DE10157024A1 - Method for treatment of patients using pulsed electromagnetic or electric fields, whereby each patient is given an electronic data storage card in which parameters and treatment details are stored for use in the treatment course - Google Patents

Abstract

Method has the following steps: provision of individual storage cards that can be used with a read-write device in the stimulation instrument; determination of patient parameters; calculation of field strength and frequency pattern for the stimulation program; storage of treatment data in the card; fixing of treatment times or numbers and storage in the card; transfer of treatment data for checking by a competent person; and adjustment of the treatment data and storage in the card and or the treatment instrument.

Description

The invention relates to a working method for operating a device for optimized stimulation of a several subjects using pulsating electromagnetic and / or electrical fields, namely in the frame the so-called magnetic field therapy in the Quantron resonance System.

The application of pulsating electromagnetic fields (PEMF) takes exceptionally positive Stimulation results in many areas of medicine a. Quittan, M., O. Schuhfried, G.F. Wiesinger and V. Fialka- Moser: Clinical efficacy of magnetic field therapy - a literature review. Acta Medica Austriaca. 27th Volume, H. 3 (2000), 61-68; Zhadin, M.N .: Review of Russian Literature on Biological Action of DC and Low-Frequency AC Magnetic fields. Bioelectromagnetics 22: 27-45 (2001)]. There is an urgent need for a stronger one scientific penetration, also based on Findings of modern conventional medicine and the molecular research. So z. B. the groundbreaking Discovery of "Vascular Nitric Oxide (NO) - Systems "[et al. Schmidt, H.H. H.W .: NO, more endogenous Messenger and cell toxin. MED. MO. PHARM. 17, 6 (1994), 168-185] by the pharmacologist Furchgott in the late 80s not only the therapeutic concepts of conventional medicine radical change, including the interpretation of results and the Further development of the QRS® magnetic field stimulation [Warnke, U .: Device for influencing electrical and magnetic fields of low frequency. European Patent EP 0 621 795 B1; Warnke, U .; Fischer, G. and H. L. König: device for transporting ions, especially protons. European patent EP 0 594 655 B1; Fischer, G. and U. Warnke: Establishment for the investigation the effect of pulsed magnetic fields on an organism. European Patent EP 0 729 318 B1; Fischer, G .: Basics of quantum therapy. Hecataeus-Verlagsanstalt 1996] is decisively influenced by this. With the through Kruglikov and Dertinger discovered "stochastic Resonance "[Kruglikov, I.L. and H. Dertinger: Stochastic Resonance as a Possible Mechanism of Amplification of Weak Electrical signals in living cells. bioelectromagnetics 15: 539-547 (1994)], especially the so-called "noise induced stability ", it can be Cell manages to amplify extremely noisy signals and generally noise as an energy source for Use information-driven processes. This scientific knowledge is full for all stimulation methods Consequences.

In addition to stimulation using pulsating magnetic fields [U. a. EP 0 621 795 B1 and EP 0 594 655 B1 as well 1st International Symposium "Quantum Medicine in Research and practice ":" QRS® magnetic field therapy: present and Future ". Darmstadt / Weiterstadt April 2, 2001] for many years stimulations with special electric fields known [u. a. König, H. L .: invisible Environment. Man in the field of electromagnetic Forces. Self-published by Herbert L. König, Munich 1986 (ISBN 3-923819-04-8); Hartmann, E .: Novel Therapy options in the tilting vibration field. Experience medicine VI, H. 12, 1958]. It had been recognized that the electric field in the Outdoors, above the ground, in terms of time and location fluctuates greatly and during rainfall and bad weather whose values deviate significantly from the fair weather values. There is a "weather sensitivity" in many people, so that obviously by a "good weather stimulation Program "appears to be possible to influence.

