Research article - (2024)23, 326 - 341 DOI: https://doi.org/10.52082/jssm.2024.326 |
Low-load Resistance Exercise with Perceptually Primed Practical Blood Flow Restriction Induces Similar Motor Performance Fatigue, Physiological Changes, and Perceptual Responses Compared to Traditional Blood Flow Restriction in Males and Females |
Robert Bielitzki1,, Tom Behrendt1, Martin Behrens2, Victoria Malczewski1, Thomas Mittlmeier3, Lutz Schega1 |
Key words: Vascular occlusion, performance fatigability, muscle oxygenation, exercise-induced muscle pain, discomfort, sex differences |
Key Points |
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Experimental Procedure |
All participants completed three laboratory visits (familiarization and two experimental trials). During the first visit, participants’ (i) arterial occlusion pressure, (ii) overlap of the elastic wrap for pBFR pressure, (iii) systolic blood flow velocity at 60% AOP in the BFR condition (pneumatic cuff) as well as with the adjusted overlap in the pBFR condition (elastic wrap), and (iv) 1RM during a unilateral isotonic knee extension were determined. Additionally, participants were comprehensively familiarized with the maximal voluntary isometric contractions (MVIC) and exercise protocol including the explanation of the perceptual ratings (i.e., effort, exercise-induced leg muscle pain, and cuff pressure-induced discomfort). In a randomized and counterbalanced cross-over design, participants completed two experimental trials consisting of low-load resistance exercise either with pBFR or BFR on two separate days. All testing sessions were separated by 7 days and were conducted at the same time of day to mitigate the influence of circadian variations. Upon arrival, participants’ blood pressure was measured and checked for hypertension. Subsequently, surface electromyography (sEMG) electrodes were applied to the three superficial quadriceps muscles of the right leg to record maximal muscle activity during MVICs and muscle activity during exercise. Furthermore, a muscular near-infrared spectroscopy (mNIRS) monitor was applied to the vastus lateralis muscle of the right thigh to measure muscle oxygenation during exercise. After completing a standardized warm-up, participants performed three MVICs of the knee extensors. The exercise protocol consisted of 4 sets of unilateral isotonic knee extensions. At the end of each set, effort and exercise-induced leg muscle pain perception were ascertained. Immediately after exercise termination, the participants had to perform one MVIC of the knee extensors ( |
Subjects |
To the best of our knowledge, there is no study that has compared the effect of pBFR and BFR on our main outcomes and therefore no effect size for a sample size calculation could be derived. Therefore, the sample size was chosen in accordance with Freitas et al. ( |
Stiffness of the elastic wrap |
In order to characterize the material properties of the elastic wrap, a stress-strain relationship was established to determine the cuff stiffness. Using a similar approach to Abe et al. ( |
Determination of BFR and pBFR pressure |
The BFR pressure was set based on participants’ AOP for the lower body. The participants were seated in an upright position with their right foot on a box (hip, knee, and ankle joint angle = 90°). The seated position during the determination of AOP was chosen to ensure an equal orthostatic position as during the exercise protocol. After resting for 10 min, a 10 x 76 cm pneumatic cuff (UT 1330-L, Ulrich Medical, Ulm, Germany) was applied at the most proximal part of the right thigh and connected to an autoregulated medical tourniquet system (Heidi™, Ulrich Medical, Ulm, Germany) that adjusted the pressure automatically. The blood flow was measured by placing a handheld, bidirectional, and highly sensitive 8 MHz Doppler probe (Dopplex DMX, Huntleigh Healthcare Ltd, Cardiff, UK) over the posterior tibial artery. The cuff was progressively inflated until the pulse could not be detected anymore. The AOP was set to the nearest 10 mmHg as the lowest cuff pressure at which the pulse was not present. The inflation protocol was performed in accordance with Loenneke et al. ( In the pBFR condition, individual priming at a pressure of 60% AOP was performed using a pneumatic cuff and, subsequently, the elastic knee wrap was applied. The pneumatic cuff was inflated to 60% AOP for about 30 s, while the participants were instructed to focus on the perceived pressure and try to remember this target pressure. Immediately after deflating and removing the pneumatic cuff, a modified 7.5 x 90 cm elastic knee wrap (C.P. Sports, Munich, Germany) was applied to the same area ( |
