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1  Systolic Blood Pressure Intervention Trial (SPRINT).
2 RD-BP) and from October 2010 to August 2015 (SPRINT).
3 d to predict regulators of mis-splicing (RNA-SPRINT).
4  Systolic Blood Pressure Intervention Trial (SPRINT).
5 n a preplanned substudy of participants from SPRINT.
6                      This performs well with SPRINT.
7 cted benefit and more predicted risk than in SPRINT.
8 ing speed in a subgroup of participants from SPRINT.
9 c mortality, calibrated to rates reported in SPRINT.
10 .S. adults meet the eligibility criteria for SPRINT.
11 ost of whom would not have been eligible for SPRINT.
12  9): one session of 4 x 30 s cycle ergometer sprints.
13 dles, which were tested in sequential 2-week sprints.
14 idual variabilities during short course 50 m sprints.
15 ons of the preliminary steps of accelerative sprinting.
16 evalent in sports involving repeated maximal sprinting.
17 e the only key aspect governing accelerative sprinting.
18 ging from walking and running to jumping and sprinting.
19  muscle recovery within the first 48 h after sprinting.
20 s (n = 24) at speeds ranging from walking to sprinting.
21 ing rules (detectable HCV RNA at week 24 for SPRINT-2 and at week 12 for RESPOND-2) could be refined
22                                       In the SPRINT-2 trial, factors that predicted a SVR to triple t
23 rom the Serine Protease Inhibitor Therapy 2 (SPRINT-2) study (treatment-naive patients) and the Retre
24                                           In SPRINT-2, a week 12 rule with an HCV RNA cutoff of >/= 1
25 rom the Serine Protease Inhibitor Therapy 2 [SPRINT-2] trial) and those who did not respond to prior
26  mm Hg), only a few would have qualified for SPRINT (27.0% and 21.9% of untreated and treated patient
27 portion of whom would have been eligible for SPRINT (5.4% untreated, 13.9% treated) or HOPE-3 (13.9%
28                  Of U.S. adults eligible for SPRINT, 51.0% (95% CI: 47.8% to 54.1%) or 8.6 million (9
29         Of the 9361 participants enrolled in SPRINT, 8828 (5578 men [63.2%]; mean [SD] age, 68.0 [9.5
30  Systolic Blood Pressure Intervention Trial (SPRINT), 9361 randomized clinical trial participants 50
31  study was a secondary analysis of data from SPRINT, a randomized clinical trial comparing intensive
32 eds might originate from intrinsically lower sprinting abilities of athletes with BKA or from more co
33 e performance was assessed by using repeated sprint ability (RSA) and Wingate tests.
34 f the primary outcome is to improve repeated sprint ability performance.
35 rength (right + left grip), speed (5 m, 20 m sprints), acceleration (10 to 20 m), agility (figure-of-
36  Systolic Blood Pressure Intervention Trial (SPRINT), adults at high risk for cardiovascular disease
37 t among the 6 key, prespecified subgroups in SPRINT: age >/=75 years, prior cardiovascular disease, c
38                                              SPRINT allows the biostatistician to concentrate on the
39 p identify subgroups of participants in both SPRINT and ACCORD-BP who had lower versus higher ARRs in
40 eed to occur at 3 times the rate observed in SPRINT and be 3 times more common in the intensive manag
41 s with SBP of 120 mm Hg or higher, including SPRINT and HOPE-3 eligibility, and estimated who may hav
42 ectives: To assess the representativeness of SPRINT and HOPE-3 relative to patients in the United Sta
43 ensor moment arms were maximized to optimize sprint and marathon running performance, and hip muscles
44 of humans worldwide and is linked to reduced sprint and power performance in both elite athletes and
45 alpha-actinin-3 deficiency is detrimental to sprint and power performance in both elite athletes and
46       Picture a predator watching their prey sprint and screech through a field.
47              Despite differences between the SPRINT and target populations, we estimated a similar be
48  correlations were found between 20-m flying sprint and the SST (p < 0.05).
