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Investigating Gains in Neurocognition in an Intervention Trial of Exercise (IGNITE): Protocol

  • Kirk I. Erickson
  • , George A. Grove
  • , Jeffrey M. Burns
  • , Charles H Hillman
  • , Arthur F Kramer
  • , Edward McAuley
  • , Eric D. Vidoni
  • , James T. Becker
  • , Meryl A. Butters
  • , Katerina Gray
  • , Haiqing Huang
  • , John M. Jakicic
  • , M. Ilyas Kamboh
  • , Chaeryon Kang
  • , William E. Klunk
  • , Phil Lee
  • , Anna L. Marsland
  • , Joseph Mettenburg
  • , Renee J. Rogers
  • , Chelsea M. Stillman
  • Bradley P. Sutton, Amanda Szabo-Reed, Timothy D. Verstynen, Jennifer C. Watt, Andrea M. Weinstein, Mariegold E. Wollam

Research output: Contribution to journalArticlepeer-review

Abstract

Despite the ubiquity of normal age-related cognitive decline there is an absence of effective approaches for improving neurocognitive health. Fortunately, moderate intensity exercise is a promising method for improving brain and cognitive health in late life, but its effectiveness remains a matter of skepticism and debate because of the absence of large, comprehensive, Phase III clinical trials. Here we describe the protocol for such a randomized clinical trial called IGNITE (Investigating Gains in Neurocognition in an Intervention Trial of Exercise), a study capable of more definitively addressing whether exercise influences cognitive and brain health in cognitively normal older adults. We are conducting a 12-month, multi-site, randomized dose-response exercise trial in 639 cognitively normal adults between 65 and 80 years of age. Participants are randomized to (1) a moderate intensity aerobic exercise condition of 150 min/week (N = 213), (2) a moderate intensity aerobic exercise condition at 225 min/week (N = 213), or (3) a light intensity stretching-and-toning control condition for 150 min/week (N = 213). Participants are engaging in 3 days/week of supervised exercise and two more days per week of unsupervised exercise for 12 months. A comprehensive cognitive battery, blood biomarkers and battery of psychosocial questionnaires is assessed at baseline, 6 and 12-months. In addition, brain magnetic resonance imaging, physiological biomarkers, cardiorespiratory fitness, physical function, and positron emission tomography of amyloid deposition are assessed at baseline and at the 12-month follow-up. The results from this trial could transform scientific-based policy and health care recommendations for approaches to improve cognitive function in cognitively normal older adults.

Original languageEnglish (US)
Article number105832
JournalContemporary Clinical Trials
Volume85
DOIs
StatePublished - Oct 2019

Keywords

  • Aging
  • Brain
  • Cognition
  • Exercise
  • MRI
  • Randomized clinical trial

ASJC Scopus subject areas

  • Pharmacology (medical)

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