pragmatic trial to evaluate clinician- and patient-directed nudges to promote SIC completion for patients with cancer. We expect the study to yield insights into the effectiveness of clinician and patient nudges as implementation strategies to improve SIC rates, and to uncover multilevel contextual factors that drive response to these strategies.Trial registrationClinicaltrials.gov, NCT04867850. Registered April 30, 2021. https://clinicaltrials.gov/ct2/show/NCT04867850?term=serious+illness&draw=2&rank=3


Author(s):  
Jeanne Marie L. Lago ◽  
Ruth Ortega-Dela Cruz

The study used experimental research design to randomly selected senior high school students in analysing their attitude and achievement in statistics when contextual teaching is implemented. In addition to structured questionnaires, semi-structured interviews with the students were also conducted to provide rich descriptions about learning experiences with contextual teaching. Results revealed that students have positive attitude towards statistics and that students learn better with contextualized instruction than direct instruction. With this, contextualized instruction must be promoted in teaching statistics. By linking it to the real world, students would be able to view statistics more than just a subject.  Thus, it makes the statistical hypothesis testing learning more enjoyable and exciting.


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