U.S. patent application number 13/151194 was filed with the patent office on 2012-05-10 for stuttering treatment methods and apparatus.
This patent application is currently assigned to SONITUS MEDICAL, INC.. Invention is credited to Amir ABOLFATHI, John SPIRIDIGLIOZZI.
Application Number | 20120116779 13/151194 |
Document ID | / |
Family ID | 40955910 |
Filed Date | 2012-05-10 |
United States Patent
Application |
20120116779 |
Kind Code |
A1 |
SPIRIDIGLIOZZI; John ; et
al. |
May 10, 2012 |
STUTTERING TREATMENT METHODS AND APPARATUS
Abstract
Stuttering treatment methods and apparatus which utilize
removable oral-based appliances having actuators which are
attached, adhered, or otherwise embedded into or upon a dental or
oral appliance are described. Such oral appliances may receive the
user's voice and process the voice to introduce a time delay and/or
a frequency shift. The altered audio feedback signal is then
transmitted back to the user through a tooth, teeth, or other bone
via a vibrating actuator element. The actuator element may utilize
electromagnetic or piezoelectric actuator mechanisms and may be
positioned directly along the dentition or along an oral appliance
housing in various configurations.
Inventors: |
SPIRIDIGLIOZZI; John; (San
Mateo, CA) ; ABOLFATHI; Amir; (Woodside, CA) |
Assignee: |
SONITUS MEDICAL, INC.
San Mateo
CA
|
Family ID: |
40955910 |
Appl. No.: |
13/151194 |
Filed: |
June 1, 2011 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
12032608 |
Feb 15, 2008 |
7974845 |
|
|
13151194 |
|
|
|
|
Current U.S.
Class: |
704/271 ;
704/E11.001 |
Current CPC
Class: |
A61F 5/58 20130101; B33Y
70/00 20141201; G10L 21/00 20130101; G10L 2021/0575 20130101; B33Y
80/00 20141201 |
Class at
Publication: |
704/271 ;
704/E11.001 |
International
Class: |
G10L 11/00 20060101
G10L011/00 |
Claims
1. A method for treating stuttering in a patient, comprising:
receiving an audio signal of a voice of the patient; introducing a
time delay in the audio signal of the patient's voice to generate
an altered audio feedback signal; and vibrationally conducting the
altered audio feedback signal to the patient through an oral
appliance whereby stuttering by the patient is diminished.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 12/032,608 filed Feb. 15, 2008, the content of
which is incorporated herein by reference in its entirety.
FIELD OF THE INVENTION
[0002] The present invention relates to methods and apparatus for
treating stuttering via altered auditory feedback. More
particularly, the present invention relates to methods and
apparatus for treating stuttering by transmitting a user's voice
which has been altered via bone conduction through teeth or bone
structures in and/or around the mouth.
BACKGROUND OF THE INVENTION
[0003] The causes of stuttering are not fully understood but
researchers believe that it may be caused by interference between
the left and right hemispheres of the brain competing against one
another to send signals to the muscles used to produce speech.
These conflicting signals ultimately impair the muscles resulting
in stuttering, which is typically characterized by interruptions in
speech flow, repetitions, prolongations, and pauses in speech.
[0004] The treatments for stuttering are varied and include methods
such as psychological therapy, drug therapy, and altered auditory
feedback (AAF). Most AAF treatments can be divided into three
categories: delayed auditory feedback (DAF), frequency-shifted
auditory feedback (FAF), and masked auditory feedback (MAF).
Treatment using DAF typically utilizes a user's own voice which is
delayed between 50 to 200 ms and then relayed back to the user,
usually through headphones or an earpiece. This type of treatment
relies on the "choral effect", which occurs when people who stutter
speak or sing in unison with others, experience a dramatic
reduction or even elimination of stuttering.
[0005] Treatments using FAF are based on changing the frequency
characteristics of the user's voice by about a half octave such
that the relayed auditory feedback sounds somewhat distorted to the
speaker. This frequency shift is believed to effect the user's
brain in the same manner as DAF treatment. The MAF treatment
involves generating a synthetic sine signal corresponding to the
user's own phonetic frequency and relaying this masking feedback to
the user.
