Sports · Part Two · Assessment and Movement

21MUSCLE

Lesson 21 / 64

Muscle Training and Power

Power is not how much force a muscle can make. It is how fast the nervous system can deliver it.

Muscle power is force multiplied by velocity, and the velocity half is set by the nervous system rather than by muscle size. Almost every explosive movement runs through the stretch-shortening cycle, where a rapid stretch loads the tendon and drives a reflex that adds force to voluntary effort. The Unified Model of Tone reads that spring as reflex responsiveness, measured at the ground.

The equation

Power equals force times velocity

Reflex gain at contact

172 percent of background

Countermovement advantage

3.4 centimeters higher

First adaptation

Neural drive before hypertrophy

The stretch-shortening cycle.

A rapid eccentric stretch, a brief amortization phase, then a concentric push. Landing and jumping again is the pattern, and it runs through every stride, cut and throw.

Reactive strength.

Jump height divided by ground contact time. It reads how much force an athlete returns in the fraction of a second the foot is on the floor.

01What the measurements show

The Numbers Behind Muscle Power

Eight findings on how the stretch-shortening cycle turns muscle into power.

3.4 centimeters from the dip
Six volleyball players jumped an average of 3.4 centimeters higher with a countermovement than from a matched static start, Bobbert 1996. Simulation traced the gain to greater joint moments at the beginning of push-off rather than to stored elastic energy.
The fascicles barely move
Ultrasound of the medial gastrocnemius during a countermovement showed fascicle length holding constant while the whole muscle-tendon unit lengthened, Kawakami 2002. The muscle worked almost isometrically and the tendon did the stretching.
172 percent at ground contact
In drop jumps from 31 centimeters, soleus H-reflexes were facilitated to 172 percent of background at the short-latency response, then fell through 133 and 123 percent to 110 percent near takeoff, Taube 2008. Reflex gain is highest in the instant the athlete lands.
The cortex arrives last
In the same drop jumps, transcranial magnetic stimulation produced no effect at the short, medium or long latency responses. Motor evoked potentials rose only at push-off, to 122 percent (P equals 0.003), Taube 2008. The spring fires before the cortex weighs in.
More force at the same speed
Against a pure concentric action, a non-fatiguing stretch-shortening cycle produced more force at a given shortening velocity while concentric muscle electrical activity stayed very low, Komi 2000. The extra force did not come from extra voluntary effort.
Doublets at 2 to 5 milliseconds
Twelve weeks of ballistic dorsiflexion training against 30 to 40 percent of maximum produced motor unit interspike intervals of 2 to 5 milliseconds, alongside earlier activation and higher peak firing frequency, Van Cutsem 1998. Recruitment order was unchanged. The timing of the discharge was not.
8.7 percent on the countermovement jump
Pooling 26 studies, plyometric training raised countermovement jump height by 8.7 percent (95 percent CI 7.0 to 10.4), against 4.7 percent for the squat jump, Markovic 2007. The jump that uses the spring gained roughly twice as much.
Tendon stiffness rose with weight training, joint stiffness with plyometrics
Over 12 weeks of unilateral training, tendon stiffness rose with weight training and not with plyometrics, while joint stiffness rose with plyometrics and not with weight training, Kubo 2007. Plyometrics improved all three jump heights and weight training improved the squat jump only.

02What power is

Power Is the Rate of Force Production, and Rate Is a Nervous System Variable

Muscle power is the rate at which an athlete produces force, and it decides almost every explosive moment in sport. A vertical jump, a first step, a punch, a swing: each is won by the athlete who expresses the most force in the shortest window. Strength sets the ceiling. Power decides how much of that ceiling reaches the ground when it counts.

The physics is simple and the biology is not. Power equals force multiplied by velocity, so an athlete can be enormously strong and still slow if the nervous system cannot deliver that strength quickly. This is why a heavy squat does not guarantee a fast sprint. The muscle holds the potential, but the speed of the signal that drives it determines how much of that potential becomes movement.