Pure low frequency signals occur Field fluctuations. These appearances have none wave-like character, they spread accordingly King does not look like an electromagnetic wave and therefore must be considered as local field fluctuations be considered. So are special because of the frequencies the ULF and the (lower) ELF range for such Apparitions predestined. You can go to King for example related to a near one Observation thunderstorms are due to lightning discharges also have spectral components up to 1 Hz. Are much more common however, such localized operations are related with electrically charged clouds, whose Turbulence apparently outwardly in the form of low frequency electrical field fluctuations appear occurs. During the "fair weather frequencies" Have frequency ranges of approx. 8-13 Hz and according to König with "Signal type I" are referred to, signal type II connected to the frequency range of the delta rhythm of the EEG's and shows, locally limited, mostly strong Weather disturbances. It thus symbolizes compared to signal type I "the opposite pole, the disturbed, restless, anomalous, Unbalanced ". Weather sensitivity as" local increased irritability "manifests itself according to Varga [Varga, A .: Electrosmog. Varga 1995] in "Weather Pain", in all her gradations "to excruciating pain, namely with pathologically altered tissue, with scars of all kinds, broken bones, amputation stumps, inflamed bursa, chronically ill joints and inflammatory tissue at all. "There exist several works that indicate that between the Weather fronts and the frequency of e.g. B. Heart attacks there is a causal relationship with acute cardiac death.

Varga points out that for over 200 years much work on the interaction between meteorological processes and biological reactions is received.

Based on these findings, König reports [Invisible environment. The man in the field electromagnetic forces. Self-published Herbert L. König, Munich 1986 (ISBN 3-923819-04-8)] on stimulation results with artificial electric fields, if their temporal Gradients (frequency content) in the basic parameters if possible well with those of the natural electric field matches. In particular, results for biological effectiveness of 10 Hz electrical fields known u. a. z. T. highly significant changes from Response times, anti-inflammatory and antispasmodic effects in acute inflammation, significant improvements in Attention Resilience for Students Who Field conditions were exposed, as well as among employees in the open plan office, significant improvements of the subjective well-being. In a wide According to König, the investigation program was the influence of artificially produced electrical 10 Hz fields on the driving and Reaction behavior of test subjects in one Motor vehicle driving simulator tested. It was found that the number of Driving errors (e.g. disregarding the right of way, of Stop signs, pedestrian crossings, etc.) of the test subjects reduced by an average of 8 to 10% under the influence of the field could be. According to König, analog 10 Hz fields were used in a high school in Munich the performance of Students examined. The evaluation of all during the School year accruing grades shows a clear positive effect of the electric field. Accordingly improved the grades here on average by 1.2%, based on a linear scale from 1 to 6. Especially the School group of the "extraverted-unstable" carried to King with an improvement of 9.4% (absolute value 0.33) in particular.

On the other hand, according to König, it is known that stimulation with artificial electrical fields similar to signal type II (3-6 Hz) headache occurred after a few minutes can, as test subjects reported. After the Headaches often became tired.

• - Statisches Feld: In zeitlicher Hinsicht ist es ein Permanentfeld, das einer sehr langsamen Umbildung unterliegt.
• - Wechselfeld: Dem statischen Feld sind scheinbar regellose Komponenten überlagert, nämlich die magnetischen Störungen oder Stürme, des weiteren solche, mit mehr oder weniger ausgeprägten Periodizitäten. Die Intensität der Stürme steht in Korrelation mit der Aktivität der Sonne und dem Auftreten von Polarlichtern, die der periodischen Variationen mit dem Gang von Sonne und Mond. Aus Erdmagnetfeldmessungen geht hervor, daß Schwingungen mit einer Variationsbreite der Periodendauer von 30 Sekunden (~ 0,03 Hz, also untere Grenze der peripheren Mikrozirkulation) bis 0,025 Sekunden (~ 40 Hz, also obere Frequenz im EEG) auftreten. Dominant (Intensität von lediglich 10^-12 Tesla) sind Schwingungen des Magnetfeldes mit der Periodendauer von 4,5 Sekunden, d. h. 0,22 Hz. Eine solche Frequenzkomponente stimmt überein mit der optimalen Atmungsfrequenz des Menschen und kann mit der Aktivität des Parasympathikus in Zusammenhang gebracht werden. Ebenfalls treten Frequenzen von 8-13 Hz auf, die mit denen des EEG-α-Bereichs übereinstimmen. Sie korrelieren mit denen des elektrischen Feldes, so daß man von einer ausgeprägten Redundanz zwischen elektrischem und magnetischem Feld sprechen kann.

