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May 2014, Vol.12, No.3 156 Journal of Integrative Medicine
Journal Homepage:
www.jcimjournal.com/jim
www.elsevier.com/locate/issn/20954964
Available also online at www.sciencedirect.com.
Copyright © 2014, Journal of Integrative Medicine Editorial office.
E-edition published by Elsevier (Singapore) Pte Ltd. All rights reserved.
● Research Article
Heart rate variability and the influence of
craniosacral therapy on autonomous nervous
system regulation in persons with subjective
discomforts: a pilot study
Wanda Girsberger1,2
, Ulricke Bänziger1
, Gerhard Lingg1
, Harald Lothaller1
, Peter-Christian Endler1
1. Interuniversity College for Health and Development, Castle of Seggau, 8042 Graz, Austria
2. Practice for Craniosacral Therapy, Kronenstrasse 48, 8006 Zurich, Switzerland
BACKGROUND: Subjective discomforts in a preclinical range are often due to imbalanced autonomic
nervous system activity, which is a focus of craniosacral therapy.
OBJECTIVE: The aim of this work was to determine any changes in heart rate variability (HRV)
in a study on craniosacral therapy.
DESIGN, SETTING, PARTICIPANTS AND INTERVENTIONS: This is a quasi-experimental
(controlled) study with cross-over design. In a private practice, measurements were performed
on 31 patients with subjective discomforts before and after a control and an intervention period.
HRV was determined using a device that requires a measuring time of 140 s and electrode contact
only with the fingertips.
Main PRIMARY OUTCOME MEASURES: HRV change under the influence of a defined one-
time intervention (test intervention) with craniosacral therapy versus control (defined rest period).
RESULTS: Standard deviation of all RR-intervals (ms) and total power of RR-interval variability
in the frequency range (ms2
) were together interpreted as an indicator of test subjects’ autonomic
nervous activity and as a measure of their ability to cope with demands on their health. Neither
of these parameters increased during the control period (P>0.05), whereas during the test
intervention period there was an increase in both (P<0.05, P<0.01). Nevertheless, interactions
between treatment and the increase were statistically not significant (P>0.05). No changes were
observed in the low frequency/high frequency ratio (sympathetic-vagal balance) in the course of
the control or the test intervention period (P>0.05).
CONCLUSION: Craniosacral treatment had a favourable effect on autonomic nervous activity.
This in itself is an interesting result, but further research will be needed to distinguish specific
effects of craniosacral therapy technique from less specific therapist-client interaction effects.
KEYWORDS: massage; autonomic nervous system; electrocardiography; adult; complementary
therapies; pilot projects
http://dx.doi.org/10.1016/S2095-4964(14)60021-2
Girsberger W, Bänziger U, Lingg G, Lothaller H, Endler PC. Heart rate variability and the influence of craniosacral
therapy on autonomous nervous system regulation in persons with subjective discomforts: a pilot study. J
Integr Med. 2014; 12(3): 156-161.
Received January 21, 2014; accepted February 24, 2014.
Correspondence: Wanda Girsberger; Tel: +41-78-791-90-20; E-mail: wanda.girsberger@hispeed.ch
May 2014, Vol.12, No.3157Journal of Integrative Medicine
www.jcimjournal.com/jim
1 Introduction
Craniosacral therapy (CST) is a non-invasive method,
derived from osteopathy, developed in the 1970s by
J. Upledger, MD[1]
. It is based on the assumption that
there is a fine rhythmic movement, which pervades the
body and can be discerned by practised therapists under
their palpating hands. This movement can be utilised for
diagnostic as well as therapeutic purposes by regulating
the flow of cerebrospinal fluid[2,3]
. The focus of craniosacral
examination and treatment lies on the craniosacral structures;
these include the bones and connective tissues (membranes
of the brain and spinal cord) of the skull and spine and
the cerebrospinal fluid. Anatomically surrounding and
physiologically sustaining the central nervous system,
these structures have a direct influence on functioning
of the autonomic nervous system[2,4]
. The effects which
can be brought about through CST are achieved through
gentle touch in the areas of the skull, face, spine and
pelvis[5]
. Treatment is not primarily aimed at symptoms,
but determined by priorities established by the therapist
during each patient examination[2]
.
Studies on the use of CST to treat migraine[6]
, fibromyalgia[7,8]
and asthma[9]
showed encouraging results. In a review
performed by Jaekel and von Hauenschild[10]
, positive clinical
outcomes were reported for pain reduction and improvement
in general well-being of patients in randomized clinical
trials; as the quality of other trials was low, the authors
stated that currently available evidence was insufficient
to draw definite conclusions on the general efficacy of this
treatment modality. A review by Ernst[11]
was less optimistic,
and concluded that “the notion that CST is associated with
more than non-specific effects is not based on evidence
from rigorous randomized clinical trials”.
Working from the observation that changes in autonomic
balance are one of the fundamental causes of bodily
discomforts, the question of whether CST has a harmonizing
influence on the regulation of autonomic nervous processes
has been raised. Heart rate variability (HRV) is a non-
invasively measurable indicator of such processes, which
has been used for diagnostic purposes since the mid-1960s.
Its range of application extends from obstetrics to stress and
regeneration research as well as sports. Determination of
HRV is regarded as a method of assessing health and coping
status[12]
. It is therefore also used in therapy evaluation[13-18]
.
