CHANGES IN RUNNING SPEEDS IN A 100 KM ULTRA-MARATHON
RACE
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MRC/UCT Research Unit for Exercise Science and Sports Medicine, Department
of Human Biology,Faculty of Health Sciences, University of Cape Town, South
Africa
| Received |
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09 March 2004 |
| Accepted |
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01
July 2004 |
| Published |
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01
September 2004 |
©
Journal of Sports Science and Medicine (2004) 3, 167 - 173
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| ABSTRACT |
| The
purpose of this study was to determine if runners who completed a
100 km ultramarathon race in the fastest times changed their running
speeds differently compared to those runners who ran an overall slower
race. Times were taken from the race results of the 1995 100 km IAU
World Challenge in Winschoten, Netherlands. Race times and 10 km split
times were analyzed. Runners (n = 67) were divided into groups of
ten with the last group consisting of seven runners. The mean running
speed for each 10 km segment was calculated using each runner's 10
km split times. Mean running speed was calculated using each runner's
race time. The first 10 km split time was normalized to 100, with
all subsequent times adjusted accordingly. The mean running speed
for each group at each 10 km split was then calculated. The faster
runners started at a faster running speed, finished the race within
15 % of their starting speed, and maintained their starting speed
for longer (approximately 50 km) before slowing. The slower runners
showed a greater percentage decrease in their mean running speed,
and were unable to maintain their initial pace for as long. It is
concluded that the faster runners: 1) ran with fewer changes in speed,
2) started the race at a faster running speed than the slower runners,
and 3) were able to maintain their initial speed for a longer distance
before slowing.
KEY
WORDS: Pacing strategy, peak performance, ultra-endurance.
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| INTRODUCTION |
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In
an attempt to improve running performance, the physiological characteristics
of elite performers and the energy demands of the athletic events
in which they participate have been studied (Robinson et al., 1991; Sparling et al., 1993; Brandon, 1995). However, changes in running
speed, either preplanned or as a consequence of fatigue during competition
may also have an effect on the outcome of a race. Pacing can be
defined as the subjective competitive strategy in which an individual
manipulates speed to achieve his/her performance goal. From a physiological
perspective pacing may be influenced by a "central programmer"
which integrates afferent signals arising from the muscle and peripheral
organs and regulates power output to optimize performance (Ulmer,
1996; Lambert et al., 2004).
The presence of this "central programmer" has been supported
in various research models (Kay et al., 2001; St Clair Gibson et al.,
2001; Kay and Marino, 2003; Marino et al., 2004).
Previous studies examining pacing have focused mainly on short duration
events lasting less than five minutes (Foster et al., 1994; van Ingen Schenau et al.,
1994) and have
generally concluded that optimal pacing is often the result of a
learning process and that it may be in the best interest of the
athlete to practise such pacing in preparation for an event (Foster
et al., 1994). Few studies have addressed the pacing of athletes
during longer endurance events (Townsend et al., 1982).
This could be due to the fact that several different mechanisms
have been identified as contributors to fatigue during prolonged
exercise (Gibson and Edwards, 1985;
Noakes, 2000), making a systematic experimental approach difficult.
Studies that have attempted to analyze the pacing of long duration
events have incorporated mathematical models into their research
design. Townsend et al. (1982)
used a mathematical model to assign values to runners' capabilities
to complete specific distances over different terrain. Through a
series of calculations, the pace at which a runner should complete
each respective segment of the race can be determined. However,
this technique is complex and thus has limited practical applications.
An alternative approach to determine the pacing of athletes during
long endurance events is to study the pacing of elite performers,
assuming that these athletes have practised such pacing in preparation
for the event (Foster et al., 1994)
and that their pacing is optimal for these events and results in
the fastest race times. Accordingly, the running speeds of the competitors
of the 1995 100 km IAU World Challenge were analyzed. The aim of
the study was to determine if the runners who completed the race
with the fastest race times changed their running speeds differently
compared to those runners who ran slower overall race times. It
was assumed that all the runners had similar racing experience,
were highly trained and were all equally motivated for the event
and were performing to the best of their abilities.