[0006] These treatments usually involve placing a device within the
ear canal of the user to completely or partially obstruct the
opening much like air-conduction hearing aids. However, such
devices are intended to be left in place even when the user is not
talking and will also obstruct ambient noises that the user may
wish to hear. Moreover, such in-ear devices (as well as other
external devices) are usually visible to others and may thus be a
deterrent for use by some users for aesthetic reasons. Other
devices utilizing such treatments are placed upon a post which is
permanently implanted into the skull of the user. However, such
devices require invasive surgery and present various complications
which may occur as a result.
[0007] Accordingly, there exists a need for methods and apparatus
for receiving and processing a user's voice and effectively
transmitting these processed signals back to the user with minimal
obstruction.
SUMMARY OF THE INVENTION
[0008] An electronic device may be attached, adhered, or otherwise
embedded into or upon a removable dental or oral appliance to form
an assembly which may conduct audio signals to a user via vibratory
conduction through bone. Such a removable oral appliance may be a
custom-made device fabricated from a thermal forming process
utilizing a replicate model of a dental structure obtained by
conventional dental impression methods. The electronic assembly may
receive incoming sounds either directly or through a receiver to
process and amplify the signals and transmit the processed sounds
via a vibrating actuator element coupled to a tooth or other bone
structure, such as the maxillary, mandibular, or palatine bone
structure.
[0009] In using an oral appliance assembly, the oral appliance may
utilize altered auditory feedback (AAF) for the treatment of
stuttering. Accordingly, in one example of treating stuttering via
delayed auditory feedback (DAF) and/or frequency-shifted auditory
feedback (FAF), the user's own voice may be received via a
microphone located upon the oral assembly or separately from the
oral appliance. The user's voice may then be processed such that
the voice data is delayed by about, e.g., 60 ms. The delay in the
auditory feedback may alternatively range anywhere from about 50 ms
to 200 ms.
[0010] In addition to delaying the auditory feedback, the auditory
feedback signal may also be shifted in frequency by about, e.g.,
+500 Hz. In other variations, the frequency may be shifted anywhere
from less than a half octave to a full octave or more, depending
upon the desired results. With the auditory feedback delayed and
shifted in frequency, the signal may be further adjusted or
equalized to account for the user's particular bone conduction
profile, which may be obtained utilizing standard bone conduction
measurements. Accounting for the user's bone conduction profile,
particularly through the skull, may facilitate optimization of the
altered auditory feedback signal by adjusting particular
frequencies or adjusting amplitude or gain such that the
vibrationally conducted altered feedback signal reaches the user's
middle and/or inner ear with minimal loss.
[0011] Once the altered feedback signal has been appropriately
adjusted for delay, frequency, bone conduction, etc., it may be
vibrationally transmitted via the removable oral appliance through
the user's tooth or teeth or other bone structure such as the
palatal or mandibular bone, etc. Thus, as the user speaks their
voice is sampled and adjusted, as described above, and then
retransmitted via the removable oral appliance to effect AAF
treatment and to reduce or eliminate stuttering.
[0012] The assembly for transmitting vibrations via at least one
tooth may generally comprise a housing having a shape which is
conformable to at least a portion of the at least one tooth, and an
actuator disposed within or upon the housing and in vibratory
communication with a surface of the at least one tooth. Moreover,
the actuator itself may be a separate assembly from the electronics
and may be positioned along another surface of the tooth, such as
the occlusal surface, or even attached to an implanted post or
screw embedded into the underlying bone.
[0013] The actuator utilized in the actuator assembly may be an
electromagnetic or piezoelectric actuator. Piezoelectric
transducers in particular may be used in various configurations due
in part to the various vibrational modes which may be utilized to
transmit the acoustic signals as vibrations through a tooth or
teeth. Any number of actuator may be utilized for particular
applications. For instance, low voltage multi-layer piezoelectric
actuator manufactured by Morgan Electro Ceramics Ltd. (Wrexham,
England) may be utilized for the applications described herein.
[0014] Aside from actuator and housing assemblies which are
positioned along or against one or more teeth, actuator assemblies
may be alternatively mounted along a retainer-like structure
configured for placement adjacent or along the palate of the user.
An arch may extend between coupling portions which are configured
to extend from the arch for placement against the lingual surfaces
of teeth on opposite sides of the user's dentition. Rather than
utilizing actuator assemblies directly upon the teeth, the actuator
may be removably or permanently integrated along the arch such that
elongational vibration of the actuator conducts the vibrations
along the arch for transmission through the coupling portions and
into the user's teeth. Alternatively, one or more actuators may be
positioned along the arch and actuated to directly conduct
vibrations through the user's palatal bone.
