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42501por Ferguson, Max, Rittenbach, Katherine, Leece, Pamela, Adams, Alison, Ali, Farihah, Elton-Marshall, Tara, Burmeister, Charlene, Brothers, Thomas D., Medley, Andrea, Choisil, Paul, Strike, Carol, Ng, Justin, Lorenzetti, Diane L., Gallant, Kat, Buxton, Jane A.“…L’objectif du présent document d’orientation est de formuler des recommandations stratégiques à l’intention des programmes fédéraux, provinciaux et territoriaux de NàE, en s’appuyant sur des données probantes issues de la documentation scientifique, de la littérature grise et des communautés, à la lumière de 11 années de distribution de NàE au Canada. …”
Publicado 2023
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42502por Lin, Yuxi, Ren, Ci, Liao, Meizhen, Kang, Dianmin, Li, Chuanxi, Jiao, Kedi, Wang, Lin, Yan, Yu, Li, Yijun, Wu, Taoyu, Cheng, Chunxiao, Zhao, Zhe, Xu, Zece, Tang, Weiming, Tucker, Joseph D, Ma, Wei“…The primary outcome was self-reported HIV testing uptake in the previous 3 months. An intention-to-treat approach was used to examine the cluster-level effect of the intervention in the 12-month study period using generalized linear mixed models and the individual-level effect using linear mixed models. …”
Publicado 2023
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42503por McKellar, Mehri, Teichner, Paula, Bettacchi, Christopher, Angel, Jonathan, Gordon, Lori A, Sutton, Kenneth, Sutherland-Phillips, Denise, Talarico, Christine L, Urbaityte, Rimgaile, Solingen-Ristea, Rodica Van, Baugh, Bryan, D’Amico, Ronald, van Wyk, Jean A“…The primary analysis was based on the prespecified modified intention-to-treat exposed (mITT-E) population (n=11 from 1 study site excluded from the ITT-E population for protocol deviation) at Month (M) 12. …”
Publicado 2023
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42504por Brand, Richard A.“…Dickson was offered a position at the new Christian Church Hospital in Kansas City. He stated, “My intention was to spend about two years in Kansas City, then return to Philadelphia” [4]. …”
Publicado 2008
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42505por Adams, Richard A, Meade, Angela M, Seymour, Matthew T, Wilson, Richard H, Madi, Ayman, Fisher, David, Kenny, Sarah L, Kay, Edward, Hodgkinson, Elizabeth, Pope, Malcolm, Rogers, Penny, Wasan, Harpreet, Falk, Stephen, Gollins, Simon, Hickish, Tamas, Bessell, Eric M, Propper, David, Kennedy, M John, Kaplan, Richard, Maughan, Timothy S“…Here, we compare arms A and C, with the primary objective of establishing whether overall survival on intermittent therapy was non-inferior to that on continuous therapy, with a predefined non-inferiority boundary of 1·162. Intention-to-treat (ITT) and per-protocol analyses were done. …”
Publicado 2011
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42506por Pontes-Arruda, Alessandro, Martins, Laércia Ferreira, de Lima, Samya Maria, Isola, Alexandre Marini, Toledo, Diogo, Rezende, Ederlon, Maia, Marcelo, Magnan, Gisele Brocco“…RESULTS: A total of 115 patients in the early stages of sepsis requiring EN were included, among whom 106 were considered evaluable. Intention-to-treat (ITT) analysis demonstrated that patients fed the EPA/GLA diet developed less severe sepsis and/or septic shock than patients fed the control diet (26.3% versus 50%, respectively; P = 0.0259), with similar results observed for the evaluable patients (26.4% versus 50.9% respectively; P = 0.0217). …”
Publicado 2011
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42507por James, Nicholas D, Sydes, Matthew R, Mason, Malcolm D, Clarke, Noel W, Anderson, John, Dearnaley, David P, Dwyer, John, Jovic, Gordana, Ritchie, Alastair WS, Russell, J Martin, Sanders, Karen, Thalmann, George N, Bertelli, Gianfilippo, Birtle, Alison J, O'Sullivan, Joe M, Protheroe, Andrew, Sheehan, Denise, Srihari, Narayanan, Parmar, Mahesh KB“…Research arms were compared pairwise against the control arm on an intention-to-treat basis. Accrual of further patients was discontinued in any research arm showing safety concerns or insufficient evidence of activity (lack of benefit) compared with the control arm. …”
