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1581por Maguire, Jonathon L, Birken, Catherine S, Loeb, Mark B, Mamdani, Muhammad, Thorpe, Kevin, Hoch, Jeffrey S, Mazzulli, Tony, Borkhoff, Cornelia M, Macarthur, Colin, Parkin, Patricia C“…METHODS/DESIGN: This study is a pragmatic randomized controlled trial. Over 4 successive winters we will recruit 750 healthy children 1–5 years of age. …”
Publicado 2014
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1582“…BACKGROUND: Recruiting to randomized controlled trials is fraught with challenges; with less than one third recruiting to their original target. …”
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1585por Tudur Smith, Catrin, Williamson, Paula, Jones, Ashley, Smyth, Alan, Hewer, Simon Langton, Gamble, Carrol“…BACKGROUND: Some level of monitoring is usually required during a clinical trial to protect the rights and safety of trial participants and to safeguard the quality and reliability of trial results. …”
Publicado 2014
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1586“…BACKGROUND: We propose a mathematical model for multichannel assessment of the trial-to-trial variability of auditory evoked brain responses in magnetoencephalography (MEG). …”
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1587por Blum, Claudine A, Nigro, Nicole, Winzeler, Bettina, Suter-Widmer, Isabelle, Schuetz, Philipp, Briel, Matthias, Bingisser, Roland, Zimmerli, Werner, Ullmer, Elke, Elsaesser, Hanno, Tarr, Philip, Wirz, Sebastian, Thomann, Robert, Hofmann, Eveline, Rodondi, Nicolas, Duplain, Hervé, Burki, Dieter, Mueller, Beat, Christ-Crain, Mirjam“…Due to discontinuing glucocorticoids without tapering after seven days, we limit duration of glucocorticoid exposition, which may reduce possible side effects. TRIAL REGISTRATION: 7 September 2009 on ClinicalTrials.gov: NCT00973154.…”
Publicado 2014
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1588“…OBJECTIVE: To evaluate the utility of the ClinicalTrials.gov registry as a data source for semi-automated trial eligibility screening. …”
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1589por Lindson-Hawley, Nicola, Coleman, Tim, Docherty, Graeme, Hajek, Peter, Lewis, Sarah, Lycett, Deborah, McEwen, Andy, McRobbie, Hayden, Munafò, Marcus R, Parrott, Steve, Aveyard, Paul“…The pragmatic study design means that results will give a realistic estimate of the success of the intervention if it were to be rolled out as part of standard smoking cessation service practice. TRIAL REGISTRATION: Current Controlled Trials ISRCTN33031001. …”
Publicado 2014
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1590por Harrold, Leslie R, Reed, George W, Harrington, J Timothy, Barr, Christine J, Saunders, Katherine C, Gibofsky, Allan, Greenberg, Jeffrey D, John, Ani, Devenport, Jenny, Kremer, Joel M“…DISCUSSION: This cluster-randomized behavioral intervention study will provide valuable insights on the outcomes and feasibility of employing a T2T treatment approach in clinical practice in the United States. TRIAL REGISTRATION: NCT01407419 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2474-15-389) contains supplementary material, which is available to authorized users.…”
Publicado 2014
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1591“…An appropriately equipped and staffed Phase I unit is critical for smooth conduct of a first-in-man clinical trial. The first-in-man prophylactic vaccine trial(s) requires basic infrastructure of clinical trial site, experienced and dedicated site staff and healthy adults as volunteers. …”
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1592por Ni, Yizhao, Kennebeck, Stephanie, Dexheimer, Judith W, McAneney, Constance M, Tang, Huaxiu, Lingren, Todd, Li, Qi, Zhai, Haijun, Solti, Imre“…Objectives (1) To develop an automated eligibility screening (ES) approach for clinical trials in an urban tertiary care pediatric emergency department (ED); (2) to assess the effectiveness of natural language processing (NLP), information extraction (IE), and machine learning (ML) techniques on real-world clinical data and trials. …”
Publicado 2015
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1593por Rose, Annika, Vinogradov, Sophia, Fisher, Melissa, Green, Michael F., Ventura, Joseph, Hooker, Christine, Merzenich, Michael, Nahum, Mor“…The purpose of the current trial (referred to as the TReatment of Social cognition in Schizophrenia Trial or TRuSST) is to compare SocialVille to an active control training condition, include a larger sample of patients, and assess both social cognitive functioning, and functional outcomes. …”
Publicado 2015
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1594por Reynolds, Penny S., Michael, Mary Jane, Cochran, Emily D., Wegelin, Jacob A., Spiess, Bruce D.“…Demonstration of significant reductions in mortality and coagulopathic/inflammatory-related morbidities as a result of pre-hospital plasma administration would be of considerable clinical importance for the management of haemorrhagic shock in both civilian and military populations. TRIAL REGISTRATION: ClinicalTrials.gov: NCT02303964 on 28 November 2014…”
Publicado 2015
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1595por Kennedy-Martin, Tessa, Curtis, Sarah, Faries, Douglas, Robinson, Susan, Johnston, Joseph“…Randomized controlled trials (RCTs) are conducted under idealized and rigorously controlled conditions that may compromise their external validity. …”
Publicado 2015
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1596“…BACKGROUND: Confidence that randomized controlled trial (RCT) results accurately reflect intervention effectiveness depends on proper trial conduct and the accuracy and completeness of published trial reports. …”
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1597por Constable, Lynda, Davidson, Tracey, Wileman, Samantha, McCormack, Kirsty, Thomas, Ruth, McDonald, Alison, Glazener, Cathryn, Norrie, JohnEnlace del recurso
Publicado 2015
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1598por Nicholson, A, Daykin, A, Macefield, R, McCann, S, Shorter, G, Sydes, M, Gamble, C, Shaw, A, Lane, JAEnlace del recurso
Publicado 2015
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1599por Fleming, J., Kamal, A., Harrison, E., Hamborg, T., Stewart-Brown, S., Thorogood, M., Griffiths, F., Robertson, W.“…BACKGROUND: Recruitment to trials evaluating the effectiveness of childhood obesity management interventions is challenging. …”
Publicado 2015
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