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| METHODS |
|
Racing
data
The 10 km split times of the 107 male runners who competed in the
1995 100 km IAU World Challenge in Winschoten, Netherlands, were
obtained from the race statistician and analyzed for the study.
The race was run over a flat course consisting of a 10 km loop and
times were recorded manually. The data of forty runners were excluded
from the analysis based on two exclusion criteria: 1) not finishing
the race, (n = 24), and 2) missing split times, (n = 16). Runners
were then divided into seven groups (A-G) by grouping the remaining
runners by time as follows: first 10 runners (A), the next 10 runners
(B), and so on. The final group (G) included only seven runners.
Analysis of running speed
Mean running speed (m·s-1) for each 10 km segment was calculated
using each runner's 10 km split times. The mean running speed (m·s-1)
for the race was calculated using each runner's race time. 'Normalized'
running speed for each runner's 10 km segment was calculated by
assigning the first 10 km running speed to 100%. All the subsequent
splits were adjusted accordingly.
The mean running speed for each 10 km split was calculated for each
group (A-G). Best-fit non-linear and linear regressions of distance
vs. mean running speed were calculated for each group (A-G). Similarly,
the mean normalized speed was calculated for each group at each
10 km split, and the line of best fit of distance vs. normalized
speed was determined for each group.
A similar analysis was done using the 10 km split-time data of the
same race in 1997. The top 10 finishers (1997) were compared with
group A (1995). The 10 finishers (1997) whose mean time was similar
to that of group F (1995) were also used for comparison. Coefficient
of variation and the relationship between mean running speed and
distance were calculated. The 1997 data were analyzed using the
same methods as were used for the 1995 data.
The 5 km splits for the 42.2 km world record established in Berlin,
Germany, in September, 2003, and the 10 km splits of the 100 km
world record (Lake Saroma, Japan, June 1998) were analyzed in a
similar way as the times from the IAU 1995 and 1997 races. Coefficient
of variation and mean running speed were calculated for the marathon
and 100 km race and the mean change in speed and mean running speed
for each split were also calculated for the 100 km race (Table
1).
Statistical
Analysis
All results are expressed as mean ± standard deviation (X
± SD). An analysis of variance (ANOVA) was used to identify
differences between groups. A Scheffe's post-hoc test was used to
identify the differences when the overall F-value of the model was
significant. Statistical significance was accepted when p < 0.05.
The relationship between running speed and distance was examined
using the coefficient of determination (R2) for linear and curvilinear
regression.
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| RESULTS |
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The
mean race time of all the 1995 groups was 7:52.05 ± 1:00.58
(h:mm.ss). The fastest time recorded was 6:18.09 and the slowest
time was 11:12.36 (h:mm.ss). The mean race time for each group (A
to G) is shown in Table 1.
Group A (1995) had a mean race time of 6:36.58 ± 0:11.39
compared to group A (1997) of 6:40.12 ± 0:08.23 (h:mm.ss)
(Table 2). Similarly, group
F (1995) had an mean race time of 8:43.25 ± 0:19.09 (h:mm.ss)
compared to group F (1997) (8:44.34 ± 0:16.52) (h:mm.ss)
(Table 2). The mean race times
of groups A-G ranged from 6:36.58 ± 0:11.39 to 10:02.04 ±
0:34.40 (h:mm.ss) (Table 1).
The
mean running speed of each runner in the seven groups is shown in
Figure 1a with the line of
best fit for each group shown in bold. Groups A-C started at a faster
and very similar running speed (4.3 ± 0.2 m·s-1)
compared to groups D-F (4.0 ± 0.3 m·s-1,
Figure 1a). Runners who finished
in group A completed the entire race at running speeds within 15%
of their initial starting speed (Figure
1b). Slower runners showed the greatest change in mean speed
from 0-10 km vs. 90-100 km (group G; 1.4 ± 0.7 m·s-1)
in contrast to group A (0.5 ± 0.2 m·s-1)
(Table 1). Figure
1a shows that runners in group A ran at relatively constant
speeds during the first half of the race. This was also true for
the second half of the race, although their pace was slower during
this period.