Systolic blood flow velocity |
Systolic peak blood flow velocity was measured in both the pBFR and BFR condition. The participants were seated in an upright position with their right foot on a box (hip, knee, and ankle joint angle = 90°). After applying the elastic wrap or the pneumatic cuff to the limb with the target pressure, the handheld, bidirectional Doppler probe was placed over the posterior tibial artery with an insonation angle of ~ 45° opposite to the direction of flow according to the manufacturer’s manual. Measurements were performed in 3 intervals of 12 s each, immediately followed by removing or deflating the elastic wrap or pneumatic cuff, respectively. After a rest period of 10 min, the second condition was applied following the same procedure. The order of application was randomized. The mean of all three intervals was used for further analysis. |
Determination of one repetition maximum |
During the familiarization session, the participants’ unilateral isotonic knee extension 1RM was determined to define the percentage load for the exercise sessions (20% 1RM). The 1RM was determined using a Biodex dynamometer (Biodex System 4 Pro, Biodex Medical Systems, Inc., Shirley, NY, USA) set in the isotonic mode. Prior to the testing procedure, participants performed a 5 min warm-up on a bicycle ergometer with 90 rpm at 100 W (males) or 80 W (females). This was followed by two submaximal knee extension sets with 8, 4, and 2 repetitions at about 50%, 70%, and 80% of the estimated 1RM, respectively. Subsequently, the load was progressively increased until the participants were incapable to lift the weight controlled through the defined range of motion (i.e., 90° knee angle to full extension (~ 0°)). The 1RM was determined within a maximum of five attempts with ~ 4 min rest between trials (Haff and Triplett, |
Maximal voluntary torque |
A Biodex dynamometer was used to measure MVT (i.e., torque during MVIC). MVICs were performed for 5 s at 70° knee and hip angle (0° = full extension). Participants completed 3 trials prior to the first exercise set and 1 trial immediately after termination of the fourth set. Prior to the testing, participants initially performed a 5 min warm-up on a bicycle ergometer with 90 rpm at 100 W (males) or 80 W (females) followed by two submaximal isometric knee extensions (50% and 80% of estimated 1RM). In each trial, participants were instructed to cross their arms in front of their chest and to push as fast and hard as possible. Strong verbal encouragement was provided to achieve maximal torque output. Visual feedback of the torque-time curve as well as feedback about the produced torque value was provided. For the pretest, 3 maximal attempts with a rest period of 60 s between each trial were recorded. If the coefficient of variation of the 3 trials was above 5%, further maximal attempts were performed until this threshold was reached within 3 consecutive trials (Behrens et al., |
Exercise protocol |
The exercise protocol followed a commonly used procedure for research and practical applications in the field of BFR (Loenneke et al., |
Maximal muscle activity and muscle activity during exercise |
Muscle activity was measured during MVIC and the exercise protocol. The sEMG recording procedure was performed as described in detail by Behrens et al. ( |
Muscle oxygenation |
During the experimental trials, muscle oxygenation was monitored using an mNIRS device (MOXY, Fortiori Design LLC, Hutchinson, MN, USA). The MOXY monitor (61 x 44 x 21 mm, 48 g) gathered changes in total tissue hemoglobin concentration (tHb) and oxygenated hemoglobin as a percentage of total hemoglobin (muscle oxygen saturation [SmO2]). Before fixing the mNIRS device, skinfold thickness of vastus lateralis (19.2 ± 9.2 mm) was measured at the halfway between the base of the patella and great trochanter using a caliper (Harpenden Ltd., British Indicators Ltd, West Sussex, Great Britain). Prior to the application, the corresponding area was shaved and cleaned with alcohol. The mNIRS device was placed on the muscle belly