Neuronetics
Malvern, Pennsylvania, 19355, United States
Location status: Recruiting
Location contact
Eleanor Cole
CONTACT
NCT Number: NCT06917339
In this study, real-world data will be used to better understand the effects patient characteristics, symptoms and TMS protocol parameters have on clinical outcomes with NeuroStar TMS.
Interested in participating?
Request Info5 year–120 year
All sexes
Observational
Malvern, Pennsylvania, 19355, United States
Location status: Recruiting
Eleanor Cole
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
non-invasive brain stimulation device
Time frame: 8 weeks
real-world efficacy of NeuroStar TMS in reducing patients' symptoms, reduction in clinical assessment score like PHQ-9
Time frame: 8 weeks
Determine the patient characteristics like age that are associated with clinical outcomes- PHQ-9 following NeuroStar TMS
Contact information is provided by the study sponsor or research team.
Eleanor Cole, PhD
CONTACT
Neha Goyal
CONTACT
Neuronetics
Other
Retrospective Analyses Evaluating the Real-World Effectiveness of NeuroStar® TMS and the Factors Associated With Clinical Outcomes
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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