FIELD OF THE INVENTION The present invention is directed to a system and method for evaluation of the performance and progress of research trials and more specifically to such a system and method, which provide benchmark metrics in real time.
DESCRIPTION OF RELATED ART In clinical trials for pharmaceuticals and the like, data must be taken over an extended period. For example, at intervals of time, typically 30 days, data must be taken on the number of patients who are participating in the trial, the number who have dropped out, the queries per patient, and the like.
However, the data are typically collected and tabulated by pharmaceutical companies to manage their project timelines. Such information is rarely shared with the physicians and health-care professionals conducting the research studies for purposes of understanding how they are performing, how other research sites are doing and/or learning from other clinicians participating in the study about how to improve their study management and performance. Currently no electronic mechanism exists that systematically, and automatically provides clinicians the ability to interact with the physicians and health-care professionals conducting the research studies for purposes of understanding how they are performing, how other research sites are doing and or learning from other clinicians participating in the study about how to improve their study management and performance. Currently no electronic mechanism exists that systematically and automatically provides clinicians and/or pharmaceutical sponsors with the ability to obtain interactive, real-time benchmarks and with those benchmarks better assess physician capabilities for matching physicians and research sites and with those data better assess physician capabilities for matching physicians and research sites for future clinical trials.
One Internet-based technique for matching experts in the biological sciences with those needing their services is disclosed in WO 01/29708, published Apr. 26, 2001. That technique provides for matching based on qualifications and times of availability as well as payment. However, once the experts and their customers are matched, there is no evaluation of the work, which the former do for the latter.
SUMMARY AND OBJECTS OF THE INVENTION It will be readily apparent from the above that a need exists in the art for an online, interactive evaluation of research performance. It is therefore a primary object of the invention to collect data concerning the progress of research and to provide an evaluation based on the collected data.
It is another object of the invention to provide an interactive, automated, online technique for doing so.
It is a further object of the invention to provide such an evaluation based on data collected at various time intervals.
It is a still further object of the invention to allow comparative evaluations among various trials.
It is a still further object of the invention to allow comparative evaluations without divulging the identity of one trial to researchers participating in another.
To achieve the above and other objects, the present invention is directed to an online, automated technique for collecting data not only for clinical trials but for other types of medical research including: marketing research, outcomes studies, disease management, etc. This type of medical research information would be information used to support the post approval product launches, marketing, product positioning, business development opportunities including licensing from clinical trials at intervals of, e.g., 30 days and for performing automated, online evaluations based on the data. The evaluations can be presented in textual or graphical formats. A common server can be used to collect data from multiple trials, with the appropriate protection of the data from each trial for privacy purposes. The comparisons, e.g., for cost per patient, can be presented anonymously; for example, the figures for the highest and lowest costs per patient can be given without identifying the sources for those figures.
Users register for the service as organizations. The system will then ask the user to register all sites and physicians that fall under the umbrella of the organization. If a physician is a solo practitioner, the physician still must complete all three profiles, although some information may be duplicated, since each profile focuses on collecting differing information. During the registration process, each user provides information to be entered into a database. For a physician, the information concerns the physician's own practice and the site, if any, at which the physician is an administrator. For a site, the information concerns such things as the facilities at the site and the physicians practicing at the site. For an organization, the information concerns such things as the type of organization and the sites and physicians within the organization.
A listing of a clinical trial opportunity (blinded synopsis) or other research opportunity (blinded synopsis) with an accompanying protocol synopsis specific questionnaire (SQQ) is posted on the website. The listing is categorized to allow browsing by prospective researchers who are members. In addition, the service can search the database to find suitable physicians, sites or organizations who preliminarily match the criteria the sponsor has provided to the service and then select which ones are to be contacted about the clinical trial opportunity. That occurs by cross-referencing project requirements with general information about the sites, physicians and organizations. Contacting members about opportunities occurs via e-mail or facsimile to invite them to consider the opportunity. Following the researchers' completion of any new data not currently in the database and contained in the SQQ, the research electronically submits the completed SQQ via email tothe service. The service summarizes all the information across all completed SQQ's for the specific research opportunity and forwards qualified and matched researchers to the sponsor. The sponsor then selects which research provided by the service they will select for the clinical trial.
Once a researcher is selected for the study, information about the study is entered into the database, e.g., at the beginning and end of the study and at 30-day intervals or less therebetween. The information concerns such things as the number of patients who have signed up and the number who have dropped out. Thus, benchmarks can be computed over time.