BRIEF DESCRIPTION OF THE DRAWINGS
[0015] FIG. 1 illustrates the dentition of a patient's teeth and
one variation of an oral appliance which is removably placed upon
or against the patient's tooth or teeth.
[0016] FIG. 2A illustrates a perspective view of the lower teeth
showing one exemplary location for placement of the removable oral
appliance.
[0017] FIG. 2B illustrates another variation of the removable oral
appliance in the form of an appliance which is placed over an
entire row of teeth in the manner of a mouthguard.
[0018] FIG. 2C illustrates another variation of the removable oral
appliance which is supported by an arch.
[0019] FIG. 2D illustrates another variation of an oral appliance
configured as a mouthguard.
[0020] FIG. 3 illustrates a detail perspective view of the oral
appliance positioned upon the patient's teeth utilizable in
combination with a transmitting assembly external to the mouth and
wearable by the patient in another variation of the device.
[0021] FIG. 4 shows an illustrative configuration of one variation
of the individual components of the oral appliance device having an
external transmitting assembly with a receiving and actuator
assembly within the mouth.
[0022] FIG. 5 shows an illustrative configuration of another
variation of the device in which the entire assembly is contained
by the oral appliance within the user's mouth.
[0023] FIG. 6 illustrates an example of how multiple oral appliance
assemblies or actuators may be placed on multiple teeth throughout
the patient's mouth.
[0024] FIG. 7 illustrates another variation of a removable oral
appliance supported by an arch and having a microphone unit
integrated within the arch.
[0025] FIG. 8A illustrates another variation of the removable oral
appliance supported by a connecting member which may be positioned
along the lingual or buccal surfaces of a patient's row of
teeth.
[0026] FIGS. 8B to 8E show examples of various cross-sections of
the connecting support member of the appliance of FIG. 8A.
[0027] FIG. 9 shows yet another variation illustrating at least one
microphone and optionally additional microphone units positioned
around the user's mouth and in wireless communication with the
electronics and/or actuator assembly.
[0028] FIG. 10 illustrates a flow chart of an optional treatment
for altering a user's voice to be retransmitted back to the user
through bone conduction via the removable oral appliance.
[0029] FIGS. 11A and 11B illustrate flow charts for alternative
treatments for altering the user's voice for retransmission back to
the user.
[0030] FIG. 12 illustrates a graph indicating a correlation between
an increase in the delay of the auditory feedback and the number of
stuttering events.
DETAILED DESCRIPTION OF THE INVENTION
[0031] In treating stuttering, methods and apparatus may utilize
altered auditory feedback (AAF) treatments. For instance, the most
commonly used treatments may include use of delayed auditory
feedback (DAF) and/or frequency-shifted auditory feedback (FAF). A
user's own voice may be modified by delaying the retransmission of
the voice back to the user and the voice may also be modified in
frequency prior to its retransmission. Rather than utilizing an
in-ear device, which obstructs the ear canal, or a device which is
coupled to a post implanted in the user, the user's voice may be
processed and transmitted via bone conduction through an
unobstructive and removable oral appliance.
[0032] The removable oral appliance may contain an electronic and
actuator device attached, adhered, or otherwise embedded into or
upon the oral appliance or other oral device to form an assembly
which may conduct audio signals to the user via vibratory
conduction through bone. Such an oral appliance may be a
custom-made device fabricated from a thermal forming process
utilizing a replicate model of a dental structure obtained by
conventional dental impression methods. The electronic and actuator
assembly may receive incoming sounds, such as the user's own voice,
either directly or through a receiver to process and amplify the
signals and transmit the processed sounds via a vibrating actuator
element coupled to a tooth or other bone structure, such as the
maxillary, mandibular, or palatine bone structure.
[0033] Detailed examples and descriptions of the oral appliance and
methods of use are more fully described in the following U.S.
patent application Ser. Nos. 11/672,239 filed Feb. 7, 2007;
11/741,648 filed Apr. 27, 2007; and 11/754,823 and 11/754,833 both
filed May 29, 2007. Each of these applications is incorporated
herein by reference in its entirety.
[0034] As shown in FIG. 1, a patient's mouth and dentition 10 is
illustrated showing one possible location for removably attaching
the oral appliance assembly 14 upon or against at least one tooth,
such as a molar 12. The patient's tongue TG and palate PL are also
illustrated for reference. An electronics and/or actuator assembly
16 may be attached, adhered, or otherwise embedded into or upon the
assembly 14, as described below in further detail.
