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641 results for “Guideline”
Data from: How well are national guidelines relating to the general sales of aspirin and paracetamol, adhered to by retail stores: a mystery shopper study
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Data from: Reporting guidelines for community-based participatory research (CBPR) did not improve the reporting quality of published studies: a systematic review of studies on smoking cessation
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Data from: First Latin American clinical practice guidelines for the treatment of systemic lupus erythematosus: Latin American Group for the Study of Lupus (GLADEL, Grupo Latino Americano de Estudio del Lupus)–Pan-American League of Associations of Rheumatology (PANLAR)
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Data from: Sustainability of professionals’ adherence to clinical practice guidelines in medical care: a systematic review
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Data from: Guidelines and considerations for designing field experiments simulating precipitation extremes in forest ecosystems
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Data from: Poor adherence to guidelines for preventing central line-associated bloodstream infections (CLABSI): results of a worldwide survey
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Data from: Intrauterine insemination: a UK survey on the adherence to NICE clinical guidelines by fertility clinics
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Data from: Cost effectiveness of the New Zealand diabetes in pregnancy guideline screening recommendations
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Guidelines for including bamboos in tropical ecosystem monitoring
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Data from: Food and nutrient gaps in rural Northern Ghana: does production of smallholder farming households support adoption of food-based dietary guidelines?
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Data from: drones as a tool to study and monitor endangered Grey Crowned Cranes (Balaerica regulorum): behavioural responses and recommended guidelines
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Dataset for "Guidelines to study and develop soft electrode systems for neural stimulation"
<p>Dataset for "Guidelines to study and develop soft electrode systems for neural stimulation"</p>
Data from: The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement: methods for arriving at consensus and developing reporting guidelines
Objective: Routinely collected health data, collected for administrative and clinical purposes, without specific a priori research questions, are increasingly used for observational, comparative effectiveness, health services research, and clinical trials. The rapid evolution and availability of routinely collected data for research has brought to light specific issues not addressed by existing reporting guidelines. The aim of the present project was to determine the priorities of stakeholders in order to guide the development of the REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement. Methods: Two modified electronic Delphi surveys were sent to stakeholders. The first determined themes deemed important to include in the RECORD statement, and was analyzed using qualitative methods. The second determined quantitative prioritization of the themes based on categorization of manuscript headings. The surveys were followed by a meeting of RECORD working committee, and re-engagement with stakeholders via an online commentary period. Results: The qualitative survey (76 responses of 123 surveys sent) generated 10 overarching themes and 13 themes derived from existing STROBE categories. Highest-rated overall items for inclusion were: Disease/exposure identification algorithms; Characteristics of the population included in databases; and Characteristics of the data. In the quantitative survey (71 responses of 135 sent), the importance assigned to each of the compiled themes varied depending on the manuscript section to which they were assigned. Following the working committee meeting, online ranking by stakeholders provided feedback and resulted in revision of the final checklist. Conclusions: The RECORD statement incorporated the suggestions provided by a large, diverse group of stakeholders to create a reporting checklist specific to observational research using routinely collected health data. Our findings point to unique aspects of studies conducted with routinely collected health data and the perceived need for better reporting of methodological issues.
Data from: Assessment of the quality of reporting in randomized controlled trials of acupuncture in the Korean literature using the CONSORT statement and the STRICTA guidelines
Objectives: This study aimed to assess the completeness of reporting of RCTs of acupuncture in the Korean literature. Design: Systematic review. Methods: We searched 12 Korean databases and 7 Korean journals to identify eligible RCTs of acupuncture published from 1996 to July 2011. We used the Consolidated Standards of Reporting Trials (CONSORT) checklist for parallel RCTs and the revised STandards for Reporting Interventions in Clinical Trials of Acupuncture (STRICTA) to assess the quality of reporting in Korean RCTs. We compared the completeness of reporting of CONSORT and STRICTA items in RCTs published in two time periods (1996-2004 referred to as the early period and 2005-2011 referred to as the late period). Results: We analysed 146 eligible RCTs using the CONSORT statement concerning RCTs of both needling and non-needling acupuncture and the STRICTA guidelines for 90 trials of needling acupuncture. Among the 103 RCTs in the late period, the proportion of RCTs that completely reported the CONSORT items of outcome definition (15.5%), sample size calculation (2.9%), randomisation (56%), allocation concealment (5.8%), implementation of allocation (11.7%), outcome assessor blinding (20.3%), flow of participants (25.2%), number of participants analysed (19.4%), ancillary analyses (0.0%), adverse events (24.3%), generalisability of findings (1.9%) and overall evidence (32.0%) remained small. Among the 61 RCTs of needling acupuncture in the late period, the STRICTA items of setting/context (24.6%) and practitioner background (27.9%) showed incomplete reporting. The completeness of reporting improved over time in several CONSORT and STRICTA items. Conclusion: The completeness of reporting of Korean RCTs of acupuncture was suboptimal according to the CONSORT and revised STRICTA statements. Trial authors and journal editors should use the CONSORT statement and the STRICTA guidelines for transparent reporting in Korean RCTs of acupuncture. The endorsement of the CONSORT and revised STRICTA statements in author instructions is also required.