The measurement that separates the two

One study makes the split concrete. In 27 active men, countermovement jump height showed no correlation with strength indices at all, and it correlated positively with maximal rate of torque development scaled to body mass Driss 2015. The men who jumped highest were not the men who could push hardest. They were the men who reached their force soonest.

Rate of force development is the variable doing that work. It describes how steeply force climbs in the first fraction of a second, before maximum force is anywhere near reached. Two athletes can share a one-repetition maximum and separate widely on the slope that gets them there.

Tissue sets part of that slope. Comparing 28 younger and 22 older men, absolute rate of torque development was 881.7 against 577.5 newton meters per second Quinlan 2018. Once the figure was normalized to quadriceps cross-sectional area, only maximum voluntary contraction and tendon stiffness remained influential. Muscle size dropped out of the equation for power. The tendon did not.

Strength is the reservoir and rate is the tap. An athlete who trains only one of them ends up with an asset they cannot spend inside the window sport allows.

03Neural before tissue

The First Weeks of a Strength Program Build the Nervous System

The earliest gains from training come from the brain and spinal cord learning to recruit motor units faster and in greater number, before any muscle fiber grows larger. A review of neural adaptation to resistive exercise names the point directly: an increase in muscular strength without noticeable hypertrophy is the first line of evidence for neural involvement in acquiring strength Gabriel 2006.

Gabriel, Kamen and Frost mapped these mechanisms. Their review traces surface electromyographic amplitude rising early in a program and reads that rise as increased neural drive to active fibers. The Brain Runs the Body carries the time course of neural gain against hypertrophy in full.

Recruitment order, and what training does not change

Motor units are recruited in a fixed order set by the Henneman size principle. Smaller, slower type I units join first, and larger, faster type II units are added as force demand climbs. Twelve weeks of ballistic training left that order intact during slow ramp contractions Van Cutsem 1998. Training does not let an athlete skip the queue.

The timing changed instead. In the same five subjects, units were activated earlier during voluntary ballistic contractions and reached a greater maximum firing frequency. The high frequency firing seen at the onset was now sustained across the spikes that followed.

The sharpest finding was the appearance of doublets: motor unit interspike intervals of 2 to 5 milliseconds, distinct from the roughly 10 millisecond pairs normally seen at the onset of a ballistic effort. Increased probability of doublet firing has been linked with training-related increases in the rate of tension development Gabriel 2006.

Why intent decides which units learn

Ballistic and explosive intent reaches the high threshold type II units that carry an athlete's speed. The Van Cutsem protocol was built on intent rather than load: ten series of ten fast dorsiflexions, five days a week, against only 30 to 40 percent of maximal strength. Light weight moved with maximum urgency rewrote motor unit behavior.

The intent of the training, not just the load, decides which units learn to fire. A bar moved slowly at 40 percent teaches almost nothing about speed. The same bar moved with intent to accelerate teaches the discharge pattern the sprint will need.

04The spring

The Stretch-Shortening Cycle Runs in Three Phases and Returns Force at the Ground

Almost every powerful athletic movement is a spring, and that spring is the stretch-shortening cycle. It runs in three phases. An eccentric phase where the muscle and tendon load and lengthen. A brief amortization phase where the joint reverses. An explosive concentric phase where the loaded structure releases.

The dip before a jump and the countermovement before a throw are not wasted motion. They are the loading of a biological spring. Six volleyball players jumped 3.4 centimeters higher with a countermovement than from a matched static start, with toe-off position identical and no sign of poor coordination in the static version Bobbert 1996.

What the spring returns

The return is measurable against a pure concentric action. A non-fatiguing stretch-shortening cycle produces more force at a given shortening velocity, and it does so while muscle electrical activity in the concentric phase stays very low Komi 2000. The athlete gets more force out for less voluntary drive in.

That is the whole economic argument for the countermovement. Force appears that the athlete did not have to command. Where that force comes from has three answers in the literature rather than one.

05Three answers, one spring

Elastic Energy, Reflex, and Timing Are Still Arguing Over the Same Jump

The stretch-shortening cycle works, and the mechanism behind it is genuinely contested. Three research programs measured the same jump and reached three conclusions, and each is right about a different part of the movement.

