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Inner Reach History
Gathering Solutions HIGS for Researchers
Our Health Information Gathering System – HiGS
HiGS for Researchers enables research institutions such as universities
and government institutions to license any agreed to combination of relevant HiGS
Histories, Assessments, and Body Systems in conjunction with their area of research.
Inner Reach HiGS is a tracking, monitoring, and following-up preventive care technology
which electronically collects, assesses, screens, teaches, tracks, stores, and retrieves
an individual’s health histories.
HiGS is a qualitative system
The Inner Reach HiGS is a qualitative system in which a user collects his or her
own health history information after answering various questions based upon our
protocols. HiGS protocols are health-psychology instruments centered on health
and preventive concerns, using a biological-physical-psychological-sociological-medical
model, including nutritional, cultural, environmental, and occupational, components.
How the Inner Reach HiGS Data Collection Works
All HiGS protocols are based upon standard Western medicine and nursing criteria
and DSM-IV psychiatric criteria. Additionally HiGS protocols can include integrative
health methods, such as Traditional Chinese Medicine (TCM), joint medicine,
Chinese Medicinal herbs (CMH), Oriental Medicine (OM) methods, and Ayurveda.
Inner Reach pioneered the way for individuals to electronically collect, manage,
update, and retrieve their own health histories which they alone control and can
print, fax, or electronically send to anyone they wish, including family, physicians,
and other healthcare professionals.
The only time a user’s personal ID information comes together with his or
her health history information is when users themselves enter their email address
and password to make that happen. Personal information and health history
information are stored in two separate HiGS data bases. In other words, only
the user ever has access to their own data with their personal identification displayed,
with the exception of when a user gives or sends their data either in printed form
or via fax or electronic email.
How HiGS Data Collection for Researchers Works
HiGS for Researchers
is an arrangement made by Inner Reach and a research institution enabling a researcher
to use specific subjects’ information collected by the HiGS
system as part of an overall research project. This system is different from
HiGS since with HiGS, only the user can enter and access their own Health History;
the user controls it completely.
As part of the overall research programs, individuals participating in a research
program will take specified histories and protocols authorized as part of the research
project. Depending upon the selections made by the research institution’s
study program, the user electronically enters answers to various HiGS Histories,
Assessments and Screenings, and Body Systems (signs and symptoms recorded for each
24 hour period).
When the individual logs onto the HiGS, in addition to entering their normal
identification information, they would enter a pre-assigned “Research Program
Identification number”. Once the individual completes the taking of
the agreed upon histories and protocols, a copy of the information will be placed
into a special “Research Program” data base under the individuals “Research
Program Identification number”.
This Research Program data base will contain copies of information from all of the
research participants under their unique Research Program Identification number.
With the Research Program data base, the researchers will have access to the research
program participants’ data without having any access to the participants private
data on the general HiGS system.
HiGS for Researchers
enables the researcher to see the study participants’ results. The resultant
data can be exported into several different formats for analysis. Study participants
must authorize the use of their information in the research project.
Privacy Matters
It is important for the public to note that any studies, performed at universities
and other research institutions, engage study participants who are aware they are
being studied and are required, as participants of the study, to authorize the institutions
use of their personal information for the purposes spelled out in each study.
Inner Reach was conceptualized and is structured to insure that individuals, and
only individuals, create and control their own personal information with HiGS.
As with any reputable institution conducting a study, authorization by HiGS users
for this type of purpose is vital.
Inner Reach Provides Grants for Certain Research Projects
Inner Reach is interested in all types of research and particularly studies which
include Traditional Chinese Medicine (TCM), and Chinese Medicinal Herbs (CMH) studies;
Breast Cancer in both genders (although rare in men); Prostate
Cancer in Men; Colon Cancer, Dementias and Elderly Issues, Metabolic Syndrome (MetS),
and all the Overweight and Obesity related diseases (see Inner Reach HiGS Dozen Dangerous Diseases White Paper
which spells out these diseases in detail).
Inner Reach® Corporation provides HiGS grants: Inner Reach is aware that obtaining
and keeping grants can pose difficulties for certain institutions and with that
understanding makes arrangements to assist research institutions in certain special
situations by providing HiGS for a particular study, waving usual fees.
For human studies of all kinds, health history data can be collected and daily signs
and symptoms can be tracked by using HiGS
for Researchers. HiGS
for Researchers can save researchers time while adding to data
collection quality and volume on a study participant.
Inner Reach Independent of Outside Influences
The Inner Reach
system is independent of any specific healthcare provider such as; private physicians,
PPOs, HMOs, insurance plans, Hospitals, Clinics etc., and not part of usual medical
mechanisms. It is strictly for and about health histories and preventive care
for individuals. The Inner
Reach HiGS is designed
for asymptomatic (not showing indications of a disease or medical condition) populations
to enable populations to learn more about themselves through history information
gathering to have and keep health and delay disease. HiGS
is not about disease but rather health and risk. If people are concerned
about having an illness or disease and or need diagnosing and treatment, their medical
care provider is the contact for their healthcare.
Related White Paper in PDF
White
Paper PDF: Inner Reach History Gathering
Solutions:
HiGS for Researchers
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