A randomized controlled trial showed positive effects of
CST on sensitive, tender points and HRV in patients with
fibromyalgia[8]
. To date there have been no studies on the
effects of CST on the regulation of the autonomic nervous
system in subjects with subjective discomforts but without
clinical diagnosis.
The following research questions were pursued in this
study: does HRV change under the influence of a defined
rest period (control rest)? does HRV change under the
influence of a defined one-time intervention (test intervention)?
are there differences between treatment periods?
2 Materials and methods
2.1 Design
This pilot study was a quasi-experimental (controlled)
study with cross-over design. The design and methods of
the study were approved by the ethics committee of the
Interuniversity College, Graz, Austria. Informed written
consent was obtained from each participant, and all data
were made anonymous before analysis.
2.2 Test subjects
Thirty-one volunteers (16 females, 15 males, average
age 46.2 years) were enrolled on the basis of the following
inclusion criteria: age 19-60 years; subjective discomforts
such as prolonged sleep latency, feeling stressed, nervous, weak
or restless as found typical for patients of complementary
therapy practices in Switzerland[19]
. These symptoms are
typical of persons seen by a craniosacral therapist, their
prime motive for seeking treatment being more often a
lack of feeling completely healthy than a clinically diagnosed
disease.
The following were exclusion criteria: cardiovascular
disease; pacemaker; diabetes with neural involvement;
acute infection; medication with β-blockers, antidepressants,
psychotropic drugs, atropine or phenylephrine. There
were no dropouts. All volunteers included in the study
completed all pre- and post-measurements.
2.3 Treatment allocation
The study was carried out in a practice for CST in Zurich,
Switzerland. Each test subject was given two appointments,
each between 10 am and 11 am on two consecutive days.
Upon their arrival on day 1, test subjects were randomly
assigned by dice either to a 30-minute session (intervention
period) or to a 30-minute control rest period for that day
(t1). Each patient was assigned to the other of the two alterna-
tives for the following day (t2) (Figure 1). In both cases
they underwent a 10-minute rest period of sitting prior to
the first measurement (t1_1 or t2_1, see below). The study
was carried out as an open study, i.e., neither participants
nor therapist were blinded to group assignment.
2.4 Intervention and control rest
A trained Swiss craniosacral therapist, with 20 years
of professional experience, gave 30-minute sessions in CST
following the 10-step protocol developed by Upledger et al[5]
,
proceeding in each case according to her observations
in the individual subject. The treatment involved gentle
touch of different parts of the fully clothed patient’s body
with the intent of resolving structural or energy restrictions.
This included techniques on the patient’s feet, sacrum,
www.jcimjournal.com/jim
May 2014, Vol.12, No.3 158 Journal of Integrative Medicine
thoracic inlet, occiput (CV4) and parietal bones (parietal
lift)[2,5]
. The expectation was that these treatments would
have an influence on HRV.
A 30-minute rest, under otherwise identical circumstances
(same participants, same time of the day, same room, same
supine position), served as a control without intervention.
2.5 Measurements
The required electrocardiogram (ECG) sequences were
recorded using a Universal Bodywave Mobile Wellness
cell phone (IMI-Health AG Co., Liechtenstein). This is a
special cell phone model with an integrated electronic single-
channel ECG recorder. Recordings are performed via
three integrated silver/silver chloride dry electrodes connected
to the tips of the index and middle fingers of both hands.
With a sampling rate of 500 Hz, common mode rejection
> 100 dB and a resolution < 2.7 µV/bit (19 bit), this system
conforms to current standards of good clinical practice.
Raw ECG data are transmitted in realtime to the cell
phone’s main memory, where they are provisionally stored
for quality control purposes, and are shown on the cell
phone display.
The cell phone is equipped with an application which
calculates all required HRV parameters in both the time
and the frequency domain. Calculation of HRV parameters
in the frequency domain involves the following calculations:
QRS detection based on a modified Pan-Tompkins algorithm;
correction of erroneous inter-beat intervals by interpolation;
dynamic resampling to 2n
to avoid discontinuities attributable
to zero-padding which are beyond the influence of the
window function; second-order detrending; application of
a cos² window function; integration of frequency bands.
Measurements were performed with test subjects seated
while resting the tips of both index and both middle fingers
on the device electrode over a 140-second interval. If the
device indicated insufficient electrode contact, the test
subject’s finger tips were wetted prior to measurement.
The data delivered by the device used were cross-checked
against and found to be compatible with the output of a
standard HRV device. A mock measurement was performed
on every test subject to allow them to become familiar
with the device and was not evaluated. On each study day,
a measurement was taken before and after the “treatment”.
We refer to these measurements on day one as t1_1 and
t1_2 respectively; similarly, on the second day of the
study we refer to the measurements as t2_1 and t2_2. See
Figure 2.
2.6 Parameters and data analysis
The following parameters were used to describe the status
of test subjects’ autonomic nervous activity:
(1) SDNN, the standard deviation (i.e., the square root
of the variance) of all RR-intervals in ms, used as an overall
measure of HRV across all frequency ranges;
(2) TP, total power of RR-interval variability in the frequency
range 0.003-0.4 Hz in ms2
, used as a supplementary measure
Figure 1 Flow of participants of the study
May 2014, Vol.12, No.3159Journal of Integrative Medicine
www.jcimjournal.com/jim
(which necessarily correlates strongly with SDNN).
