Method and treatment with transcranially applied electrical signals

• US 4,646,744 A
• Filed: 06/29/1984
• Issued: 03/03/1987
• Est. Priority Date: 06/29/1984
• Status: Expired due to Fees

• Current Assignee: ZION Foundation
• Original Assignee: ZION Foundation
• Inventors: Capel, Ifor D.
• Primary Examiner(s): Kamm, William E.
• Application Number:
  US06/626,335
• Time in Patent Office: 977 Days
• Field of Search: 128/419 R, 128/421, 128/422, 128/423 R
• US Class Current: 607/58
• CPC Class Codes: A61N 1/328 for improving the appearance of the skin, e.g. facial toning or wrinkle treatment

Abstract

A method of applying an electrical signal transcranially includes the steps of generating a series of signal trains and applying the signal trains across the head of a subject, wherein each of the trains comprises a number of pulses and is separated from other trains by off periods, during which the signal is not applied. The signal trains are of such short duration that substantially no nerves within the subject'"'"'s brain that receive the signal trains are demyelinized. In certain embodiments, the signal trains and the off periods are of irregular duration such that the activation of nerves of the brain by a signal is of a substantially continuous rate as the application of the signal train proceeds. The invention also includes particular characteristics of signals used to treat respective afflictions, including drug addictions and habituations, appetite disturbances, stress, insomnia, and pain.

Claims

1. A method of treating a subject with an electrical signal transcranially comprising

a first step of generating a first signal train comprising a plurality of pulses and applying said train across a subject'"'"'s head,

a second step of terminating the applying of said first signal train,

a third step of applying no signal across said subject'"'"'s head for a duration of a first off period,

a fourth step of generating a successive signal train comprising a plurality of pulses and applying said trains across said subject'"'"'s head,

a fifth step of terminating the applying of said successive signal train,

a sixth step of varying the duration of the applying of said successive train in respect to a duration of the applying of a preceding train,

a seventh step of applying no signal across said subject'"'"'s head for a duration of a successive off period,

an eighth step of varying the duration of said successive off period in respect to a duration of a preceding off period, and

a ninth step of repeating said fourth, fifth, sixth, seventh, and eighth steps such that an activation of nerves of said brain by said signal, comprising a series of trains and off periods the durations of which are varied in accordance with said sixth and eighth steps, is at a substantially continuous rate as the application of said trains and off periods proceeds.

2. The method of claim 1, wherein said signal has a frequency of at least about 100 Hz.

3. The method of claim 2, further comprising the step of substituting said signal with a signal having a frequency of at most about 35 Hz. when said subject experiences an adverse reaction to said method.

4. The method of claim 1, wherein said signal has a frequency of at most about 35 Hz.

5. The method of claim 4, further comprising the step of substituting said signal with a signal having a frequency of at least about 100 Hz. when said subject experiences an adverse reaction to said method.

6. The method of claim 1, further comprising the step of inhibiting the production of neurotransmitter in the brain.

7. The method of claim 1, further comprising the step of stimulating the production of neurotransmitter in the brain.

8. The method claim 1, wherein said signal has a frequency of about 100 Hz. and said method is used in the treatment of an addiction to drugs that are received by opiate receptors.

9. The method of claim 1, wherein said signal has a pulse width of about 0.22 milliseconds and said method is used in the treatment of an addiction to drugs that are received by opiate receptors.

10. The method of claim 1, wherein said signal has a frequency of about 10 Hz. and said method is used in the treatment of an addiction to drugs that are received by opiate receptors.

11. The method of claim 1, wherein said signal has a pulse width of about 1.5 milliseconds and said method is used in the treatment of an addiction to drugs that are received by opiate receptors.

12. The method of claim 1, wherein said signal has a frequency of about 25 to 35 Hz. and said method is used in the treatment of an habituation to barbiturates or barbiturate-like sedatives.

13. The method of claim 2, wherein said signal has a pulse width of about 0.1 milliseconds and said method is used in the treatment of an habituation to barbiturates or barbiturate-like sedatives.

