Effects of Soft Tissue Mobilization (Rolfing Pelvic Lift) on Parasympathetic in Two Age Groups

From "Physical Therapy"


From "Physical Therapy"

Mobilization of the bony pelvis and the surrounding soft tissues has been used in medical practice since the beginning of recorded history. Ancient Chinese, Egyptian, and Greek medical accounts all describe pelvic manipulations and associated changes in breathing, arterial pulse, body temperature, and muscle tone(1). Several schools of manual therapy, including chiropractic, osteopathic, and Rolfing, have rediscovered and further developed these mobilization practices in the United States in the last century.(2-4) A resurgence of interest in soft tissue manipulative techniques is evident in the physical therapy and medical literature of the last two decades.(5-7) Advocates of these techniques have recommended pelvic mobilization for various clinical problems that involve autonomic nervous system (ANS) dysfunctions.

Scientific evaluation of soft tissue manipulative treatments is difficult because of the scarcity of experimental studies, the difficulty in quantifying treatment outcomes and the speculative nature of the neurophysiologic mechanisms of ANS action.(8,9) Homogeneous subject samples undergoing standardized treatment procedures must be examined to establish the ANS responses associated with a given manipulation. Such information will allow more appropriate selection of manual therapy for specific conditions.

This study examined the pelvic lift mobilization procedure and associated changes in ANS tone. Pelvic lift is a soft tissue manipulation from the Rolfing method of manual therapy and movement education. It involves a combination of posterior tilting and pelvic traction with concurrent moderate pressure to the epigastrium.(4-10) Lumbosacral decompression, a similar technique, is involved in osteopathic manipulative techniques.(11) Both the pelvic lift and the lumbosacral decompression maneuvers have been associated with an increase in parasympathetic nervous system (PNS) tone and a corresponding decrease in sympathetic nervous system (SNS) activity.(10,11)

Pelvic lift also is comparable to the facilitated pelvic tilt exercise described in the physica] therapy and occupational therapy literature.(12,13) The pelvic tilt originally was devised by Paul Williams as part of a series of back exercises.(13) The facilitated pelvic tilt and related pelvic mobilization techniques, however, currently are used with adults, children, and infants in various therapeutic contexts: 1) to activate selected thoracic and abdominal breathing patterns,(1,14) 2) to inhibit hyperactive behaviors, (1,14) 3) to inhibit shoulder elevation and retraction,(14-17) 4) to reduce hyperextensive neck and back patterns,(6,7,15-17) and 5) to reduce chronic soft tissue pain associated with excessive SNS activity.(1,14,16,17) The posterior pelvic tilt has been demonstrated to reduce electromyographic activity in the lumbosacral regions of healthy young adults when compared with anterior pelvic tilt and baseline measurements.(13)

The results of experimental investigations of ANS reflexes and tactile stimulation also support the clinical observations that pelvic mobilization appears to be correlated with increased PNS activity. Overall, the studies indicate that deep mechanical pressure to the abdominal region, slow stroking to the back, and sustained pressure to the pelvis produce increases in PNS reflex responses, including increased electrical activity in sacral and vagal fibers, increased peripheral skin temperatures, synchronous electroencephalographic patterns, and decreased EMG activity.(14-22) These studies have also demonstrated that autonomic and somatic responses are integrated, not two independent motor systems.(22)

Age also appears to be an important factor in determining the responsiveness of the ANS of human subjects to a given stimulus (e.g., tactile). Studies on aging have demonstrated that subjects over 60 years of age show slower and diminished ANS than younger subjects.(23)

We decided to measure PNS tone in this study because tactile stimulation of the pelvis, back, and abdominal regions enhances PNS activity. The method we selected to assess PNS activity involved the analysis and isolation of rhythmic variations in the heart rate pattern that are correlated with PNS cardiac innervation through the vagus nerve. Katona and Jih,(24) in a study of anesthetized dogs, and Eckberg,(25) in a study of conscious human subjects, demonstrated that measuring the amplitude of the heart rate oscillations associated with respiration could be used as an index of cardiac PNS tone. Respiratory sinus arrhythmia (RSA ) is the rhythmic increase in heart rate associated with inspiration and the decrease in heart rate associated with expiration (Fig.1).

