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TRENA: Trial of Enhanced Neurostimulation for Anorexia

Sponsor
The George Institute (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05788042
Collaborator
The University of New South Wales (Other)
70
Enrollment
1
Location
4
Arms
26.7
Anticipated Duration (Months)
2.6
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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).

Condition or Disease Intervention/Treatment Phase
  • Device: MagPro TMS device (ARTG: 204659)
  • Device: tDCS mini-CT Stimulator (Soterix, USA: ARTG: 284637)
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Double-blind, randomised, sham-controlled trial, parallel group design. Participants will be randomised to one of four groups (2:1:2:1 ratio): Active or sham tDCS, or Active or sham rTMS. The brain stimulation protocols involve 84 sessions of tDCS (active or sham) or 56 sessions of rTMS (active or sham) over the 8 week acute treatment period.Double-blind, randomised, sham-controlled trial, parallel group design. Participants will be randomised to one of four groups (2:1:2:1 ratio): Active or sham tDCS, or Active or sham rTMS. The brain stimulation protocols involve 84 sessions of tDCS (active or sham) or 56 sessions of rTMS (active or sham) over the 8 week acute treatment period.
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
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. The following measures will be taken to ensure preservation of blinding to treatment allocation: Unblinded personnel (i.e., Neurostimulation Nurse(s) and/or tDCS research assistant), will be present during rTMS treatment delivery. tDCS will be self administered in the presence of ward staff. Team members involved in conducting blinded assessments for mood (i.e., MADRS) must not be present in the room during research treatment delivery. Knowledge of the code (i.e., which of 'A', 'B', 'C' or 'D' refers to which randomised treatment) will only be known to study staff responsible for treatment delivery, the study CI and study statistician involved in the study.
Primary Purpose:
Treatment
Official Title:
Randomised Controlled Trial of Neurostimulation for Symptoms of Anorexia Nervosa
Anticipated Study Start Date :
Apr 10, 2023
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Jul 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Active transcranial Direct Current Stimulation (tDCS)

It will be given continuously for 30 minutes at 2 mA, twice daily (separated by >=2 hours) over the first 4 weeks, and daily over the second 4 weeks of the 8 week acute treatment period (84 sessions total).

Device: tDCS mini-CT Stimulator (Soterix, USA: ARTG: 284637)
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.
Sham Comparator: Sham transcranial Direct Current Stimulation (tDCS)

It will involve an initial ramping up to 0.5 mA and then a ramp down to 0 mA for the remainder of each treatment. The same number of sessions as active tDCS will be administered.

Device: tDCS mini-CT Stimulator (Soterix, USA: ARTG: 284637)
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.
Active Comparator: Active Repetitive Transcranial Magnetic Stimulation (rTMS)

Active rTMS twice per day (separated by ≥ 2 hours) over the first 4 weeks. Two sessions per day (separated by ≥ 2 hours), given on 2 days each week for the following 4 weeks. The total number of rTMS sessions over the 8 week acute treatment period will be 56.

Device: MagPro TMS device (ARTG: 204659)
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.
Sham Comparator: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)

Sham rTMS twice per day (separated by ≥ 2 hours) over the first 4 weeks. Two sessions per day (separated by ≥ 2 hours), given on 2 days each week for the following 4 weeks. The same number of sessions as active rTMS will be administered.

Device: MagPro TMS device (ARTG: 204659)
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.

Outcome Measures

Primary Outcome Measures

  1. Effectiveness - Eating Disorder Examination Questionnaire (EDE Q) [Change from baseline at 8 weeks]

    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.

  2. Acceptability [8 weeks]

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

Secondary Outcome Measures

  1. Weight [Change from baseline at 4 weeks]

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

  2. Weight [Change from baseline at 8 weeks]

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

  3. Weight [Change from baseline at 20 weeks]

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

  4. Mood - Montgomery Asberg Depression Rating Score (MADRS) [Change from baseline at 4 weeks]

    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.

  5. Mood - Montgomery Asberg Depression Rating Score (MADRS) [Change from baseline at 8 weeks]

    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.

  6. Mood - Montgomery Asberg Depression Rating Score (MADRS) [Change from baseline at 20 weeks]

    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.

  7. Neurocognition - Trail Making Test parts A and B (TMT: attention and cognitive flexibility) [Change from baseline at 8 weeks]

    Deficits in set shifting has been found to be common in people with AN.

  8. Neurocognition - Trail Making Test parts A and B (TMT: attention and cognitive flexibility) [Change from baseline at 20 weeks]

    Deficits in set shifting has been found to be common in people with AN.

  9. Neurocognition - Embedded Figures Test (EFT: field dependence vs independence). [Change from baseline at 8 weeks]

    This task assesses central coherence, or the degree of focus on details in processing information. Poor central coherence is a potential etiologic or maintaining factor for people with eating disorders.

