Research

The background to this Association is that Tourette Syndrome is a little known disability that afflicts a percentage of Australia’s population.

Many people with TS go through life without having their disorder properly diagnosed.  Many also suffer discrimination in schooling, housing and employment because the symptoms of their disorder are not recognised by teachers, doctors or employers.  The Association aims to increase awareness of this disorder to help sufferers to live a normal life, gain public acceptance and to assist medical research into the disorder.

As such our activities support research into Tourette Syndrome and available forms of treatment.

Current supported projects are listed below.

TSAA also supports raising funds for research into the causes and cure for Tourette Syndrome.


CLICK HERE TO DONATE

Help fund research into Tourette Syndrome


Call for members to join a Research Database

TSAA are building an electronic database of members who are willing to be invited to participate in research in the field of TS. This research may be conducted directly by TSAA, or on behalf of organisations approved by the TSAA committee (e.g. universities). The research subject matter will vary and those on the database might be invited to participate in anything from a casual group discussion to a university-funded study. You might be somebody with TS, or a parent, partner or other close relation of somebody with TS.

There is no pressure to participate if you are on the database and your personal details and research responses will be confidential unless you agree otherwise. The database will be owned by TSAA.


CLICK HERE TO SIGN UP

Add your name to our database


Pilot study of transcranial Direct Current Stimulation (tDCS) as a therapeutic intervention for Tourette Syndrome

Researchers at the University of New South Wales and Macquarie University are seeking volunteers with a diagnosis of Tourette Syndrome, aged 12 years or older, to participate in research trialling a new intervention for Tourette Syndrome. The intervention, called transcranial Direct Current Stimulation (tDCS) is a non-invasive brain stimulation technique. Please see the files below for further information.

Information for parents or guardians of interested child participants

Information for interested adult participants

Genetic Study of Tourette Syndrome

Australian researchers and colleagues of TSA Australia are conducting a research project into the genetics of Tourette Syndrome. This project is being advertised to all current and past members of the TSA Australia and with the support of the TSA Australia.
Information for Participants

You are invited to participate in a study evaluating genes that have been linked to Tourette Syndrome. This study aims to further understanding of the genetic mechanisms involved in this condition.

The study is being conducted by:
Prof. Valsamma Eapen, Professor and Chair of Infant, Child, and Adolescent Psychiatry, UNSW;
Prof. Perminder Sachdev, Professor of Neuropsychiatry, UNSW; and
Dr. Raymond Clarke, Principal Scientific Officer, St George Hospital.

Who can participate in the research?
Individuals with Tourette Syndrome who are aged over 8 years.

For further details please contact Professor Valsamma Eapen, Level 1, Mental Health Centre, Liverpool Hospital, Liverpool, NSW 2170, Tel: +61 2 9616 4205, Fax: +61 2 9601 2773