Study (clinical trial/protocol) specific benchmarks from one researcher, site and or organization can be anonymously compared with those from other researchers, sites and/or organizations. In one example of a comparison, four values of a benchmark are given: the highest and lowest values from the researcher, site and organization participating in the study, the median from all researchers, sites and/or organizations, and the actual value from the researcher, site and/or organization with which the person viewing the results is linked in which the person viewing the results is participating. The identities of the other researchers, sites and/or organizations from which the information is provided are not given, thus preserving confidentiality. The user can thus see how their researcher, site and or organization performance results for the study compares with other researcher, site and/or organization performance results for the study and can use that information, e.g., to see where efficiency can be improved, budgets should be reallocated, patients that qualify for the study can be found, training is required or to make the case for an increase in the research budget.
BRIEF DESCRIPTION OF THE DRAWINGS A preferred embodiment of the present invention will be set forth in detail with reference to the drawings, in which:
FIG. 1 shows a hardware architecture on which the preferred embodiment can be implemented;
FIGS. 2, 2A-2I, 3, 3A-3D, 4 and 4A-4C show flow charts and screen shots of the registration and data inputting process for new users;
FIGS. 5A and 5B show a physician registration page;
FIG. 6 shows a search page;
FIG. 7 shows a search result page;
FIG. 8 shows a flow chart of the processes involved in posting a CTO or ORO description;
FIGS. 8A-8E show screen shots of the processes of FIG. 8;
FIG. 9 shows a merge page;
FIGS. 10 and 11 show pages used in collecting progress data;
FIGS. 12 and 13 show pages used in displaying benchmark data; and
FIG. 14 shows a flow chart of operation of an enhancement to the service which allows physicians to obtain information on fees.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT A preferred embodiment of the present invention will now be set forth in detail with reference to the drawings, in which like reference numerals refer to like elements or process steps throughout.
FIG. 1 shows an example of a hardware architecture on which the preferred embodiment can be implemented. The design of the hardware architecture has been selected to follow the industry-standard N-tier architecture, separating site navigation and design from stored procedures and data. In that way, one part of the site can be redesigned without breaking another part of the site. For instance, the HTML which provides the user interface can be changed without affecting the stored procedures and tables of the database.
FIG. 1 shows such a hardware architecture 100. Client devices 102, which can be microcomputers or any other devices capable of communicating over the Internet, connect via any suitable connections 104, such as dial-up or cable modem connections, to the Internet 106, and thence via a full-time Internet connection 108 to a Web server 110. The client devices are used by physicians, research sponsors, research sites such as hospitals, and others participating in the operations of the preferred embodiment. The Web server 110 provides business services, such as site navigation and design, and is connected via a full-time dedicated connection 112 to a database server 114 storing the stored procedures and database tables. Thus, the client devices 102 access the stored procedures and database tables in the database server 114 only through the Web server 110. It is preferable to implement the Web server 110 and the database server 114 on separate, dedicated machines to facilitate backups and restarts with a minimum of disruption. The Web server 110 implements interactive HTML pages through known technologies, such as CGI or ASP.
The database stored in the database server 114 is populated when physicians and organizations register and provide the information required for registration. As is known in the art, the Web server 110 provides persons accessing it from client devices 102 with several options, including physician registration and organization registration.
A user registers as an organization; physician registration and site registration are part of organizational registration. As noted above, a solo practitioner still registers as an organization. The organizational registration has two parts, the first part resulting in temporary status and the second part resulting in active status.
FIG. 2 shows an overview of organization registration. At step 202, the user is prompted for the name and address of the organization and for the type of organization (see the Web page of FIG. 2A). The latter is preferably selected through check boxes, so that multiple choices may be selected, although it may be selected through a drop-down menu or radio buttons if only one choice is allowed. At step 204, once that information is received, a temporary user identification and password are generated and provided to the user (or the user can select them; see FIG. 2B). The user is then allowed to view more detailed descriptions of the research opportunities; however, if any particular opportunity is selected, the user must proceed to the second part of the registration.
That second part begins at step 206, in which the user is prompted to complete an organizational profile (see FIG. 2C). When the User is completing the site location section of the organization profile, the first page of the organization profile asks “how many site locations” at step 208, and this automatically generates, at step 210, a table (see FIG. 2D) on page two of the organization profile with the necessary number of rows for all site locations. The User must complete this table in order to advance to page three of the organization profile; that will generate the correct number of site profiles. At step 212, the user completes a physician profile (see FIG. 2E) for each physician within the organization, until it is determined at step 214 (see FIG. 2F) that profiles have been completed for all physicians within the organization; step 214 can be performed like step 210. Identifications and passwords are generated for the organization as a whole, for each site, and for each physician at steps 216, 218 and 220, respectively (see FIG. 2G). At step 222, it is indicated in the database that the organization's status is that of an active member (see FIG. 2H). At step 224, the identifications and passwords are sent to the organization. At step 226, a responsible person at the organization has the option to change the identification and password for the organization (see FIG. 2I). The organization representative has the ability to change any data about the organization, sites or physicians and has complete access to all three profiles. The representative cannot add further sites or physicians or edit the name of a physician.
