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Biomechanics 2
Laboratory Report
1. Introduction
According to Cheng et al. (2008), people are accustomed to jumping with an arm swing
which suggests jumps without an arm swing may not be optimal in attaining maximum
height. Moreover, previous findings have shown that arm swing facilitated an increase of
above 10% in jump height (Shetty and Etnyre, 1989; Harman et al., 1990; Feltner et al.,
1999). Cheng et al. (2008) found that increased take-off (TO) velocity of the centre of mass
(CoM) contributed nearly two thirds to increased jump height which also reflected Lees et
al.’s findings of 72% contribution to increased jump height (2004). Further research has been
conducted as to what exactly causes the effect of arm swing to increase jump height through
increased TO velocity.
Hara et al. (2006) suggested that increased jump height was due to increased activity
of the lower extremity muscles from the additional load on the lower extremity from an arm
swing. It was noted that increased work by the hip suggested an increased activation of the
biceps femoris, which acts as a hip extensor (Umberger, 1998). However, this was not
validated as this study did not directly examine electromyography (EMG) which would have
been beneficial in determining individual muscle activity in different types of jump (Rota et
al., 2013). Although Hara et al.’s study did examine the effect of arm swing during maximal
jumping, squat jumps were performed thus not making this study a direct representation of
countermovement jumps which would have provided more concrete research for this specific
topic.
Although the direct study of EMG in countermovement jumping with an arm swing is
limited, Lees et al. (2004) found some interaction between muscle activity and arm swing,
especially for muscles acting at the hip which would support Hara et al.’s assumption.
However, Lees et al. found a significant decrease in biceps femoris activity. Furthermore,
Lees et al. concluded that increased height and TO velocity from arm swing was not
exclusively due to the different levels of activity in the lower extremity muscles but rather to
a complex series of mechanisms acting collectively. Nonetheless, this study could have
Payne et al. (1968, cited in Lees et al. 2004) proposed the ‘transmission of force’
theory as the explanation for the increased TO velocity due to arm swing. This theory
suggests a greater impulse is produced as vertical ground reaction force (GRF) is increased
due to a downward force acting on the body as the arms are propelled upwards. However,
Dapena (1999, cited in Cheng et al., 2008) viewed this theory as too simplistic in a simulation
investigation. Additionally, Feltner et al. (2004) reported that greater impulse was not due to
increased vertical GRF but rather a complex series of mechanisms which supported Lees et
However, according to more recent findings, Akl (2013) suggested the use of arm
swing contributed to augmented jump height through the acquisition of additional impulse.
This was due to increased maximal vertical GRF, which was also found to have a strong
correlation with arm swing during countermovement jumping. This study reflected the
previous research of Harman et al. (1990) who reported greater vertical GRF, resulting in an
increased net impulse, being the direct cause for increased jump height.
The purpose of this report is to support the findings that arm swing does enhance
performance during a countermovement jump and to investigate and examine further the
2. Method
2.1. Participants
Thirteen injury-free undergraduate students (mean ± S.D.: age = 20.5 ± 2.1 years;
stature = 1.77 ± 0.1 m; mass = 74.4 ± 13.2 kg) were required to perform two variations of
maximal countermovement vertical jump. There were eleven male participants and two
female participants, all wearing shoes. All trials were to follow the same protocol and
procedure. The participants were made aware of the purpose and risks of the experiment and
A Kistler 9281B force plate, recording at 500 Hz, was used to record GRF with
Bioware software. An amplifier was used to strengthen the signal and A/D converter to
digitise the data to the computer. While on the force plate, the participant’s body mass would
be subtracted using the Bioware software so that GRF would be set at a constant zero before
each jump.
A Delsys Bagnoli 8 channel box, recording at 1000 Hz was used to record raw EMG
readings from lower extremity muscles with EMGWorks 4.1 software. An amplifier was used
to strengthen the signal and A/D converter to digitise the data to the computer. The weight of
the channel box was negligible therefore would not have a significant effect on the mass of
the participant.
Both the force plate and EMG equipment were synchronised to the computer to record
data simultaneously during a window of 5 seconds from the touch of a button (Figure. 1).
The participants performed a maximal vertical jump on the force plate two different
ways (Figure. 2): countermovement jump with arm swing (CMJAS) and countermovement
jump without arm swing (CMJ). A countermovement jump is a type of bilateral vertical jump,
that incorporates a stretch-shortening cycle (Magee et al., 2007), with preceding flexion of
the ankle, knee and hip joints and subsequent extension of these briefly flexed joints
(Radcliffe and Farentinos, 1999). CMJ was performed with hands placed on the iliac crest to
The rectus femoris (RF) and biceps femoris (BF) were marked because these bi-
articular muscles act to flex and extend both the hip and knee which are essential movements
To reduce the effect of cross-talk, these muscles were identified through performing a
seated isometric knee extension and lying hip extension respectively against manual
resistance and then palpating the belly of the muscle. The surface of the skin was shaved and
cleansed with ethanol wipes before placing the mono-polar electrodes over it with the wires
facing upwards. A reference electrode was placed over the bony prominence of the patella.