of the vastus lateralis of the right thigh half distance between patellar base and trochanter major. To avoid the irradiation of external light sources, a light protection rubber cap (diameter = 125 mm) was attached around the mNIRS device and fixed to the thigh with elastic adhesive tape. The location of the mNIRS device was marked to reproduce its application in the subsequent test session. SmO2 and tHb were recorded at rest in a seated position 60 s before the cuff or wrap application (baseline) and throughout the exercise protocol. The mNIRS data were recorded at a sampling rate of 2 Hz and filtered with a 4th order low-pass zero-phase Butterworth filter with a cutoff frequency of 0.2 Hz (Husmann et al., |
Effort, exercise-induced leg muscle pain, and cuff pressure-induced discomfort perception |
For the assessment of effort and exercise-induced leg muscle pain perception, standardized instructions were used (Behrens et al., |
Statistical analysis |
Data analyses were conducted using JASP Statistics (Version 0.16.2, University of Amsterdam, Amsterdam, Netherlands). All data were screened for normality of distribution and homogeneity of variance using the Shapiro-Wilk and Levene’s tests, respectively. Since studies revealed that analysis of variance (ANOVA) is robust against moderate and even severe violation of normality and homogeneity, nonparametric tests were not used to check for differences (Blanca et al., |
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All 30 participants successfully completed the exercise protocol in both conditions. Due to data loss, there were missing values for systolic blood flow velocity (2 males and 1 female) and maximal muscle activity (1 female) as well as muscle activity of quadriceps femoris during exercise (1 female) due to sensor and measurement errors. As most statistical analyses resulted in no differences, only the significant correlations between the conditions as well as interactions and main effects are presented within the result section. All statistical results of the ANOVA and sex-specific data are shown in supplemental material |
Systolic blood velocity |
There was a strong correlation between systolic blood velocity recorded in the pBFR and BFR condition (r = 0.85, p < 0.001) without differences between conditions ( |
Maximal voluntary torque |
A moderate correlation (r = 0.56, p = 0.001) between conditions for ∆MVT was found. There was a time × sex (F1,28 = 15.384, p < 0.001, ηp2 = 0.355) and condition × sex interaction (F1,28 = 5.277, p = 0.029, ηp2 = 0.159) as well as a main effect of time (F1,28 = 84.158, p < 0.001, ηp2 = 0.750) and sex (F1,28 = 21.913, p < 0.001, ηp2 = 0.439). Post-hoc analysis revealed that, irrespective of time, MVT was higher in males during both the pBFR (MD = 92.58 Nm (95% CI: 41.69 to 143.46 Nm), p < 0.001, d = 1.65) and BFR condition (MD = 71.03 Nm (95% CI: 20.15 to 121.92 Nm), p = 0.003, d = 1.27) compared to females with no differences between conditions. Moreover, irrespective of the condition, MVT was higher in males before (MD = 116.38 Nm (95% CI: 62.14 to 170.61 Nm), p < 0.001, d = 2.07) but not after exercise (p = 0.122) compared to females, indicating a higher decline in MVT in males compared to females. Means ± SD of ∆MVT in pBFR and BFR are shown in |
Maximal muscle activity during MVIC |
A moderate correlation (r = 0.46, p = 0.013) was found for the decline in muscle activity of the quadriceps femoris muscle during MVIC between conditions. There was a main effect of time (F1,27 = 16.713, p < 0.001, ηp2 = 0.382) and sex (F1,27 = 12.347, p = 0.002, ηp2 = 0.314). Post-hoc analysis revealed that maximal muscle activity of quadriceps femoris during MVIC was higher in males compared to females (MD = 122.34 µV (50.90 to 193.78 µV), p = 0.002, d = 1.12). Means ± SD of decline in muscle activity of the quadriceps femoris muscle during MVIC are shown in |
Muscle activity during exercise |