Start with the answer that got ruled out. Feeding measured kinematics and electromyography into a musculoskeletal model, storage and reutilization of elastic energy was ruled out as the explanation for the countermovement advantage Bobbert 1996. The countermovement instead let the jumpers reach greater joint moments at the start of push-off, so more work could be produced over the first part of joint extension.

That means the countermovement buys time. Force takes time to build, and dipping first means the athlete is already at high force when the push begins.

The tendon does more than the muscle

Then ultrasound looked directly at the tissue. During maximal-effort plantar flexion with a countermovement in six men, fascicle length rose slightly with little electrical activity, then held constant while the whole muscle-tendon unit went on lengthening Kawakami 2002. Peak force, average power and work at the Achilles tendon were all significantly greater than without the countermovement.

Muscle fibers work almost isometrically and leave the storing and releasing of elastic energy to the tendon. Elasticity is doing real work in the stretch-shortening cycle. It is simply not stored where the older account placed it.

What the drop jump recording settles

The third answer is the reflex, and it is the one with the cleanest numbers. Recording H-reflexes and motor evoked potentials at distinct moments after ground contact in drop jumps from 31 centimeters, soleus H-reflexes were facilitated to 172 percent of background activity at the short-latency response Taube 2008.

Then they decayed: 133 percent at the medium-latency response, 123 percent at the long-latency response, and 110 percent near takeoff. The authors read the early facilitation as substantial Ia afferent input reaching the alpha motor neurons in the instant the foot loads.

The cortex was doing something else entirely. Motor evoked potentials rose only at push-off, to 122 percent. The spinal loop carries the landing and the cortex arrives for the departure.

Reactive strength is therefore not a metaphor for a fast athlete. It is a reflex gain that has been measured, that changes across 120 milliseconds, and that a force plate reads indirectly every time an athlete drops onto it.

06Training the spring

Plyometric Training Moves the Jump, and Not the Tissue Most People Expect

Plyometric training is the deliberate use of the stretch-shortening cycle through jumps, bounds and ballistic throws, and the pooled evidence is specific about what it delivers. Across 26 studies, plyometric training raised countermovement jump height by 8.7 percent, with a 95 percent confidence interval of 7.0 to 10.4 percent Markovic 2007.

Squat jump height rose 4.7 percent in the same analysis. The jump that loads the spring gained roughly twice what the jump starting from a static squat gained.

Weight training stiffened the tendon and plyometrics stiffened the joint

One study separated the mechanisms by training each leg differently. Ten subjects trained plantar flexors for 12 weeks, four days a week, with plyometrics on one side and 80 percent of one repetition maximum on the other. Tendon stiffness rose significantly with weight training and not with plyometrics. Joint stiffness rose with plyometrics and not with weight training Kubo 2007.

The performance split followed the stiffness split. Plyometric training raised squat jump, countermovement jump and drop jump heights, while weight training raised the squat jump alone. Electrical activity in the measured muscles did not differ between the two protocols.

So the training that improved the spring did not stiffen the tendon. It stiffened the joint, which is a regulated quantity set by how the nervous system co-activates around the ankle in the moment before contact. The spring is tuned, not rebuilt.

Contact time is the cheap instrument

Reactive strength is measured as jump height divided by ground contact time, and it is the field instrument closest to the reflex physiology. In 21 professional rugby league players, the drop-jump reactive strength index averaged 0.90 plus or minus 0.22, against 0.47 plus or minus 0.08 for the countermovement jump variant McMahon 2021.

The two variants correlated at r equals 0.524, which is 22 percent shared variance. The drop jump version reads the fast spring, because its denominator is genuine ground contact rather than time to takeoff.

Sequencing, and the foundation underneath

Explosive work sits on a foundation of balance, eccentric strength, joint integrity and clean movement patterns. Reviewing power development, Cormie and colleagues conclude that an athlete cannot possess a high level of power without first being relatively strong Cormie 2011. Movement pattern, load and velocity specificity then govern how the power work itself is programmed.

