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IQCare Frequently Asked Questions

Who is developing IQCare?
- Futures is leading the IQCare software development initiative
in collaboration with other AIDSRelief consortium members’, Catholic
Relief Services and the University of MD, Institute of Human Virology.
A consortium steering committee provides guidance on financial and
scope change issues. A working group, which includes US and local
experts, is responsible for gathering the business requirements,
developing, testing, and implementing the software
Where has IQCare been deployed and in how many
locations?
- IQCare has been installed in several countries throughout Africa,
Kenya, Uganda, Nigeria and Tanzania. 70 facilities are currently using
IQCare in these countires.
Can a clinic add its own questions or custom
fields to the IQCare forms?
- Yes. Additional questions or custom fields can be added to all
of the IQCare forms. Text, numeric, date, and yes/no fields, select
list and multi select lists can be added. There is no restriction
to the number of custom fields or the field types that can be added.
What kind of reporting capabilities does IQCare
have?
- IQCare provides both pre-defined reports as well as robust custom
reporting capabilities. Pre-defined reports include: PEPFAR Track
1.0, Missed ARV report, Missed ARV Pick up report, Enrollment by
month, Patient profile.
IQCare provides a flexible custom reporting module that allows users
to create almost any report needed using all of the data that is
captured in the system.
What are the minimum computer requirements
to run IQCare?
Software components
- XP Professional operating system with service pack 2
- Internet Explorer 6.0 or higher
- Java Runtime Environment 5
Hardware components
How much training is required to learn how
to use IQCare?
The amount of training required to use IQCare
depends on how familiar the clinical team is with their data capture
process. As well, the size of the clinic and amount of IT support
available will impact the number of hours of training needed. For
those clinics that are new to gathering data (site activation), clinical
and technical training is recommended, including setting and reviewing
the hardcopy data process at the clinic (1 week) and then the computer
set up, data entry and report creation process (1-2 weeks). Please
contact us for more information about our train-the-trainer program
and training materials customized to fit your needs.
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