49 t high performance motor activities, such as sprinting and jumping.
50 howing that hip musculature is vital to both sprinting and marathon running.
51 imal distribution of added muscle volume for sprinting and marathon running.
52                                 For example, sprinting and running are fundamental to many forms of s
53 ffective for enhancing knee joint mechanics, sprint, and agility recovery post-fatigue, while SS is o
54  cultures: Texel DCM-1, Texel LM-30, Biostar Sprint, and SM-181.
55 ing the fatigue response to repeated maximal sprints are unclear.
56 ly agile, scrambling ibex Capra sibirica and sprinting argali Ovis ammon-responded to predation risk
57                                       Humans sprinting around banked bends change the duration of foo
58  Spectral Parameterization Resolved in Time (SPRiNT) as a novel method for decomposing complex neural
59 care, Eighth Joint National Committee based, SPRINT based) using nationally representative data to an
60 h optimal brain health improved with optimal SPRINT-based BP treatment implementation versus usual ca
61                                              SPRINT-based BP treatment increased the number of years
62                    Optimal implementation of SPRINT-based BP treatment strategy, compared with usual
63  lived free of ASCVD events were greater for SPRINT-based than Eighth Joint National Committee-based
64 ith CKD who met the eligibility criteria for SPRINT between January 1 and December 31, 2019, in the V
65                          The current body of sprinting biomechanics literature together with the fron
66           The 2004 Olympic women's 100-metre sprint champion, Yuliya Nesterenko, is assured of fame a
67  Systolic Blood Pressure Intervention Trial (SPRINT), conducted from October 20, 2010, to August 20,
68  Systolic Blood Pressure Intervention Trial (SPRINT), conducted November 2010 through July 2018.
69 and determine the broader population to whom SPRINT could be generalized.
70 ), Maximal Sprinting Speed Test (20-m flying sprint), Countermovement Jump (CMJ), and Standing Long J
71                       Overall, 22.2% met the SPRINT criteria, representing 116.2 (95% CI 107.5 to 124
72 nese adults aged 45 years and older who meet SPRINT criteria.
73  Systolic Blood Pressure Intervention Trial (SPRINT) demonstrated the benefit of lowering systolic bl
74 ning distance (HSR; 19.81-25.2 km h(-1)) and sprinting distance (SprD; > 25.2 km h(-1)) were analysed
75 , and characteristics of U.S. adults meeting SPRINT eligibility criteria and determine the broader po
76 treated hypertension, the percentage meeting SPRINT eligibility criteria increased with older age, wa
77                                              SPRINT eligibility criteria were applied to the 1999 to
78 adults who would qualify for treatment under SPRINT eligibility criteria.
79 on) adults with treated hypertension met the SPRINT eligibility criteria.
80                                              SPRINT eligibility included age >/=50 years, SBP of 130
81    Main limitations include lack of specific SPRINT eligibility information in the CHARLS survey, unc
82  intensive SBP treatment among those meeting SPRINT eligibility.
83 nd quality-adjusted life-years (QALYs) among SPRINT-eligible adults, under 2 alternative treatment st
84 national sources to a hypothetical cohort of SPRINT-eligible adults.
85 six randomised controlled trials (ACCORD BP, SPRINT, ESPRIT, BPROAD, STEP, and CRHCP).
86  Systolic Blood Pressure Intervention Trial (SPRINT) estimated the effect of intensive systolic blood
87 uding total distance covered (TD), number of sprints, fast run distance, accelerations, and decelerat
88                                              Sprint Fidelis (Fidelis) implantable cardioverter-defibr
89  safety and feasibility of extraction of the Sprint Fidelis (Medtronic, Minneapolis, Minnesota) lead.
90 onsecutive patients undergoing extraction of Sprint Fidelis (models 6930, 6931, 6948, 6949) leads at
91                                              Sprint Fidelis (SF) (Medtronic, Inc., Minneapolis, Minne
92 urvival analyses on our 3-center database of Sprint Fidelis and Quattro Secure implantable cardiovert
93 cardioverter-defibrillator leads such as the Sprint Fidelis are limited.