Strong correlations between conditions were found for muscle activity during exercise for all sets (set 1: r = 0.79, p < 0.001, set 2: r = 0.74, p < 0.001, set 3: r = 0.80, p < 0.001, set 4: r = 0.73, p < 0.001). There was a time × condition × sex interaction (F1.7,46.6 = 6.679, p = 0.004, ηp2 = 0.198) and a main effect of time (F1.3,34.7 = 44.950, p < 0.001, ηp2 = 0.625). Post-hoc tests showed that muscle activity in both conditions was significantly higher in set 3 (pBFR: MD = 5.17% (95% CI: 0.66 to 9.69%), p = 0.007, d = 0.58; BFR: MD = 8.02% (95% CI: 3.51 to 12.53%), p < 0.001, d = 0.90) and set 4 (pBFR: MD = 7.33% (95% CI: 2.81 to 11.84%), p < 0.001, d = 0.83; BFR: MD = 12.06% (95% CI: 7.55 to 16.58%), p < 0.001, d = 1.36) compared to set 1 in males, while muscle activity in females was significantly higher only in set 4 (pBFR: MD = 8.45% (95% CI: 3.78 to 13.13%), p < 0.001, d = 0.95; BFR: MD = 6.79% (95% CI: 2.12 to 11.46%), p < 0.001, d = 0.77), but not in set 3 (p ≥ 0.133) compared to set 1. However, there were no differences between conditions and sexes in each set. Means ± SD of muscle activity during exercise are presented in |
Muscle oxygenation |
∆SmO2: Strong to very strong correlations for ∆SmO2 between conditions were found for all sets (set 1: r = 0.88, p < 0.001; set 2: r = 0.87, p < 0.001; set 3: ρ = 0.92, p < 0.001; set 4: r = 0.89, p < 0.001) and rest intervals (rest 1: r = 0.87, p < 0.001; rest 2: r = 0.83, p < 0.001; rest 3: r = 0.81, p < 0.001). There was a time × sex interaction (F1.8,49,7 = 3.966, p = 0.030, ηp2 = 0.124) as well as a main effect of time (F1.8,49,7 = 15.302, p < 0.001, ηp2 = 0.353) and sex (F1,28 = 42.517, p < 0.001, ηp2 = 0.603) for ∆SmO2 during sets. Post-hoc tests revealed that the decline in SmO2 was higher in set 3 (MD = -6.17% (95% CI: -11.20 to -1.14%), p = 0.004, d = 0.36) and set 4 (MD = -9.36% (95% CI: -14.38 to -4.33%), p < 0.001, d = 0.54) compared to set 1 in females but not in males. Furthermore, the decline in SmO2 was higher in males compared to females during each set (set 1: MD = -38.49% (95% CI: -58.74 to -18.25%), p < 0.001, d = 2.21; set 2: MD = -41.11% (95% CI: -61.36 to -20.86%), p < 0.001, d = 2.37; set 3: MD = -37.26% (95% CI: -57.51 to -17.02%), p < 0.001, d = 2.14; set 4: MD = -33.65% (95% CI: -53.89 to -13.40%), p < 0.001, d = 1.94). Moreover, a time × condition (F1.5,42.7 = 7.708, p = 0.003, ηp2 = 0.216) and time × sex interaction (F1.3,35.1 = 8.984, p = 0.003, ηp2 = 0.243) as well as a main effect of time (F1.3,35.1 = 6.870, p = 0.009, ηp2 = 0.197), condition (F1,28 = 5.452, p = 0.027, ηp2 = 0.163), and sex (F1,28 = 35.636, p < 0.001, ηp2 = 0.560) was found for ∆SmO2 during rest intervals. Post-hoc analyses showed that the decline in SmO2 was higher in rest interval 2 (MD = -3.01% (95% CI: -5.77 to 0.25%), p = 0.022, d = 0.20) and rest interval 3 (MD = -4.59% (95% CI: -7.35 to -1.83%, p < 0.001, d = 0.30) compared to rest interval 1 in BFR but not in pBFR with no differences between conditions during each rest interval. However, the main condition effect revealed a higher decline in SmO2 during BFR compared to pBFR (MD = -4.91% (95% CI: -9.22 to -0.60%), p = 0.027, d = 0.33) over all rest intervals. Regarding sex differences, the decline in SmO2 was higher in rest interval 3 compared to rest interval 1 (MD = -6.17% (95% CI: -9.55 to -2.80%), p < 0.001, d = 0.41) in females but not in males. In addition, ∆SmO2 was higher in males compared to females during each rest interval (rest 1: MD = -33.14% (95% CI: -49.31 to -16.98%), p < 0.001, d = 2.19; rest 2: MD = -29.61% (95% CI: -45.78 to -13.45), p < 0.001, d = 1.96; rest 3: MD = -26.56% (95% CI: -42.72 to -10.39%), p < 0.001, d = 1.76). ∆tHb: A moderate correlation for ∆tHb between conditions was found for set 1 (r = 0.42, p = 0.022) as well as and a strong correlation for set 2 (r = 0.72, p < 0.001), set 3 (r = 0.72, p < 0.001), and set 4 (ρ = 0.79, p < 0.001). Furthermore, there were strong correlations for ∆tHb between conditions for each rest interval (rest interval 1: ρ = 0.81, p < 0.001; rest interval 2: ρ = 0.87, p < 0.001; rest interval 3: ρ = 0.86, p < 0.001). There was a time × sex interaction (F1.7,47.1 = 9.408, p < 0.001, ηp2 = 0.251) as well as a main effect of time (F1.7,47.1 = 40.685, p < 0.001, ηp2 = 0.592), condition (F1,28 = 6.875, p = 0.014, ηp2 = 0.197), and sex (F1,28 = 31.631, p < 0.001, ηp2 = 0.530) for ∆tHb during sets. Post-hoc tests showed a higher ∆tHb in BFR compared to pBFR (MD = 0.86% (95% CI: 0.19 to 1.53%), p = 0.014, d = 0.52) over all sets. With regard to sex differences, tHb was higher in set 2 compared to set 1 (MD = 1.38% (95% CI: 0.65 to 2.11%), p < 0.001, d = 0.83) in females but not in males. Furthermore, the increase in tHb was higher in females compared to males during each set (set 1: MD = 1.62% (95% CI: 0.01 