Parameters used to measure parasympathetic activation:
(1) HF (high-frequency power, 0.15-0.4 Hz, in ms2
);
(2) HF% (proportion of HF in relation to TP).
Parameters reflecting sympathetic activation (amongst
other processes):
(1) LF (low-frequency power, 0.04-0.15 Hz, in ms2
);
(2) LF% (proportion of LF in relation to TP).
Parameter of sympathetic-vagal balance: LF/HF ratio.
Furthermore, heart rate (HR, in beats per minute) was
measured. No attempt was made to calculate the power of
very low frequency (0.003-0.04 Hz) from the data of this
short-term ECG.
Average freedom from artifacts was 97%.
2.7 Statistical analysis
IBM SPSS Statistics 20 was used for all statistical analyses.
Data were evaluated with analysis of variance with repeated
measures of the parameters in a pre-post design and the
treatments as independent variables. This procedure can
identify whether experimental parameters change over
the course of a treatment by comparing before and after
measurements. It can also determine whether the magnitude
of change in measured parameters is statistically different
among experimental groups.
LF/HF ratios were calculated on the basis of the individual
measurements and not on the basis of LF and HF means.
Results with an error probability P < 0.05 were considered
significant.
3 Results
3.1 Basic characteristics of the patients
Thirty-one volunteers (16 females, 15 males, average
46.2 years) were enrolled. Baseline measures for all
parameters did not differ between the groups (P > 0.05).
3.2 SDNN and TP
Both control rest and the intervention gave significant
increase of SDNN, but while the increase was +15% (P <
0.05) in the control period, it was +32% (P < 0.05) in the
test period. TP value did not increase significantly in the
control period (+19%; P > 0.05), but showed high significance
in the test intervention period (+126%; P < 0.01).
Although interactions were not statistically significant,
the increase was more marked in the test than in the
control rest period. With regard to SDNN, this statistical
finding might be due to the data characteristics. The
interaction between treatment and increase of TP was only
marginally above the level of significance (P = 0.057).
The measured values showed remarkably high variability.
Further analysis revealed that this was not attributable to
measurement quality (freedom from artifacts) but to the
values obtained from test subjects with SDNN > 100 ms.
SDNN values in this range may result from above-average
physical fitness, amongst other causes.
3.3 LF/HF ratio
No changes in the LF/HF ratio (sympathetic-vagal balance)
were observed in the course of the control or the test intervention
period (P > 0.05).
3.4 Heart rate
A highly significant decrease in heart rate (P < 0.01)
was observed after the CST as compared to that after the
rest period.
No significant adverse events or side effects were reported.
Table 1 shows the values for the parameters for pre-
measurement points t1_1/t2_1 (immediately before – upper
line) and post-measurement points t1_2/t2_2 (immediately
after – lower line) for the control rest period and the test
intervention period. Significant P value obtained in the
control rest period was change in HR (beats per minute).
In the test intervention period SDNN (ms), TP (ms2
), HF
(ms2
), LF (ms2
) and HR (beats per minute) showed significant
change.
4 Discussion
In this study on CST given to test subjects with subjective
discomforts, SDNN and TP were used as a global measure
of autonomic nervous activity and as an indicator of test
subjects’ability to cope with demands on their health (regulatory
capacity)[12]
. Before the control rest and before the test
intervention period, mean values (65.95 ms/2 161.3 ms2
and 55.2 ms/1 375.7 ms2
, respectively) were within the
range expected from the literature[13,20]
. SDNN and TP values
both did not increase significantly in the control period
(+15%/+19%; P > 0.05), but increased significantly in the
test intervention period (+32%/+126%; P < 0.05/P < 0.01).
In preliminary studies performed by the team, a rest period
of several minutes led to no changes or to an increase in
SDNN (range about 0 to 10 ms difference) and TP (range
0 to 400 ms2
)[18]
.
Further studies using the device compared the HRV pa-
rameters on two subsequent days at identical times of day
for each participant. No significant differences between
SDNN, TP or LF/HF values were found (P > 0.05)[18]
.
Figure 2 Sequence of heart rate variability measurements (dark-
shaded arrows) and control or test period (light-shaded arrows)
on day 1 (t1_1 and t1_2) and day 2 (t2_1 and t2_2)
www.jcimjournal.com/jim
May 2014, Vol.12, No.3 160 Journal of Integrative Medicine
it had been decided to admit test subjects across a wide
age range and of very different levels of fitness. This
brought with it a high variability in measured parameters.
For follow-on studies it could be of interest to define more
limiting inclusion criteria for test subjects’ age and physical
fitness, and to include matched instead of randomised par-
ticipants in the cross-over design. Furthermore, the criteria
for freedom from artifacts should be tightened.
The results are in line with the literature, in that they
indicate that HRV may be a useful tool to determine effects
of interventions, including complementary and alternative
medicine[13-18]
. The measurement device used seems to be
a promising tool for practical application studies of this kind.
5 Conclusion
In this pilot study on test subjects with subjective discomforts,
CST had a favourable effect on autonomic nervous activity.
This, in itself, is an interesting result, considering the frequency
persons with subjective discomforts electing to be treated
by a craniosacral therapist in Switzerland. Nevertheless,
further research will be needed to distinguish specific effects
of CST technique from less specific therapist/client-interaction
effects.