Publicado 2012
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42508por Mukherjee, Somnath, Hurt, Christopher N, Bridgewater, John, Falk, Stephen, Cummins, Sebastian, Wasan, Harpreet, Crosby, Tom, Jephcott, Catherine, Roy, Rajarshi, Radhakrishna, Ganesh, McDonald, Alec, Ray, Ruby, Joseph, George, Staffurth, John, Abrams, Ross A, Griffiths, Gareth, Maughan, Tim“…The primary endpoint was 9-month progression-free survival, analysed by intention to treat including only those patients with valid CT assessments. …”
Publicado 2013
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42509Publicado 2013“…Primary efficacy endpoints were new WHO stage 4 events or death for monitoring and change in CD4 percentage at 72 and 144 weeks for ART-strategy randomisations; the co-primary toxicity endpoint was grade 3 or 4 adverse events. Analysis was by intention to treat. This trial is registered, ISRCTN24791884. …”
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42510por Jefferson, Tom, Jones, Mark, Doshi, Peter, Spencer, Elizabeth A, Onakpoya, Igho, Heneghan, Carl J“…Main outcome measures Time to first alleviation of symptoms, influenza outcomes, complications, admissions to hospital, and adverse events in the intention to treat population. Results From the European Medicines Agency and Roche, we obtained clinical study reports for 83 trials. …”
Publicado 2014
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42511por Tilbrook, H.E., Hewitt, C.E., Aplin, J.D., Semlyen, A., Trewhela, A., Watt, I., Torgerson, D.J.“…SUMMARY OF BACKGROUND DATA: A large multicentre RCT using intention-to-treat (ITT) analysis found that participants with chronic low back pain who were offered a 12-week progressive programme of yoga plus usual GP care had better back function than those offered usual GP care alone. …”
Publicado 2014
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42512por Baker, Valerie L., Jones, Christopher A., Doody, Kevin, Foulk, Russell, Yee, Bill, Adamson, G. David, Cometti, Barbara, DeVane, Gary, Hubert, Gary, Trevisan, Silvia, Hoehler, Fred, Jones, Clarence, Soules, Michael“…Both formulations were well-tolerated, with no difference in serious adverse events. Analysis with the intention-to-treat population also demonstrated no difference for any outcomes between the treatment groups. …”
Publicado 2014
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42513por Watson, Sinead, Woodside, Jayne V, Ware, Lisa J, Hunter, Steven J, McGrath, Alanna, Cardwell, Christopher R, Appleton, Katherine M, Young, Ian S, McKinley, Michelle C“…RESULTS: Retention rates for the intervention and control groups at 3 months were 78% (25/32) vs 97% (32/33), at 6 months were 66% (21/32) vs 94% (31/33), and at 12 months were 53% (17/32) vs 88% (29/33). Intention-to-treat analysis, using baseline observation carried forward imputation method, revealed that the intervention group lost more weight relative to the control group at 3 months (mean –3.41, 95% CI –4.70 to –2.13 kg vs mean –0.52, 95% CI –1.55 to 0.52 kg, P<.001), at 6 months (mean –3.47, 95% CI –4.95 to –1.98 kg vs mean –0.81, 95% CI –2.23 to 0.61 kg, P=.02), but not at 12 months (mean –2.38, 95% CI –3.48 to –0.97 kg vs mean –1.80, 95% CI –3.15 to –0.44 kg, P=.77). …”
Publicado 2015
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42514por Huang, Yunda, Follmann, Dean, Nason, Martha, Zhang, Lily, Huang, Ying, Mehrotra, Devan V., Moodie, Zoe, Metch, Barbara, Janes, Holly, Keefer, Michael C., Churchyard, Gavin, Robb, Merlin L., Fast, Patricia E., Duerr, Ann, McElrath, M. Juliana, Corey, Lawrence, Mascola, John R., Graham, Barney S., Sobieszczyk, Magdalena E., Kublin, James G., Robertson, Michael, Hammer, Scott M., Gray, Glenda E., Buchbinder, Susan P., Gilbert, Peter B.“…We predefined two co-primary analysis cohorts for assessing the vaccine effect on HIV-1 acquisition. The modified-intention-to-treat (MITT) cohort included all randomly assigned participants HIV-1 uninfected at study entry, who received at least the first vaccine/placebo, and the Ad5 cohort included MITT participants who received at least one dose of rAd5-HIV vaccine or rAd5-placebo. …”