FIG. 3 shows an overview of the physician registration process of step 212. At step 302 (see FIG. 3A), the Web server asks whether the physician is an administrator at the site at which the physician works. If it is determined at step 304 that the physician has answered in the affirmative, the physician is prompted at step 306 (see FIG. 3B) for information about the site, in a manner which will be described in detail below. If not, the physician is prompted at step 308 for the name of an administrator at that site. Either way, the physician's information is taken in a physician information form at step 310 (see FIG. 3C). A user identification (ID) and password (PW) are generated for the physician at step 312 (see FIG. 3D).
FIG. 4 shows an overview of the site registration of step 210. The number of sites input by the user is received at step 402 (see FIG. 4A). As noted above, a table of site locations, having a sufficient number of rows, is generated at step 404 (see FIG. 4B). The user completes the table, including information for each site, at step 406 (see FIG. 4C).
The data entry forms will now be described. In general, a data entry form can be implemented in HTML as one page or several; if it is implemented in several pages, each page ends with “Next Page” (or if the last page of the form “Submit”), “Discard Changes and Exit” or “Save Changes and Exit” options. Also, the same forms can be used to add information about new users and to update information for existing users.
FIG. 5A shows the first page of the physician's form. The first page 502 includes an area 504 for contact information, an area 506 for medical licensing and DEA information, and an area 508 in which the physician can identify specialties through drop-down menus. Other information, such as professional affiliations with one or more medical schools and hospitals, can be solicited here. There are also “Next Page” (or if the last page of the form “Submit”), “Main Page” and “Save Changes and Exit” buttons 510, 512 and 513, as mentioned above.
FIG. 5B shows a subsequent page 514 of the physician's form. As shown in FIG. 5B, the physician is asked about experience as a principal investigator in a clinical trial. Detailed experience on each clinical trial can be solicited in further pages, as well as information on any FDA or sponsor audit that the physician or the site has undergone, any administrative roles that the physician plays at the site, any articles or presentations in which the physician is named as an author, and any organizations and associations in which the physician is actively involved.
The pages requesting organization and site information are similar. In addition, the organization pages request the type of organization, while the site pages request what facilities the site has, among other things. Pages can also be provided to transfer a physician from one site or organization to another or to transfer a site from one organization to another. This function is accessible solely to employees of the service, not registered users.
The administrator of the database server 114 can accept the information as given or can take various steps to verify it. For example, the administrator can verify that a given facsimile number or e-mail address words, check a given medical license number, or interview either the person submitting the information or those persons named as references.
Once all of the data concerning participating physicians, organizations, and sites have been entered into the database, the database can be searched. FIG. 6 shows a search page for searching for physicians. The search page 600 uses text boxes and drop-down menus, although other suitable interface elements can be used as needed. In any text box, wildcard searching can be allowed.
Physicians can be searched by name, site, organization, or any combination of the three by use of the text boxes 602, 604, 606. The drop-down menu 608 allows the search to be conducted for physicians who are members, non-members, or either. The person conducting the search can select a state through a drop-down menu 610 or a region through a drop-down menu 612. A specialty can be selected through a drop-down menu 614. Key words can be entered in a text box 616. The page 600 can be designed to include any other search criteria, such as those relating to clinical trial experience. Once all of the search criteria are entered, the user clicks on the “Find Physicians” button 618.
Clicking on the “Find Physicians” button 618 causes the database server 114 to search for physician records matching the search criteria. The database server 114 passes the search results to the Web server 110 which formats them as shown in FIG. 7. The search results page 700 shows the search results in the form of a table 702. At the far left is a select column 704, which allows the user to select individual physicians for further consideration or to select all physicians through a “Select all” check box 706. The name column 708 lists the physicians by name, with links to their profiles in the database. The specialty column 710 gives each physician's specialty. The organization column 712 and the site column 714 identify the organization and site, respectively, with which each physician is associated and include links to those organizations' and sites' profiles. A telephone number column 716 and a facsimile number column 717 give that information for each physician. The membership status column 718 identifies each physician as a member or non-member. The CTO column 720 and the ORO column 722 list CTO's and ORO's, respectively, with which the physician is or has been involved. Columns can be sorted by clicking on the name of the column. An indicator 726 identifies the number of physicians who have matched the query. The merge buttons 728 and 730 allow the user to merge the records for the selected physicians with a CTO or ORO in a manner to be explained below.