The mean linear and curvilinear lines of best fit for each group
are shown in Figure 2a. For
the graph of mean running speed vs. distance, both linear and curvilinear
lines were calculated for each group's mean values. However, the
curvilinear calculations produced better fit lines (R2
= 0.61 vs. R2 = 0.90, mean linear vs. mean curvilinear
regressions, respectively; Table
1). Therefore, curvilinear
lines are shown in Figure 1a
and figure 2a.
The slopes of the normalized running speeds ranged from -0.16 ±
0.06 to -4.60 ± 1.50 (groups A to G) (Table
1). The slopes of groups A, B, C and D were significantly less
than the slopes of groups E, F and G (P < 0.01), suggesting that
groups A-D ran at a more even speed compared to groups E-G (Table
1).
Figure 2b shows the combined
graphs of groups A and F for 1995 and 1997. Group A (1995) had an
mean speed of 4.2 ± 0.1 m·s- 1 compared to Group A
(1997) (4.2 ± 0.1 m·s-1) (Table
2). Group F (1995) had an mean speed of 3.2 ± 0.1 m·s-1
compared to group F (1997) (3.2 ± 0.1 m.s-1) (Table
2). It is clear from Figure
2b that specific trends regarding distance vs. speed exist between
the two data sets.
The time for the marathon world record (2003) was 2:04.55 (h:mm.ss)
(Table 2). The mean running
speed was 5.6 m·s-1, and the CV was 1.2% (Table
2). The time for the 100 km world record is 6:13.33 (h:mm.ss)
(Table 2). The mean running
speed is 4.5 m·s-1, and the CV is 3.2% (Table
2).
|
| DISCUSSION |
The
aim of this study was to describe the changes in running speed of
national class runners in a 100 km ultra-marathon race to determine
if the faster runners showed different changes in their running speeds
compared to the slower runners. Runners in group A completed the race
at running speeds within 15% of their starting speed (0-10 km) (Figure
1b). Runners from other groups had a greater difference between
starting and finishing speeds than the top runners (Table
1, Figure 1b). For example,
group G had the greatest difference between starting (0-10 km) and
finishing (90-100 km) speeds (1.4 ± 0.8 m·s-1)
vs. group A (0.5 ± 0.2 m·s-1) (Table
1). The slower runners had greater variation in running speed
compared to faster runners. This is shown by the greater mean change
in running speed and the greater CV for mean running speed in slower
runners (Table 1, Figure
1a and 1b).
The faster runners maintained their initial running speed up to a
distance of approximately 50 km before they decreased their running
speed (Figure 1a). Their reduction
in running speed thereafter was relatively small as the race progressed.
In contrast, runners with slower race times were unable to maintain
their initial speed as long as the faster runners, and decreased their
speed more rapidly. The design of this study does not allow us to
explain the mechanisms causing the differences in the rate at which
running speed changed, particularly as the perception of effort may
be dissociated from running speed (Hampson et al., 2004). However, we can speculate that the inability to
maintain running speed may be attributed to physiological mechanisms
(Milvy, 1977).
It is suggested that although runners utilize about 65% VO2
max during a 100 km race (Davies and Thompson, 1979),
there is a large variation in resistance to fatigue and running economy-
which would account for different levels of performance (Sjodin and
Svedenhag, 1985). Fatigue after prolonged
exercise is associated with glycogen depletion (Bosch et al. , 1993),
which would occur after 40 - 50 km running at about 65% VO2
max (Karlsson and Saltin, 1971).
An alternative explanation for the decreased running speed after about
50 km is that there are neuromuscular changes caused by repetitive
eccentric muscle actions, resulting in fatigue and impaired muscle
function (Nicol et al., 1991).