to 3.24%), p = 0.049, d = 0.98; set 2: MD = 2.31% (95% CI: 0.69 to 3.93%), p < 0.001, d = 1.39; set 3: MD = 2.74% (95% CI: 1.12 to 4.36%), p < 0.001, d = 1.65; set 4: MD = 3.26% (95% CI: 1.64 to 4.88%), p < 0.001, d = 1.96). Moreover, a time × condition (F1.4,39.7 = 6.973, p = 0.006, ηp2 = 0.199) and time × sex interaction (F1.2,34.6 = 18.765, p < 0.001, ηp2 = 0.401) as well as a main effect of time (F1.2,34.6 = 81.659, p < 0.001, ηp2 = 0.745), condition (F1,28 = 6.206, p = 0.019, ηp2 = 0.181), and sex (F1,28 = 28.319, p < 0.001, ηp2 = 0.503) was found for ∆tHb during rest intervals. Post-hoc analyses showed no differences between conditions during each rest interval. However, the main condition effect revealed a higher ∆tHb during BFR compared to pBFR (MD = 0.95% (95% CI: 0.18 to 1.72%), p = 0.017, d = 0.51) over all rest intervals. Regarding sex differences, there were no time-related differences between males and females. However, the increase in tHb was higher in females compared to males during each rest interval (rest 1: MD = 2.53% (95% CI: 0.75 to 4.30%), p = 0.001, d = 1.36; rest 2: MD = 2.94% (95% CI: 2.94% (95% CI: 1.17 to 4.72%), p < 0.001, d = 1.59; rest 3: MD = 3.32% (95% CI: 1.54 to 5.09%), p < 0.001, d = 1.79). Means ± SDs of ∆SmO2 and ∆tHb as well as ∆SmO2 and ∆tHb split by sex are presented in |
Effort, exercise-induced leg muscle pain, and cuff pressure-induced discomfort perception |
A moderate correlation for effort perception between conditions was only found for set 4 (ρ = 0.67, p < 0.001). There was a time × sex interaction (F1.6,44,7 = 4.575, p = 0.022, ηp2 = 0.140) and a main effect of time (F1.6,44.7 = 55.906, p < 0.001, ηp2 = 0.666) for effort perception. Post-hoc analysis revealed that effort perception was higher in set 2 compared to set 1 (MD = 1.63 a.u. (95% CI: 0.37 to 2.90 a.u.), p = 0.002, d = 0.85) in males but not in females. A moderate correlation for exercise-induced leg muscle pain perception between conditions was observed for set 1 (ρ = 0.42, p = 0.022), set 2 (ρ = 0.50, p = 0.005), and set 3 (r = 0.54, p = 0.002) as well as and a strong correlation for set 4 (ρ = 0.71, p < 0.001). There was a main effect of time (F1.4,40.0 = 74.211, p < 0.001, ηp2 = 0.726) for exercise-induced leg muscle pain. A moderate correlation between conditions was found for cuff pressure-induced discomfort perception before (ρ = 0.57, p < 0.001) and a strong correlation after exercise (ρ = 0.71, p < 0.001). There was a main effect of time (F1,28 = 7.426, p = 0.011, ηp2 = 0.210) and condition (F1,28 = 16.244, p < 0.001, ηp2 = 0.367) for cuff pressure-induced discomfort perception. The post-hoc test showed that cuff pressure-induced discomfort perception was generally lower in the pBFR compared to the BFR condition (MD = -0.87 a. u. (95% CI: -1.83 to -0.42 a. u.), p < 0.001, d = 0.74). Means ± SD of perceptual responses are shown in |
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The present study investigated whether low-load resistance exercise combined with perceptually primed pBFR using an elastic knee wrap is suitable to induce similar changes in motor performance fatigue (i.e., decrease in MVT) as well as physiological (i.e., muscle activity, muscle oxygenation) and perceptual responses (i.e., effort, exercise-induced leg muscle pain, and cuff pressure-induced discomfort perception) compared to traditional BFR using a pneumatic nylon cuff in males and females. The main findings are: (i) the decrease in MVT and maximal muscle activity were moderately correlated and did not differ between conditions, (ii) during exercise, there were strong correlations for muscle activity as well as no to moderate correlations and moderate to strong correlations for effort and exercise-induced leg muscle pain perception, respectively, with no differences between conditions, (iii) there were moderate to very strong correlations with a lower decline and greater increase in ∆SmO2 and ∆tHb, respectively, in pBFR compared to BFR during rest intervals, (iv) ∆SmO2 was higher while ∆tHb was lower in males compared to females during exercise, and (v) perception of cuff pressure-induced discomfort was lower in the pBFR condition. In the present study, we applied a pBFR pressure using perceptual priming based on the individuals’ %AOP. It was shown that the individuals’ 60% AOP positively correlated with the applied absolute