Transcranial Magnetic Stimulation of the Prefrontal Cortex: Effects on Risky Decision Making and Temporal Discounting.

NCT ID: NCT01098864

Last Updated: 2015-03-04

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-05-31
• Study Completion Date: 2014-01-31

Brief Summary

The main objective of this study is to examine the effects of magnetic stimulation on the prefrontal cortex. We plan to use low frequency, repeated transcranial magnetic stimulation (1 Hz rTMS) to temporarily inhibit activity in the prefrontal cortex and measure the resulting effect on two decision-making tasks. The prefrontal cortex is thought to mediate or control cognitive functions like decision-making, planning, memory, and inhibit impulsive behavior.Previous research has indicated that rTMS over the right dorsal lateral prefrontal cortex will lead to preferences for riskier alternatives. Our hypothesis is that rTMS over the right DLPFC will lead to greater preference for the riskier alternative and greater temporal discounting.

Conditions

Decision Making

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Blinding Strategy: NONE

Interventions

transcranial magnetic stimulation

low frequency (1 Hz) repeated transcranial magnetic stimulation will be delivered to the dorsal lateral prefrontal cortex (DLPFC) area for a period of 15 minutes to test for effect on executive function (e.g., decision choice and subjective value). Four sessions will be conducted per subject; 2 active stimulations,(1 left DLPFC, 1 right DLPFC) and 2 sham stimulations (1 left DLPFC, 1 right DLPFC) with a minimum of 48 hours between every stimulation. Pre and post stimulations measures of cognitive and executive function will be collected and analyzed for significant differences.

Intervention Type: DEVICE

Other Intervention Names

Magstim Super Rapid 2 Stimulator w/ 70mm figure eight stimulating coil

Eligibility Criteria

Inclusion Criteria

• Healthy participants willing to give informed consent to participate
• complete the Transcranial magnetic stimulation Adult Safety Screen
• have a MRI scan
• wear ear plugs during rTMS
• receive rTMS over the designated course of days
• complete cognitive assessments and decision making tasks.
• return for post-testing on all tasks after completing all rTMS sessions

Exclusion Criteria

• Diagnosed neurological and/or psychiatric disorders requiring hospitalization or medication
• pregnancy or the possibility of pregnancy at the time of consent
• a history of tinnitus
• metal implants in head or neck or a pacemaker
• poorly-controlled migraines
• a history of head injury, stroke, previous brain neurosurgery, or loss of consciousness due to head injury lasting greater than 10 minutes
• a personal or family history of epilepsy or seizures

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Arkansas

OTHER

Sponsor Role: lead

Responsible Party

UAMS

Principal Investigators

Mark S Mennemeier, PhD

Role: PRINCIPAL_INVESTIGATOR

Universtiy of Arkansas for Medical Sciences

Other Identifiers

109639

Identifier Type: -

Identifier Source: org_study_id