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Pelvic floor muscles after birth: Do unstable shoes have an effect on pelvic floor activity and can this be measured reliably? – A feasibility study / Der Beckenboden nach der Geburt: Verändern instabile Schuhe die Aktivität und kann diese reliabel gemessen werden? – Eine Machbarkeitsstudie


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Introduction

Pregnancy and childbirth are risk factors for the development of urinary incontinence (Danforth et al., 2006; Fritel, Ringa, Quiboeuf, & Fauconnier, 2012; Menezes, Pereira, & Hextall, 2010; Milsom et al., 2009; Sangsawang & Sangsawang, 2013; Zhou et al., 2018). During a women’s first 3 months postpartum, the overall prevalence of urinary incontinence is 33%, with 12% of all women suffering from weekly and 3% from daily incontinence (Thom & Rortveit, 2010; Wesnes, Hunskaar, & Rortveit, 2012). Urinary incontinence often continues for several years after pregnancy (Gyhagen, Bullarbo, Nielsen, & Milsom, 2013; Hansen, Svare, Viktrup, Jørgensen, & Lose, 2012; MacArthur et al., 2006). In middle-aged or older women, the prevalence of urinary incontinence is between 30% and 60% and increases with age (Milsom et al., 2009). The large variation in the prevalence of urinary incontinence may be due to different study designs, different methods used to assess urinary incontinence, different definitions of urinary incontinence, and a selection bias (Milsom et al., 2009; Pregazzi et al., 2002; Thom & Rortveit, 2010; Wesnes et al., 2012).

The exact etiology and pathophysiology of urinary incontinence after pregnancy and birth are still unknown (Fritel et al., 2012; Fuselier, Hanberry, Lovin, & Gomelsky, 2018; Živković et al., 2016). A potential cause seems to be a weakness of the pelvic supportive structures (Hilde, Stær-Jensen, Ellström Engh, Brækken, & Bø, 2012; Mørkved, Salvesen, Bø, & Eik-Nes, 2004; Sangsawang, 2014; Sangsawang & Sangsawang, 2013; Van Geelen, Ostergard, & Sand, 2018). During pregnancy, hormonal changes as well as changes in collagen structure occur, making the pelvic floor more elastic and preparing it for birth. These changes can lead to weakening of the pelvic floor musculature (Bartling & Zito, 2016; Sangsawang & Sangsawang, 2013). The growing uterus and the weight gained by the fetus and the childbearing woman lead to an increased intra-abdominal pressure, which may also play a role in developing urinary incontinence (Allahdin & Kambhampati, 2012; Bartling & Zito, 2016; Fuselier et al., 2018; Sangsawang, 2014).

Pelvic floor muscle training before and after birth is an evidenced-based intervention to prevent urinary incontinence and its symptoms (Dumoulin, Cacciari, & Hay-Smith, 2018; Dumoulin, Glazener, & Jenkinson, 2011; Mørkved & Bø, 2014; Price, Dawood, & Jackson, 2010; Wesnes & Lose, 2013). In fact, for women with urinary incontinence, pelvic floor muscle training should be a first-line therapy (Bø, 2012). It is simple to perform and available to all women (Allahdin & Kambhampati, 2012).

While most women are aware of the effectiveness of pelvic floor muscle training (Hermansen, O’Connell, & Gaskin, 2010), prevention methods are not used enough (Hermansen et al., 2010). Few women perform regular pelvic floor muscle training antenatally and postpartum (Allahdin & Kambhampati, 2012; Bø, Haakstad, & Voldner, 2007). After childbirth, women are busy caring for their newborns. They often suffer from insomnia and exhaustion (Corwin & Arbour, 2007). Unless urinary incontinence causes distress, training of the pelvic floor musculature is not a priority, especially in households with small children.

However, urinary incontinence during pregnancy and after delivery usually has just a mild to moderate effect on the quality of life (Abdullah et al., 2016; Arrue et al., 2010; Dolan et al., 2004; Hansen et al., 2012; Kocaöz, Talas, & Atabekoğlu, 2010; Martínez Franco, Parés, Lorente Colomé, Méndez Paredes, & Amat Tardiu, 2014). According to Kocaöz et al. (2010), one reason for this might be that women perceive urinary incontinence during pregnancy and birth as temporary. In addition, urinary incontinence is still a big taboo (Elenskaia et al., 2011; Marecki & Seo, 2010).

