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Exercise, Cognitive Function and Neuroplasticity in Healthy Adults

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University of Miami

Status

Completed

Conditions

Sedentary Lifestyle

Treatments

Behavioral: High intensity exercise.
Behavioral: Moderate intensity exercise.

Study type

Interventional

Funder types

Other

Identifiers

NCT02994134
20161059

Details and patient eligibility

About

The overall goal of the proposed study is to compare the effects of 4 weeks of moderate or high intensity aerobic exercise on neuroplasticity, cognitive performance and gait and postural control in sedentary healthy adults.

Full description

The primary aim of the study is to compare the effects of a moderate intensity aerobic exercise intervention (delivered at 55-64% age-predicted maximal heart rate) with a high intensity aerobic exercise intervention (delivered at 65%-90% age-predicted maximal heart rate) on measures that probe cortical synaptic plasticity using transcranial magnetic stimulation (TMS) in sedentary healthy adults.

Enrollment

19 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult males and females aged 18-70 years old
  • Primary language is English
  • Sedentary (defined as not engaging in purposeful physical activity more than 2 times over the last two months)
  • Exercise clearance

Exclusion criteria

  • Presence of cognitive, neurologic or orthopedic conditions that could affect performance of the testing and training procedures

  • History of migraines.

  • History of fainting spells of unknown or undetermined etiology that might constitute seizures

  • History of seizures, diagnosis of epilepsy, history of abnormal (epileptiform) EEG or family history of treatment resistant epilepsy

  • Any current history of a psychiatric illness

  • Any unstable medical condition

  • No medication is an absolute exclusion from TMS. Medications will be reviewed by the Principal Investigator and a decision about inclusion will be made based on the following:

    • The subject's past medical history, drug dose, history of recent medication changes or duration of treatment, and combination with other CNS active drugs.
    • The published TMS guidelines review medications to be considered with TMS (Rossi, Hallett, Rossini, Pascual-Leone, & Safety of TMS Consensus Group, 2009).
  • Any metal in the brain, skull or elsewhere unless approved by the responsible MD

  • Any medical devices (i.e. Cardiac pacemaker, deep brain stimulator, medication infusion pump, cochlear implant, vagal nerve stimulator)

  • Intracranial lesion

  • Substance abuse or dependence within the past six months Subjects who, in the Investigator's opinion, might not be suitable for the study

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

19 participants in 2 patient groups

Moderate intensity exercise.
Active Comparator group
Description:
Moderate intensity aerobic exercise intervention (delivered at 55-64% age-predicted maximal heart rate), 4 times per week for 4 weeks.
Treatment:
Behavioral: Moderate intensity exercise.
High intensity exercise
Experimental group
Description:
High intensity aerobic exercise intervention (delivered at 65%-90% age-predicted maximal heart rate), 4 times per week for 4 weeks.
Treatment:
Behavioral: High intensity exercise.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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