"Earth's magnetism" means the magnetic field occurring in the immediate area of the earth, the amount of which averages around 50 µTesla (= 0.5 Gauss) and hardly exceeds about 70 µTesla. According to König [invisible environment. Man in the field of electromagnetic forces. Self-published by Herbert L. König, Munich 1986 (ISBN 3-923819-04-8)] consisting of 2 components:

• - Static field: In terms of time, it is a permanent field that is subject to a very slow transformation.
• - Alternating field: Apparently irregular components are superimposed on the static field, namely the magnetic disturbances or storms, furthermore those with more or less pronounced periodicities. The intensity of the storms is correlated with the activity of the sun and the occurrence of polar lights, and the periodic variations with the course of the sun and moon. Earth's magnetic field measurements show that vibrations occur with a variation in the period from 30 seconds (~ 0.03 Hz, i.e. lower limit of the peripheral microcirculation) to 0.025 seconds (~ 40 Hz, i.e. upper frequency in the EEG). The dominant (intensity of only 10 ^-12 Tesla) are vibrations of the magnetic field with a period of 4.5 seconds, ie 0.22 Hz. Such a frequency component corresponds to the optimal breathing frequency of the person and can be associated with the activity of the parasympathetic nervous system become. Frequencies of 8-13 Hz also occur, which correspond to those of the EEG-α range. They correlate with those of the electric field, so that one can speak of a pronounced redundancy between the electric and magnetic fields.

• - elektrisches Feld über eine entsprechende Antenne,
• - magnetisches Feld über spezielle Applikatoren [EP 0 594 655 B1].

So if certain biological processes are caused by natural electric and magnetic fields, it must be possible to imitate nature as far as possible with special fields and to stimulate humans and animals if there is a deficit. Such stimulation is possible according to EP 0 621 795 B1 and EP 0 594 655 B1 by means of special "pulsating magnetic fields", on the other hand by radiation of characteristic electric fields via an antenna. Obviously, the accuracy of such a simulation of the natural electrical and magnetic fields is improved in terms of optimization if, according to the invention, these fields are emitted simultaneously (in parallel):

• - electric field via a corresponding antenna,
• - magnetic field via special applicators [EP 0 594 655 B1].

A crucial role in the best possible Stimulation of patients using special electrical or generally electromagnetic fields optimal communication between doctor and patient, so both by appropriate procedures as well Devices, too. In the present invention, these are intended Devices are called "modules" between the modules appropriate communication takes place.