Heavy strength work raises the force ceiling. Eccentric and ballistic work sharpens the rate at which force arrives. Plyometric work ties those layers together at the ground. Core stability belongs in the foundation with a narrower claim than it usually receives, and Beyond the Core Strength Myth carries the evidence on that.

07Where care meets power

Explosive Power Is a Signal Quality Question Before It Is a Tissue Question

Every motor unit that fires in a jump is commanded through the corticospinal tract, and the reflex that adds force at ground contact is driven by Ia afferents from muscle spindles. Both halves of the stretch-shortening cycle are neurological traffic. That is a statement about what power is made of, not a claim about what any treatment does to it.

Joint and spinal movement quality sits directly on that traffic. Spindles report length and rate of length change, and the H-reflex facilitation Taube and colleagues measured at 172 percent of background is that afferent volley reaching the motor neuron pool Taube 2008. The accuracy of the incoming signal is the input to the loop that produces reactive strength.

What is actually being assessed

A performance neurology assessment measures the loop rather than the muscle. Joint position sense, reflex timing, balance under load, eye movements and motor control all read the same central integrative state that schedules a contraction. Proprioception and Joint Position Sense covers the receptor side of that in detail, and The Functional Neurology Workup covers the battery.

We do not add force to a muscle. The work is on the path the force travels. Care is drug free and fully anti-doping compliant, which matters for any athlete competing under testing.

08What we corrected

Three Claims Changed on This Page

This page previously listed tighter motor unit synchronization alongside firing rate as an established neural adaptation. The review it drew on is more careful. Synchronization is a possible mechanism for strength increases that has yet to be definitely demonstrated Gabriel 2006. It stays here as a candidate rather than a finding.

The page also stated that the research is clear that weaker athletes should build maximal strength before emphasizing power. The strength-first relationship is supported Cormie 2011. The certainty was not.

A quotation attributed to Dr. Jason Dulberg appeared here and was not drawn from anything he said or wrote. It has been removed. The page also promised that care makes recruitment faster, amortization shorter and rate of force development better. No trial supports that sequence, so the claim is gone and the mechanism stands in its place.

09The model's claim

The Stretch-Shortening Cycle Is Reflex Responsiveness Measured at the Ground

Two layers run through this page. The established science is the countermovement simulation, the fascicle ultrasound, the H-reflex and motor evoked potential recordings during drop jumps, the plyometric meta-analysis, and the motor unit training data. Each of those belongs to the laboratory that produced it.

The Unified Model of Tone reads the stretch-shortening cycle as a reflex readout. Reflex responsiveness is one of the readouts the model uses to track the organization of the nervous system, and the stretch-shortening cycle is that readout expressed mechanically. Reactive strength is reflex gain with a force plate under it.

The model also supplies the frequency scale the argument runs on. The motor units driving a muscle fire from around five per second when they first switch on to roughly fifty at high force. A drop jump asks a pool at the top of that range to change its discharge pattern inside 120 milliseconds.

Why three mechanisms is the expected answer

The elastic account, the timing account and the reflex account have been treated as rivals for decades. The model predicts exactly this pattern, because the effect of an input is determined by how that event interacts with the tone already there. A stiff ankle, a fatigued spindle and a fresh one are three different systems meeting the same landing.

Fatigue makes the point measurable. Exhaustive stretch-shortening cycle work reduces stretch reflex sensitivity and muscle stiffness together, and recovery runs a bimodal course rather than a straight one Komi 2000. The same drop height lands on a different athlete on day two than on day zero.

The prediction this page makes

The model treats reactive strength as a regulatory reading rather than a muscular property. That is a claim about how power is organized rather than a claim about what treatment does, and sport already owns every instrument it needs.

Record four things in one squad across a season. Drop-jump reactive strength index. Ground contact time in milliseconds. Soleus H-reflex amplitude at the short-latency response after landing, expressed against background electromyography. Time to return to baseline after a standardized drop jump battery.

If reactive strength index, ground contact time, short-latency H-reflex gain and time to return to baseline are shown to move together within the same athletes across a season, the unification claim is confirmed.