In order to achieve high adherence to a training regimen, it needs to be easy for the target group of young mothers to integrate pelvic floor muscle training into a daily routine. Little is known to date about extrinsic factors that may activate the pelvic floor muscles. There is no research on measuring the effect of gait on the pelvic floor, although it has been shown that reduced foot flexibility may lead to increased impact forces, which may, in turn, be related to urinary incontinence (I. E. Nygaard, Glowacki, & Saltzman, 1996). Changes to the foot are also known to alter the kinematics of the hip, pelvis, and thorax (Khamis & Yizhar, 2007; Lee, 2018; Tateuchi, Wada, & Ichihashi, 2011). In light of this, footwear designed to change the kinematics of walking and standing may influence the pelvic region.

Studies performed on the Masai Barefoot Technology (MBT) shoe have shown that wearing unstable footwear can lead to altered muscle activation and sway while standing (Landry, Nigg, & Tecante, 2010; Nigg, Hintzen, & Ferber, 2006) as well as walking (Nigg et al., 2006; Stöggl, Haudum, Birklbauer, Murrer, & Müller, 2010). The kyBoot produced by kybun AG (Roggwil, Switzerland) is another example of an unstable shoe, it has a soft-elastic outsole and an air buffer in the center. It is assumed that the findings for the MBT shoe also apply to the kyBoot shoe. In both cases, more stabilization is needed while walking and standing than while barefoot. Wearing kyBoot shoes could, therefore, exercise the pelvic floor musculature.

The activity of the pelvic floor muscles in dynamic situations can be measured noninvasively with vaginal electromyography (EMG; Luginbuehl et al., 2013). This has a limited reliability (Luginbuehl et al., 2013) and is, therefore, unfit for repeated measurements. For a possible longitudinal study examining the effect of unstable shoes on the pelvic floor muscles, it would be necessary to have a more reliable method. There may be other more reliable variables providing information on pelvic floor activity that can be quantified in a movement laboratory, such as kinematic variables or skeletal muscle activation.

Previous research has provided evidence of co-activation of the pelvic floor muscles and abdominal muscles (Junginger, Baessler, Sapsford, & Hodges, 2010; Neumann & Gill, 2002; Sapsford & Hodges, 2001; Sapsford et al., 2001). Those studies used fine-wire EMG to record intramuscular activity. This approach is invasive and its application in a study design involving walking is limited. Finding a surrogate marker that can be recorded noninvasively would allow for a longitudinal study measuring the effectiveness of an intervention such as unstable shoes on the pelvic floor.

Aim of the study

The primary purpose of this feasibility study was to determine if there is a change in the activation of the pelvic floor muscles in postpartum women with different extrinsic parameters (barefoot versus kyBoot shoes). Second, we wanted to define variables that can be measured with high reliability in the laboratory and can be correlated with the activity of the pelvic floor muscle activity.

Methods
Design

The study was designed as a cross-sectional, within-subject comparison, feasibility study.

Sample

A total of 20 women who were 8 weeks to 6 months postpartum with no previous experience with unstable footwear were recruited for the study, and the data of 15 women were analyzed (mean ± std age: 32 ± 2.7 years; height: 1.7 ± 0.7 m; mass: 63.2 ± 8.2 kg). The main exclusion criteria were severe incontinence (according to ICIQ-UI short form), urinary tract infections, chronic diseases, or injuries affecting the participant’s gait pattern. Five data sets had to be excluded because of missing data or premature termination of the data collection. Participants were all free of diseases or injuries and had, if any, only mild stress incontinence. All women signed informed written consent approved by the local ethics committee (ID: KEK-ZH-Nr. 2015-0126).

Data collection process

Two footwear conditions (“barefoot” and “kyBoot”, Figure 1) were tested in random order by each participant. The participants performed three tasks: walking at self-selected speed (walk), standing for 15 s with an active pelvic floor (stance active), and standing for 15 s without pelvic floor activation (stance passive). The participants were instructed to stand upright during stance passive and to contract their pelvic floor as much as possible during stance active.

Figure 1

kyBoot used for data collection

Three-dimensional kinematics of the body were recorded using a marker-based 12-camera system (200 Hz, Vicon Motion Systems, Oxford, UK). Markers were placed on the body according to the Plug-In Gait (PiG) full body marker set (Davis, Õunpuu, Tyburski, & Gage, 1991). The joint angles in the sagittal plane of the ankle, knee, and hip, as well as the global orientation in the sagittal plane of the pelvis were calculated. The activity of the following muscles (left and right) was recorded using surface EMG (1000 Hz, myon AG, Schwarzenberg, Switzerland): M. Obliquus Externus (ObliExt), M. Rectus Abdominis (RectAbd), M. Erector Spinae (ErecSpi), M. Multifidii Lumbalis (MultLum), and M. Gluteus Maximus (GlutMax). Electrodes (Ambu BlueSensor, Ambu, Ballerup, Denmark) were placed on the prepared skin (shaven and cleaned) according to the SENIAM guidelines (Hermens et al., 1999) and recorded by the Vicon system synchronized with the marker data. The activity of the pelvic floor was recorded using a vaginal electrode (MultiBioSensors) and NeXus-10 (Mind Media BV, Herten, The Netherlands) at 2,048 Hz.