These were connected to the Delsys Bagnoli 8 channel box, tucked in the participant’s shorts.
Following appropriate warm-up and familiarity with the movement, three successful
trials for CMJAS were first completed followed by three successful trials for CMJ. There was
a rest period of approximately two minutes between trials to maximise jump performance.
The data from each participant’s final trial of each jump condition was to be analysed.
Finally, an isometric maximal voluntary contraction (MVC) was recorded for the RF
and BF from performing a seated knee extension and lying hip extension respectively against
manual resistance.
2.3. Analysis
phase, minimal vertical GRF, maximal vertical GRF, net impulse, TO velocity of CoM, jump
height, peak average rectified EMG (PAVEMG) and normalised EMG for each muscle and
total PAVEMG.
The start and end points of both TO and flight phase were noted by visually identifying
significant changes in vertical GRF patterns. Thus, the difference between the start and end
For vertical GRF data, the minimum and maximum values were identified using a
spreadsheet. Net impulse was calculated through the following equation: impulse (N∙s) =
F∙∆t. Thereafter, take-off velocity was subsequently calculated through the impulse-
momentum relationship (Hamill and Knutzen, 2008), also known as Newton’s Second Law of
Raw EMG and MVC data was processed into AVEMG using a spreadsheet by
converting all of the data into absolute values and calculating the mean. In order to compare
the level of muscle activity from the jumps as a percentage of muscle activity from the
Normalised EMG would also verify the accuracy of the raw EMG recordings by assuming
the MVCs would be greater than the PAVEMG recorded from the jumps.
Descriptive statistics were implemented on IBM SPSS to calculate the mean and
standard deviation of each variable and to determine the normality of the data through
Skewness, Kurtosis and Shapiro-Wilk. The difference of the variables between the two jump
conditions was also determined through paired samples T-tests since the same group of
people performed both conditions. If parametric assumptions were broken due to non-
normally distributed data, a Wilcoxon-Signed Ranks test (statistic Z) was used. A value of p ≤
3. Results
Table 1 displays the points in time and duration of the TO and flight phases in both
jump conditions. TO duration was greater in CMJ than CMJAS by 0.02 s, but with non-
significant difference (p > 0.05). This indicates there was greater duration spent performing
countermovement and TO during CMJ. However, flight duration was significantly greater in
CMJAS than CMJ by 0.04 s (Z = 2.981, p < 0.05). This indicates that there was greater
Table 1. Mean (±S.D.) temporal data associated with two different jump conditions (N=13).
CMJ CMJ
AS
Mean SD Mean SD
TO phase Start (s) 0.84 0.34 0.82 0.22
End (s) 1.72 0.36 1.72 0.25
Duration (s) 0.88 0.20 0.90 0.14**
Flight phase End (s) 2.30 0.39 2.24 0.27
Duration (s) 0.58 0.11 0.52 0.06 *
* indicates a significant difference between the CMJAS and CMJ condition (p < 0.005).
**indicates a non-significant difference between the CMJAS and CMJ condition (p > 0.005).
Table 2 displays the kinetic variables and figure 3 displays the net impulse in both jump
conditions. CMJAS produced significantly greater jump height by the CoM than CMJ by
0.07 m (Z = 3.19, p ≤ 0.001). CMJAS also produced significantly greater TO velocity than
CMJ by 0.25 m·s-1 (p < 0.001). The maximal vertical GRF value was significantly greater (p ≤
0.05) in CMJAS than CMJ by 87 N (0.12 BW) and the minimal value was lower in CMJ than
CMJAS by 21 N (0.04 BW), but with non-significant difference (p > 0.05). Furthermore, net
impulse was significantly greater in CMJAS than CMJ by 18.9 N·s (p ≤ 0.001). Figure 4
depicts one participant’s vertical GRF pattern (Fz in Figure 4) application over time, which
displays greater maximal vertical GRF of 1099 N for CMJAS compared to that of 917 N for
CMJ and lower minimal vertical GRF of -589 N for CMJ compared to that of -412 N for
CMJAS. This was a true reflection of the greater mean maximal vertical GRF in CMJAS and
Table 2. Mean (±S.D.) kinetic data associated with two different jump conditions (N=13).