10The tone reading

The Spring Is a Regulated State, Not a Stored Quantity

Three signatures of tone appear in the power measurements on this page.

Gain

Soleus H-reflexes run at 172 percent of background at landing and 110 percent by takeoff. Reflex gain is set moment to moment.

Time course

The countermovement advantage is bought with time to build force, and the whole exchange closes inside 120 milliseconds.

Constraint

Plyometrics raised joint stiffness and left tendon stiffness alone. The spring is tuned by how tightly the ankle is held.

The rest of the library carries the same logic through its other foundations. Oscillation is the rhythm underneath motor unit discharge, which runs from roughly five per second at recruitment to about fifty at high force. Prediction is the feedforward model that preactivates the calf before the foot lands, and input-quality is the accuracy of the spindle signal that the reflex then amplifies. Coupling is what links the eccentric and concentric halves into one action, while load is the drop height the system is asked to organize. Set-point is the joint stiffness the athlete defends on contact, and time-course governs the bimodal recovery after exhaustive jumping. The full framework is set out in the Unified Model of Tone.

11Where this sits

How This Page Relates to the Rest of the Library

Seven places this argument continues, each with the claim that earns the link.

The Brain Runs the Body

Owns the neural-drive thesis and the motor unit recordings showing training changes how the pool is driven.

Reaction Time and Motor Control

Measures reflex responsiveness as latency, where this page measures it as force returned at the ground.

Cortical Drive and Force

Carries the transcranial magnetic stimulation evidence that quantifies the descending half of the loop.

Clinical Biomechanics

Explains the lever mechanics and moment arms that decide what the spring has to work against.

Proprioception and Joint Position Sense

The spindle afferents whose volley becomes the reflex facilitation measured at ground contact.

Beyond the Core Strength Myth

Holds the evidence on trunk stability training and narrows what the foundation under explosive work actually requires.

Tone and the Athlete's Edge

The keystone lesson, where reflex responsiveness joins the other three readouts in one study design.

12Questions athletes ask

Questions Athletes Ask

Why does explosive power come from the nervous system and not just muscle size?

Power is force multiplied by velocity, and velocity is governed by how fast the signal arrives. In 27 active men, countermovement jump height showed no correlation with strength indices and did correlate with maximal rate of torque development scaled to body mass. Comparing younger and older men, once rate of torque development was normalized to quadriceps cross-sectional area, only maximum voluntary contraction and tendon stiffness stayed influential. Muscle size dropped out. A large muscle fed by a slow, disorganized signal stays slow.

What is the stretch-shortening cycle and why does a countermovement help?

It is the three-phase spring underneath almost every explosive movement: a rapid eccentric stretch, a brief amortization phase as the joint reverses, then a concentric push. Six volleyball players jumped 3.4 centimeters higher with a countermovement than from a matched static start. A non-fatiguing stretch-shortening cycle produces more force at a given shortening velocity while concentric muscle electrical activity stays very low. The dip before a jump and the countermovement before a throw are the loading of a biological spring.

Is the extra force stored elastic energy or a reflex?

The literature genuinely disagrees, and each answer is right about part of the movement. Simulation ruled out stored elastic energy as the explanation for the countermovement jump advantage and traced it instead to greater joint moments at the start of push-off, meaning time to build force. Ultrasound showed calf fascicles holding nearly isometric while the tendon stretched, so elasticity does real work in the tendon. Recordings during drop jumps put soleus reflex facilitation at 172 percent of background at landing. All three contribute.

What does reactive strength index actually measure?

Jump height divided by ground contact time, which reads how much force an athlete returns in the fraction of a second the foot is on the floor. In 21 professional rugby league players the drop-jump version averaged 0.90 plus or minus 0.22, against 0.47 plus or minus 0.08 for the countermovement jump variant. They correlated at r equals 0.524, or 22 percent shared variance, so the two are not interchangeable. The drop jump version reads the fast spring, because its denominator is real ground contact.

Does plyometric training work, and what exactly does it change?