An employee of the service can enter a CTO or ORO as shown in FIG. 8. At step 802, the following are selected through drop-down menus or other suitable interface elements. (see FIG. 8A): the specialty concerned (e.g., urology), the estimated number of patients, and the duration. At step 804, the following are input as free-form text (see FIG. 8B): a descriptive title of the study, one or more inclusion criteria for patients (e.g, male patient aged 40-85 years), one or more exclusion criteria for patients (e.g., no previous prostatic surgery within two weeks of base line), and a per-patient budget (this can be indicated as “to be negotiated”). The criteria can also be selected through drop-down menus, in which case there will be an option to add criteria not appearing in the menus. The criteria can also be assigned a sorting order. Through a Design SQQ/PQQ Interface, the relevant SQQ or PQQ is designed and posted on the web at step 806 (see FIG. 8C). A number is manually assigned at step 808 (see FIG. 8D). The opportunity can be made viewable to network members only by an employee of the service at step 810 (see FIG. 8E). The CTO or ORO can be made viewable to persons viewing the organization's or site's profile or in a list sorted by specialty; preferably, both are done.
Once the CTO or ORO is entered, the search results from FIG. 7 can be merged into the CTO or ORO. Once the button 728 or 730 is clicked, the merge page 902 or 904 in the merge area 900 of FIG. 9 appears. The user can select the Merge CTO or Merge ORO 902 or 904 and click the “Merge” button 906 or may cancel by closing the window. If the “Merge” button 906 is clicked, all of the selected search results from FIG. 7 are linked to the description of the CTO or ORO in the database. Checking for duplicate records is done automatically.
The physicians, organizations, or sites merged into the listing can be invited to consider the CTO or ORO. Since anyone found in the search results will have provided some contact information, the invitation can be made by e-mail, facsimile, or any other suitable channel.
Thus, the service (or, in an alternative embodiment, a sponsor of a CTO or ORO) can initiate contact with a physician, organization or site which may be suited to conduct that CTO or ORO, as described above with reference to FIG. 9. Either way, the questionnaire is completed and returned to the sponsor. The sponsor considers the questionnaire and can send a person to interview the physician or otherwise visit the organization or site at which the trial or other research would take place. A Web page can be provided to indicate the reasons why any particular physician, organization or site was accepted or declined. That Web page is accessible only by employees of the service or network members who have registered to use the system.
Once a physician, organization or site is selected to conduct the trial, data are collected for benchmarking. General (industry) benchmarks include the following: revenue per primary investigator per year, patients enrolled per number of coordinator FTE's, average revenue per patient, distribution of revenue by type, average enrollment as a percentage of goal, split of patient recruitment between in-house and advertised, average number of protocols per year, average number of years in clinical research, percentage of studies through third party, percentage of studies directly from CRO or sponsor, number of sponsors with which a particular physician, site or organization has worked, and number of CRO's with which a particular physician, site or organization has worked. Benchmarks specific to a particular study include the following: time to first patient enrolled, total patients enrolled after the first thirty days, actual enrollment as a percentage of the enrollment goal, per-patient budget, number of queries per patient, enrollment as a percentage of total patients screened, and elapsed time from notification of award of study to initiation visit. Data entered into the Web Form (Site Status Summary, or SSS) are used to compute the benchmarks specific to a particular study. Those data are collected on a per-protocol basis, are specific to that protocol and are not stored for future protocols. On the other hand, information collected in the profiles can be used to update the SQQ/PQQ.
Examples of Web pages for taking data associated with a particular study are shown in FIGS. 10 and 11 as 1000 and 1100, respectively. The page 1100 is only partially shown, since the data are taken not simply at the end of 30 days, but rather at the end of every 30-day interval until the end of the study; for instance, the page 1100 may ask for the number of patients screened after 720 days, etc. At the end of the study, data may be collected, such as the date of the study close-out visit and the number of queries generated.
The benchmarks are calculated automatically by the system. The more data inputted, the more an organization can access. They do not have to wait until the study is over until they can view benchmarks, but as soon as the relevant data are input the benchmark is viewable. Once all of the data are input and the study is concluded, or once the data currently available are input if benchmarking during the study is required, benchmarking can be performed using straightforward calculations on the data. Two examples of data outputs are shown; those skilled in the art will recognize that many other types of data outputs can be provided as needed.