Publicado 2015
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42515por Oza, Amit M, Cook, Adrian D, Pfisterer, Jacobus, Embleton, Andrew, Ledermann, Jonathan A, Pujade-Lauraine, Eric, Kristensen, Gunnar, Carey, Mark S, Beale, Philip, Cervantes, Andrés, Park-Simon, Tjoung-Won, Rustin, Gordon, Joly, Florence, Mirza, Mansoor R, Plante, Marie, Quinn, Michael, Poveda, Andrés, Jayson, Gordon C, Stark, Dan, Swart, Ann Marie, Farrelly, Laura, Kaplan, Richard, Parmar, Mahesh K B, Perren, Timothy J“…The primary endpoint was progression-free survival; the study was also powered to detect a difference in overall survival. Analysis was by intention to treat. This trial is registered as an International Standard Randomised Controlled Trial, number ISRCTN91273375. …”
Publicado 2015
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42516por Wilkins, Anna, Mossop, Helen, Syndikus, Isabel, Khoo, Vincent, Bloomfield, David, Parker, Chris, Logue, John, Scrase, Christopher, Patterson, Helen, Birtle, Alison, Staffurth, John, Malik, Zafar, Panades, Miguel, Eswar, Chinnamani, Graham, John, Russell, Martin, Kirkbride, Peter, O'Sullivan, Joe M, Gao, Annie, Cruickshank, Clare, Griffin, Clare, Dearnaley, David, Hall, Emma“…The CHHiP trial completed accrual on June 16, 2011, and the QoL substudy was closed to further recruitment on Nov 1, 2009. Analysis was on an intention-to-treat basis. The primary endpoint of the QoL substudy was overall bowel bother and comparisons between fractionation groups were done at 24 months post-radiotherapy. …”
Publicado 2015
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42517por Wilson, Emma, Free, Caroline, Morris, Tim P, Kenward, Michael G, Syred, Jonathan, Baraitser, Paula“…All analyses will be based on the intention-to-treat (ITT) principle. RESULTS: This study is funded by Guy’s and St Thomas’ Charity and it has received ethical approval from NRES Committee London-Camberwell St Giles (Ref 14/LO/1477). …”
Publicado 2016
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42518por Taylor, Stephanie J. C., Carnes, Dawn, Homer, Kate, Kahan, Brennan C., Hounsome, Natalia, Eldridge, Sandra, Spencer, Anne, Pincus, Tamar, Rahman, Anisur, Underwood, Martin“…Analyses followed the intention-to-treat principle, accounted for clustering by course in the intervention arm, and used multiple imputation for missing or incomplete primary outcome data. …”
Publicado 2016
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42519por DeFronzo, Ralph A., Buse, John B., Kim, Terri, Burns, Colleen, Skare, Sharon, Baron, Alain, Fineman, Mark“…A total of 26 randomised participants were included in study 2: 24 had at least one dose of study medication and at least one post-dose pharmacokinetic/pharmacodynamic assessment and were included in the pharmacokinetic/pharmacodynamic intent-to-treat analysis; and 12 completed all treatment periods and were included in the evaluable population. …”
Publicado 2016
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42520por Boeree, Martin J, Heinrich, Norbert, Aarnoutse, Rob, Diacon, Andreas H, Dawson, Rodney, Rehal, Sunita, Kibiki, Gibson S, Churchyard, Gavin, Sanne, Ian, Ntinginya, Nyanda E, Minja, Lilian T, Hunt, Robert D, Charalambous, Salome, Hanekom, Madeleine, Semvua, Hadija H, Mpagama, Stellah G, Manyama, Christina, Mtafya, Bariki, Reither, Klaus, Wallis, Robert S, Venter, Amour, Narunsky, Kim, Mekota, Anka, Henne, Sonja, Colbers, Angela, van Balen, Georgette Plemper, Gillespie, Stephen H, Phillips, Patrick P J, Hoelscher, Michael“…Patients without evidence of rifampicin resistance on phenotypic test who took at least one dose of study treatment and had one positive culture on liquid or solid media before or within the first 2 weeks of treatment were included in the primary analysis (modified intention to treat). Time-to-event data were analysed using a Cox proportional-hazards regression model and adjusted for minimisation variables. …”
Publicado 2017
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