CMJAS CMJ
Mean SD Mean SD
Minimum (N) -442 202.4 -463 192.9 **
(BW) -0.39 0.53 -0.35 0.58
Maximum (N) 1021 193.8 934 182.5 *
(BW) 1.42 0.26 1.30 0.24
Net impulse (N∙s) 201.8 46.3 182.9 42.0 *
-1
T/O velocity (m∙s ) 2.70 0.3 2.45 0.3 *
Jump height (m) 0.38 0.1 0.31 0.1 *
* indicates a significant difference between the CMJAS and CMJ condition (p ≤ 0.005).
**indicates a non-significant difference between the CMJAS and CMJ condition (p > 0.005).
210
*
200
190
Impulse (N∙s)
180
170
160
150
CMJAS CMJ
Figure 3. Mean (±S.D.) net impulse associated with two different jump conditions (N=13).
* indicates a significant difference between the CMJAS and CMJ condition (p < 0.001).
1500
CMJ CMJAS
1000
500
Fz (N)
0
0. 2
0. 0
0. 8
0. 6
0. 4
0. 2
0. 0
0. 8
0. 6
0. 4
1. 2
1. 0
1. 8
1. 6
1. 4
1. 2
1. 0
1. 8
1. 6
1. 4
1. 2
1. 0
1. 8
1. 6
1. 4
1. 2
1. 0
1. 8
1. 6
1. 4
2
50
55
59
64
69
74
79
83
88
93
98
03
07
12
17
22
27
31
36
41
46
51
55
60
65
70
75
79
84
89
94
0.
-500
-1000
Time (s)
Figure 4. Vertical GRF plotted against time at TO during two different jump conditions.
PAVEMG for RF was greater for CMJ than CMJAS by 0.0348 mV (Table. 3) but with
non-significant difference (Z = -0.384, p > 0.05). Therefore, the normalised EMG for RF was
greater by 5% for CMJ, which was 112%, than CMJAS, which was 107%, with non-
significant difference (Z = 0.944, p > 0.05). This suggests RF muscle activity was greater
PAVEMG for BF was greater for CMJAS than CMJ by 0.1368 mV but with non-
significant difference (Z = 1.503, p > 0.05). Therefore, the normalised EMG for BF was
greater by 10% for CMJAS, which was 49%, than CMJ, which was 39%, but with significant
difference (p ≤ 0.05). This suggests BF muscle activity was lower during both jump
Total PAVEMG for both muscles was greater for CMJAS than CMJ by 0.1019 mV
with non-significant difference (Z = -0.384, p > 0.05). This suggests greater muscle activity
Table 3. Mean (±S.D.) EMG data associated with two different jump conditions (N=13).
CMJAS CMJ
Mean SD Mean SD
PAVEMG RF (mV) 0.3356 0.3 0.3704 0.3 **
Normalised RF (%) 107 30.3 112 37.6 **
PAVEMG BF (mV) 0.3118 0.4 0.1750 0.2 **
Normalised BF % 49 13.7 39 12.4 *
Total PAVEMG (mV) 0.6474 0.6 0.5455 0.5 **
* indicates a significant difference between the CMJAS and CMJ condition (p ≤ 0.05).
**indicates a non-significant difference between the CMJAS and CMJ condition (p > 0.05).
Discussion
CMJ and provided further insight and points for discussion on the mechanisms behind this
effect.
Current values for temporal and kinetic variables displaying significant difference
were directly compared with values of previous related investigations in order to compare
outcome and similarity of results. CMJAS produced significant increase in flight phase
duration with 0.58 s compared to CMJ with 0.52 s. Harrison and Moroney (2007) displayed
results also between 0.50 s and 0.60 s for both conditions with the same outcome, stating
CMJAS produced significant increase in jump height with 0.38 m compared to CMJ
with 0.31 m while Lees et al. (2004) procured similar results of 0.39 m and 0.33 m for
CMJAS and CMJ respectively. This increase of approximately 23% relates to previous
findings which have shown that arm swing facilitated an increase above 10% (Shetty and
Etnyre, 1989; Harman et al., 1990; Feltner et al., 1999). According to Cheng et al. (2008),
increased TO velocity of the CoM contributed nearly two thirds to increased jump height
which also reflected 72% contribution in Lees et al (2004). CMJAS produced significant
increase in TO velocity with 2.70 m·s-1 compared to CMJ with 2.45 m·s-1 while Hara et al.
(2006) procured similar results of 2.73 m·s-1 and 2.46 m·s-1 for CMJAS and CMJ respectively.
To investigate the explanation for increased TO velocity due to arm swing, net
impulse was analysed. CMJAS produced significant increase in net impulse with 201.8 N·s
compared to CMJ with 182.9 N·s while Akl (2013) procured related net impulses of 233.6
multiplied by change in time (Hamill and Knutzen, 2008). Therefore, since net impulse was
greater in CMJAS than CMJ, maximal vertical GRF was also significantly greater with 1021
N for CMJAS compared to 934 N for CMJ. These were similar to those from Akl (2013) with
1236 N and 956 N for CMAS and CMJ respectively and were therefore analysed in the same
unit of measurement. These support the assumptions of Payne et al. (1968, cited in Lees et al.
