Status:

COMPLETED

Effect of Transcranial Magnetic Stimulation on Memory

Lead Sponsor:

National Institute of Mental Health (NIMH)

Conditions:

Healthy

Healthy Volunteer

Eligibility:

All Genders

Brief Summary

This study will examine the effect of transcranial magnetic stimulation (TMS) on short-term memory in healthy adults. Healthy people use their brains to answer short-term memory questions in a differe...

Detailed Description

Psychiatrists have recognized cognitive dysfunction as the principal impediment to recovery and psychosocial rehabilitation of patients with schizophrenia since the first edition of Emil Kraepelin's 1...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • 1\. Male and Female subjects, age 18-55
  • EXCLUSION CRITERIA:
  • Significant psychiatric, or severe chronic medical illness at the time of the study, or by history. This criterion includes the absence of substance abuse histories, learning disabilities or any other DSM-IV AXIS I or II disorder with documented cognitive impairment. The P.I. or his designate will evaluate medical histories. Medical conditions that are judged not to interfere with the study may be allowed.
  • Pregnancy, personal or family history of epilepsy, concurrent use of tricyclic antidepressants, neuroleptic agents, or any licit or illicit drugs that could lower the seizure threshold, or history of complicated migraine.
  • Persons with surgically or traumatically implanted ferro-magnetic objects in the head that may pose a physical hazard during magnetic stimulation will also be excluded.
  • Use of psychotropic substances in the last 3 months.
  • Head injury with a period of more than 15 minutes unconsciousness, or head trauma with any duration loss of consciousness in the last year, or any evidence of functional impairment due to and persisting after head trauma.
  • Use of caffeine or tobacco in the 2 hours preceding the test.
  • Subjects who have been previously excluded from NIH MRI or TMS protocols for safety reasons.
  • Subjects who are found to have eye lesions on exam.
  • First degree relative with a history of cognitive disorder with onset before age 55 by subject report, and by collateral report of at least one other family member, if necessary.

Exclusion

    Key Trial Info

    Start Date :

    March 1 2005

    Trial Type :

    OBSERVATIONAL

    End Date :

    February 1 2006

    Estimated Enrollment :

    80 Patients enrolled

    Trial Details

    Trial ID

    NCT00105118

    Start Date

    March 1 2005

    End Date

    February 1 2006

    Last Update

    March 4 2008

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    National Institute of Mental Health (NIMH)

    Bethesda, Maryland, United States, 20892