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42201“…Repeated measures multivariate analysis of covariance (intention-to-treat) found that breast cancer e-support + care as usual participants had significant better health outcomes at 3 months regarding self-efficacy (21.05; 95% CI 1.87-40.22; P=.03; d=0.53), symptom interference (−0.73; 95% CI −1.35 to −.11; P=.02; d=−0.51), and quality of life (6.64; 95% CI 0.77-12.50; P=.03, d=0.46) but not regarding social support, symptom severity, anxiety, and depression compared with care as usual participants. …”
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42202por Griffin, Damian R, Dickenson, Edward J, Wall, Peter D H, Achana, Felix, Donovan, Jenny L, Griffin, James, Hobson, Rachel, Hutchinson, Charles E, Jepson, Marcus, Parsons, Nick R, Petrou, Stavros, Realpe, Alba, Smith, Joanna, Foster, Nadine E“…The primary outcome was hip-related quality of life, as measured by the patient-reported International Hip Outcome Tool (iHOT-33) 12 months after randomisation, and analysed in all eligible participants who were allocated to treatment (the intention-to-treat population). This trial is registered as an International Standard Randomised Controlled Trial, number ISRCTN64081839, and is closed to recruitment. …”
Publicado 2018
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42203por Howard, Robert, Cort, Elizabeth, Bradley, Rosie, Harper, Emma, Kelly, Linda, Bentham, Peter, Ritchie, Craig, Reeves, Suzanne, Fawzi, Waleed, Livingston, Gill, Sommerlad, Andrew, Oomman, Sabu, Nazir, Ejaz, Nilforooshan, Ramin, Barber, Robert, Fox, Chris, Macharouthu, Ajay Verma, Ramachandra, Pranathi, Pattan, Vivek, Sykes, John, Curran, Val, Katona, Cornelius, Dening, Tom, Knapp, Martin, Gray, Richard“…The primary, secondary, and safety endpoints were all analysed in participants given at least one dose of study treatment in modified intention-to-treat analyses. This study is registered with EudraCT, number 2010-022184-35, and ISRCTN, number ISRCTN45593573. …”
Publicado 2018
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42204por Li, Jinshuo, Parrott, Steve, Sweeting, Michael, Farmer, Andrew, Ross, Jamie, Dack, Charlotte, Pal, Kingshuk, Yardley, Lucy, Barnard, Maria, Hudda, Mohammed, Alkhaldi, Ghadah, Murray, Elizabeth“…The primary analysis was based on intention-to-treat, using multiple imputation to handle the missing data. …”
Publicado 2018
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42205por Cohen, Stanley B., Alten, Rieke, Kameda, Hideto, Hala, Tomas, Radominski, Sebastiao C., Rehman, Muhammad I., Palaparthy, Ramesh, Schumacher, Karl, Schmitt, Susanne, Hua, Steven Y., Ianos, Claudia, Lea Sewell, K.“…Week 14 ACR20 in the intention-to-treat population was 62.7% for PF-06438179/GP1111 and 64.1% for infliximab-EU. …”
Publicado 2018
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42206por Geense, Wytske W, van Gaal, Betsie GI, Knoll, Jaqueline L, Maas, Nienke M, Kok, Gerjo, Cornelissen, Elisabeth AM, Nijhuis-van der Sanden, Maria WG“…We used linear mixed models to evaluate the potential effectiveness and effect sizes using the intention-to-treat and per-protocol analyses. In the process evaluation, we evaluated recruitment, reach, the dose received, and context using a questionnaire sent to the parents, log-in data, and a focus group interview with health care professionals. …”
Publicado 2018
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42207por Fleischmann, Roy M., Alten, Rieke, Pileckyte, Margarita, Lobello, Kasia, Hua, Steven Y., Cronenberger, Carol, Alvarez, Daniel, Bock, Amy E., Sewell, K. Lea“…The observed week-12 ACR20 values were 68.7% (PF-06410293) and 72.7% (adalimumab-EU) in the intention-to-treat population. With non-responder imputation, the treatment difference in week-12 ACR20 was −2.98% and corresponding CIs—95% CI (−10.38%, 4.44%) and 90% CI (−9.25%, 3.28%)—were entirely contained within the equivalence margins (symmetric and asymmetric, respectively). …”