6 Acknowledgements
Thanks are due to the IMI-Health AG Co., Liechtenstein
for providing the measurement device.
Table 1 The values for the parameters for pre-measurement points t1_1/t2_1 and post-measurement points t1_2/t2_2
(Mean ± standard deviation)
Group n
Measurement
point
SDNN (ms) TP (ms2
) HF (ms2
) HF (%)
Control rest period 31
Pre 65.95±45.32 2 161.26±2 680.72 599.33±952.06 26.97±17.26
Post 75.92±50.52*#
2 575.48±2 555.28 556.12±807.00 23.23±18.88
Test intervention period 31
Pre 55.21±43.34 1 375.70±1 756.80 414.25±899.22 26.10±15.37
Post 72.97±40.01*
3 113.29±3 526.84**
754.84±1 431.92 **
23.81±16.17
Group n
Measurement
point
LF (ms2
) LF (%) LF/HF HR (beats/min)
Control rest period 31
Pre 677.03±936.50 32.55±17.13 3.55±8.43 67.45±10.13
Post 1 006.05±1 183.89 37.81±18.39 3.59±4.08 65.26±9.28*
Test intervention period 31
Pre 480.48±596.20 34.03±18.03 2.25±2.41 68.45±11.22
Post 1 143.33±1 239.16 **
36.39±15.70 3.06±4.08 64.52±9.45**
*
P< 0.05, **
P< 0.01, vs pre-measurement point.
#
An additional non-parametric Wilcoxon-test, executed due to a non-normal distribution of data, shows a slightly significant difference
(P = 0.044).
SDNN: the standard deviation of all RR-intervals; TP: total power of RR-interval variability; HF: high-frequency power; LF: low-
frequency power; HR: heart rate.
Conditions during the control rest period and the test
intervention period were otherwise identical, so that it
can be assumed that if there were any nonspecific influences,
relating for example, to the person conducting the
experiment or her relationship with the test subject, they
cancelled each other out. Thus, any differences observed
between the control regimen and the test intervention in
the degree of change occurring during the experiment
should be attributed to the test intervention.
The LF/HF ratio (sympathetic-vagal balance) in this
study was interpreted as a measure of the balance between
activation and relaxation[12]
. Mean baseline values (3.6 in
the control group, 2.3 in the test group) were classified
as sympathicotonia according to literature data. No sig-
nificant changes in the LF/HF ratio were observed in the
course of the control or the test intervention period (P >
0.05). In preparatory studies performed by the team, mean
LF/HF ratio ranged about 1.0 to 2.0 in various groups of
healthy volunteers. A rest period led to no changes or to a
decrease in the LF/HF ratio (ranged about 0 to 0.5).
The dropout rate of zero has strengthened the study. It
might be due to the applied therapy that was not invasive
and without any reported adverse effects. On the other
hand the weakness of this study is the lack of blinding,
which sets the standard for experimental design in the
clinical setting. Taking this into consideration, each
participant received both an intervention and a control
rest, on two consecutive days.
In order to reflect the everyday routine of a CST practice,
May 2014, Vol.12, No.3161Journal of Integrative Medicine
www.jcimjournal.com/jim
7 Competing interests
The authors declare that there are no competing interests.
REFERENCES
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Research article

  • 1. May 2014, Vol.12, No.3 156 Journal of Integrative Medicine Journal Homepage: www.jcimjournal.com/jim www.elsevier.com/locate/issn/20954964 Available also online at www.sciencedirect.com. Copyright © 2014, Journal of Integrative Medicine Editorial office. E-edition published by Elsevier (Singapore) Pte Ltd. All rights reserved. ● Research Article Heart rate variability and the influence of craniosacral therapy on autonomous nervous system regulation in persons with subjective discomforts: a pilot study Wanda Girsberger1,2 , Ulricke Bänziger1 , Gerhard Lingg1 , Harald Lothaller1 , Peter-Christian Endler1 1. Interuniversity College for Health and Development, Castle of Seggau, 8042 Graz, Austria 2. Practice for Craniosacral Therapy, Kronenstrasse 48, 8006 Zurich, Switzerland BACKGROUND: Subjective discomforts in a preclinical range are often due to imbalanced autonomic nervous system activity, which is a focus of craniosacral therapy. OBJECTIVE: The aim of this work was to determine any changes in heart rate variability (HRV) in a study on craniosacral therapy. DESIGN, SETTING, PARTICIPANTS AND INTERVENTIONS: This is a quasi-experimental (controlled) study with cross-over design. In a private practice, measurements were performed on 31 patients with subjective discomforts before and after a control and an intervention period. HRV was determined using a device that requires a measuring time of 140 s and electrode contact only with the fingertips. Main PRIMARY OUTCOME MEASURES: HRV change under the influence of a defined one- time intervention (test intervention) with craniosacral therapy versus control (defined rest period). RESULTS: Standard deviation of all RR-intervals (ms) and total power of RR-interval variability in the frequency range (ms2 ) were together interpreted as an indicator of test subjects’ autonomic nervous activity and as a measure of their ability to cope with demands on their health. Neither of these parameters increased during the control period (P>0.05), whereas during the test intervention period there was an increase in both (P<0.05, P<0.01). Nevertheless, interactions between treatment and the increase were statistically not significant (P>0.05). No changes were observed in the low frequency/high frequency ratio (sympathetic-vagal balance) in the course of the control or the test intervention period (P>0.05). CONCLUSION: Craniosacral treatment had a favourable effect on autonomic nervous activity. This in itself is an interesting result, but further research will be needed to distinguish specific effects of craniosacral therapy technique from less specific therapist-client interaction effects. KEYWORDS: massage; autonomic nervous system; electrocardiography; adult; complementary therapies; pilot projects http://dx.doi.org/10.1016/S2095-4964(14)60021-2 Girsberger W, Bänziger U, Lingg G, Lothaller H, Endler PC. Heart rate variability and the influence of craniosacral therapy on autonomous nervous system regulation in persons with subjective discomforts: a pilot study. J Integr Med. 2014; 12(3): 156-161. Received January 21, 2014; accepted February 24, 2014. Correspondence: Wanda Girsberger; Tel: +41-78-791-90-20; E-mail: wanda.girsberger@hispeed.ch