Training habits (Lambert and Keytel, 2000)
and genotype (Bouchard et al., 1992)
of the runners are additional explanations for the varying reductions
in running speed after about 50 km. Also, in accordance with the findings
of Foster et al., (1994),
the slower runners may not have sufficiently practised their pacing
strategies over the longer distance. This observation is interesting
and needs further investigation, particularly if it is related to
training habits.
It is clear that the runners who had faster race times regulated their
speed more accurately than the slower runners, and had fewer changes
in running speed than the slower runners. This seems to be a consistent
finding as groups A and F in 1995 and 1997 had similar patterns of
changes in running speed. In accordance with these findings, the current
marathon world record of 2:04.55 held by Paul Tergat (Berlin, Germany,
September 2003) and the 100 km world record of 6:13.33 held by Takahiro
Sunada (Lake Saroma, Japan, June 1998) are additional examples of
races run at an almost even pace (CV = 1.2 and 3.2 %, marathon and
100 km world records respectively, Table
2). These examples show that elite world record performances are
run with very few changes in running speed.
Due to the nature of this study and the information available, certain
assumptions had to be made. We assumed that all runners produced similar
effort and were equally tired at the end of the race; and that all
runners had similar racing experience. In addition, in the analysis
we also assumed that the runners were highly motivated and trained
because they were representing their countries at an international
event. A limitation to this study was that training histories and
biographical information were not available. These data would have
added more interpretive value to this study, and should be included
in future studies of this nature.
|
| CONCLUSIONS |
These
results indicate that the faster runners in the 1995 IAU 100 km World
Challenge: 1) ran with fewer changes in running speed compared to
the slower runners; 2) started the race at a faster running speed
than the slower runners; and 3) were able to maintain their initial
running speed for longer distances than slower runners. Future studies
need to determine whether running performance in ultra-endurance events
is enhanced by adopting a more even running speed as a pacing strategy,
or whether the ability to run at even running speeds is dependent
on a combination of the physiological, psychological, and training
habits of the runner.
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| ACKNOWLEDGEMENTS |
These
results indicate that the faster runners in the 1995 IAU 100 km World
Challenge: 1) ran with fewer changes in running speed compared to
the slower runners; 2) started the race at a faster running speed
than the slower runners; and 3) were able to maintain their initial
running speed for longer distances than slower runners. Future studies
need to determine whether running performance in ultra-endurance events
is enhanced by adopting a more even running speed as a pacing strategy,
or whether the ability to run at even running speeds is dependent
on a combination of the physiological, psychological, and training
habits of the runner.
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| KEY
POINTS |
|
Faster
runners in the 100 km race;
- ran
with fewer changes in running speed compared to the slower runners;
- started
the race at a faster running speed than the slower runners;
- were
able to maintain their initial running speed for longer distances
than slower runners.
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| AUTHORS
BIOGRAPHY |
Mike I. LAMBERT
Employment: Associate Professor, University of Cape Town
Degree: PhD.
Research interests: Adaptations to exercise training
and their relationship to performance
E-mail: mlambert@sports.uct.ac.za
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Jonathan
P. DUGAS
Employment: Postgraduate student, University of Cape Town
Degree: BSc(Med)(Hon) Exercise Science
Research interests: Fluid ingestion and prolonged
exercise
E-mail:
jdugas@sports.uct.ac.za
|
|
Mark C. KIRKMAN
Employment: Postgraduate student, University of Cape Town
Degree: BSc(Med)(Hon) Exercise Science
Research interests: Training adaptations after high intensity
running training
E-mail: mkirkman@sports.uct.ac.za
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Gaonyadiwe G. MOKONE
Employment: Postgraduate student, University of Cape Town
Degree: BSc(Med)Hons
Research interests: Genetic basis of tendon injuries
E-mail: gmokone@sports.uct.ac.za |
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Miriam
R. WALDECK
Employment: Postgraduate student, University of Cape Town
Degree: B.Curr (Ed et Admin)
Research interests: Heart rate and monitoring performance
E-mail: mwaldeck@sports.uct.ac.za
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