[0035] FIG. 2A shows a perspective view of the patient's lower
dentition illustrating the assembly 14 comprising a removable oral
appliance 18 and the electronics and/or actuator assembly 16
positioned along a side surface of the assembly 14. In this
variation, oral appliance 18 may be fitted upon two molars 12
within tooth engaging channel 20 defined by oral appliance 18 for
stability upon the patient's teeth, although in other variations, a
single molar or tooth may be utilized. Alternatively, more than two
molars may be utilized for the oral appliance 18 to be attached
upon or over. Moreover, electronics and/or actuator assembly 16 is
shown positioned upon a side surface of oral appliance 18 such that
the assembly 16 is aligned along a buccal surface of the tooth 12;
however, other surfaces such as the lingual surface of the tooth 12
and other positions may also be utilized. The figures are
illustrative of variations and are not intended to be limiting;
accordingly, other configurations and shapes for oral appliance 18
are intended to be included herein.
[0036] FIG. 2B shows another variation of a removable oral
appliance in the form of an appliance 15 which is placed over an
entire row of teeth in the manner of a mouthguard. In this
variation, appliance 15 may be configured to cover an entire bottom
row of teeth or alternatively an entire upper row of teeth. In
additional variations, rather than covering the entire rows of
teeth, a majority of the row of teeth may be instead be covered by
appliance 15. Assembly 16 may be positioned along one or more
portions of the oral appliance 15.
[0037] FIG. 2C shows yet another variation of an oral appliance 17
having an arched configuration. In this appliance, one or more
tooth retaining portions 21, 23, which in this variation may be
placed along the upper row of teeth, may be supported by an arch 19
which may lie adjacent or along the palate of the user. As shown,
electronics and/or actuator assembly 16 may be positioned along one
or more portions of the tooth retaining portions 21, 23. Moreover,
although the variation shown illustrates an arch 19 which may cover
only a portion of the palate of the user, other variations may be
configured to have an arch which covers the entire palate of the
user.
[0038] FIG. 2D illustrates yet another variation of an oral
appliance in the form of a mouthguard or retainer 25 which may be
inserted and removed easily from the user's mouth. Such a
mouthguard or retainer 25 may be used in sports where conventional
mouthguards are worn; however, mouthguard or retainer 25 having
assembly 16 integrated therein may be utilized by persons,
stutterers, hearing impaired or otherwise, who may simply hold the
mouthguard or retainer 25 via grooves or channels 26 between their
teeth for receiving instructions remotely and communicating over a
distance.
[0039] Generally, the volume of electronics and/or actuator
assembly 16 may be minimized so as to be unobtrusive and
comfortable to the user when placed in the mouth. Although the size
may be varied, a volume of assembly 16 may be less than 800 cubic
millimeters. This volume is, of course, illustrative and not
limiting as size and volume of assembly 16 and may be varied
accordingly between different users.
[0040] Moreover, removable oral appliance 18 may be fabricated from
various polymeric or a combination of polymeric and metallic
materials using any number of methods, such as computer-aided
machining processes using computer numerical control (CNC) systems
or three-dimensional printing processes, e.g., stereolithography
apparatus (SLA), selective laser sintering (SLS), and/or other
similar processes utilizing three-dimensional geometry of the
patient's dentition, which may be obtained via any number of
techniques. Such techniques may include use of scanned dentition
using intra-oral scanners such as laser, white light, ultrasound,
mechanical three-dimensional touch scanners, magnetic resonance
imaging (MRI), computed tomography (CT), other optical methods,
etc. Examples for manufacturing the oral appliance are described in
further detail in U.S. patent application Ser. No. 11/841,477 filed
Aug. 20, 2007, which is incorporated herein by reference in its
entirety.
[0041] In forming the removable oral appliance 18, the appliance 18
may be optionally formed such that it is molded to fit over the
dentition and at least a portion of the adjacent gingival tissue to
inhibit the entry of food, fluids, and other debris into the oral
appliance 18 and between the actuator assembly and tooth surface.
Moreover, the greater surface area of the oral appliance 18 may
facilitate the placement and configuration of the assembly 16 onto
the appliance 18.