  • 2. May 2014, Vol.12, No.3157Journal of Integrative Medicine www.jcimjournal.com/jim 1 Introduction Craniosacral therapy (CST) is a non-invasive method, derived from osteopathy, developed in the 1970s by J. Upledger, MD[1] . It is based on the assumption that there is a fine rhythmic movement, which pervades the body and can be discerned by practised therapists under their palpating hands. This movement can be utilised for diagnostic as well as therapeutic purposes by regulating the flow of cerebrospinal fluid[2,3] . The focus of craniosacral examination and treatment lies on the craniosacral structures; these include the bones and connective tissues (membranes of the brain and spinal cord) of the skull and spine and the cerebrospinal fluid. Anatomically surrounding and physiologically sustaining the central nervous system, these structures have a direct influence on functioning of the autonomic nervous system[2,4] . The effects which can be brought about through CST are achieved through gentle touch in the areas of the skull, face, spine and pelvis[5] . Treatment is not primarily aimed at symptoms, but determined by priorities established by the therapist during each patient examination[2] . Studies on the use of CST to treat migraine[6] , fibromyalgia[7,8] and asthma[9] showed encouraging results. In a review performed by Jaekel and von Hauenschild[10] , positive clinical outcomes were reported for pain reduction and improvement in general well-being of patients in randomized clinical trials; as the quality of other trials was low, the authors stated that currently available evidence was insufficient to draw definite conclusions on the general efficacy of this treatment modality. A review by Ernst[11] was less optimistic, and concluded that “the notion that CST is associated with more than non-specific effects is not based on evidence from rigorous randomized clinical trials”. Working from the observation that changes in autonomic balance are one of the fundamental causes of bodily discomforts, the question of whether CST has a harmonizing influence on the regulation of autonomic nervous processes has been raised. Heart rate variability (HRV) is a non- invasively measurable indicator of such processes, which has been used for diagnostic purposes since the mid-1960s. Its range of application extends from obstetrics to stress and regeneration research as well as sports. Determination of HRV is regarded as a method of assessing health and coping status[12] . It is therefore also used in therapy evaluation[13-18] . A randomized controlled trial showed positive effects of CST on sensitive, tender points and HRV in patients with fibromyalgia[8] . To date there have been no studies on the effects of CST on the regulation of the autonomic nervous system in subjects with subjective discomforts but without clinical diagnosis. The following research questions were pursued in this study: does HRV change under the influence of a defined rest period (control rest)? does HRV change under the influence of a defined one-time intervention (test intervention)? are there differences between treatment periods? 2 Materials and methods 2.1 Design This pilot study was a quasi-experimental (controlled) study with cross-over design. The design and methods of the study were approved by the ethics committee of the Interuniversity College, Graz, Austria. Informed written consent was obtained from each participant, and all data were made anonymous before analysis. 2.2 Test subjects Thirty-one volunteers (16 females, 15 males, average age 46.2 years) were enrolled on the basis of the following inclusion criteria: age 19-60 years; subjective discomforts such as prolonged sleep latency, feeling stressed, nervous, weak or restless as found typical for patients of complementary therapy practices in Switzerland[19] . These symptoms are typical of persons seen by a craniosacral therapist, their prime motive for seeking treatment being more often a lack of feeling completely healthy than a clinically diagnosed disease. The following were exclusion criteria: cardiovascular disease; pacemaker; diabetes with neural involvement; acute infection; medication with β-blockers, antidepressants, psychotropic drugs, atropine or phenylephrine. There were no dropouts. All volunteers included in the study completed all pre- and post-measurements. 2.3 Treatment allocation The study was carried out in a practice for CST in Zurich, Switzerland. Each test subject was given two appointments, each between 10 am and 11 am on two consecutive days. Upon their arrival on day 1, test subjects were randomly assigned by dice either to a 30-minute session (intervention period) or to a 30-minute control rest period for that day (t1). Each patient was assigned to the other of the two alterna- tives for the following day (t2) (Figure 1). In both cases they underwent a 10-minute rest period of sitting prior to the first measurement (t1_1 or t2_1, see below). The study was carried out as an open study, i.e., neither participants nor therapist were blinded to group assignment. 2.4 Intervention and control rest A trained Swiss craniosacral therapist, with 20 years of professional experience, gave 30-minute sessions in CST following the 10-step protocol developed by Upledger et al[5] , proceeding in each case according to her observations in the individual subject. The treatment involved gentle touch of different parts of the fully clothed patient’s body with the intent of resolving structural or energy restrictions. This included techniques on the patient’s feet, sacrum,
