Trial of Enhanced Neurostimulation for Anorexia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16+
SponsorThe George Institute

About this trial

Preliminary open-label studies have suggested that non-invasive brain stimulation methods of both transcranial direct current stimulation (tDCS) and repetitive transcranial magnetic stimulation (rTMS) have clinical benefits for improving psychological and eating disorder related symptoms, which can persist at long-term follow ups after acute treatment (i.e., at 6 and 12 months).

Here the investigators propose to conduct the first double-blinded, randomised sham-controlled study to directly compare the therapeutic effectiveness and acceptability of both treatment modalities.

Participants will be recruited and treated at one inpatient setting (Northside Clinic, St Leonards, Sydney). This facility is one of the largest specialist eating disorder settings in Australia with approximately 130 new admissions every year (2019 data). All participants who give consent and who fulfill the eligibility criteria will be randomised to receive active tDCS, sham (placebo) tDCS, active rTMS or sham rTMS over 8 weeks. Trial participants, their treating psychiatrist, ward staff, and a study staff member (who will conduct blinded assessments of mood secondary outcome measures) will be blinded after assignment to intervention until the database is locked and the primary analysis completed. All participants will complete assessments of eating disorder symptoms, mood, psychological symptoms, neurocognition and functioning at baseline, end of week 4, 8 and 20.

Expected outcomes include data on the relative effectiveness and acceptability for both treatment modalities in the inpatient and at-home setting (i.e., for at-home tDCS). The investigators expect that both active treatment arms will produce clinical benefits and have high acceptability, and that clinical benefits will be maintained with long-term at-home tDCS continuation treatment. These outcomes have potential to assist in reducing hospital stay and emergency re-admissions and improving day to day functioning in participants. Health economic data for both treatment modalities will additionally have utility from a service perspective, given the disparity in resource requirements between the two treatments (TMS, tDCS) in terms of costs for patients and access to treatment for people living in remote and rural areas (i.e., for at-home tDCS).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged ≥16 years,

A current Diagnostic and Statistical Manual of Mental Disorders (5th edition DSM-5) diagnosis of anorexia nervosa

Willing and able to participate and comply with study requirements

Worked or studied in a context requiring some proficiency in spoken English (to ensure validity of neuropsychological testing)

Disqualifiers

Inability to provide informed consent

Contraindications to tDCS/rTMS

Failed to respond to an adequate course or rTMS (4 weeks) within the current illness course

Had ECT in the last 3 months

Trial design

Design model

Parallel

Treatments tested in this trial

  • MagPro TMS device (ARTG: 204659)

    Device

    rTMS will be administered using a MagPro TMS device (ARTG: 204659) which is approved for its intended use in this trial. rTMS involves the application of transient magnetic pulses which induce small currents in the underlying cortex via the principal of electromagnetic induction. rTMS will be administered using a patterned frequency stimulus called intermittent theta-burst stimulation (iTBS).This form of rTMS was chosen because a recent large multicentre trial showed 3 minutes of iTBS attained the same therapeutic effect as 30 minutes of standard rTMS, leading to FDA approval for depression. Each treatment session will comprise an extended iTBS session, i.e., 6.6 mins, delivered at 100% resting motor threshold (RMT). It will be targeted to the left DLPFC (F3 using the 10-20 International EEG system), consistent with the prior RCT of rTMS for AN.

  • tDCS mini-CT Stimulator (Soterix, USA: ARTG: 284637)

    Device

    tDCS will be self-administered using the 1x1 tDCS mini-CT Stimulator (Soterix, USA: ARTG: 284637) with two saline-soaked sponge electrodes held in place on the scalp using the Soterix Ole-2 headband. The device is intended to treat different neurological and psychiatric disorders. tDCS involves the passing of weak electrical current through the brain via electrodes placed upon the scalp. The current modulates the resting membrane potential of stimulated neurons which causes changes in neuronal excitability. The anode will be placed over the left F3 (10-20 System) and the cathode over F4 (electrode sizes 5 x 5cm, 25cm2). This montage was chosen to target the left DLPFC, consistent with prior pilot studies of tDCS in AN.

Treatment groups

70 Participants
are divided into 4 treatment groups
Group A: Active transcranial Direct Current Stimulation (tDCS)Active comparator 1 intervention
Group B: Sham transcranial Direct Current Stimulation (tDCS)Sham comparator 1 intervention
Group C: Active Repetitive Transcranial Magnetic Stimulation (rTMS)Active comparator 1 intervention
Group D: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)Sham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Effectiveness - Eating Disorder Examination Questionnaire (EDE Q)

Self-report instrument that measures eating disorder behaviors and attitudes. Eating Disorder Examination Questionnaire; 28-items; rating scale 0 - 6; Higher scores on the global scale and subscales indicate more problematic eating behaviours and attitudes.

Time frame
Change from baseline at 8 weeks
2

Acceptability

Number of completed sessions for active tDCS and active rTMS in the acute 8 week RCT period.

Time frame
8 weeks

Secondary outcomes

1

Weight

Change in Body Mass Index. Weight status in AN is considered a key determinant of remission from illness.

Time frame
Change from baseline at 4 weeks
2

Weight

Change in Body Mass Index. Weight status in AN is considered a key determinant of remission from illness.

Time frame
Change from baseline at 8 weeks
3

Weight

Change in Body Mass Index. Weight status in AN is considered a key determinant of remission from illness.

Time frame
Change from baseline at 20 weeks
4

Mood - Montgomery Asberg Depression Rating Score (MADRS)

Depressive symptomology is a common psychiatric comorbidity of AN and both tDCS and rTMS significantly improve mood symptoms. 10-items; rating scale 0- 6; Higher score indicates more severe depression.

Time frame
Change from baseline at 4 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The George Institute

Lead sponsor

The University of New South Wales

Collaborator