Publicado 2018
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42208por Kyrios, Michael, Ahern, Claire, Fassnacht, Daniel B, Nedeljkovic, Maja, Moulding, Richard, Meyer, Denny“…RESULTS: No pretreatment differences were found between the 2 conditions. Intention-to-treat analysis revealed significant pre-post improvements in OCD symptom severity for both conditions (P<.001). …”
Publicado 2018
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42209por Tang, Weiming, Wei, Chongyi, Cao, Bolin, Wu, Dan, Li, Katherine T., Lu, Haidong, Ma, Wei, Kang, Dianmin, Li, Haochu, Liao, Meizhen, Mollan, Katie R., Hudgens, Michael G., Liu, Chuncheng, Huang, Wenting, Liu, Aifeng, Zhang, Ye, Smith, M. Kumi, Mitchell, Kate M., Ong, Jason J., Fu, Hongyun, Vickerman, Peter, Yang, Ligang, Wang, Cheng, Zheng, Heping, Yang, Bin, Tucker, Joseph D.“…The proportion of individuals receiving an HIV test during the intervention periods within a city was 8.9% (95% confidence interval [CI] 2.2–15.5) greater than during the control periods. In addition, the intention-to-treat analysis showed a higher probability of receiving an HIV test during the intervention periods as compared to the control periods (estimated risk ratio [RR] = 1.43, 95% CI 1.19–1.73). …”
Publicado 2018
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42210por Adams, Richard, Brown, Ewan, Brown, Louise, Butler, Rachel, Falk, Stephen, Fisher, David, Kaplan, Richard, Quirke, Phil, Richman, Susan, Samuel, Leslie, Seligmann, Jenny, Seymour, Matt, Shiu, Kai Keen, Wasan, Harpreet, Wilson, Richard, Maughan, Tim“…The final analysis was assessed by intention to treat. This trial is registered at controlled-trials.com, ISRCTN 90061546. …”
Publicado 2017
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42211por Berkley, James A, Ngari, Moses, Thitiri, Johnstone, Mwalekwa, Laura, Timbwa, Molline, Hamid, Fauzat, Ali, Rehema, Shangala, Jimmy, Mturi, Neema, Jones, Kelsey D J, Alphan, Hassan, Mutai, Beatrice, Bandika, Victor, Hemed, Twahir, Awuondo, Ken, Morpeth, Susan, Kariuki, Samuel, Fegan, Gregory“…Secondary endpoints were nutritional recovery, readmission to hospital, and illness episodes treated as an outpatient. Analysis was by intention to treat. This trial was registered at ClinicalTrials.gov, number NCT00934492. …”
Publicado 2016
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42212por McConnell, Tracey, Best, Paul, Davidson, Gavin, McEneaney, Tom, Cantrell, Cherry, Tully, Mark“…Yet, despite these good intentions, the literature on coproduction has struggled to keep pace with the coproduction ‘movement’. …”
Publicado 2018
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42213por Grijalva-Eternod, Carlos S., Jelle, Mohamed, Haghparast-Bidgoli, Hassan, Colbourn, Tim, Golden, Kate, King, Sarah, Cox, Cassy L., Morrison, Joanna, Skordis-Worrall, Jolene, Fottrell, Edward, Seal, Andrew J.“…Primary outcomes were the mean Child Dietary Diversity Score in the household cohort and the incidence of first episode of acute malnutrition in the child cohort, defined by a mid-upper arm circumference < 12.5 cm and/or oedema. Analyses were by intention-to-treat. For the household cohort we assessed differences-in-differences, for the child cohort we used Cox proportional hazards ratios. …”
Publicado 2018