  10. Neurocognition - Embedded Figures Test (EFT: field dependence vs independence). [Change from baseline at 20 weeks]

    This task assesses central coherence, or the degree of focus on details in processing information. Poor central coherence is a potential etiologic or maintaining factor for people with eating disorders.

  11. Neurocognition - STROOP Colour Word Test (response inhibition). [Change from baseline at 8 weeks]

    The STROOP task assesses inhibitory control, which has been shown to be reduced in people with eating disorders.

  12. Neurocognition - STROOP Colour Word Test (response inhibition). [Change from baseline at 20 weeks]

    The STROOP task assesses inhibitory control, which has been shown to be reduced in people with eating disorders.

  13. Neurocognition - Wisconsin Card Sorting Test (WSCT: perseveration). [Change from baseline at 8 weeks]

    This task has been found to be sensitive to set shifting deficits in people with AN.

  14. Neurocognition - Wisconsin Card Sorting Test (WSCT: perseveration). [Change from baseline at 20 weeks]

    This task has been found to be sensitive to set shifting deficits in people with AN.

  15. Psychological Symptoms - Depression Anxiety and Stress Scale (DASS-21) [Change from baseline at 8 weeks]

    Self reported questionnaire designed to measure the severity of a range of symptoms common to both Depression and Anxiety. 21-items; rating scale 0- 3; Higher scores on subscales indicate more severe depression, anxiety and stress.

  16. Psychological Symptoms - Depression Anxiety and Stress Scale (DASS-21) [Change from baseline at 20 weeks]

    Self reported questionnaire designed to measure the severity of a range of symptoms common to both Depression and Anxiety. 21-items; rating scale 0- 3; Higher scores on subscales indicate more severe depression, anxiety and stress.

  17. Functioning - The Assessment of Quality of Life Instrument (AQoL-4D) [Change from baseline at 8 weeks]

    Measures quality of life for independent living, mental health, relationships, and senses. It as chosen as measures can be used for economic evaluation based on Quality Adjusted Life Years (QALYs). 12-items; scale 1-4; Higher score indicates lower health-related quality of life.

  18. Functioning - The Assessment of Quality of Life Instrument (AQoL-4D) [Change from baseline at 20 weeks]

    Measures quality of life for independent living, mental health, relationships, and senses. It as chosen as measures can be used for economic evaluation based on Quality Adjusted Life Years (QALYs). 12-items; scale 1-4; Higher score indicates lower health-related quality of life.

  19. Change in Circumplex Scales of Interpersonal Efficacy (CSIE-32) [Change from baseline at 8 weeks]

    Change in Circumplex Scales of Interpersonal Efficacy: 32-items; scale 0-10; Higher score indicate confidence that one can engage in variety of interpersonal behaviours.

  20. Change in Circumplex Scales of Interpersonal Efficacy (CSIE-32) [Change from baseline at 20 weeks]

    Change in Circumplex Scales of Interpersonal Efficacy: 32-items; scale 0-10; Higher score indicate confidence that one can engage in variety of interpersonal behaviours.

  21. Total cost of costs of rTMS and tDCS administration [Through study completion, an average of 20 weeks]

    Total cost of costs of rTMS and tDCS administration

  22. Duration of inpatient hospital stay as recorded by clinical staff [Through study completion, an average of 20 weeks]

    Duration of inpatient hospital stay as recorded by clinical staff

  23. Number of re-admissions as reported by clinical staff. [From date of randomization until the date of study completion, assessed up to 20 weeks.]

    Number of re-admissions as reported by clinical staff

  24. Number of psychology sessions [Through study completion, an average of 20 weeks]

    Number of psychology sessions

  25. Cost of psychology sessions [Through study completion, an average of 20 weeks]

    Cost of psychology sessions in $ AUD

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • 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)

  • Under ongoing care by his/her own treating psychiatrist (to ensure patient safety during the study)

Exclusion Criteria:

  • 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

  • MoCA score of <26

  • Significant risk of significant self harm or suicide as assessed by study psychiatrist(s)

  • Currently enrolled in another interventional clinical trial or using an investigational device/product

Contacts and Locations

Locations

Site City State Country Postal Code
1 Northside Clinic Sydney New South Wales Australia 2031

Sponsors and Collaborators

  • The George Institute
  • The University of New South Wales

Investigators

  • Principal Investigator: Sloane Madden, Assoc. Prof., University of Sydney, Ramsay Health Care

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
The George Institute
ClinicalTrials.gov Identifier:
NCT05788042
Other Study ID Numbers:
  • 2021-016
First Posted:
Mar 28, 2023
Last Update Posted:
Mar 28, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The George Institute
Anorexia Nervosa
Repetitive Transcranial Magnetic Stimulation
Transcranial Direct Current Stimulation
Non-invasive brain stimulation
Additional relevant MeSH terms:
Anorexia
Anorexia Nervosa

Study Results

No Results Posted as of Mar 28, 2023