FIG. 12 shows a bar chart 1200 in which the total budget per patient is broken down into overhead, procedure and lab fees, the study coordinator, and the investigator fees. FIG. 13 shows a bar chart 1300 showing a particular benchmark by its value in the user's study compared to its high, low, and average values from among all organizations participating in the same opportunity monitored by the database server 114. The identities of the other organizations are not identified. Each of the bars of the bar chart 1300 can be broken up like the bar in the bar chart 1200.
The benchmarks can be displayed to the sponsor of the study, the physician, site or organization conducting the study, or both. Non-numerical information, such as the identities of the physicians involved in the study and information about them, can also be reported.
An enhancement to the service provides a customizable search page for the “study budget project” where physicians can search for a price range for their service. The search is intuitive enough to allow physicians to select predetermined criteria to focus their search. Physicians will also be able to download their study budget information in a standard template usable in a spreadsheet program (e.g., Microsoft Excel).
At step 1402, a study budget system is provided, which is a separate module from the service previously described. At step 1404, the user logs in. Members will pay a yearly license fee, billed monthly. Existing users will be able to retrieve their user name and password information by entering their e-mail address.
If the system determines at step 1406 that the user is a new user, or is an existing member using the system for the first time, the user will be required to complete an activation form at step 1408. On confirmation of the user's credit card, the user will receive a welcome message and information about their subscription via e-mail.
At step 1410, the user will choose from standard study questions about that user's procedure type, which sets the parameters for the query. At step 1412, the user receives high, average, and low fees for the selected query.
At step 1414, a study budget template is provided in order to be populated with the user's information. The study budget template provides automatic calculations and a printable template. At step 1416, on completion of the template, the information is updated to the database.
While the disclosure set forth above is believed to provide an enabling disclosure of the present invention and a best mode for carrying out the present invention, an administrative-level user's guide will now be set forth for the sake of completeness. For ease of understanding, the user's guide is organized in tabular form.
Question Topic Response
What happens New Site If it is completed on-line,
when a site Applications E-mail Copy automatically goes to the service.
completes their Completing The Site Recruiter then logs onto
application on- Reference Check www.rapidtrials.com/orge.asp
line or hard Information on They select the organization name from the drop
copy? Rapidtrials down list and hit EDIT
Activating a New They move using ALT+N or Next Page to the last
Site page of the profile
The last page lists the references
They also list whether the references were:
“outstanding”
“Average”
“Unfavorable”
Once the reference checks are done, these are
changed as appropriate
The date the contract is signed is inputted into the
first page, as well as some other contract
information.
Once the site is ready to be a member of the
network the site recruiter goes to the first page of
the organization profile, by going to
www.rapidtrials.com/orge.asp, members admin,
selecting the org name from the drop down and
hitting EDIT
Members admin page drop down list of
organizations If the organization is in black it is an
active member of the network, if the org is in blue
or any other color you can check the status by
going to Edit and looking at the status drop down
halfway down page one of the organization profile.
Halfway down the first page is a status drop down.
The status is:
Active
Terminated
Contact
Hold
Pending
Inactive
The organization status is changed to Active. This
automatically creates a second browser window
with the User ID and Passwords for that
organization.
You then select Export to XLS, and these can be
printed out from XLS and faxed to the
organization.
You then close the second browser window and
select ‘Save changes and Exit’
This organization is now an Active member of the
network and has full access to the member's
section.
How do I put a Posting a New The Project manager identifies a new CTO
new clinical Clinical Trial Log on to Rapidtrials.com
trial Opportunity on This will take you to CTO Admin or
opportunity on Rapidtrials www.rapidtrials.com/cto/asp
Rapidtrials Creating a PCRS Click New
Tracking Number Enter the CTO name
Enter the Tracking Number
Enter if the CTO is recruiting Yes/No (When a
CTO is no longer recruiting this must be changed to
No)
Enter if the CTO is to be shown on the web Yes/No
(When the CTO is no longer to be viewed on the
web must be changed to NO)
Enter Project Manager Name
Enter which of the following are applicable (to be
update, as information becomes available over
time)
Sponsor
Sponsor contact Name
Sponsor Contract Name
CRO
CRO contact name
CRO contract name
Then select save
How do I create Creating a Synopsis Click CTO description
a CTO Online for a Clinical Trial This is where you create the synopsis for the
(CTO) clinical trial
For those choices that appear in blue, click on the
blue link, type in the text that is to appear under
that link, click save and click return
Select Therapeutic Area and indication from the
dropdown
Date CTO sent to sites
CTO Phase
Study design
Status-Proposed or awarded
Study Objective
Investigator specialty, up to three from dropdown
Clinical Experience, do they have to have
experience or can they be trial naive
Is a certain number of past clinical trials necessary,
indicate this here
IRB Utilization-Central or Local
Type of site, check all that apply
Is it Inpatient/Outpatient?