  • 3. www.jcimjournal.com/jim May 2014, Vol.12, No.3 158 Journal of Integrative Medicine thoracic inlet, occiput (CV4) and parietal bones (parietal lift)[2,5] . The expectation was that these treatments would have an influence on HRV. A 30-minute rest, under otherwise identical circumstances (same participants, same time of the day, same room, same supine position), served as a control without intervention. 2.5 Measurements The required electrocardiogram (ECG) sequences were recorded using a Universal Bodywave Mobile Wellness cell phone (IMI-Health AG Co., Liechtenstein). This is a special cell phone model with an integrated electronic single- channel ECG recorder. Recordings are performed via three integrated silver/silver chloride dry electrodes connected to the tips of the index and middle fingers of both hands. With a sampling rate of 500 Hz, common mode rejection > 100 dB and a resolution < 2.7 µV/bit (19 bit), this system conforms to current standards of good clinical practice. Raw ECG data are transmitted in realtime to the cell phone’s main memory, where they are provisionally stored for quality control purposes, and are shown on the cell phone display. The cell phone is equipped with an application which calculates all required HRV parameters in both the time and the frequency domain. Calculation of HRV parameters in the frequency domain involves the following calculations: QRS detection based on a modified Pan-Tompkins algorithm; correction of erroneous inter-beat intervals by interpolation; dynamic resampling to 2n to avoid discontinuities attributable to zero-padding which are beyond the influence of the window function; second-order detrending; application of a cos² window function; integration of frequency bands. Measurements were performed with test subjects seated while resting the tips of both index and both middle fingers on the device electrode over a 140-second interval. If the device indicated insufficient electrode contact, the test subject’s finger tips were wetted prior to measurement. The data delivered by the device used were cross-checked against and found to be compatible with the output of a standard HRV device. A mock measurement was performed on every test subject to allow them to become familiar with the device and was not evaluated. On each study day, a measurement was taken before and after the “treatment”. We refer to these measurements on day one as t1_1 and t1_2 respectively; similarly, on the second day of the study we refer to the measurements as t2_1 and t2_2. See Figure 2. 2.6 Parameters and data analysis The following parameters were used to describe the status of test subjects’ autonomic nervous activity: (1) SDNN, the standard deviation (i.e., the square root of the variance) of all RR-intervals in ms, used as an overall measure of HRV across all frequency ranges; (2) TP, total power of RR-interval variability in the frequency range 0.003-0.4 Hz in ms2 , used as a supplementary measure Figure 1 Flow of participants of the study
  • 4. May 2014, Vol.12, No.3159Journal of Integrative Medicine www.jcimjournal.com/jim (which necessarily correlates strongly with SDNN). Parameters used to measure parasympathetic activation: (1) HF (high-frequency power, 0.15-0.4 Hz, in ms2 ); (2) HF% (proportion of HF in relation to TP). Parameters reflecting sympathetic activation (amongst other processes): (1) LF (low-frequency power, 0.04-0.15 Hz, in ms2 ); (2) LF% (proportion of LF in relation to TP). Parameter of sympathetic-vagal balance: LF/HF ratio. Furthermore, heart rate (HR, in beats per minute) was measured. No attempt was made to calculate the power of very low frequency (0.003-0.04 Hz) from the data of this short-term ECG. Average freedom from artifacts was 97%. 2.7 Statistical analysis IBM SPSS Statistics 20 was used for all statistical analyses. Data were evaluated with analysis of variance with repeated measures of the parameters in a pre-post design and the treatments as independent variables. This procedure can identify whether experimental parameters change over the course of a treatment by comparing before and after measurements. It can also determine whether the magnitude of change in measured parameters is statistically different among experimental groups. LF/HF ratios were calculated on the basis of the individual measurements and not on the basis of LF and HF means. Results with an error probability P < 0.05 were considered significant. 3 Results 3.1 Basic characteristics of the patients Thirty-one volunteers (16 females, 15 males, average 46.2 years) were enrolled. Baseline measures for all parameters did not differ between the groups (P > 0.05). 3.2 SDNN and TP Both control rest and the intervention gave significant increase of SDNN, but while the increase was +15% (P < 0.05) in the control period, it was +32% (P < 0.05) in the test period. TP value did not increase significantly in the control period (+19%; P > 0.05), but showed high significance in the test intervention period (+126%; P < 0.01). Although interactions were not statistically significant, the increase was more marked in the test than in the control rest period. With regard to SDNN, this statistical finding might be due to the data characteristics. The interaction between treatment and increase of TP was only marginally above the level of significance (P = 0.057). The measured values showed remarkably high variability. Further analysis revealed that this was not attributable to measurement quality (freedom from artifacts) but to the values obtained from test subjects with SDNN > 100 ms. SDNN values in this range may result from above-average physical fitness, amongst other causes. 