Actively Recruiting
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
Eligibility Criteria
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
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
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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