94             The reported failure rate of the Sprint Fidelis defibrillator lead has increased to a ran
95                                          The Sprint Fidelis implantable cardioverter-defibrillator le
96                            Extraction of the Sprint Fidelis lead can be performed safely by experienc
97       Recommendations regarding prophylactic Sprint Fidelis lead extraction may warrant reconsiderati
98                                              Sprint Fidelis leads are prone to pace-sense lead fractu
99        Between May 2005 and August 2009, 349 Sprint Fidelis leads were extracted from 348 patients.
100                              A total of 3169 Sprint Fidelis leads were implanted in 11 centers with a
101                  The animal's probability of sprinting forward in response to a mechanosensory stimul
102          The Systolic BP Intervention Trial (SPRINT) found that intensive versus standard systolic BP
103                                     Overall, SPRINT-Gly is 18% and 50% higher in Matthews correlation
104                           The method, called SPRINT-Gly, achieved consistent results between ten-fold
105  no differences in the quantity or length of sprints (&gt;24 km h(-1)) between CON and HOT.
106 reat Britain is only weakly heritable across sprint (h(2) = 0.124), middle-distance (h(2) = 0.122) an
107  initial recovery following repeated maximal sprinting in humans.
108 CK-based profiling of in vitrotranscription (SPRINT), in vitro transcribed RNA sequence-specifically
109                                          The SPRINT inclusion criteria were age >/=50 years, SBP 130
110          Here, we show that repeated maximal sprints induce neuromuscular fatigue accompanied with a
111 quantify the potential benefits and risks of SPRINT intensive goal implementation, we estimated the d
112 xcess serious adverse events incurred if the SPRINT intensive SBP treatment goal were implemented in
113 ntly, in the Systolic BP Intervention Trial (SPRINT), intensive lowering of clinic systolic BP to a t
114                                           In SPRINT, intensive BP reduction decreased both acute deco
115 nged in a coordinate manner in response to a sprint interval exercise training regimen in humans and
116                 Second, we hypothesized that sprint interval training (SIT) also promotes increases i
117                                              Sprint interval training (SIT) and traditional endurance
118 e exercise performance in adult humans after sprint interval training (SIT) has been attributed to mi
119                                              Sprint interval training (SIT) has been proposed as a ti
120                                              Sprint interval training (SIT) has been proposed as a ti
121                                              Sprint interval training (SIT) has been proposed as a ti
122           We report that a single session of sprint interval training (SIT), but not of moderate inte
123                           In human subjects, sprint interval training primarily stimulated synthesis
124 andomized controlled trial and observed that sprint-interval exercise (SIE; n = 14), compared to mode
125 ive phosphorylation (OXPHOS) proteins, while sprint-interval training (SIT) improves respiratory func
126  Systolic Blood Pressure Intervention Trial (SPRINT) is a multicenter randomized clinical trial that
127             The Simple Parallel R INTerface (SPRINT) is a wrapper around such parallelised functions.
128 ximal exercises (i.e. less than 1 min - e.g. sprints, jumps, isometric contractions) exhibits diurnal
129 d, where addition of starter culture Biostar Sprint (Lactobacillus sakei, Staphylococcus carnosus, St
130 resent study provides evidence that repeated sprinting leads to significant decreases in average spee
131 ne in the control group were able to achieve SPRINT levels without antihypertensives.
132      The kinematic changes immediately after sprinting likely protected fatigued hamstrings from exce
133 rdized approach to BP management, as used in SPRINT, may help ensure equitable care and could reduce
134 s with BKA or from more complex adaptions in sprinting mechanics due to the biomechanical and morphol
135  Systolic Blood Pressure Intervention Trial (SPRINT MIND), a multicenter randomized clinical trial th
136 r individuals at risk, most notably from the SPRINT-MIND trial.