• - offline: Ausgehend von einer ärztlichen Diagnose bzw. durch entsprechendes Feedback werden im Master-Modul die für den Patienten zum aktuellen Zeitpunkt optimalen Stimulationsdaten auf einer Chipkarte oder einen anderen Datenträger (z. B. Diskette) gespeichert. Damit ist eine automatische Aktivierung des Patienten-Moduls zum Zwecke der häuslichen Patienten-Stimulation möglich.
  Die notwendige Kontrolle des Stimulationsergebnisses erfolgt nach einem festgelegten Zeitpunkt durch den Arzt, so daß er eine Präzisierung der zukünftigen Stimulationsdaten für seinen Patienten auf der Chipkarte (bzw. Datenträger) vornehmen kann. Der Arzt beendet die gesamte Behandlung, wenn bei seinem Patienten entsprechende quantitative oder qualitative Parameter erreicht werden bzw. in einem festgelegten Unsicherheitsbereich liegen.
  Als weitere Variante ist vorgesehen, die Gültigkeitsdauer der durch den Arzt auf dem Datenträger codierten Stimulationsdaten zeitlich zu begrenzen und danach eine Löschung der Daten vorzunehmen. Dazu wird in beiden Modulen eine Uhr integriert.
  Das Quantron-Resonanz-System QRS® nach EP 0 621 795 B1 und EP 0 594 655 B1 ist ein offenes Stimulierungs-System mittels spezieller pulsierender Magnetfelder und ohne Rückkopplung von aktuellen Herz-Kreislauf-Parametern eines Patienten auf den QRS®-Eingang. Stimuliert wird nach Intensität des Magnetfeldes, wobei erkannt wurde, daß es u. a. bei niedrigen Intensitäts-Stufen eines solchen Feldes zu einer gefäßerweiternden Wirkung mit Reduzierung des Blutdruckes sowie der Herzfrequenz kommen kann, andererseits bei höheren Stufen sich dies umkehrt, der Sympathikotonus sich erhöht. Der Frequenzinhalt des Feldes wird nicht verändert, lediglich die Signal-Intensität. Erfindungsgemäß ist deshalb als weitere Variante das Biofeedback-Stimulations-System vorgesehen, d. h. den Master-Modul mit einem Sensor- Modul zu koppeln, wo auf der Grundlage der bekannten Remissions-Photoplethysmographie (NIRP-Prinzip genannt) [EP 0 913 120 A1] bzw. Transmissions-Photoplethysmographie (mit NIRT-Prinzip bezeichnet) nichtinvasiv von einem peripheren Meßort (Finger- oder Großzehenbeere) sowohl zentrale als auch periphere Kreislauf-Parameter (z. B. Puls-/Herzfrequenz, arterielle und mikrovaskuläre Durchblutung am Meßort, Blutgefäß-Tonus) kontinuierlich erfaßt und über eine Code-Tabelle daraus Stellbefehle für ein Stimulationssystem abgeleitet und eingestellt werden. Damit liegt eine Rückkopplung bzw. ein Biofeedback vor. In diesem Sinne ist auch die Stimulationsdauer nur bedingt frei wählbar, da sie im Falle von den (bekannten) Normalbereichen weglaufenden Kreislauf- Parametern automatisch beendet wird. In der Regel wird auf Grund praktischer Erfahrungen eine Stimulationsdauer von 8 bis 24 Minuten gewählt, Verkürzungen sowie Verlängerungen sind möglich. Die so bei dem Patienten erhaltenen Stimulationsdaten werden auf einem Datenträger gespeichert, so daß eine häusliche Patienten-Stimulation automatisch durchgeführt werden kann. Die dargestellte Vorrichtung mit Rückkopplung ist so gestaltet, daß zu jeder Zeit manuell durch den Arzt die Stimulation beendet werden kann.
• - online: Die Informationsübertragung erfolgt über das World Wide Web. Dazu erhalten beide Module eine Rechnerschnittstelle. Von einem mit dem Patienten-Modul gekoppelten Sensor-Modul werden beim Patienten in Echtzeit abgeleitete Herz-Kreislauf-Daten (z. B. Puls-/Herzfrequenz, arterielle und mikrovaskuläre Durchblutung am Meßort, Blutgefäß-Tonus) zum Master-Modul (Arzt-Modul) übertragen, dort bewertet und die entsprechenden Stimulationssignale zwecks individueller Behandlung zum Peripherie-Modul (Patienten-Modul) zurückgesendet. Die individuelle Stimulation wird beendet, wenn entsprechende Parameter erreicht werden bzw. in einem festgelegten Unsicherheitsbereich liegen. Der Master-Modul ist wiederum gekoppelt mit einem Rechner zum Zweck der Patientenverwaltung, Speicherung der Stimulationsdaten und Eintragung von Befunden.

According to the invention, the doctor module (master) is in mutual communication with the patient module (peripheral module). Communication takes place either in offline or online mode:

• - offline: Based on a medical diagnosis or by means of appropriate feedback, the optimal stimulation data for the patient at the current time are saved on a chip card or another data carrier (e.g. floppy disk) in the master module. This enables the patient module to be activated automatically for the purpose of domestic patient stimulation.
  The necessary control of the stimulation result is carried out by the doctor after a fixed point in time, so that he can make a precise specification of the future stimulation data for his patient on the chip card (or data carrier). The doctor ends the entire treatment if the patient achieves appropriate quantitative or qualitative parameters or is within a defined uncertainty range.
  As a further variant, provision is made to limit the validity period of the stimulation data encoded by the doctor on the data carrier and then to delete the data. For this purpose, a clock is integrated in both modules.
  The Quantron resonance system QRS® according to EP 0 621 795 B1 and EP 0 594 655 B1 is an open stimulation system using special pulsating magnetic fields and without feedback from a patient's current cardiovascular parameters to the QRS® input. The stimulation is based on the intensity of the magnetic field, it being recognized that, at low intensity levels of such a field, a vasodilating effect with a reduction in blood pressure and heart rate can occur, on the other hand this reverses at higher levels, the sympathetic tone increases. The frequency content of the field is not changed, only the signal intensity. According to the invention, the biofeedback stimulation system is therefore provided as a further variant, ie to couple the master module to a sensor module, where on the basis of the known remission photoplethysmography (called NIRP principle) [EP 0 913 120 A1] or Transmission photoplethysmography (designated by the NIRT principle) non-invasively from a peripheral measurement site (finger or big toe berries) both central and peripheral circulatory parameters (e.g. pulse / heart rate, arterial and microvascular blood flow at the measurement site, blood vessel tone) ) are continuously recorded and control commands for a stimulation system are derived and set from them via a code table. This results in feedback or biofeedback. In this sense, the duration of the stimulation can only be freely selected to a limited extent, since it is automatically ended in the event of circulatory parameters running away from the (known) normal ranges. As a rule, a stimulation duration of 8 to 24 minutes is selected based on practical experience, shortening and lengthening are possible. The stimulation data obtained in this way with the patient are stored on a data carrier, so that domestic patient stimulation can be carried out automatically. The device shown with feedback is designed so that the stimulation can be ended manually by the doctor at any time.
• - online: Information is transmitted via the World Wide Web. For this purpose, both modules are provided with a computer interface. Cardiovascular data derived from the patient in real time (e.g. pulse / heart rate, arterial and microvascular blood flow at the measurement site, blood vessel tone) are transferred from a sensor module coupled to the patient module to the master module (doctor's Module), evaluated there and the corresponding stimulation signals sent back to the peripheral module (patient module) for individual treatment. The individual stimulation is ended when corresponding parameters are reached or are within a defined uncertainty range. The master module is in turn coupled to a computer for the purpose of patient management, storage of the stimulation data and entry of findings.