Key Inclusion Criteria
Key exclusion Criteria
Removal of patients from therapy
Length in enrollment in months
Note: This generates the correct amount of 30 day
increments for the benchmarking
Expected enrollment
Duration of therapy
Number of patient visits
Investigator Meeting
Anticipated Start Date
Special request/equipment
Budget
There are then 5 extra criteria, which you can label
and then enter text for
Click Save
How do I create Creating an SQQ Click SQQ design
a Site Using the same If there is another SQQ already created that you
Qualification template as a know is identical to the one you wish to create, or
Questionnaire previously very similar so that you would change just one or
(SQQ) Online developed SQQ two things-
Creating Custom Click Load SQQ pattern from another CTO
Questions Select CTO Name and click OK
Say OK
This will create the same SQQ for your clinical trial
OR
To create a brand new SQQ
Click SQQ design
There will be a list of standard questions, these are
questions that if they are completed on the profiles
will pre fill for the Investigators
Select those you wish to delete
Note: The one that is blank is actually Board
Certification
If you wish to create specialized questions, in
addition to the standard questions, click Further
Criteria
Click Simple Questions
A Question Interface appears
Let's use some examples:
How far away is the nearest airport?
in miles
Which of the following apply to your site? Small,
Medium or Large
Check all that your site has ECG, Sleep Lab, Study
Coord
What date is your next IRB meeting?
Using the Interface Label-
1. Question One
Label = How far away is your site
After Label = miles
Question Type = Text box
Question Data Type = Text
Multiple Choices =
2. Question Two
Label = Which of the following
apply to your site?
After Label =
Question Type = Combo Box (only one
answer allowed)
Question Data Type = Numeric
Multiple Choices = Small, Medium,
Large
3. Question Three
Label = Check all that your site has
After Label =
Question Type = Multiple Choices (allows
for more than one answer)
Question Data Type = Numeric Multiple Choices = ECG,
Sleep
Lab, Study Coord
4. Question Four
Label = What date is your next IRB
meeting
After Label =
Question Type = Text box
Question Data Type = Date
Multiple Choices =
Then Click Save
This saves your question and it shows up under the
Criteria Label
Continue clicking Simple Questions and then
creating questions until you are done
To change any question you have already created,
click the blue link and make your changes and click
save
When you are done Click SQQ combination, this
merges the standard questions and the special
questions
Click re number, and then number the questions so
that they appear in the correct order.
To delete a question click the delete box then save
To make further changes to the special questions
click Edit further criteria and click on the blue links
and make the change, click save and then SQQ
combination
When you are satisfied with the order click Save
Then click Save Changes and Exit
TO send The project manager will provide with the new
automatic CTO a list of specialties who need to be informed
emails to the about this trial
orgs to inform From CTO admin, click search, this appears above
them of a new the matched site window
CTO This will take you to the search page
Select enable - Membership Status
The choices are member, non-member, or all
Select member
Under Investigator specialty, click enable and
choose the specialty from the drop down box
Note; The search by specialty is an AND search,
not an OR search. So choose only one specialty at a
time.
Click Find Physicians
At the bottom of the search results page, click
select all
Review the list and those that you do not wish to
inform of the clinical trial unselect them by clicking
on the checkmark on the left-hand side so that the
box is empty.
Then click merge CTO
Select the CTO name
Click Merge
This will dump the sites you selected into the
matched window on the CTO admin page
Repeat with each specialty until completed
From CTO admin
Click Select All next to matched window
Click Send SQQ and description
This will create an email and fax list of all the
matched organizations
To send the email click send mail all
One email is sent to each organization contact
person that you identified, the email lists all the
suitable investigators at that site.