137  Systolic Blood Pressure Intervention Trial (SPRINT; N=9361), the Action to Control Cardiovascular Ri
138  RNA was quantified on a NanoString nCounter SPRINT (NanoString Technologies, Seattle, WA).
139 of a heart attack and the leg pain of a 30 s sprint--occurs when muscle gets too little oxygen for it
140 e step from a transition state by a unitary "sprint" of approximately 7.8 nm.
141 t during recovery from an exhaustive 1-2 min sprint on a bicycle ergometer with a workload of 400 W.
142                          When executed using SPRINT on an HPC resource of eight processors this compu
143 ed how the Namib Day Gecko, Rhoptropus afer, sprints on ecologically relevant substrates.
144 verage speed between the fastest and slowest sprint (p < 0.001; d = 2.27).
145                           Compared with 9361 SPRINT participants (mean [SD] age, 67.9 [9.4] years; 60
146                                  Among 8,828 SPRINT participants (mean age 67.9 years, 35% women), 60
147                                        Among SPRINT participants above BP target goal, this cross-sec
148                                     Of 6,554 SPRINT participants analyzed (mean age 65 years, 37% wom
149           Self-identified non-Hispanic Black SPRINT participants free of diabetes at baseline were in
150                                              SPRINT participants in the highest predicted benefit sub
151 r rates of dialysis or transplantation among SPRINT participants randomized to intensive treatment, b
152                              A total of 7918 SPRINT participants were included in the analysis; 3989
153                                  Of the 8685 SPRINT participants who were prevalent users of antihype
154                             Similarly, among SPRINT participants with baseline LVH (n=605, 7.4%), tho
155 the composite of ADHF events and death among SPRINT participants with baseline malignant LVH.
156                                        Among SPRINT participants with CKD, worse tubular secretion wa
157                              Data from 9,069 SPRINT participants with complete data on covariates wer
158                                              SPRINT participants with higher baseline predicted CVD r
159                                        Among SPRINT participants without baseline CVD, the relative r
160                                        Among SPRINT participants without baseline LVH (n=7559), inten
161                             Among 2466 Black SPRINT participants, a higher European ancestry proporti
162                                   Among 9361 SPRINT patients, 755 patients (8.1%) had a MACE or death
163 ation, body weight loss as well as post-game sprint performance were similar between the two conditio
164  technique modifications affect accelerative sprinting performance and assess whether the hypothetica
165                In this secondary analysis of SPRINT, prevalent users of regimens that contain exclusi
166 e randomized systolic BP intervention on the SPRINT primary cardiovascular composite and all-cause mo
167 tensive (versus standard) BP lowering on the SPRINT primary CVD outcome (a composite of myocardial in
168 and quantified using the NanoString nCounter SPRINT Profiler.
169 mine the acute effects of a maximum repeated sprint protocol on (1) hamstring shear modulus and (2) k
170 ction, before and after a 10 x 30 m repeated sprint protocol.
171  Systolic Blood Pressure Intervention Trial (SPRINT) provide background information and context on th
172 ignificantly positively correlated with 30-m sprinting (r = 0.604, p < 0.05).
173 red horse population that are best suited to sprint racing.
174  Systolic Blood Pressure Intervention Trial (SPRINT) randomized clinical trial compared the efficacy
175                                        These SPRINT reactions are easily adaptable to portable format
176                                   We foresee SPRiNT responding to growing neuroscientific interests i
177 ors have questioned the ability to translate SPRINT results into routine clinical practice, in which
178                           We generalized the SPRINT results to US adults who would qualify for treatm
179  Systolic Blood Pressure Intervention Trial (SPRINT) results, we propose a systolic blood pressure ta
180                   The follow-up protocol for SPRINT routinely assessed two laboratory monitoring AEs
181 monstrate, with naturalistic synthetic data, SPRiNT's capacity to reliably recover time-varying spect
182 on with the release of detailed results from SPRINT's primary analysis.