3.3 LF/HF ratio No changes in the LF/HF ratio (sympathetic-vagal balance) were observed in the course of the control or the test intervention period (P > 0.05). 3.4 Heart rate A highly significant decrease in heart rate (P < 0.01) was observed after the CST as compared to that after the rest period. No significant adverse events or side effects were reported. Table 1 shows the values for the parameters for pre- measurement points t1_1/t2_1 (immediately before – upper line) and post-measurement points t1_2/t2_2 (immediately after – lower line) for the control rest period and the test intervention period. Significant P value obtained in the control rest period was change in HR (beats per minute). In the test intervention period SDNN (ms), TP (ms2 ), HF (ms2 ), LF (ms2 ) and HR (beats per minute) showed significant change. 4 Discussion In this study on CST given to test subjects with subjective discomforts, SDNN and TP were used as a global measure of autonomic nervous activity and as an indicator of test subjects’ability to cope with demands on their health (regulatory capacity)[12] . Before the control rest and before the test intervention period, mean values (65.95 ms/2 161.3 ms2 and 55.2 ms/1 375.7 ms2 , respectively) were within the range expected from the literature[13,20] . SDNN and TP values both did not increase significantly in the control period (+15%/+19%; P > 0.05), but increased significantly in the test intervention period (+32%/+126%; P < 0.05/P < 0.01). In preliminary studies performed by the team, a rest period of several minutes led to no changes or to an increase in SDNN (range about 0 to 10 ms difference) and TP (range 0 to 400 ms2 )[18] . Further studies using the device compared the HRV pa- rameters on two subsequent days at identical times of day for each participant. No significant differences between SDNN, TP or LF/HF values were found (P > 0.05)[18] . Figure 2 Sequence of heart rate variability measurements (dark- shaded arrows) and control or test period (light-shaded arrows) on day 1 (t1_1 and t1_2) and day 2 (t2_1 and t2_2)
  • 5. www.jcimjournal.com/jim May 2014, Vol.12, No.3 160 Journal of Integrative Medicine it had been decided to admit test subjects across a wide age range and of very different levels of fitness. This brought with it a high variability in measured parameters. For follow-on studies it could be of interest to define more limiting inclusion criteria for test subjects’ age and physical fitness, and to include matched instead of randomised par- ticipants in the cross-over design. Furthermore, the criteria for freedom from artifacts should be tightened. The results are in line with the literature, in that they indicate that HRV may be a useful tool to determine effects of interventions, including complementary and alternative medicine[13-18] . The measurement device used seems to be a promising tool for practical application studies of this kind. 5 Conclusion In this pilot study on test subjects with subjective discomforts, CST had a favourable effect on autonomic nervous activity. This, in itself, is an interesting result, considering the frequency persons with subjective discomforts electing to be treated by a craniosacral therapist in Switzerland. Nevertheless, further research will be needed to distinguish specific effects of CST technique from less specific therapist/client-interaction effects. 6 Acknowledgements Thanks are due to the IMI-Health AG Co., Liechtenstein for providing the measurement device. Table 1 The values for the parameters for pre-measurement points t1_1/t2_1 and post-measurement points t1_2/t2_2 (Mean ± standard deviation) Group n Measurement point SDNN (ms) TP (ms2 ) HF (ms2 ) HF (%) Control rest period 31 Pre 65.95±45.32 2 161.26±2 680.72 599.33±952.06 26.97±17.26 Post 75.92±50.52*# 2 575.48±2 555.28 556.12±807.00 23.23±18.88 Test intervention period 31 Pre 55.21±43.34 1 375.70±1 756.80 414.25±899.22 26.10±15.37 Post 72.97±40.01* 3 113.29±3 526.84** 754.84±1 431.92 ** 23.81±16.17 Group n Measurement point LF (ms2 ) LF (%) LF/HF HR (beats/min) Control rest period 31 Pre 677.03±936.50 32.55±17.13 3.55±8.43 67.45±10.13 Post 1 006.05±1 183.89 37.81±18.39 3.59±4.08 65.26±9.28* Test intervention period 31 Pre 480.48±596.20 34.03±18.03 2.25±2.41 68.45±11.22 Post 1 143.33±1 239.16 ** 36.39±15.70 3.06±4.08 64.52±9.45** * P< 0.05, ** P< 0.01, vs pre-measurement point. # An additional non-parametric Wilcoxon-test, executed due to a non-normal distribution of data, shows a slightly significant difference (P = 0.044). SDNN: the standard deviation of all RR-intervals; TP: total power of RR-interval variability; HF: high-frequency power; LF: low- frequency power; HR: heart rate. Conditions during the control rest period and the test intervention period were otherwise identical, so that it can be assumed that if there were any nonspecific influences, relating for example, to the person conducting the experiment or her relationship with the test subject, they cancelled each other out. Thus, any differences observed between the control regimen and the test intervention in the degree of change occurring during the experiment should be attributed to the test intervention. The LF/HF ratio (sympathetic-vagal balance) in this study was