[0042] Additionally, the removable oral appliance 18 may be
optionally fabricated to have a shrinkage factor such that when
placed onto the dentition, oral appliance 18 may be configured to
securely grab onto the tooth or teeth as the appliance 18 may have
a resulting size slightly smaller than the scanned tooth or teeth
upon which the appliance 18 was formed. The fitting may result in a
secure interference fit between the appliance 18 and underlying
dentition.
[0043] In one variation, with assembly 14 positioned upon the
teeth, as shown in FIG. 3, anextra-buccal transmitter assembly 22
located outside the patient's mouth may be utilized to receive
auditory signals for processing and transmission via a wireless
signal 24 to the electronics and/or actuator assembly 16 positioned
within the patient's mouth, which may then process and transmit the
processed auditory signals via vibratory conduction to the
underlying tooth and consequently to the patient's inner ear.
[0044] The transmitter assembly 22, as described in further detail
below, may contain a microphone assembly as well as a transmitter
assembly and may be configured in any number of shapes and forms
worn by the user, such as a watch, necklace, lapel, phone,
belt-mounted device, etc.
[0045] FIG. 4 illustrates a schematic representation of one
variation of oral appliance assembly 14 utilizing an extra-buccal
transmitter assembly 22, which may generally comprise microphone or
microphone array 30 (referred to "microphone 30" for simplicity)
for receiving sounds and which is electrically connected to
processor 32 for processing the auditory signals. Processor 32 may
be connected electrically to transmitter 34 for transmitting the
processed signals to the electronics and/or actuator assembly 16
disposed upon or adjacent to the user's teeth. The microphone 30
and processor 32 may be configured to detect and process auditory
signals in any practicable range, but may be configured in one
variation to detect auditory signals ranging from, e.g., 50 Hertz
to 20,000 Hertz.
[0046] With respect to microphone 30, a variety of various
microphone systems may be utilized. For instance, microphone 30 may
be a digital, analog, and/or directional type microphone. Such
various types of microphones may be interchangeably configured to
be utilized with the assembly, if so desired. Moreover, various
configurations and methods for utilizing multiple microphones
within the user's mouth may also be utilized, as further described
below.
[0047] Power supply 36 may be connected to each of the components
in transmitter assembly 22 to provide power thereto. The
transmitter signals 24 may be in any wireless form utilizing, e.g.,
radio frequency, ultrasound, microwave, Blue Tooth.RTM. (BLUETOOTH
SIG, INC., Bellevue, Wash.), etc. for transmission to assembly 16.
Assembly 22 may also optionally include one or more input controls
28 that a user may manipulate to adjust various acoustic parameters
of the electronics and/or actuator assembly 16, such as acoustic
focusing, volume control, filtration, muting, frequency
optimization, sound adjustments, and tone adjustments, etc.
[0048] The signals transmitted 24 by transmitter 34 may be received
by electronics and/or actuator assembly 16 via receiver 38, which
may be connected to an internal processor for additional processing
of the received signals. The received signals may be communicated
to actuator 40, which may vibrate correspondingly against a surface
of the tooth to conduct the vibratory signals through the tooth and
bone and subsequently to the middle ear to facilitate hearing of
the user. Actuator 40 may be configured as any number of different
vibratory mechanisms. For instance, in one variation, actuator 40
may be an electromagnetically actuated actuator. In other
variations, actuator 40 may be in the form of a piezoelectric
crystal having a range of vibratory frequencies, e.g., between 250
to 15,000 Hz.
[0049] Power supply 42 may also be included with assembly 16 to
provide power to the receiver, actuator, and/or processor, if also
included. Although power supply 42 may be a simple battery,
replaceable or permanent, other variations may include a power
supply 42 which is charged by inductance via an external charger.
Additionally, power supply 42 may alternatively be charged via
direct coupling to an alternating current (AC) or direct current
(DC) source. Other variations may include a power supply 42 which
is charged via a mechanical mechanism, such as an internal pendulum
or slidable electrical inductance charger as known in the art,
which is actuated via, e.g., motions of the jaw and/or movement for
translating the mechanical motion into stored electrical energy for
charging power supply 42.
[0050] In another variation of assembly 16, rather than utilizing
an extra-buccal transmitter, hearing aid assembly 50 may be
configured as an independent assembly contained entirely within the
user's mouth, as shown in FIG. 5. Accordingly, assembly 50 may
include at least one internal microphone 52 in communication with
an on-board processor 54. Internal microphone 52 may comprise any
number of different types of microphones, as described below in
further detail. At least one processor 54 may be used to process
any received auditory signals for filtering and/or amplifying the
signals and transmitting them to actuator 56, which is in vibratory
contact against the tooth surface. Power supply 58, as described
above, may also be included within assembly 50 for providing power
to each of the components of assembly 50 as necessary.