183                                 We emphasize SPRiNT's specific strengths compared to other time-frequ
184 lder receiving treatment for hypertension, a SPRINT SBP level of 120 mm Hg or lower was not associate
185                                  With design sprints, Scrum, Model-View-Controller, and Representatio
186  to explore the correlation between repeated sprint sets (RSS) ability and several physical attribute
187 ic capacity and short repeated accelerations/sprint sets for overall competitive performance in socce
188  Systolic Blood Pressure Intervention Trial (SPRINT) showed significant reductions in death and cardi
189  Systolic Blood Pressure Intervention Trial (SPRINT) showed that intensive blood pressure control red
190  Systolic Blood Pressure Intervention Trial (SPRINT) showed that intensive control of systolic blood
191  Systolic Blood Pressure Intervention Trial (SPRINT) showed that intensive lowering of systolic BP in
192 lgus, fastest take-off time; d = 0.43-1.89), sprint speed (d = 0.57-0.71), and agility (d = 0.80-0.92
193                                         Fast sprint speed evolved several times in lizards, including
194 the subdigital adhesive toe pad may increase sprint speed in this species.
195 1)) by 26% in HOT compared to CON), but peak sprint speed was 4% higher (P<0.05) in HOT than in CON,
196 ment jump (CMJ) (assessed via OpenCap), 20-m sprint speed, and Illinois agility test performance.
197 veral physical attributes, including maximum sprint speed, maximal aerobic speed, maximal anaerobic s
198                                However, peak sprinting speed and execution of successful passes and c
199 bic Shuttle Running Test (V(MASRT)), Maximal Sprinting Speed Test (20-m flying sprint), Countermoveme
200                      We found slower maximum sprinting speeds in athletes with BKA, but did not find
201 ss and elastic energy storage at running and sprinting speeds.
202 s ran at self-selected endurance running and sprinting speeds.
203                                 The MCL-002 (SPRINT) study was a randomised, phase 2 study of patient
204 f diabetes or dementia were screened for the SPRINT substudy from 6 sites in the US.
205  Systolic Blood Pressure Intervention Trial (SPRINT) suggested that a SBP level of lower than 120 mm
206                 Coaches should be aware that sprint swimmers produce significant differences in the s
207                                              Sprinting, swimming, and jumping performance of ectother
208                  This study pooled data from SPRINT (Systolic Blood Pressure Intervention Trial) and
209                                              SPRINT (Systolic Blood Pressure Intervention Trial) demo
210 g one, and 19.5% (95% CI, 18.5-20.5) met the SPRINT (Systolic Blood Pressure Intervention Trial) elig
211                                   Among 2089 SPRINT (Systolic Blood Pressure Intervention Trial) part
212 Joint National Committee recommendations and SPRINT (Systolic Blood Pressure Intervention Trial) prot
213 re (SBP) treatment goal is in question, with SPRINT (Systolic Blood Pressure Intervention Trial) sugg
214 is for the primary end point considering the SPRINT (Systolic Blood Pressure Intervention Trial) targ
215             We evaluated the participants of SPRINT (Systolic Blood Pressure Intervention Trial) to a
216                                              SPRINT (Systolic Blood Pressure Intervention Trial) was
217             A total of 8,820 participants in SPRINT (Systolic Blood Pressure Intervention Trial) were
218        This study was a post hoc analysis of SPRINT (Systolic Blood Pressure Intervention Trial), a r
219                                           In SPRINT (Systolic Blood Pressure Intervention Trial), a s
220                                       In the SPRINT (Systolic Blood Pressure Intervention Trial), int
221                                           In SPRINT (Systolic Blood Pressure Intervention Trial), pat
222             This was a secondary analysis of SPRINT (Systolic Blood Pressure Intervention Trial).
223 baseline and 1 year from stored specimens in SPRINT (Systolic Blood Pressure Intervention Trial).
224                         Subgroup analyses of SPRINT (Systolic Blood Pressure Intervention Trial).
225 lure (ADHF) was a frequent common outcome in SPRINT (Systolic Blood Pressure Intervention Trial).