TO add a Go to CTO admin
doctor that has Under CTO name drop down list, select the name
submitted for a and click Edit
clinical trial OR
Enter tracking number on the top bar and click
EDIT
IF
Doctor appears in matched window
Doctor does not appear in matched window
1. Select his name by clicking on it
Click SSS
Then click EDIT under Update
Compete the first page:
Date of submission deadline
Date of submission
Date notified of submission
Note: This last field sends an automatic email to the
site when it is completed. See attached email
Click Save changes and Exit
His status will now be Submitted pending selection
2. From CTO admin halfway down
Select Org Name
Select Site
Select Physician
Click ADD
He will go in to the top of the matched window
Follow above steps
To get a list of Go to responded window
doctors Click on first name in the box
submitted for a Click Shift
study (not Click on last name in the box
including those Click Show Info
whose status is Print report
not submitted)
To remove a Click on his name
doctor from a Click remove
trial To view info for a doctor
Click his name
Click view info
Info is shown as: Name, Site, Org, Specialty, Tel #,
Fax #, Status, Last Change
To update SSS Click his name
Click SSS
Click Edit under Update
To view SQQ
Click his name
Click SQQ
To add a new Click New next to Sponsor
Sponsor Enter Info
Click Save
Click Return
Same for Sponsor Contact, Sponsor Contract, CRO,
CRO Contact, and CRO Contract
Search Page Every criteria you enable limits your search
It is a wild card to search:
To search for Bill Jones, enable physician name
and enter
Bill
Jones
Bi
Ll
Jo
Nes
Etc
Click find physicians to get results
Results are shown as Org, Site, Physician, Phone,
Fax, Specialty, Status (member/non-member),
CTO, ORO
The results can be sorted by any of the column
headings, simply click on them
Clicking on the physician's name takes you to his
profile
Clicking on the site name takes you to the site
profile
Clicking on the org name takes you to the
organization profile
To transfer a doctor If a doctor moves from one organization, or more
likely someone entered him in the wrong
organization profile
Search for the physicians
From the results page select doctor to be transferred
Member Admin Page
Organization Level
To create a new org, click new
To edit an existing org, select name from drop
down list and click edit
Click Transfer
Select Org and Site he is to be transferred to
Click Transfer
To view (in read only mode) an existing org, select
name from drop down list and click show
To view the sites for that org, select site name from
drop down and click site
Site Level
To create a new site, click new
To edit an existing site, select name from drop
down list and click edit
To view (in read only mode) an existing site, select
name from dropdown list and click show
To view the members for that site, select site name
from drop down and click members
To view the SSS for a site (all the trials that they
are linked with) click SSS
To delete a site, select the site name from the drop
down and click delete
Members Level
To create a new member, click new
To edit an existing member, select name from drop
down lists and click edit
To view (in read only mode) an existing member,
select name from dropdown list and click show
To view the SSS for member (all the trials that they
are linked with) click SSS
To delete a member, select the member name from
the drop down and click delete
Please Note
If you change the organization name at the
organization level, the site level and the member
level DOES NOT AUTOMATICALLY CHANGE.
You must click Site and Member again to ensure
the information you are looking at is relevant to the
site that you are viewing
To view the SSS for and org (all the trials that they
are linked with) click SSS
To delete an org, select the org name from the drop
down and click delete
SSS Search Mini search for CTO Issues
Criteria Results are always shown as CTO Number, Org
Name, Site Name, Physician, Specialty, Phone,
Fax, Sponsor/CRO, Status, Last Change, Access to
SSS
You can search by
Tracking Number
Organization Name
Site Name
Physician Name
The more information you enter the more limited
your search
After you enter the search criteria, click find
To get to CTO admin, click CTO
To reset search criteria, click reset
Passwords Click Passwords Link
Select the organization that you want to get
passwords for
Click Update
Make changes and to save click update
To print, click print
To export to XLS, click export to XLS
Tracking of Web These are tracked by
Site Changes SSS changes
SQQ changes
Profile changes
It tracks-Tracking number, Physician, Site, Org,
Date and Time of change, Location of change
(form name and page)
Physician History View which CTO have been sent to a physician and
whether they responded (yes or no)
Search by name, site, organization or institution
(for ORO doctors)
Limit as much as you want, more info, more
limited search, another wild card search
Hit Find
Then select which physician and click View
History
History shown as CTOs offered responded Yes/No
OROs offered responded Yes/No
Sponsor Requests
Results of tell us
about your needs
Marketer Requests
Results of See what
we can do for you
Various other enhancements can be made to the present invention. They will now be set forth.
Functionality Description
Best Practices Extension of the benchmarking capability, this would be accessible to
Across All Sites members. Based on benchmarking metrics, those sites with the best
Benchmarked practices will be identified by the service, contacted and interviewed on
how they obtained the results in this trial. This information will be shared
confidentially with other sites in the same protocol. This will promote
information exchange amongst sites, help research naive sites, or poorer
performing sites to achieve better results on studies, and identify problems
before a study closeout situation occurs
Secure Bulletin Each clinical trial listed on Rapidtrials and whose status is on-going will
Board have a one (1) way (from the service outboard) Bulletin Board where
sponsors can post information about a study including Q&A type
information In addition, Sponsor project managers can use the bulletin
Board to share information about the study on a on-going basis
Rapid Budget Separate Web Module accessible from the current website (rapidtrials.com).
