CareSolutionsTM ConCERT-D is an advanced clinical solution designed to manage dementia patients and dementia research by easily identifying patients and carers who have provided consent for inclusion in research. Developed in collaboration with leading NHS Clinicians and Researchers at West London Mental Health Trust, ConCERT-D is an information system that provides clinicians with the granularity of data required for effective care and assessment of dementia patients that cannot usually be found in more traditional EPR solutions. The system also identifies patients, along with their families and care supporters, who would be willing to participate in research studies and clinical trials.
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CareSolutions ConCERT-D
1. www.6pmsolutions.com
Research is vitally important to help develop a better
understanding of neurodegenerative conditions and possible
new treatments. The aim of research is to find better ways of
looking after patients, keeping them healthy and improving
their quality of life.
Developed in collaboration with leading NHS Researchers
at West London Mental Health Trust, CareSolutions™
ConCERT-D provides a registry of people, along with their
families and care supporters, who would be willing to
participate in research studies. These will be used to answer
some of the key questions faced by service users and
providers.
An Electronic Care
Record System
for Dementia that
manages Clinical
Research developed by
Clinicians for Clinicians.
ConCERT-D is an advanced clinical solution designed to
manage dementia patients and dementia research by
easily identifying patients and carers who have provided
consent for inclusion in research.
2. Solution
ConCERT-D is a registry of people, grouped together on
the basis of their clinical conditions, and their carers to
provide the basis for efficient and appropriate identification
of patients who are suitable for and would welcome the
opportunity to participate in research studies. This patient
registry is being designed and developed with the purpose
to be used in the NHS for Research Management and Patient
Recruitment for local and national research projects.
ConCERT-D can be used to identify and recruit
consenting participants for research studies
Examples of the Patient Search function and Score Graph Overview
“Linking people with dementia with high quality
research has historically been very problematic.
Registering an individual’s interest has proved very
effective in earlier pilot work with DemReg but the new
ConCERT-D system will allow us to embed the register
fully in clinical practice as it acts as both a Research
Register and an Electronic Patient Record. This will
allow even more people to gain access to the high
quality dementia research we undertake.”
Dr Craig Ritchie,
Honorary Consultant and R&D Director, WLMHT
Senior Lecturer, Imperial College London
3. Provides a registry of patients
and carers who are suitable for a
study and have given consent to
participate in research.
A clinical database system which
supports clinical practice, audit
and service planning.
Provides infrastructure to link
selected patients into well-
designed and highly organised
clinical studies.
Supports the process of inviting
patients and carers to join a
research registry, providing a
platform to record their research
preferences and activity.
Holds a minimum dataset of
information assigned to the
Cognitive Impairment and
Dementia Care Pathway.
Supports very accurate feasibility
for both the commercial and non-
commercial sector for new trials.
Stores clinical details of all
patients assigned to the Cognitive
Impairment and Dementia care
Pathway.
Provides capability for in-depth
patient searching for research,
audit and clinical practice.
Facilitates identification and
recruitment of appropriate /
suitable patients for clinical
research.
Provide a clinical database
system to complement RiO, to
facilitate clinical activity and audit
/ service planning / pharmacy
monitoring etc.
Holds information about
contributors’ consent to the
research registry, to enable
appropriate matching of registry
members to research projects.
Key Benefits Financial Drivers:
4. The Data Protection Act requires all patients who are identified for research projects to have given their consent
to be identified in this way. ConCERT-D is a registry of people who have consented to be approached, allowing
efficient identification of these patients while avoiding the delay of prospective identification of subjects.
Patients and their carers who have consented to participate
and are willing to be approached for their involvement
in research studies have their clinical data drawn into
ConCERT-D and this is visible to local researchers. This
enables them, once selected, to then be approached to be
involved in a variety of clinical research projects, all of which
are subject to separate ethics approval, RD registration and
consent. This may include cohort studies, intervention studies
and other epidemiological enquiries.
ConCERT-D patients in the registry are assembled through
specialist services for people with cognitive impairment and
dementia (e.g. memory clinics, old age psychiatry outpatients
and day hospitals and care homes).
LET US DEMONSTRATE HOW ConCERT-D CAN ADD VALUE
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