Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT05900271

Dutch-Depression Outcome Trial Comparing 5 Day Multi Daily Neuronavigated Theta Burst Sessions With 6 Weeks rTMS

Led by Amsterdam UMC, location VUmc · Updated on 2024-04-05

108

Participants Needed

4

Research Sites

211 weeks

Total Duration

On this page

Sponsors

A

Amsterdam UMC, location VUmc

Lead Sponsor

R

Radboud University Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

INTRODUCTION Recent findings from three small studies (total n=59) suggest that three changes in repetitive Transcranial Magnetic Stimulation (rTMS) protocols, called the Stanford Neuromodulation Therapy (SNT) protocol, contribute to extreme high overall remission of 79% in patients with treatment resistant depression (TRD), whereas remission using a standard 10 Hz rTMS protocol is 25%. The improvement using the SNT protocol is achieved by combining 1) accelerated treatment with multiple sessions per day, 2) applying a higher overall pulse dose of stimulation, using intermittent Theta Burst Stimulation (iTBS), and 3) precise targeting of the region in the left dorsolateral prefrontal cortex (DLPFC), using functional MRI guided neuronavigation. OBJECTIVE To determine if the SNT protocol is more (cost-) effective compared to standard 10 Hz rTMS in patients with TRD, even though the number of pulses given in both protocols is equal, i.e., 90,000. STUDY DESIGN Multicenter randomized controlled trial comparing SNT with standard 10Hz rTMS with a follow-up of 25 weeks. STUDY POPULATION 108 Patients with TRD (no response to 2 or more evidence-based treatments). INTERVENTION 50 sessions using the SNT protocol in 5 days. The region of the left DLPFC most anticorrelated with the subgenual anterior cingulate cortex in each participant will be targeted based on subject-specific functional resting state MRI. COMPARISON 30 standard daily 10 Hz rTMS sessions in six weeks, targeting the left DLPFC based on standard measurement procedures of the skull. OUTCOME MEASURES * Remission, based on the Hamilton depression rating scale * Cost effectiveness, based on healthcare resource use * Quality of life and positive mental health * Tolerability and safety * Relapse * Description of opportunities and difficulties with regard to implementation SAMPLE SIZE The investigators will enrol 108 patients (α=0.05, power is 0.80) including adjustment for attrition. COST EFFECTIVENESS ANALYSIS SNT is faster and possibly more effective than 10Hz rTMS leading to a total cost reduction of 22 million each year considering less expensive healthcare, reduced illness duration and absence from work. TIME SCHEDULE Within 36 months, the investigators will recruit and treat 108 patients with TRD: each center will recruit 9 patients per year. After the last follow-up assessments, the investigators will finalise the study within 12 months and report the results.

CONDITIONS

Official Title

Dutch-Depression Outcome Trial Comparing 5 Day Multi Daily Neuronavigated Theta Burst Sessions With 6 Weeks rTMS

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Sufficient spoken and written Dutch
  • Ability to freely provide written informed consent
  • Current DSM-5 diagnosis of a depressive episode confirmed by MINI-S
  • Hamilton depression rating score above 16 points
  • Treatment-resistant depression defined as no remission after two adequate evidence-based treatments
  • Stable antidepressant medication for at least 6 weeks; benzodiazepines allowed up to 3.0 mg lorazepam equivalent and can be reduced during study based on clinical judgement
Not Eligible

You will not qualify if you...

  • Bipolar disorder
  • Current psychotic disorder including psychotic depression
  • Suspected dementia (score less than 20 on MOCA or clinical/neuroimaging signs)
  • Active suicidal thoughts with intent to act
  • Metallic devices implanted above the neck
  • Diagnosis of epilepsy
  • Substance abuse within 4 weeks before study, including benzodiazepine over 3.0 mg lorazepam equivalent
  • Inability to understand or comply with study requirements
  • Pregnancy

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Trial Site Locations

Total: 4 locations

1

Radboud UMC

Nijmegen, GL, Netherlands, 6525GA

Actively Recruiting

2

GGZinGeest

Amsterdam, North Holland, Netherlands, 1081JC

Actively Recruiting

3

Amsterdam UMC location AMC

Amsterdam-Zuidoost, North Holland, Netherlands, 1105AZ

Actively Recruiting

4

Maastricht UMC

Maastricht, Netherlands

Not Yet Recruiting

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Research Team

A

Annemiek Dols, MD PhD

CONTACT

E

Eric van Exel, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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