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Electrodes implanted into the region of the brain involved in mediating sustained stress and anxiety
Electrodes implanted into the region of the brain involved in mediating sustained stress and anxiety © Õ¬Äе¼º½.
21 April 2021

Deep brain stimulation has been found to help people with severe obsessive compulsive disorder (OCD) that has not responded to other treatment, in a clinical trial led by researchers.

Study lead author from the , CSIRO and the said the trial produced some remarkable results given the lifetime of disability experienced by participants.

“For example, one participant has married, started a business and now has a young family after participating in the study,” Dr Mosley said.

“We have demonstrated that deep brain stimulation is a promising treatment, and our ultimate goal is for this to become an approved therapy for those sufferers with extreme and treatment-resistant OCD.”

People with – a psychiatric condition affecting between one and two per cent of the population – experience intrusive, anxiety-provoking thoughts (obsessions) that may be accompanied by mental acts or behaviours (compulsions). 

Time dealing with these behaviours profoundly interferes with their day-to-day life, and reduces occupational and social functioning.

Dr Mosley said the team had imaged the brains of participants to understand exactly how deep brain stimulation was providing a therapeutic benefit.

“The brain imaging has provided valuable information that will help us to repeat these positive findings in the future.”

This trial was a first for Australia, was randomised and double-blind placebo controlled, strengthening the reliability of the findings.

It targeted a region of the brain involved in mediating sustained stress and anxiety – and involved nine participants with severe OCD who had not responded to years of extensive pharmaceutical or psychological treatment.

The implantations were performed by QBI’s Associate Professor Terry Coyne (neurosurgeon) and (neurologist), world leaders in deep brain stimulation.

In the first part of the trial, half of the participants received active stimulation and half received placebo stimulation for three months.

The clinical trial showed further gains in the second phase of the trial, when all participants received active stimulation for a further nine months, and a course of cognitive behavioural therapy once they had responded to stimulation.

QBI Director said delivered by implanted electrodes was well-established for treating movement disorders like Parkinson’s disease.

“Deep brain stimulation is like a pacemaker for the brain – the electrodes deliver a continuous electrical impulse to a targeted region of the brain, a treatment that is both adjustable and reversible,” Professor Sah said.

“The trial showed a statistically and clinically-significant reduction in OCD symptoms during active stimulation when compared to placebo.”

The researchers gratefully acknowledge the commitment of the participants who contributed their time to the study, which was funded by QBI in partnership with Medtronic.

The clinical trial results are published in the Nature Journal, Translational Psychiatry (). 

Media: QBI Communications, communications@qbi.uq.edu.au, +61 (0) 405 661 856.