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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
23 rom the Serine Protease Inhibitor Therapy 2 (SPRINT-2) study (treatment-naive patients) and the Retre
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%
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
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
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
53 ffective for enhancing knee joint mechanics, sprint, and agility recovery post-fatigue, while SS is o
56 ly agile, scrambling ibex Capra sibirica and sprinting argali Ovis ammon-responded to predation risk
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
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
67 Systolic Blood Pressure Intervention Trial (SPRINT), conducted from October 20, 2010, to August 20,
70 ), Maximal Sprinting Speed Test (20-m flying sprint), Countermovement Jump (CMJ), and Standing Long J
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
81 Main limitations include lack of specific SPRINT eligibility information in the CHARLS survey, unc
83 nd quality-adjusted life-years (QALYs) among SPRINT-eligible adults, under 2 alternative treatment st
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
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
92 urvival analyses on our 3-center database of Sprint Fidelis and Quattro Secure implantable cardiovert
106 reat Britain is only weakly heritable across sprint (h(2) = 0.124), middle-distance (h(2) = 0.122) an
108 CK-based profiling of in vitrotranscription (SPRINT), in vitro transcribed RNA sequence-specifically
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
115 nged in a coordinate manner in response to a sprint interval exercise training regimen in humans and
118 e exercise performance in adult humans after sprint interval training (SIT) has been attributed to mi
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
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
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
137 Systolic Blood Pressure Intervention Trial (SPRINT; N=9361), the Action to Control Cardiovascular Ri
139 of a heart attack and the leg pain of a 30 s sprint--occurs when muscle gets too little oxygen for it
141 t during recovery from an exhaustive 1-2 min sprint on a bicycle ergometer with a workload of 400 W.
151 r rates of dialysis or transplantation among SPRINT participants randomized to intensive treatment, b
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
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
169 mine the acute effects of a maximum repeated sprint protocol on (1) hamstring shear modulus and (2) k
171 Systolic Blood Pressure Intervention Trial (SPRINT) provide background information and context on th
174 Systolic Blood Pressure Intervention Trial (SPRINT) randomized clinical trial compared the efficacy
177 ors have questioned the ability to translate SPRINT results into routine clinical practice, in which
179 Systolic Blood Pressure Intervention Trial (SPRINT) results, we propose a systolic blood pressure ta
181 monstrate, with naturalistic synthetic data, SPRiNT's capacity to reliably recover time-varying spect
184 lder receiving treatment for hypertension, a SPRINT SBP level of 120 mm Hg or lower was not associate
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
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
199 bic Shuttle Running Test (V(MASRT)), Maximal Sprinting Speed Test (20-m flying sprint), Countermoveme
205 Systolic Blood Pressure Intervention Trial (SPRINT) suggested that a SBP level of lower than 120 mm
210 g one, and 19.5% (95% CI, 18.5-20.5) met the SPRINT (Systolic Blood Pressure Intervention Trial) elig
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
223 baseline and 1 year from stored specimens in 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
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
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
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
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
249 METHODS AND Cox models were derived from SPRINT trial data and validated on ACCORD-BP trial data
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
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