The participants were instructed on how to insert the electrode and inserted the lubricated electrode themselves. To synchronize the pelvic floor EMG signal with the remaining data, an external trigger was added to the NeXus-10 device, which sent a trigger signal to the Vicon system as well as the NeXus-10. Before the tasks were performed, participants were instructed to perform a maximum voluntary contraction (MVC) task by contracting their pelvic floor as hard as possible three times in a row at their own rate of contraction. The measurement was used to normalize the signal of the pelvic floor activity signal during the subsequent tasks.

Data analysis

All kinematic data were filtered using a mean-squared-error Woltring filter with a smoothing level of 10 mm2, and joint angles were calculated following the PiG procedure in Vicon Nexus 2.7. The surface EMG signals of the skeletal muscles were filtered (second-order Butterworth bandpass filter 10-450 Hz), rectified, and a root-mean-square (RMS) envelope was calculated. The EMG of the pelvic floor was filtered (second-order Butterworth bandpass filter 10-1000 Hz), rectified, and an RMS envelope calculated. Subsequently, all data were synchronized, with gait data being expressed from 0% to 100% of a gait cycle. All data processing and analysis were performed in MATLAB (The MathWorks, Natick, USA).

Variables

To address the first aim of the study, the maximum activity of the pelvic floor during the stance (active and passive) and walking trials was compared between barefoot and kyBoot using a paired t-test with a significance level of 0.05. Also, the pelvic floor muscle activity was compared between footwear conditions during 0.5 s in the middle of the standing trials.

To answer the secondary aim, the joint angles (ankle-, knee-, and hip-joint angles in the sagittal plane) and skeletal muscle activity were correlated with the activity of the pelvic floor at the moment of maximal pelvic floor activity for all tasks using the Pearson correlation coefficient.

Results

Pelvic floor activity while walking in kyBoot shoes or barefoot showed two peaks, at around 20% and 70% of the gait cycle (0% of gait cycle represent initial foot-ground contact, 100% of gait cycle represents consecutive foot-ground contact of the same foot; Figure 2). The maximum activity was significantly higher (p-value: 0.02) for the barefoot than for the kyBoot condition (112% vs. 90% of MVC; see Table 1). For the standing trials (stance active and passive), no significant differences between the conditions were observed for maximal and mid activities of the pelvic floor (Table 1).

Figure 2

Pelvic floor activity (in % of MVC) over the gait cycle for barefoot (light grey) and kyBoot (dark grey). The vertical lines represent foot-off.

Mean maximum and mid pelvic floor activity for “kyBoot” and “barefoot” for all tasks. The last column lists p-values of comparison. Bold indicates a significant difference between “kyBoot” and “barefoot” based on a significance level of p<0.05.

Mean pelvic floor activity (in % MVC)p-Value
kyBootBarefoot
WalkingMaximal activity90.0112.20.02
Stance activeMaximal activity76.064.30.59
Mid activity57.252.60.84
Stance passiveMaximal activity16.017.70.72
Mid activity14.315.60.79

The Pearson correlation coefficient between maximum pelvic floor activity and a variety of variables (measured at the same time point) was calculated to determine if the activity of the pelvic floor could be determined by a surrogate variable. The data were analyzed separately for the two conditions “kyBoot” and “barefoot” (Table 2). The highest correlation coefficient for joint angles was observed for the knee angle during stance active with kyBoot (0.48). However, the same variable for other conditions or tasks was much smaller. For the muscles, all correlation coefficients were ≤ 0.26 (Table 2).

Pearson correlation coefficient between pelvic floor activity and kinematic/skeletal muscles variables for “kyBoot” and “barefoot.”