Pooling 26 studies, plyometric training raised countermovement jump height by 8.7 percent, with a 95 percent confidence interval of 7.0 to 10.4 percent, against 4.7 percent for the squat jump. The tissue effect is not the obvious one. Training one leg with plyometrics and the other with 80 percent of a one repetition maximum for 12 weeks raised tendon stiffness only on the weight-trained side, and joint stiffness only on the plyometric side. Plyometrics tunes how the joint is held.

Should I build maximal strength before training power?

Reviewing power development, Cormie and colleagues conclude that an athlete cannot possess a high level of power without first being relatively strong, so maintaining maximal strength underpins long-term power development. Movement pattern, load and velocity specificity then govern the power work itself. Intent matters as much as load. Twelve weeks of fast dorsiflexions against only 30 to 40 percent of maximum produced earlier motor unit activation, higher peak firing frequency, and doublets at intervals of 2 to 5 milliseconds. Light and urgent teaches speed.

How does a performance neurology assessment relate to power?

It measures the loop rather than the muscle. Every motor unit in a jump is commanded through the corticospinal tract, and the force added at ground contact comes from spindle afferents driving a reflex measured at 172 percent of background during drop jumps. So joint position sense, reflex timing, balance under load, eye movements and motor control all read the state that schedules a contraction. That is a statement about what power is made of. The assessment is drug free and fully anti-doping compliant.

13The sources

References

1
Bobbert MF, Gerritsen KG, Litjens MC, Van Soest AJ. Why is countermovement jump height greater than squat jump height?. Med Sci Sports Exerc. 1996. PMID 8933491
2
Kawakami Y, Muraoka T, Ito S, Kanehisa H, Fukunaga T. In vivo muscle fibre behaviour during counter-movement exercise in humans reveals a significant role for tendon elasticity. J Physiol. 2002. PMID 11956349
3
Komi PV. Stretch-shortening cycle: a powerful model to study normal and fatigued muscle. J Biomech. 2000. PMID 10899328
4
Taube W, Leukel C, Schubert M, Gruber M, Rantalainen T, Gollhofer A. Differential modulation of spinal and corticospinal excitability during drop jumps. J Neurophysiol. 2008. PMID 18199811
5
Van Cutsem M, Duchateau J, Hainaut K. Changes in single motor unit behaviour contribute to the increase in contraction speed after dynamic training in humans. J Physiol. 1998. PMID 9782179
6
Gabriel DA, Kamen G, Frost G. Neural adaptations to resistive exercise: mechanisms and recommendations for training practices. Sports Med. 2006. PMID 16464122
7
Markovic G. Does plyometric training improve vertical jump height? A meta-analytical review. Br J Sports Med. 2007. PMID 17347316
8
Kubo K, Morimoto M, Komuro T, Yata H, Tsunoda N, Kanehisa H, Fukunaga T. Effects of plyometric and weight training on muscle-tendon complex and jump performance. Med Sci Sports Exerc. 2007. PMID 17909408
9
McMahon JJ, Suchomel TJ, Lake JP, Comfort P. Relationship Between Reactive Strength Index Variants in Rugby League Players. J Strength Cond Res. 2021. PMID 29401201
10
Cormie P, McGuigan MR, Newton RU. Developing maximal neuromuscular power: part 2 - training considerations for improving maximal power production. Sports Med. 2011. PMID 21244105
11
Driss T, Lambertz D, Rouis M, Jaafar H, Vandewalle H. Musculotendinous stiffness of triceps surae, maximal rate of force development, and vertical jump performance. Biomed Res Int. 2015. PMID 25710026
12
Quinlan JI, Maganaris CN, Franchi MV, Smith K, Atherton PJ, Szewczyk NJ, Greenhaff PL, Phillips BE, Blackwell JI, Boereboom C, Williams JP, Lund J, Narici MV. Muscle and Tendon Contributions to Reduced Rate of Torque Development in Healthy Older Males. J Gerontol A Biol Sci Med Sci. 2018. PMID 28977366

12 primary sources, each linked to its record. Figures quoted on this page were checked against the published abstract.

Related evidence

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