interpreted as a measure of the balance between activation and relaxation[12] . Mean baseline values (3.6 in the control group, 2.3 in the test group) were classified as sympathicotonia according to literature data. No sig- nificant changes in the LF/HF ratio were observed in the course of the control or the test intervention period (P > 0.05). In preparatory studies performed by the team, mean LF/HF ratio ranged about 1.0 to 2.0 in various groups of healthy volunteers. A rest period led to no changes or to a decrease in the LF/HF ratio (ranged about 0 to 0.5). The dropout rate of zero has strengthened the study. It might be due to the applied therapy that was not invasive and without any reported adverse effects. On the other hand the weakness of this study is the lack of blinding, which sets the standard for experimental design in the clinical setting. Taking this into consideration, each participant received both an intervention and a control rest, on two consecutive days. In order to reflect the everyday routine of a CST practice,
  • 6. May 2014, Vol.12, No.3161Journal of Integrative Medicine www.jcimjournal.com/jim 7 Competing interests The authors declare that there are no competing interests. REFERENCES 1 Upledger JE. Craniosacral therapy. Phys Ther. 1995; 75(4): 328-330. 2 Agustoni D. Craniosacral-Rhythmus: Praxisbuch zu einer sanften Körpertherapie. Kandern: Kösel Verlag. 2006. German. 3 Lomba J, Schröder G. Craniosacrale Osteopathie in der Kinder- und Erwachsenenpraxis. Kandern: Pflaum Verlag. 2005. German. 4 Liem T. Kraniosakrale Osteopathie. Ein praktisches Lehrbuch. Stuttgart: Hippokrates. 2001. German. 5 Upledger JE, Vredevoogd JD. Lehrbuch der Craniosacral Therapie. Heidelberg: Georg Thieme Verlag. 2002. German. 6 Arnadottir TS, Sigurdardottir AK. Is craniosacral therapy effective for migraine? Tested with HIT-6 Questionnaire. Complement Ther Clin Pract. 2013; 19(1): 11-14. 7 Matarán-Peñarrocha GA, Castro-Sánchez AM, García GC, Moreno-Lorenzo C, Carreño TP, Zafra MD. Influence of craniosacral therapy on anxiety, depression and quality of life in patients with fibromyalgia. Evid Based Complement Alternat Med. 2011; 2011: 178769. 8 Castro-Sánchez AM, Matarán-Peñarrocha GA, Sánchez- Labraca N, Quesada-Rubio JM, Granero-Molina J, Moreno- Lorenzo C. A randomized controlled trial investigating the effects of craniosacral therapy on pain and heart rate variability in fibromyalgia patients. Clin Rehabil. 2011; 25(1): 25-35. 9 Mehl-Madrona L, Kligler B, Silverman S, Lynton H, Merrell W. The impact of acupuncture and craniosacral therapy interventions on clinical outcomes in adults with asthma. Explore (NY). 2007; 3(1): 28-36. 10 Jaekel A, von Hauenschild P. A systematic review to evaluate the clinical benefits of craniosacral therapy. Complement Ther Med. 2012; 20(6): 456-465. 11 Ernst E. Craniosacral therapy: A systematic review of the clinical evidence. Focus Altern Complement Ther. 2012; 17(4): 197-201. 12 Wittling W, Wittling RA. Herzschlagvariabilität: Frühwarnsystem, Stress- und Fitnessindikator. Heiligenstadt: Eichsfeld Verlag. 2012. German. 13 Agelink MW, Sanner D, Eich H, Pach J, Bertling R, Lemmer W, Klieser E, Lehmann E. Does acupuncture influence the cardiac autonomic nervous system in patients with minor depression or anxiety disorders? Fortschr Neurol Psychiatr. 2003; 71(3): 141-149. German with abstract in English. 14 Trappe HJ. The effects of music on the cardiovascular system and cardiovascular health. Heart. 2010; 96(23): 1868-1871. 15 Field T. Tai Chi research review. Complement Ther Clin Pract. 2011; 17(3): 141-146. 16 Mishra N, Muraleedharan KC, Paranjpe AS, Munta DK, Singh H, Nayak C. An exploratory study on scientific investigations in homeopathy using medical analyzer. J Altern Complement Med. 2011; 17(8): 705-710. 17 Courtney R, Cohen M, van Dixhoorn J. Relationship between dysfunctional breathing patterns and ability to achieve target heart rate variability with features of “Coherence” during biofeedback. Altern Ther Health Med. 2011; 17(3): 38-44. 18 Pizzinato E, Muller J, Lingg G, Dapra D, Lothaller H, Endler PC. Heart rate variability in a study on Reiki treatment. Open Complement Med J. 2012; 4: 12-15. 19 Melchart D, Mitscherlich F, Amiet M, Eichenberger R, Koch P. Programm Evaluation Komplementärmedizin (PEK), Schlussbericht. Bern: Schweizerisches Bundesamt für Gesundheit. 2005: 61. German. 20 Nunan D, Sandercock GRH, Brodie DA. A quantitative systematic review of normal values for short-term heart rate variability in healthy adults. Pacing Clin Electrophysiol. 2010; 33(11): 1407-1417. Submission Guide Journal of Integrative Medicine (JIM) is an international, peer-reviewed, PubMed-indexed journal, publishing papers on all aspects of integrative medicine, such as acupuncture and traditional Chinese medicine, Ayurvedic medicine, herbal medicine, homeopathy, nutrition, chiropractic, mind-body medicine, Taichi, Qigong, meditation, and any other modalities of complementary and alternative medicine (CAM). Article types include reviews, systematic reviews and meta-analyses, randomized controlled and pragmatic trials, translational and patient-centered effectiveness outcome studies, case series and reports, clinical trial protocols, preclinical and basic science studies, papers on methodology and CAM history or education, editorials, global views, commentaries, short communications, book reviews, conference proceedings, and letters to the editor. ● No submission and page charges ● Quick decision and online first publication For information on manuscript preparation and submission, please visit JIM website. Send your postal address by e-mail to jcim@163.com, we will send you a complimentary print issue upon receipt.