<img src=’https://novo.pedroprado.com.br/imgs/1988/1083-1.jpg’>

Complex mechanisms control the relationship between RSA and cardiac vagal tone. Some cardiovascular physiologists traditionally have considered RSA to be produced by nonneural factors rather than by cardiac vagal reflexes. Strong evidence currently exists, however, that respiration, through either a central mechanism or a peripheral feedback loop to medullary areas, phasically inhibits, or “gates,” the source nuclei of the vagal cardioinhibitory fibers.(24-27) Respiration is involved in the phasic modulation of the vagal influences to the heart, with the maximal inhibition occurring during the mid- to late-inspiratory phase and the maximal output occurring during the expiratory phase.(28-31) Because the vagal cardioinhibitory neurons by definition slow the heart rate and exhibit a respiratory frequency, their impact on heart rate should be a slowing of heart rate during the expiratory phase of respiration. The greater the vagal efferent output to the heart, the greater the slowing of heart rate during expiration. Thus, RSA is a peripheral manifestation of the influence of the vagal cardioinhibitory neurons on the heart (i.e., cardiac vagal tone), and a strong argument can be made that quantification of the amplitude of RSA is an accurate index of cardiac vagal tone.(32)

Porges developed a unique method of accurately quantifying RSA with time series procedures.(33) This method of assessing cardiac PNS activity has been validated experimentally. Pharmacological and electrophysiological manipulations of cardiac vagal efferent tone in rats, cats, and humans were found to be reliably reflected in the amplitude of RSA.(32, 34-36) Because of the direct relationship between this method of quantifying RSA and cardiac PNS tone, the statistical description of the RSA amplitude has been termed vagal tone.

The purpose of this study was to examine the immediate PNS responses of two age groups of healthy male subjects to 1) the application of a single soft tissue pelvic procedure, the Rolfing pelvic lift, and 2) a control manipulative procedure involving sustained tactile pressure, durational touch.

We formulated two hypotheses based on the literature review. First, the pelvic lift would elicit a somatovisceral-PNS reflex and increase PNS tone, but the durational touch would not produce such an increase. Second, a group of young, healthy male subjects would demonstrate greater autonomic responsiveness (i.e., larger increases in PNS tone) to the pelvic lift than a group of older healthy male subjects.



Two groups of men were selected for this study. Group I consisted of 20 healthy men aged 26 to 41 years (X = 32 years), and Group 2 consisted of 10 healthy men aged 55 to 68 years (X = 63 years). All subjects were nonsmokers and reported no known health problems. The subjects were oriented to soft tissue therapy before testing. All subjects were selected on a volunteer basis from the professional practice of the primary investigator (J.T.C.). Each subject signed an informed consent form to participate in the study. The study procedure was approved by the Frances Nelson Health Center Board of Directors. Two subjects from Group 1 and one subject from Group 2 were eliminated from the data analysis because of problems with the ECG signal.


We placed electrodes bilaterally on the ventral wrists of the subjects and monitored ECG activity with an ECG amplifier.(*) The output of the ECG amplifier was fed into a Vagal Tone Monitor,(&) a microcomputer that calculates vagal tone and heart rate. A quiet environment was maintained with an average temperature of 24°C (range = 23°- 25°C).

* Scope Service, inc. 1015 W Main, Urbana, IL 61801.

(&) Delta-Biometrics, inc. 9411 Locust Hill Rd. Bethesda, MD 20814.


During each testing session before data collection, the subjects were positioned supine on a treatment table with the electrodes placed on their wrists. Five minutes was allowed for adaptation to the environment. We gave the subjects instructions about the testing procedure during this interval.