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42214por Baskerville, Neill Bruce, Struik, Laura Louise, Guindon, Godefroy Emmanuel, Norman, Cameron D, Whittaker, Robyn, Burns, Catherine, Hammond, David, Dash, Darly, Brown, K Stephen“…Moreover, 45.34% (725/1599) of participants completed baseline, 3-, and 6-month follow-up. Intention-to-treat analysis (last observation carried forward) showed that continuous abstinence (N=1599) at 6 months was not significantly different at 7.8% (64/820) for CTC versus 9.2% (72/779) for OnRQ (odds ratio; OR 0.83, 95% CI 0.59-1.18). …”
Publicado 2018
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42215por Tavares, Daniela Regina Brandao, Okazaki, Jane Erika Frazao, Rocha, Aline Pereira, Santana, Marcia Valeria De Andrade, Pinto, Ana Carolina Pereira Nunes, Civile, Vinicius Tassoni, Santos, Fania Cristina, Fregni, Felipe, Trevisani, Virginia Fernandes Moça“…The data will be analyzed using the principle of intention-to-treat. RESULTS: This study was approved by the institutional review board with the protocol number 1685/2016. …”
Publicado 2018
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42216por Rockstroh, Jurgen K, Bhagani, Sanjay R, Orkin, Chloe, Soto-Malave, Ruth, Lacombe, Karine, Zhang, Zhenzhen, Wang, Stanley, Mensa, Federico, Trinh, Roger“…Baseline demographics are shown in Tables 1 and 2. The overall intention-to-treat (ITT) SVR12 rate was 98.2% (165/168), with no virologic failures among non-cirrhotic patients treated for 8 weeks; mITT rate (excluding non-virologic failures) was 99.4% (167/168). …”
Publicado 2018
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42217por Alexander, Elizabeth, Goldberg, Lisa, Das, Anita, Moran, Gregory J, Sandrock, Christian, Gasink, Leanne B, Spera, Patricia, Sweeney, Carolyn, Paukner, Susanne, Wicha, Wolfgang W, Schranz, Jennifer“…The US FDA primary endpoint was early clinical response (ECR) (96 ± 24 h after first dose) in the intent-to-treat (ITT) population. The EMA coprimary endpoints (FDA secondary endpoints) were investigator assessment of clinical response (IACR) at test of cure (TOC) (5–10 days after last dose) in the modified ITT (mITT) and clinically evaluable (CE) TOC populations. …”
Publicado 2018
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42218por Gravenstein, Stefan, Davidson, H Edward, Mcconeghy, Kevin, Han, Lisa, Canaday, David, Saade, Elie, Baier, Rosa R, Mor, Vincent“…For the subset of long-stay NH residents (>100 days in facility as of October 1, 2016) aged ≥65 years, we determined how many were hospitalized from November 1, 2016 to June 1, 2017 on an intent-to-treat basis. We obtained all-cause hospitalization, patient-, and facility-level characteristics from Minimum Data Set and Certification and Survey Provider Enhanced Reporting data. …”
Publicado 2018
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42219por Reimer, Jens, Stoehr, Albrecht, Naumann, Uwe, Teuber, Gerlinde, Zamani, Carsten, Mauss, Stefan, Qurishi, Nazifa, Lohmann, Kristina, Kleine, Henning, Pangerl, Andreas, Christensen, Stefan“…There were no virologic failures: of three early discontinuations, one OST patient was lost to follow-up and two non-OST patients discontinued treatment due to adverse events (AE). In the modified intention-to-treat population which excluded non-virologic failures, SVR12 was 100% for both OST and non-OST patients. …”
Publicado 2018
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42220por File, Thomas, Goldberg, Lisa, Paukner, Susanne, Das, Anita, Gelone, Steven P, Saviski, John, Sweeney, Carolyn, Seltzer, Elyse, Talbot, George H, Gasink, Leanne B“…Primary outcomes were early clinical response (ECR) in the intent-to-treat (ITT) population (FDA endpoint), and investigator assessment of clinical response (IACR) at test of cure in the modified ITT (mITT) and clinically evaluable (CE-TOC) populations (co-primary EMA endpoints). …”
Publicado 2018
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