226 , using individual participant data from the SPRINT (Systolic Blood Pressure Intervention Trial; N=93
227                In this secondary analysis of SPRINT (Systolic Pressure Intervention Trial), participa
228 dulus, the only significant change after the sprint task was in the biceps femoris long head (BFlh) w
229 lite players during the games and a repeated sprint test was conducted after the two game trials.
230 , countermovement jumps [CMJ]), the 20-meter sprint test, and the Yo-Yo intermittent recovery test (Y
231 Phe levels are increased following a Wingate sprint test.
232 regulator of dynein-dependent transport) and Sprint (the guanine nucleotide exchange factor for Rab5)
233  Systolic Blood Pressure Intervention Trial (SPRINT), the longer-term incidence of needing dialysis o
234 atistically significant improvements in 40-m sprint time in study I (compared to LR) and in star dril
235 ilance test), and athletic performance (40-m sprint time, long jump distance, and star drill time) in
236 correlations between tlim100 and SST (sum of sprint times), and large negative correlations between Y
237 r study aimed to assess the applicability of SPRINT to Chinese adults.
238               To translate the findings from SPRINT to clinical practice, we developed prediction mod
239                               Lastly, we use SPRiNT to demonstrate how aperiodic dynamics relate to m
240                               Second, we use SPRiNT to illustrate how aperiodic spectral features flu
241  Systolic Blood Pressure Intervention Trial (SPRINT) to estimate treatment effects and adverse event
242     Athletes increasingly engage in repeated sprint training consisting in repeated short all-out eff
243 en healthy young men performed nine repeated sprint training sessions in either normoxia (F(I)O(2) =
244     We used a microsimulation model to apply SPRINT treatment effects and health care costs from nati
245                     Although adoption of the SPRINT treatment strategy would increase the number of C
246 rt disease classification, and data from the SPRINT trial (Systolic Blood Pressure Intervention Trial
247 pertension but no diabetes mellitus from the SPRINT trial (Systolic Blood Pressure Intervention Trial
248 ts that closely resemble participants of the SPRINT trial (Systolic Blood Pressure Trial).
249     METHODS AND Cox models were derived from SPRINT trial data and validated on ACCORD-BP trial data
250  and explore how ambulatory BP data from the SPRINT trial may inform this discussion.
251                                          The SPRINT trial was conducted between November 1, 2010, and
252            In this secondary analysis of the SPRINT trial, participants with higher baseline projecte
253 sistent with the estimates from the original SPRINT trial.
254 associated with intensive BP lowering in the SPRINT trial.
255 ed on a level surface while contributions to sprinting uphill are more evenly distributed among motio
256 l tournament, using squat, bench press, 30-m sprint, vertical jump, pull-ups and abdominal endurance
257                                              SPRINT was an open-label, multicentre, randomised contro
258                                              SPRINT was terminated early due to benefit observed in t
259                    In a post hoc analysis of SPRINT, we defined change in eGFR as the percentage chan
260 -level data from 9361 randomized patients in SPRINT, we developed models to predict risk for MACE or
261  covariate, treatment, and outcome data from SPRINT were combined with covariate data from these popu
262 7%] women) who had been randomly assigned in SPRINT were enrolled in the substudy (1448 received inte
263 d the increase in adverse events observed in SPRINT were largely transportable to trial-eligible CKD
264 absolute risks for serious adverse events in SPRINT were used to estimate the number of potential dea
265  Systolic Blood Pressure Intervention Trial (SPRINT), which recruited individuals 50 years or older w
266  Systolic Blood Pressure Intervention Trial (SPRINT), which recruited participants from 102 sites in
267 nsive therapy in mild to moderate CKD, where SPRINT will help to inform practice, as well as where ga
268 ale and eight female swimmers performed 25 m sprints with five isotonic loads (1-2-3-4-5 kg for femal
269 ation of this conceptual scaffold in 'design sprint' workshops for graduate students in the life scie

 
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