We monitored the subjects’ ECG activity during five consecutive three-minute conditions: 1) baseline, 2) manipulation, 3) baseline, 4) manipulation, and 5) baseline. The vagal tone monitoring device was located in an adjacent room so that the investigator did not have access to the heart rate data during the testing session. Fifteen subjects experienced the pelvic lift manipulation first, and the other 15 subjects experienced the durational touch manipulation first. We administered the pelvic lift with the subjects in a supine position with their knees flexed. The experimenter placed one hand under the subject’s sacrum so that his fingertips rested on the lumbosacral junction. He then applied traction to tilt the pelvis in a posterior direction (i.e., tilting the anterior superior spines posterior to the pubic symphysis in the sagittal plane). The experimenter placed his other hand on the subject’s epigastrium with moderate pressure. The control manipulation of durational touch involved moderate bilateral pressure by the experimenter’s hands to the subject’s anterior deltoid muscles. The manipulative techniques were administered by the primary investigator (J.T.C.), a certified advanced Rolfing practitioner.

Data Quantification and Analysis

We assessed the dependent variables of vagal tone and heart rate during sequential 30-second periods within each three-minute condition. Heart rate in beats per minute was calculated as twice the number of interbeat intervals within each 30-second period. We calculated the vagal tone index by extracting the amplitude of RSA from the beat-to-beat pattern. This procedure necessitated the following steps: 1) conducting a time-series analysis, 2) applying a moving polynomial filtering procedure that removes the heart rate variability associated with baseline trends and periodic activity slower than respiration, 3) band pass filtering the residual series to allow only the heart rate pattern in the frequency band associated with spontaneous respiration to pass, 4) calculating the variance of band-pass series that represents the RSA amplitude, and 5) calculating the natural logarithm of this variance to normalize its distribution.(37)

We calculated analyses of variance (ANOVAs) for vagal tone and heart period with age group and order of treatment as between-subject factors and treatment as a within-subject repeated measure.(37) An alpha level of .05 was used for statistical significance.


For the dependent variable of vagal tone, the ANOVA demonstrated a significant group by treatment interaction (F = 2.7; df = 4,92; p <.05) (Table).

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Simple-effects post hoc tests of univariate ANOVAs for Groups I and 2 demonstrated that only Group I exhibited significant differences among the five treatment conditions (F= 12.5; df= 4,64; p < .0005). Examination of the treatment means and standard errors in Group I clearly indicated that this significant variance was related solely to the increase in vagal tone during the pelvic lift (Fig. 2). The control treatment of durational touch did not significantly influence vagal tone. A significant group effect (F = 8.4; df = 1,23; p < .01) indicated that the young subjects in Group I had a higher overall vagal tone than the older subjects in Group 2.

<img src=’https://novo.pedroprado.com.br/imgs/1988/1083-3.jpg’>

Heart rate as a dependent variable was not sensitive to the manipulations (Fig. 3). A significant group effect (F = 7.7; df= 1,23; p < .05) demonstrated that the young subjects in Group I had a lower heart rate than the older subjects in Group 2. The order of manipulation did not significantly influence the two dependent variables.

<img src=’https://novo.pedroprado.com.br/imgs/1988/1083-4.jpg’>


To our knowledge, this study represents the first attempt to quantify the effects of a soft tissue mobilization procedure on ANS function (i.e., cardiac vagal tone) under controlled conditions. The data clearly demonstrate that the Rolfing pelvic lift produces an increase in cardiac vagal tone in young, healthy male subjects. Neither durational touch nor the baseline conditions influenced the level of PNS tone. The increased vagal tone during the pelvic lift returned to the initial baseline level upon cessation of the maneuver, indicating that the elicited response did not persist after removal of the stimulus. This finding supports the initial hypothesis that a somatovisceral-PNS reflex would be elicited by the pelvic lift.(22)

