Hi Merrie,
Oakrise CAMHS has been developing and using an integrated outcomes assessment
database(Clinical Outcome and Tracking System(COaTS)). We are using HONOSCA at the moment
but only because our state mental health service has begun using a system called OARS(from
NSW, Wentworth Area Health I think). Prior to this we were using the SOPISCA(Severity of
Psychiatric Illness Scale- Adolescent). We are using FACES-III as a way of tracking family
functioning and the Ohio Youth Problem, Functioning and Satisfaction Scales to gather
parental and client information about symptoms and satisfaction.
Part of the implementation of all this has been to develop as low-profile a data
collection system as possible. Probably 98-100% of our clients complete the initial
assessments prior to the first appointment. The data is entered into our database by the
clinicians as part of the initial registration of clients. We then have a protocol for
follow-up assessments at 6 month intervals whilst the case is open and then a final
assessment 6 months after discharge.
We have now been collecting data for 2 years (about 950 initial assessments)and are in
the process of analysing some of the instruments used in terms of whether they provide a
useful and integrated picture of client issues. The main problem with the whole approach
is that we have been getting very low return of follow-up assessments(<100). I am
thinking about using the next 12 months to trial a simple 7 question outcome format which
can be gathered in 5-10 minutes over the phone. We used this methodology in some research
we did on single sessions and it provided excellent data but we have done nothing further
in looking at validity and etc.
Obviously most of this stuff should be looked at on a national basis. But, it certainly
seems like that process has stalled and in the meantime CAMHS in Tasmania has been getting
pressure to adopt the adult database which doesn't assess what we would like and comes
with a range of Federal Govt DHAC data collection agendas.
One of the things that I am most pleased about is that we developed and introduced this
data collection system as a team of clinicians. All the clinicians are as interested and
involved in the design of the data system and it's implementation as the developer(me). We
truly 'own' this as a team and I have not worked in any other team where the issue of data
collection has been worked on collaborativley by clinicians. Usually IT and management
impose a system which is then maintained and implemented incredibly poorly. Interestingly
I read some documentation regarding the development of outcomes assessment systems for
CAMHS that recommended that clinicians not be involved in the design and delivery phase!!
If anything I think that this would be a recipe for corrupt data.
I would be happy to communicate(there doesn't seem to be an email equivalent to
"talk"). If you have ICQ or MSN Messanger perhaps we could set up a time to chat
about it? Maybe we could identify a group of people in CAMHS and have an online forum
about this... not dominated by the existing power heirachy - whoever that is - as this
whole area seems to bring out the territorial imperative in most of the people that I have
talked to.
Alistair Campbell
Senior Clinical Psychologist/Manager: CAMHS(N)
Ph:03-6336-2867
ICQ#:34159422
Email: Alistair.Campbell@utas.edu.au <mailto:Alistair.Campbell@utas.edu.au>