The invention will be explained in more detail using exemplary embodiments and figures. Here, FIG. 1 shows an example of a patient chip card with the possibility of four special programs to save (Memo 1 to 4)

Fig. 2, the general communication between the master module and the patient module (peripheral module),

Fig. 3, the special communication between doctor and patient,

Fig. 4 shows an embodiment of a feedback QRS® biofeedback stimulation system, including data acquisition at the measurement locations finger and / or big toe Berry,

FIG. 5 shows a QRS® code table on which the example according to FIG. 4 is based, for pulse / heart frequencies derived at the measurement location finger finger under stimulation and

Fig. 6 is a representation of changes in peripheral and central cardiovascular parameters under a QRS®- stimulation derived from a fingertip of a cancer patient by means of non-invasive NIRP method.

• - Pulsfrequenz,
• - mikrovaskuläre Durchblutung am Meßort,
• - arterielle Durchblutung der entsprechenden Peripherie.

From the NIRP measurements (see FIG. 6), before, under and also after stimulation, it can be determined continuously and as mean values per minute:

• - pulse rate,
• - microvascular blood flow at the measurement site,
• - arterial blood flow to the corresponding periphery.

The associated normal ranges can be seen on the surface in FIG. 6. In order to immediately recognize optically from the derived parameters, from when a stimulation was started, a mark ("T" in FIG. 6) is automatically set in FIG. 6 as an example after the 7th minute of the measurements before the stimulation. It can be seen in the present case that both the microvascular and arterial blood flow represent non-normal values before the QRS stimulation, which deviate even further from the normal range under stimulation. On the basis of the internal code table, the signal intensity level 2 is determined at the start of the QRS stimulation with a set "vital program", which is reduced to "sensitive" (level Se) after a stimulation time of 1 minute, after the 3rd Minutes of stimulation to zero and the stimulation ended. The cause of such behavior is free oxygen radicals, not shown here, which occur more frequently in this cancer patient.

Fig. 1 shows an exemplary ISO-Standard chip card, which can be found in the inventive working method for operating the device for stimulating by means of magnetic field therapy application. This card contains one or more semiconductor memories which interact with a read / write device via conventional contact fields, so-called contactless chip cards also being able to be used, ie those which allow inductive or capacitive communication are used.

The master module according to FIG. 2 is used to create one or more special stimulation programs tailored to the respective test subjects or patients, which can be transferred using the chip card as a storage medium and then read out in the patient module. Since the invention provides for application times and / or the number of applications when the stimulation program (s) is executed to be stored in the memory card as log data and there is still the possibility of recording treatment results or successes, the corresponding data must be transferred back to and transferred to the master Module an assessment by the attending doctor possible, who is then in turn able to optimize the respective stimulation program patient-specific. This process can of course run with software support, so that the doctor is largely freed from manual programming and thus updating of the stimulation program data.

According to FIG. 3, a first or repeated treatment can be carried out in the presence of the attending doctor with the help of the master module, in order to create a basic program via a feedback measurement taking into account the cardiovascular parameters of the respective patient or subject, which can then be performed by the subject or Patients in home operation can be executed repeatedly using the patient module there.

In order to be able to objectively evaluate the result of the treatment or the stimulation by means of magnetic field therapy, according to FIG. 4 there is the possibility of recording cardiovascular parameters, the microvascular blood flow at the measurement location and the arterial blood flow to the corresponding periphery. After an evaluation of the signals preprocessed by the sensor module, these evaluation results are transferred to the master module, in order to be incorporated in the programming of the stimulation program data.