The study results also demonstrate that vagal tone is a more sensitive ANS index for assessing pelvic lift than heart rate. This finding may be due to the specificity of the vagal tone assessment. Vagal tone was defined as the component of the heart rate variability that is associated with respiration’s phasic modulation of the vagal cardioinhibitory efferents (i.e., RSA amplitude).(28-32) Heart rate, in contrast, is a more global ANS index of heart rate variability that involves PNS and several other (eg, SNS, intrinsic, and mechanical) components.(32)

In the older age group, the pelvic lift did not elicit an ANS response. This finding is supported by studies on aging and ANS activity. Elderly subjects have shown more difficulty than younger subjects in responding to changes in ambient room temperature and in recovering resting pulse rate and respiratory volume after displacement by exercise.(23) Subjects over 60 years of age also have exhibited less predictability in the ANS reflexes that control heart rate, pupil size, and gastrointestinal tract.(23) Other research has demonstrated that the aging process is associated with less sudomotor activity (i.e., sweating), progressive increase in rigidity of the aorta and peripheral arteries, and reduced ANS conditionability.(38) The older subject group may have exhibited reduced sensitivity in receptor response to the tactile stimuli provided by the pelvic lift.(23, 38) Another possible explanation, supported by the significantly lower levels of vagal tone found in Group 2 than in Group 1, is that aging is associated with a general reduction in brain stem cardiac vagal outflow. which limits the somatovisceral-PNS response to the pelvic lift.(26,27,32)

What aspects of the pelvic lift account for its somatovisceral-PNS consequences? The pelvic lift has two distinct mechanical components: 1) moderate sustained pressure to the epigastrium and 2) firm posterior tilting and traction to the pelvis. Experimental studies on ANS reflexes have demonstrated that both deep pressure to the abdominal region and tactile stimulation to the back and sacral nerve roots produce PNS cardiovascular reflexes and alterations in respiratory patterns.(14,18-20) Both mechanical components of the pelvic lift, therefore, probably contribute to the somatovisceral-PNS response. Additional experimental investigation is needed to evaluate the relative importance of the two mechanical elements and whether they act synergically to elicit the observed somatovisceral-PNS reflex.

Although we conducted this study on healthy adults, the results have possible clinical implications. Our finding that the older subjects did not exhibit a vagotonic reflex response to the pelvic lift implies that elderly clinical populations may not be as responsive to soft tissue mobilization as younger populations. The assessment of a patient’s PNS tone to a given soft tissue procedure may provide a useful criterion for determining the appropriateness of manual therapy.

Another clinical implication of this study pertains to the finding that in the younger subjects, pelvic lift produced a transient increase in PNS tone, suggesting a relaxed, nurturing physiological state. This finding contrasts with the heightened arousal and “fight-night” activity associated with increased SNS tone.(14, 18) Furthermore, ANS investigations by Gellhorn have demonstrated a general law of reciprocity: When one ANS division is excited, the other division is inhibited to maximize the response of the stimulated branch.(18) The increased PNS tone elicited by the pelvic lift in our study may be associated with a corresponding reduction in SNS tone.

From a therapeutic perspective, this combination of enhanced PNS activity and suppressed SNS tone may explain in part the successful clinical reports of pelvic mobilization as a treatment modality (1,6,7,14-17) Such an ANS response would indicate favorable conditions for the reduction of muscle spasm and peripheral vasoconstriction commonly correlated with myofascial pain syndromes (e.g., primary fibromyalgia).(39) Other musculoskeletal disorders in infants, children, and adults that involve autonomic stress (e.g., chronic SNS) may benefit from pelvic mobilization, including the treatment of restricted breathing patterns, hyperactive behaviors, and hyperextensive neck and back patterns.(40)

We must emphasize, however, that this study demonstrated only a transient, reflexive increase in vagal tone in young, healthy adults to a single pelvic mobilization technique. The long-term ANS effects of pelvic lift and other soft tissue mobilization techniques can be established on a scientific basis only through additional research. We currently are designing a study that will compare two matched groups of healthy adults. One subject group will receive a sequence of Rolfing sessions, and the other group will receive a series of control treatments. We will assess both ANS activity and joint range of motion.