overlap of the elastic wrap, meaning that subjects with a higher AOP need a greater overlap, when a %AOP is applied for exercise or training. Therefore, a fixed overlap value (Yamanaka et al., The results of the present study have shown that 4 sets of low-load knee extension exercise combined with either perceptually primed pBFR or traditional BFR have led to a similar significant decline in maximal motor performance (i.e., decrease in MVT) and maximal muscle activity indicating a comparable effect of pBFR and BFR on neuromuscular function. This notion is supported by the correlations found between changes in MVT and maximal muscle activity recorded in the pBFR and BFR condition, respectively. Our results are in accordance to those of Thiebaud et al. ( Furthermore, ∆SmO2 and muscle activity during exercise sets showed strong correlations and did not differ between the pBFR and the BFR condition. For the latter, similar results were observed by Freitas et al. ( The perceptual responses during exercise increased in both the pBFR and BFR condition with a moderate correlation only in the last set for effort perception and moderate (set 1-3) to strong correlations (set 4) for exercise-induced leg muscle pain perception with no differences between conditions. These findings are in contrast to those of Miller et al. ( This is also in line with the similar increase in exercise-induced leg muscle pain perception during exercise in both conditions. It could be suggested that the limited blood flow has led to comparable local hypoxic environment during exercise sets resulting in an increased nociceptive group III/IV muscle afferent input in both conditions similarly (Mauger, However, there was a lower cuff discomfort during pBFR, which was also found by Miller et al. ( Regarding sex differences, it was shown that MVT was lower in females compared to males. According to the findings by Miller et al. ( Nevertheless, the present study was not without limitations. The participants’ AOP and 1RM were determined only during the familiarization session, which might have led to different %AOP and %1RM during the test trials, respectively. However, Husmann et al. ( |
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The present study has shown that low-load resistance exercise combined with a pBFR pressure individually primed to the pressure perception to the individuals’ %AOP induces similar changes in motor performance fatigue as well as muscle activity, muscle oxygenation, and perceptual responses during exercise sets compared with traditional BFR. However, changes in muscle oxygenation were slightly lower in the pBFR compared to BFR condition during rest intervals, which could have contributed to a lower perception of cuff pressure-induced discomfort in the pBFR condition. These results indicate that low-load resistance exercise combined with perceptually primed pBFR is a convenient and less discomfort inducing alternative to traditional BFR. This is especially relevant for BFR training in group settings regarding cost minimizing, given that this kind of pBFR technique requires only one pneumatic cuff device for the validation of the pBFR pressure. Moreover, using elastic wraps for pBFR exercise might be more favorable for individuals who have a low cuff pressure-induced discomfort tolerance. Furthermore, applying an elastic wrap in relation to the limb circumference might be more precise compared to a fixed overlap value, when a specific %AOP is required for BFR exercise or training. Of note, elastic wraps should be stretched to the maximum extent before the first application to ensure constant material properties afterwards, because our data indicate that an initial slight slackening might occur when using new cuffs. |
ACKNOWLEDGEMENTS |
The authors show appreciation to all individuals participating in the present study. The authors would also like to thank Frank Feldhege for his support in developing the matlab routine for the mNIRS data analyzes. The authors declare that there are no conflicts of interest. The experiments comply with the current laws of the country where they were performed. The data that support the findings of this study are available on request from the corresponding author. |
AUTHOR BIOGRAPHY |
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REFERENCES |
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