The device for optimized stimulation has a predetermined number of intensive levels (see QRS level according to FIG. 5) and the duration of treatment can be individually entered via an input unit. Various basic programs are part of the basic software of the patient module. A partner circuit enables the connection of several applicators, e.g. B. in a double bed, with at least two programs running in succession. All therapy parameters last set are saved in the device and can be called up and activated for quick repetition via a memo function key. The chip cards can also optionally be used as quasi cash cards for studios and fitness centers that provide the appropriate devices. Rental cards for corresponding rental devices are also conceivable, although all other functions remain unaffected.

Basic chip cards contain certain clinically tested ones and proven stimulation programs that target specific Target indications. These initial programs can then taking into account individual patient data be adjusted so that the programming effort in In individual cases further reduced. The stimulation device interacts with a coil mat that creates a magnetic field different strength depending on the setting. The Magnetic field strength can range from 0.3 µT to 30 µT lie. The magnetic field is preferred this way set it to be even across the length and width of the Coil mat is distributed. Are also used Coil pillow or combined pillow and mat.

In summary, the working method according to the invention to operate a device for optimized Stimulation of one or more subjects using pulsating electromagnetic and / or electrical Fields characterized in that at least one Memory card is provided, which is individually programmed can be and which with one in the Stimulation device arranged read / write unit interacts. On the output side, the optimum is first biological amplitude window of the respective subject preferably determined according to EP 0 729 318 B1. Farther the cardiovascular function of the respective subjects. This is followed by a calculation or Determine field strength and frequency patterns for the Stimulation program taking into account the aforementioned sample-typical data.

The stimulation program data is stored on the Memory card and / or in another, in the device existing data storage. In the application or execution of the stimulation program Application times and / or the number of applications preferred in a protected area of the memory card as Log data recorded. The protocol and Stimulation program data is used for review by a authorized and qualified person to do what preferably done by reading the memory card. Out the protocol and stimulation program data then exists the possibility of an updated stimulation program to create and this new or changed program on the memory card or in the to take over device-internal data storage, in order then when it is renewed Program execution an improved or therapeutic goal adapted treatment success achieve.

Claims (9)

1. Working method for operating a device for optimized stimulation of one or more test persons by means of pulsating electromagnetic and / or electrical fields with the following steps: Provision of an individually programmable memory card which interacts with a read / write unit arranged in the stimulation device, Determining the biological amplitude window of the respective subject or subjects, - determination of the cardiovascular functions of the respective subject, Calculating field strengths and frequency patterns for a stimulation program from the test-specific previously determined or determined functions or data, Storing the stimulation program data on the memory card and / or in a further data memory present in the device, Recording of application times and / or number of applications when executing the stimulation program, preferably in a protected area of the memory card as log data, - Acceptance of the protocol and stimulation program data for verification by an authorized and qualified person, - Creation of new updated stimulation program data and transmission of this to the memory card and / or in the device-internal data memory. 2. Working method according to claim 1, characterized in that a standard chip card is used as the memory card. 3. Working method according to claim 1 or 2, characterized in that environmental data such as during stimulation treatment Temperature, air pressure, air humidity, acoustic loads or the like is detected and these are stored. 4. Working method according to claim 3, characterized in that the exceeding of certain specified limits Environmental data is determined and saved. 5. Working method according to claim 3 or 4, characterized in that saving the environmental data or limit values mentioned on the memory card. 6. Working method according to one of the preceding Expectations, characterized in that the pulse rate during stimulation treatment, the microvascular blood flow at the measurement site and arterial Blood flow to the corresponding periphery of the test subject recorded and in the sense of a biofeedback to evaluate the Stimulation success and at least the Evaluation results can be saved. 7. Working method according to claim 6, characterized in that current biofeedback reviews Determines stimulation program data and this in the manner of a quasi self-learning system and saved for a new one or continued treatment can be used. 8. Working method according to one of the preceding Expectations, characterized in that an additional active during stimulation electromagnetic field of low frequency and lower Field strength generated to maintain a reproducible bioclimate becomes. 9. Working method according to claim 8, characterized in that the frequency of the additional electromagnetic field in the range of essentially 5 to 20 Hz, preferred 10 Hz.