With a group of young, healthy adult male subjects, a soft tissue mobilization procedure, Golfing pelvic lift, was found to significantly increase PNS tone (cardiac vagal tone) for the duration of the manipulation, followed by a return of vagal tone to baseline levels. A control manipulation, durational touch, produced no change in PNS tone. A second group of older, healthy male subjects did not demonstrate a significant vagotonic response to pelvic lift. Possible neurophysiological mechanisms of the pelvic lift effect were discussed in terms of a somatovisceral-PNS reflex.

The increase of PNS tone produced by the pelvic lift in the group of younger subjects and the probable concurrent reciprocal inhibition of SNS tone may explain why pelvic mobilization techniques have been used successfully in various clinical applications for musculoskeletal disorders associated with ANS dysfunction.


We thank Gregory A. Miller, PhD, Department of Psychology, University of Illinois at Urbana-Champaign, for his assistance in developing the experimental design and Georgia DeGangi, MS, ORT, Department of Psychology, University of Maryland at College Park, for her comments and suggestions in preparing this manuscript.


1. Cottingham JT: Healing Through Touch: A History and a Review of the Physiological Evidence. Boulder, CO, Rolf Institute, 1985, pp.93-180

2. Palmer DD: The Science, Art, and Philosophy of Chiropractic. Portland, OR, Portland Printing House, 1910

3. Still AT: Philosophy of Osteopathy. Kirksville, MO, A T Still Publisher, 1899

4. Rolf IP: Rolfing: The Integration of Human Structures. Santa Monica CA, Dennis-Landman Publications, 1977, pp 101-151

5. Cookson JC, Kent BE: Orthopedic manual therapy-An overview. Part 1: The extremities. Phys Ther 59:136-146,1979

6. Cibulka MT, Rose SJ, Delitto A, et al: Hamstring muscle strain treated by mobilizing the sacroiliac joint. Phys Ther 66:1220-1223,1986

7. Perry J. Jones MH, Thomas L: Functional evaluation of Rolfing in cerebral palsy. Dev Med Child Neurol 23:717-729,1981

8. Di Fabio RP: Clinical assessment of manipulation and- mobilization of the lumbar spine: A critical review of the literature. Phys Ther 66:51-54,1986

9. Haldeman S: The clinical basis for discussion of mechanisms of manipulative therapy. In Korr IM fed): The Neurobiologic Mechanisms in Manipulative Therapy. New York, NY, Plenum Publishing Corp, 1978, pp 53-75

10. Rolf IP: Structural integration: A contribution to the understanding of stress. Confinia Psychiatrica 16(2):69-79,1973

11. Upledger JE, Vredevoogd JD: Craniosacral Therapy. Chicago, IL, Eastland Press, 1983, pp 79-81

12. Cailliet R: Low Back Pain Syndrome, ed 3.Philadelphia, PA, F A Davis Co, 1981, pp 115-116

13. Blackburn SE, Portney LG: Electromyographic activity of back musculature during Williams’flexion exercises. Phys Ther 61:878-885,1981

14. Heiniger MC, Randolph SL: Neurophysiological Concepts in Human Behavior. The Tree of Learning. St. Louis, MO, C V Mosby Co, 1981, pp 3-208

15. Hollis M: Practical Exercise Therapy, ed 2. St. Louis, MO, C V Mosby Co, 1981, pp 36-50, 174-223

16. Trombly CA: Occupational Therapy for Physical Dysfunction, ed 2. Baltimore, MD, Williams & Wilkins, 1982, pp 73-229

17. Daniels L, Worthingham C: Therapeutic Exercise for Body Alignment and Function, ed 2. Philadelphia, PA, W B Saunders Co, 1977, pp 46-89