[0051] In order to transmit the vibrations corresponding to the
received auditory signals efficiently and with minimal loss to the
tooth or teeth, secure mechanical contact between the actuator and
the tooth is ideally maintained to ensure efficient vibratory
communication. Accordingly, any number of mechanisms may be
utilized to maintain this vibratory communication.
[0052] For any of the variations described above, they may be
utilized as a single device or in combination with any other
variation herein, as practicable, to achieve the desired hearing
level in the user. Moreover, more than one oral appliance device
and electronics and/or actuator assemblies may be utilized at any
one time. For example, FIG. 6 illustrates one example where
multiple actuator assemblies 60, 62, 64, 66 may be placed on
multiple teeth. Although shown on the lower row of teeth, multiple
assemblies may alternatively be positioned and located along the
upper row of teeth or both rows as well. Moreover, each of the
assemblies may be configured to transmit vibrations within a
uniform frequency range. Alternatively in other variations,
different assemblies may be configured to vibrate within
overlapping or non-overlapping frequency ranges between each
assembly. As mentioned above, each actuator 60, 62, 64, 66 can be
programmed or preset for a different frequency response such that
each actuator may be optimized for a different frequency response
and/or transmission to deliver a relatively high-fidelity sound to
the user.
[0053] Moreover, each of the different actuators 60, 62, 64, 66 can
also be programmed to vibrate in a manner which indicates the
directionality of sound received by the microphone worn by the
user. For example, different actuators positioned at different
locations within the user's mouth can vibrate in a specified manner
by providing sound or vibrational queues to inform the user which
direction a sound was detected relative to an orientation of the
user, as described in further detail below. For instance, a first
actuator located, e.g., on a user's left tooth, can be programmed
to vibrate for sound detected originating from the user's left
side. Similarly, a second actuator located, e.g., on a user's right
tooth, can be programmed to vibrate for sound detected originating
from the user's right side. Other variations and queues may be
utilized as these examples are intended to be illustrative of
potential variations.
[0054] FIG. 7 illustrates another variation 70 which utilizes an
arch 19 connecting one or more tooth retaining portions 21, 23, as
described above. However, in this variation, the microphone unit 74
may be integrated within or upon the arch 19 separated from the
actuator assembly 72. One or more wires 76 routed through arch 19
may electrically connect the microphone unit 74 to the assembly 72.
Alternatively, rather than utilizing a wire 76, microphone unit 74
and assembly 72 may be wirelessly coupled to one another, as
described above.
[0055] FIG. 8A shows another variation 80 which utilizes a
connecting member 82 which may be positioned along the lingual or
buccal surfaces of a patient's row of teeth to connect one or more
tooth retaining portions 21, 23. Connecting member 82 may be
fabricated from any number of non-toxic materials, such stainless
steel, Platinum, etc. and affixed or secured 84, 86 to each
respective retaining portions 21, 23. Moreover, connecting member
82 may be shaped to be as non-obtrusive to the user as possible.
Accordingly, connecting member 82 may be configured to have a
relatively low-profile for placement directly against the lingual
or buccal teeth surfaces. The cross-sectional area of connecting
member 82 may be configured in any number of shapes so long as the
resulting geometry is non-obtrusive to the user. FIG. 8B
illustrates one variation of the cross-sectional area which may be
configured as a square or rectangle 90. FIG. 8C illustrates another
connecting member geometry configured as a semi-circle 92 where the
flat portion may be placed against the teeth surfaces. FIGS. 8D and
8E illustrate other alternative shapes such as an elliptical shape
94 and circular shape 96. These variations are intended to be
illustrative and not limiting as other shapes and geometries, as
practicable, are intended to be included within this
disclosure.
[0056] In yet another variation for separating the microphone from
the actuator assembly, FIG. 9 illustrates another variation where
at least one microphone 102 (or optionally any number of additional
microphones 104, 106) may be positioned within the mouth of the
user while physically separated from the electronics and/or
actuator assembly 100. In this manner, the one or optionally more
microphones 102, 104, 106 may be wirelessly or by wire coupled to
the electronics and/or actuator assembly 100 in a manner which
attenuates or eliminates feedback from the actuator, also described
in further detail below.