2004) and Harman et al. (1990) which depict the ‘transmission of force’ theory which further
suggests greater vertical GRF resulting in increased net impulse as being the direct cause for
increased jump height. Additionally, this is reciprocated by Dowling and Vamos (1993) who
reported that a high maximum force was necessary for enhanced performance and that the
pattern of force application was the most crucial aspect in vertical jump performance.
However, it was also noted that high maximal force was also not sufficient for enhanced
velocity due to arm swing which meets the assumption of Feltner et al. (2004).
Rota et al. (2013) reported that investigating EMG would be beneficial in determining
individual muscle activity in different jump conditions. However, normalised EMG appeared
inaccurate because mean RF values for both jump conditions were greater than MVC, which
may reflect data error. Due limited EMG-related studies on this particular topic, current
values could not be directly compared with values from previous studies even in Lees et al.
where EMG was only reported in figure format and change of percentage. Therefore,
outcome of results was compared for variables displaying both significant and non-significant
difference.
PAVEMG and normalised EMG for RF were greater for CMJ than CMJAS, but with
non-significant difference to further emphasise this statement while Lees et al. also reported a
PAVEMG and normalised EMG for BF were greater for CMJAS than CMJ while
Lees et al. reported significant decrease in BF activity. It was noted that PAVEMG produced
However, Hara et al.’s investigation (2006) contradicts Lees et al.’s findings but
matches this study in terms of increased BF activation as it was suggested that increased
work by the hip increased involvement of this hip extensor due to increased activity of lower
extremity muscles from the additional load on the lower extremity due to arm swing. This
was also supported by the findings of Blache and Monteil (2012) who concluded that greater
It was noted for this assumption that Hara et al. (2006) did not directly examine EMG
and squat jumps were performed thus not making this study a direct representation of
where greater muscle force is produced due to the force-velocity relationship in which
upward acceleration of the arms can trigger a downward reaction force to act on the rest of
the body. Lees et al.’s investigation (2004) further contradicts this theory because lower joint
power was produced during jumps with arm swing. However, increased total PAVEMG in
this study suggests greater muscle activity produced from the lower extremity as reported as
corresponding to joint activation in Bobbert and Cassius (2005, cited in Cheng et al. 2008).
Hara et al. (2006) also stated arm swing to act as an additional load due partly to
increased shoulder joint torque applied to the trunk. However, Cheng et al. (2008) later
argued that this force on the shoulders is not closely related to changes in vertical GRF, thus
supporting Lees et al. (2004) in questioning the ‘transmission of force’ theory. Cheng et al.
also questioned the ‘joint work augmentation’ theory as this only applied in the hips while
knee joint work decreased due to shorter duration of torque generation. It is interesting to
note that, contrary to the outcome in Lees et al. (2004), increased BF activity in this study
would decrease knee extension torque, thus supporting the ‘joint work augmentation’ theory,
as the BF is a knee flexor (Hara et al. 2006). However, this cannot be clarified since joint
According to more recent findings, Akl (2013) suggested that arm swing contributed
to augmented jump height through the acquisition of additional impulse which matches the
findings of this study. This was due to increased maximal vertical GRF reflecting the research
of Harman et al. (1990), which Akl also found to have a strong correlation with arm swing
As noted previously, there was potential for error in either or both the raw EMG and
MVC recordings due to mean RF normalised EMG in both jump conditions being greater
than MVC. Considering the error to be in MVC recording, Noreau and Vachon (1998)
muscle test implemented in this study. Arm swing technique may have differed between
participants as there was likelihood, at university, to have used individuals who played sports
that require maximal vertical jumps such as basketball, therefore more accustomed to this
skill (Umberger, 1998). The use of non-parametric tests in data analysis was not ideal as these
are less likely to find significant differences. However, they were deemed appropriate as even
with the initial removal of outliers, additional outliers appeared in the data and the sample of
the difference in jump height between CMJAS and CMJ, which supports the ‘transmission of
force’ theory proposed by previous studies. Where EMG in relation to arm swing was directly
measured in limited research, the results of this study contradict the findings, albeit with the
limitations of this study. Where it was suggested a more active state in the muscles,
particularly those of the hip, the results were not clarified through the ‘joint work
the ‘transmission of force’ theory in relation to arm swing in jump performance, future
studies should aim to measure the many complex series of mechanisms that have been related
to the effect of arm swing, particularly EMG. This report has supported the findings that arm
swing does enhance performance during a countermovement jump and has provided further
points for discussion based on present theories examining the factors behind this effect.
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