Pelvic floor activity versusPearson correlation coefficient
WalkingStance activeStance passive
kyBootBarefootkyBootBarefootkyBootBarefoot
Ankle angle−0.060.030.250.140.090.10
Knee angle0.150.180.48−0.100.150.33
Hip angle0.040.100.390.020.270.38
Pelvis angle0.100.230.280.180.290.29
ObliExt0.02−0.090.25−0.180.14−0.01
RectAbd0.00−0.030.09−0.35−0.10−0.17
ErecSpi−0.11−0.09−0.12−0.40−0.080.06
MultLum−0.07−0.09−0.04−0.41−0.26−0.10
GlutMax0.260.230.17−0.35−0.27−0.27
Discussion

The primary aim of this study was to determine if unstable footwear was able to alter the activation of the pelvic floor muscles in postpartum women. The second aim was to identify the variables that can be reliably measured in a movement laboratory, which provide information on the activation of the pelvic floor muscles.

The pelvic floor activity during walking yielded significantly more activation while barefoot compared with “kyBoot.” No difference in activation was observed for the standing tasks. Therefore, the initial hypothesis that the pelvic floor may need to be activated more while wearing an unstable shoe had to be rejected. The kyBoot has a soft-elastic outsole with an air cushion in the center. This could result in more cushioning for the foot during landing than while barefoot. A more cushioned landing of the foot may actually require less activity in the pelvic floor despite the instability caused by the shoe. However, there is a lack of knowledge about the effect that walking has on the pelvic floor muscles, which is why it was impossible to consult other studies about this phenomenon.

This study compared the pelvic floor activation while wearing kyBoot shoes with that while barefoot. This approach was chosen because it was felt that bare feet may best represent the situation of women at home after childbirth. It is unknown how the activity of the pelvic floor is affected by the wearing of standard outdoor footwear. It is possible that wearing kyBoot shoes would result in an increase of pelvic floor activity compared with regular footwear. However, such a hypothesis needs to be examined in future studies.

This study measured the short-term effect of unstable footwear on the activity of the pelvic floor muscles while walking and standing. Ultimately, it would be of interest to know if unstable shoes are able to introduce a training effect on the pelvic floor muscles for a prolonged period of time. Future research is needed to investigate this.

A serious limitation is the limited reliability of vaginal EMG (Luginbuehl et al., 2013). The placement of the electrode only has limited reliability. The participants were asked to place the prominent bulge of the electrode ventrally. However, there is no suitable way to standardize the placement according to specific anatomical landmarks that would ensure equal placement for different measurement sessions. Furthermore, the vaginal electrode can shift or vibrate during dynamic tasks such as walking because of the impulse that needs to be absorbed by the body. In fact, several women reported the feeling that the vaginal electrode may have shifted. Owing the lack of instruments to control for this, it could not be checked. Consequently, it is possible that there is a measurement error inherent to the data.

For a possible longitudinal study, we were looking for a surrogate marker for the pelvic floor activity that can be quantified reliably in a movement laboratory. Therefore, the activity of M. Obliquus Externus, M. Rectus Abdominis, M. Erector Spinae, M. Multifidii Lumbalis, and M. Gluteus Maximus was measured using surface EMG. Three-dimensional kinematics of the body was recorded, and the joint angles in the sagittal plane of the ankle, knee, and hip as well as the global orientation in the sagittal plane of the pelvis were calculated.

Using the Pearson correlation coefficient, we were unable to find any strong correlation between maximal pelvic floor activity and any of the potential surrogate markers. Consequently, different surrogate markers need to be found before embarking on a longitudinal study assessing the training effect of unstable shoes on the pelvic floor muscles.

In this study, only women between 8 weeks and 6 months postpartum with no or a mild urinary incontinence were included. The results of this study cannot be translated to different populations, such as women with more than mild urinary incontinence or older women, in whom the pelvic floor activity and urinary incontinence are of high relevance (Fritel et al., 2012; Menezes et al., 2010; Milsom et al., 2009).

The recruitment of women for this study was difficult. One reason for this could be the fact that women between 8 weeks and 6 months postpartum are too busy caring for their infant. They often suffer from fatigue (Corwin & Arbour, 2007). As a result, the time needed to travel to and from our laboratory and the time spent there (duration of data collection: approximately 3 hours) might have prevented many from participating in this study. Another reason for the difficulty in recruiting women could be that for this sample, symptoms had to be mild, so women may have been less motivated to support research about this topic. These assumptions may be supported by the study results showing that postpartum women’s willingness to participate in pelvic floor muscle training is limited because of a variety of factors (Moossdorff-Steinhauser et al., 2015). Finally, many women may have been hesitant about using a vaginal electrode.

Conclusions

With regard to the pelvic floor musculature, it is not possible to make a recommendation concerning unstable shoes. We did not measure any short-term effect on the pelvic floor musculature caused by walking and standing in kyBoot shoes compared with walking and standing while barefoot. Whether or not the regular wearing of kyBoot shoes has a long-term effect on the pelvic floor needs to be addressed in future research.

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