[0057] In utilizing multiple actuators and/or processing units,
several features may be incorporated with the oral appliance(s) to
effect any number of enhancements to the quality of the conducted
vibratory signals and/or to emulate various perceptual features to
the user to correlate auditory signals received by a user for
transmitting these signals via bone conduction through teeth or
bone structures in and/or around the mouth. Examples of various
processing methods and systems for simulating directionality as
well as for processing algorithms for filtering out undesirable
signals, among other features, are shown and described in further
detail in U.S. patent application Ser. No. 11/672,239 filed Feb. 7,
2007, which is incorporated herein by reference in its entirety.
The features shown and described may be utilized with any of the
variations described herein and in any number of combinations as
practicable.
[0058] In using any of the variations of the oral appliance
assembly described herein, the oral appliance may utilize AAF for
the treatment of stuttering, as illustrated in one example in the
flow chart of FIG. 10. Accordingly, in one example of treating
stuttering via DAF and FAF, the user's own voice may be received
via a microphone 100 located upon the oral assembly or separately
from the oral appliance. The user's voice may then be processed,
e.g., by processor 54, such that the voice data is delayed 112 by
about, e.g., 60 ms. The delay in the auditory feedback may
alternatively range anywhere from about 50 ms to 200 ms.
[0059] In addition to delaying the auditory feedback, the auditory
feedback signal may also be shifted in frequency 114 by about,
e.g., +500 Hz. In other variations, the frequency may be shifted
anywhere from less than a half octave to a full octave or more,
depending upon the desired results. With the auditory feedback
delayed and shifted in frequency, the signal may be further
adjusted or equalized to account for the user's particular bone
conduction profile 116, which may be obtained utilizing standard
bone conduction measurements. Accounting for the user's bone
conduction profile, particularly through the skull, may facilitate
optimization of the altered auditory feedback signal by adjusting
particular frequencies or adjusting amplitude or gain such that the
vibrationally conducted altered feedback signal reaches the user's
middle and/or inner ear with minimal loss.
[0060] Once the altered feedback signal has been appropriately
adjusted for delay, frequency, bone conduction, etc., it may be
vibrationally transmitted via the removable oral appliance 118
through the user's tooth or teeth or other bone structure such as
the palatal or mandibular bone, etc. Thus, as the user speaks their
voice is sampled and adjusted, as described above, and then
retransmitted via the removable oral appliance to effect AAF
treatment and to reduce or eliminate stuttering.
[0061] In other variations, rather than utilizing both DAF and FAF
in altering the auditory feedback signal, DAF treatment may be
utilized alone, as illustrated in the flowchart of FIG. 11A. In
this example, the user's voice signal 110 may be delayed 112, as
above by 60 ms or anywhere from 50 ms to 200 ms. The delayed
auditory feedback signal may then be further adjusted to account
for the user's bone conduction profile 116 and then the resulting
feedback signal may be transmitted via vibrational conduction 118
through the removal oral appliance. In yet another variation,
rather than utilizing DAF treatment, FAF treatment may be utilized
alone, as illustrated in the flowchart of FIG. 11B. In this case,
the user's voice signal 110 may be shifted in frequency 114 by,
e.g., +500 Hz, and then further adjusted for the user's bone
conduction profile 116 and then transmitted via vibration
conduction 118 through the removal oral appliance. In these and
other examples, adjustment of the user's auditory feedback signal
by their (or a standard) bone conduction profile 116 may be
performed prior to adjustment of the delay or frequency shift.
[0062] In determining the amount of delay to adjust the auditory
feedback signal, it may be delayed anywhere from about 50 ms to 200
ms, as mentioned above. As shown in chart 120 in FIG. 12, curve 122
illustrates the relationship between an increase in delayed
auditory feedback (in milliseconds) and a reduction in the number
of stuttering events from the speaker. Generally, as the amount of
delay in the auditory feedback is increased, the number of
stuttering events decreases exponentially, particularly delay times
of 25 ms or greater.
[0063] The applications of the devices and methods discussed above
are not limited to the treatment of hearing loss but may include
any number of further treatment applications. Moreover, such
devices and methods may be applied to other treatment sites within
the body. Modification of the above-described assemblies and
methods for carrying out the invention, combinations between
different variations as practicable, and variations of aspects of
the invention that are obvious to those of skill in the art are
intended to be within the scope of the claims.
* * * * *