Data from: ALS drug development guidances and trial guidelines: consensus and opportunities for alignment
The Food and Drug Administration (FDA) developed a draft guidance for drug development in Amyotrophic Lateral Sclerosis (ALS) that was issued in February 2018. The FDA draft guidance considered the recommendations developed by the ALS community which incorporated the views of a large group of clinical investigators, industry representatives, advocacy groups, patients, and caregivers. This external input from the ALS community reviewed the current state of clinical research in ALS and made suggestions over a wide range of drug development topics and served as an educational tool to provide the Agency with additional inputs about ALS, the state of the science and the community's views on key topics. In parallel to this effort, there was an independent effort to revise and update the ALS clinical trial guidelines. We discuss the areas of agreement of these three documents, and the areas that provide opportunities to improve the efficiency of drug development in ALS. It is likely that further research into biomarkers, efficacy endpoints, and predictive algorithms will provide greater alignment among community stakeholders and increase clarity on drug development efforts going forward. Continued patient engagement and inclusion of patient experience data in every aspect of the drug development process will further facilitate the approval of new treatments.
Data from: Translocation tactics: a framework to support the IUCN Guidelines for wildlife translocations and improve the quality of applied methods
1. Translocation is a popular conservation tool, but the outcomes are variable. Many tactics can be used to improve the probability of success, but a comprehensive summary of these does not exist. This increases the risk that valuable tactics will be overlooked, and inhibits effective communication. 2. We assess the diversity of 'translocation tactics' used in mammal and bird translocations, by reviewing the IUCN/SSC Guidelines for Reintroduction and other Conservation Translocations, 195 peer-reviewed articles and 73 case studies from the IUCN/SSC Global Reintroduction Perspectives Series.3. We recorded descriptions of every technique used to influence the post-release performance of translocated wildlife. We developed the Translocation Tactics Classification System (TTCS) which defines a collection of 30 tactics and organize them into an ecologically relevant framework. We also assess the occurrence of tactics within the Guidelines, the primary literature and the case studies to evaluate how tactics are communicated within these mediums. 4. Our results indicate that the Guidelines are a valuable resource, but do not exhaustively cover tactics, and that detailed methodological accounts are rarely made publicly accessible. This highlights the need to develop context-specific resources to support the Guidelines, and to develop and exploit mediums that facilitate recording of methodological detail, the tactical rationale behind the design and evaluations of effectiveness. Although some forms of grey literature address this issue, the general lack of information limits the ability to investigate the relationship between tactics and translocation success. 5. Synthesis and applications. The Translocation Tactics Classification System (TTCS) provides a checklist which ensures that the full diversity of tactics is considered when developing translocation processes. Standardizing the communication of tactics, and encouraging detailed accounts of applied methodologies to be recorded, along with the tactical reasoning behind the design, will provide operational models and the data required to conduct broad-scale meta-analyses.
Annotation Guideline of LRE corpus
<p>本文書は、場所参照表現タグ付きコーパスのアノテーションのためのガイドラインです。一部、作業手順書的な内容を含んでいます。</p>
Assessing Garousi's Guidelines - A Focus Group Research
<p>Replication package of the study conducted to assess Garousi's Guidelines.</p>
Supplementary material 1 from: Dang NA, Jackson BM, Tomscha SA, Lilburne L, Burkhard K, Tran DD, Phi LH, Benavidez R (2022) Guidelines and a supporting toolbox for parameterising key soil hydraulic properties in hydrological studies and broader integrated modelling. One Ecosystem 7: e76410. https://doi.org/10.3897/oneeco.7.e76410
Supplementary Material S1
Supplementary material 2 from: Dang NA, Jackson BM, Tomscha SA, Lilburne L, Burkhard K, Tran DD, Phi LH, Benavidez R (2022) Guidelines and a supporting toolbox for parameterising key soil hydraulic properties in hydrological studies and broader integrated modelling. One Ecosystem 7: e76410. https://doi.org/10.3897/oneeco.7.e76410
Supplementary Material S2
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.