14. The method of claim 1, wherein said signal has a frequency of about 10 Hz. and a pulse width of about 1.5 milliseconds and is used to encourage sleep in a treatment for an habituation to barbiturates or barbiturate-like sedatives.

15. The method of claim 1, wherein said signal has a frequency of about 200 Hz. and said method is used in the treatment of an addiction to benzodiazeapines.

16. The method of claim 1, wherein said signal has a pulse width of about 0.5 milliseconds and said method is used in the treatment of an addiction to benzodiazeapines.

17. The method of claim 1, wherein said signal has a frequency of about 30 Hz. and said method is used in the treatment of an addiction to cocaine.

18. The method of claim 1, wherein said signal has a pulse width of about 0.1 milliseconds and said method is used in the treatment of an addiction to cocaine.

19. The method of claim 1, wherein said signal has a frequency of about 200 Hz. and said method is used in the treatment of an addiction to amphetamines.

20. The method of claim 1, wherein said signal has a pulse width of about 0.5 milliseconds and said method is used in the treatment of an addiction to amphetamines.

21. The method of claim 1, wherein said signal has a frequency of about 200 Hz. and a pulse width of about 1.5 milliseconds and is used to encourage sleep in a treatment for an addiction to amphetamines.

22. The method of claim 1, wherein said signal has a frequency of about 5 to about 10 Hz. and said method is used in the treatment of an habituation to nicotine.

23. The method of claim 1, wherein said signal has a pulse width of about 0.1 or 0.22 milliseconds and said method is used in the treatment of an habituation to nicotine.

24. The method of claim 1, wherein said signal has a frequency of about 10 Hz. and said method is used in the treatment of an addiction to alcohol.

25. The method of claim 1, wherein said signal has a pulse width of about 0.1 milliseconds and said method is used in the treatment of an addiction to alcohol.

26. The method of claim 1, wherein said signal has a frequency of about 30 Hz. and a pulse width of about 1.5 milliseconds and is used to encourage sleep in a treatment for an addiction to alcohol.

27. The method of claim 1, wherein said signal has a frequency of about 200 Hz. and said method is used in the treatment of an habituation to hallucinogenic drugs.

28. The method of claim 1, wherein said signal has a pulse width of about 0.5 milliseconds and said method is used in the treatment of an habituation to hallucinogenic drugs.

29. The method of claim 1, wherein said signal has a frequency of about 200 Hz. and said method is used in the treatment of pain.

30. The method of claim 1, wherein said signal has a pulse width of about 1.5 milliseconds and said method is used in the treatment of pain.

31. The method of claim 1, wherein said signal has a frequency of about 10 Hz. and said method is used in the treatment of pain.

32. The method of claim 1, wherein said signal has a pulse width of about 0.22 milliseconds and said method is used in the treatment of pain.

33. The method of claim 1, further comprising the step of standardizing said subject prior to said applying step, said standardization step comprising the steps of clinically administering a dosage of a drug to which said subject is addicted or habituated, or a drug that is functionally equivalent to said drug to which said subject is addicted or habituated, to said subject and applying said signal after effects of said drug or said functionally equivalent drug have subsided and before said subject experiences withdrawal symptoms.

34. The method of claim 1, wherein said signal has a rectangular wave form.

35. The method of claim 1, further comprising the step of generating said signal in a rectangular wave form comprising a spike that occurs at the onset of positive segments of the pulses of said signal.

36. The method of claim 1, wherein the voltage of said applied signal is about 1 volt.

37. The method of claim 1, further comprising the step of monitoring characteristics of said signal on an oscilloscope.

38. The method of claim 1, further comprising the step of determining the duration of said trains and said off periods by an arithmetic progression.

39. The method of claim 1, wherein the pulses applied across said subject'"'"'s head have an equal amount of positive and negative segments such that there is a zero net voltage applied across said subject'"'"'s head.

40. The method of claim 1, wherein the duration of off periods between pulse trains in between 5 and 10 seconds.