rTMS for Neuroenhancement

Description

The purpose of this pilot study is to evaluate the effects of Repetitive Transcranial Magnetic Stimulation (rTMS) on Sleep Quality, Mood and Memory.

Conditions

Sleep

Study Overview

Study Details

Study overview

The purpose of this pilot study is to evaluate the effects of Repetitive Transcranial Magnetic Stimulation (rTMS) on Sleep Quality, Mood and Memory.

A Prospective Study To Evaluate Safety and Effectiveness of Repetitive Transcranial Magnetic Stimulation (rTMS) For Neuroenhancement

rTMS for Neuroenhancement

Condition
Sleep
Intervention / Treatment

-

Contacts and Locations

Vienna

Gerrish MedEsthetics, Vienna, Virginia, United States, 22180

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Male or female, 22 to 70 years of age
  • * Freely provides written informed consent
  • * In good general health, as ascertained by medical history
  • * If female, not breastfeeding, no known or suspected pregnancy, a status of non- childbearing potential or use of an acceptable form of birth control
  • * If subject is in menopausal transition, the subject must be stabilized on hormonal treatment.
  • * Subject scored a 2 or higher on PHQ-9 sleep related question (#3), OR subject scored 2 or more on at least 2 QIDS-SR sleep related questions (#'s 1-4)
  • * If subject is on any psychiatric or sleep medication, dose must be stable for two weeks prior to enrollment and remain stable throughout the trial.
  • * Subject satisfies any one or more of the contraindications for TMS Therapy per current treatment guidelines as determined by the PI.
  • * History of head trauma associated with loss of consciousness or diagnosed as concussion.
  • * History of fainting, syncope, hearing problems or ringing in the ears (tinnitus)
  • * Has any metallic implant(s) in or near the head (e.g., pacemaker, defibrillator, neurostimulator, etc.) including any splinters, fragments, clips, etc.
  • * Has an implanted stimulator device (including device leads) in or near the head.
  • * Has medication infusion device.
  • * Subjects with any prior TMS or MRI complications which, in the opinion of the investigator, might interfere with safety, study participation, or which might confound data interpretation,
  • * Current diagnosis of a Substance Use Disorder (Abuse or Dependence, as defined by DSM-IV-TR), with the exception of nicotine dependence.
  • * Current diagnosis or known history of neurologic or neuropsychiatric disease (e.g., epilepsy, convulsion, seizure)
  • * Has a clinically significant abnormality on the screening examination that might affect safety, study participation, or confound interpretation of study results.
  • * Participation in any clinical trial with an investigational drug or device within the past month or concurrent with study participation.

Ages Eligible for Study

22 Years to 70 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Gerrish MedEsthetics,

Study Record Dates

2024-11