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Repetitive Transcranial Magnetic Stimulation
Dash Protocol for Depression (Comfort Start Trial)
N/A
Waitlist Available
Research Sponsored by Neuronetics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 10 days
Awards & highlights
Summary
This trial will compare the standard NeuroStar TMS protocol with a new feature that alters the strength of the pulses, in order to find which is more comfortable for patients.
Eligible Conditions
- Depression
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 10 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~10 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Evaluate comfort of TMS treatment
Secondary outcome measures
Ability to reach prescribed treatment intensity
Trial Design
2Treatment groups
Active Control
Group I: Dash ProtocolActive Control1 Intervention
Patients will be randomized after consent to receive standard Dash protocol
Group II: Modified Dash protocol with the New feature enabledActive Control1 Intervention
Patients will be randomized after consent to receive modified Dash protocol with the New feature enabled
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Who is running the clinical trial?
NeuroneticsLead Sponsor
23 Previous Clinical Trials
7,542 Total Patients Enrolled
12 Trials studying Depression
7,087 Patients Enrolled for Depression
Steve A Erickson, BSStudy DirectorNeuronetics
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You cannot take pain medication before your TMS therapy sessions.You have been diagnosed with Major Depressive Disorder (MDD) by a healthcare professional using specific diagnostic criteria.You have taken at least one anti-depressant medication in the past, but it did not improve your symptoms.
Research Study Groups:
This trial has the following groups:- Group 1: Dash Protocol
- Group 2: Modified Dash protocol with the New feature enabled
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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