Members pay a yearly fee, billed monthly. They can apply for membership
via the website (rapidtrials.com), with payment accepted via credit card. A
new user will be required to complete an activation form; this will collect
basic data on the physician and his organization. The module will ask them
questions about the type of study they wish to budget for and which
procedures are involved. Users receive a high, average, low, and your site
(which allows them to view what they charged for the procedure the last
time they used the system). The system then asks them to choose a price for
each procedure, this feeds into a basic per patient clinical trial specific study
budget template which when they have completed choosing their ranges
they can print the complete budget worksheet from the website. This
information then updates the underlying sequel table, so it will be available
to be used in the calculation for the next user.
RapidTraining Current Training Program owned by the service is for Novice Sites and or
as a refresher course for experienced sites. Currently we have the program
on CD and will Migrate the CD based training program to the Web as a
standalone serviced
Rapid Meeting Investigator CD platform currently exists. Will be migrated to the Web.
Rapidpatient This will be a guide Clinical Research sites in selecting strategies and
Recruitment tactics to aid in the clinical trial patient recruitment and retention activities.
Based upon a users description of the patient recruitment and retention
objectives they are attempting to support, the Rapidtrials web module will
suggest appropriate tactics to support the objectives. This module will also
include IRB/FDA regulations governing patient recruitment advertising and
recruitment guidelines. This module of the Rapidtrials website will be a
portal for ordering mugs, t-shirts, ads, media buying, plaques and other
promotional items through the service to enhance patient recruitment and
retention in clinical trials. A catalog of items, which are IRB/FDA
compliant that they can order through us.
Rapid Assessment A Rapidtrials web module that uses a psycho-behavioral assessment
(similar to Myers Briggs) that has been validated by the service using
historical performance and behavioral assessment response correlation's to
identify sites with a high probability of succeeding in clinical trials.
Investigators and coordinators will complete this behavioral assessment on-
line as a predictive tool for the practice of future success in clinical trials.
Gaps in attributes will be identified for Sites as a means of guiding them in
clinical research program recruitment. For sponsors involved in site
selection, or preparing to invest in site development it will give them
another performance indicator prior to selecting sites to participate in a
clinical trial.
Industry Generated by data entered into members organization, site and Investigator
Benchmarking profiles, these benchmarks will be displayed by Type of Organization (I.e.
solo practice, SMO etc): Total number of protocols per year, Total grant
value per protocol, total number of patients enrolled in a clinical trial/year,
total number of Study coordinators, total number of sites doing research,
Total number of Patients per study coordinator FTE's, Average number of
Patients per year, Number of Physicians, Number of PI's, Overhead as a
percentage of total per patient budget, Study Coordinator costs as a
percentage of Total per patient budget, Investigator Fees as a percentage of
total per patient budget, Procedure, lab fees as a percentage of total per
patient budget, total number of sponsors worked for/year, Total number of
CROs/year, Actual Enrollment/Enrollment
Goal.
Site Capabilities Data capture approved by field based consultants to gather information on
Assessment Data sites developing research programs or preparing to participate in clinical
Capture and trial. Migration of proprietary data capture tools to the web.
Reporting
Site Operations Data capture pages used by field based consultants to gather information on
Specialists Site sites developing research programs or preparing to participate in clinical
Specialists Site sites developing research programs or preparing to participate in clinical
Development trial. Migration of proprietary data capture tools to the web. This is the
eWorkbook same as the above.
Site Operations Data Capture Pages, tools and presentations to use in preparing for and
Specialists Site monitoring site performance on a clinical trial. Migration of Proprietary
Management Data Capture tools to the web
eWorkbook
While a preferred embodiment of the present invention has been set forth in detail, those skilled in the art who have reviewed the present disclosure will readily appreciate that other embodiments can be realized within the scope of the present invention. For example, the utility of the invention is not limited to the medical field. Also, any benchmarks can be calculated, in which case the forms for collecting the data are modified accordingly. Further, the benchmarks can be displayed as text, as any suitable chart, or as a combination of the two. In addition, either the Web server or the database server can incorporate the ability to handle payments from one participant to another, as well as from participants to the company operating the servers. Moreover, any mention of a specific software package (e.g., Microsoft Excel) should be construed as illustrative rather than limiting. Therefore, the present invention should be construed as limited only by the appended claims.