18. Gellhorn E: Principles of Autonomic-Somatic Integrations: Physiological Basis and Psychological and Clinical implications. Minneapolis, MN, University of Minnesota Press, 1967, pp 52-163

19. Folkow B: Cardiovascular reactions during abdominal surgery. Ann Surg 156:905-913, 1962

20. Johansson B: Circulatory response to stimulation of somatic afferents. Acta Physiol Scand 62(Suppl 198):1-91,1962

21. Pompeiano O. Swett JE: EEG and behavioral manifestations of sleep induced by cutaneous nerve stimulation in normal cats. Arch Ital Biol 100:311 -342,1962

22. Kuizumi K, Brooks C: The integration of autonomic system reactions: A discussion of autonomic reflexes, their control and their association with somatic reactions. Ergeb Physiol 67:1-68, 1972

23. Rockstein M, Sussman M: Biology of Aging. Belmont, CA, Wadsworth Publishing Co, 1979, pp 47-147

24. Katona PG, Jih F: Respiratory sinus arrhythmia: Non-invasive measure of parasympathetic cardiac control. J Appl Physiol 39:801-805, 1975

25. Eckberg DL: Human sinus arrhythmia as an index of vagal tone. J Appl Physiol: Respirat Environ Exercise Physiol 54:961-966,1983

26. McGrady JD, Vallbona C, Hoff HE: Neural origin of the respiratory heart-rate response. Am J Physiol 211:323-328,1966

27. Lopes OV, Palmer JF: Proposed respiratory gating mechanism for cardiac slowing. Nature 264:454-456,1976

28. Iriuchjima J. Kumada M: Activity of single vagal fibers efferent to the heart. Jpn J Physiol 14:479-487,1964

29. Jewett DL: Activity of single efferent fibers in the cervical vagus nerve of the dog, with special reference to possible cardio-inhibitory fibers. J Physiol (Lond) 175:321-357,1964

30. Katona PG, Poitras JW, Barnett GO, et al: Cardiac vagal efferent activity and heart period in the carotid sinus reflex. Am J Physiol 218:1030-1037,1970

31. Kunze DL: Reflex discharge patterns of cardiac vagal efferent fibers. J Physiol (Lond)222:115,1972

32. Porges SW: Respiratory sinus arrhythmia: Physiological basis, quantitative methods, and clinical implications. In Grossman P. et al (eds): Cardiorespiratory and Cardiosomatic Psychophysiology. New York, NY, Plenum Publishing Corp, 1986, pp 101-115

33. Porges SW: Method and Apparatus for Evaluating Rhythmic Oscillations in Apehodic Physiological Response Systems. Washington, DC, US Patent Office, 1985

34. Yongue BG, McCabe PM, Porges SW, et al: The effects of phammacological manipulations that influence vagal control of the heart on heart period, heart period variability, and respiration in rats. Psychophysiology 19:426-432, 1982

35. McCabe PM, Yongue BG, Porges SW, et al: Changes in heart period, heart period variability, and a spectral analysis estimate of respiratory sinus arrhythmia during aortic nerve stimulation in rabbits. Psychophysiology 21:149-158,1984

36. McCabe PM, Yongue BG, Ackles PK, et al: Changes in heart period, heart period variability, and a spectral analysis estimate of respiratory sinus arrhythmia in response to pharmacological manipulations of the baroreoeptor reflex in cats. Psychophysiology 22:195-203, 1985

37. Winer BJ: Statistical Principles in Experimental Design. New York, NY, McGraw-Hill Book Co, 1962, pp 140-374

38. Porges SW, Fox NA: Developmental psychophysiology. In Coles MGH, et al (eds): Psychophysiology. New York, NY, The Guilford Press, 1986, pp 611 -625

39. Coulehan JL: Primary fibromyalgia. Am Fam Physician 32:170-177,1985

40. Levine P: Stress. In Coles MGH, et al (eds): Psychophysiology. New York, NY, The GuiHord Press, 1986, pp 331-353

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