2021
DOI: 10.1186/s13063-021-05096-w
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Sympathetic Nervous System and Exercise Affects Cognition in Youth (SNEACY): study protocol for a randomized crossover trial

Abstract: Background There is an increasing prevalence of physical inactivity during childhood, which is associated with a variety of health problems. However, the mechanisms by which acute exercise benefits cognition in childhood remains unknown. Here we describe the protocol for a randomized crossover trial called SNEACY (Sympathetic Nervous System & Exercise Affects Cognition in Youth), a study designed to better understand mechanisms linking acute exercise and cognition in 9–10-year-old healthy, … Show more

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Cited by 5 publications
(9 citation statements)
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References 40 publications
(24 reference statements)
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“…The two trials include relatively healthy older individuals (65–80 years, 23% non-white) from three different geographical sites in the U.S. (Pittsburgh, PA; Boston, MA; Kansas City, KS), and typically developing children (8–10-years, 42% non-white) from Boston, MA, see Table 1 for participant demographics. Recruitment strategies, eligibility, testing protocols, BMI measurements, and CRF protocols were published before the start of the pandemic ( 36 , 37 ) and did not change over the course of the pandemic. All participants provided written informed consent (or assent in the case of children) in accordance with the Institutional Review Board at their testing site.…”
Section: Methodsmentioning
confidence: 99%
“…The two trials include relatively healthy older individuals (65–80 years, 23% non-white) from three different geographical sites in the U.S. (Pittsburgh, PA; Boston, MA; Kansas City, KS), and typically developing children (8–10-years, 42% non-white) from Boston, MA, see Table 1 for participant demographics. Recruitment strategies, eligibility, testing protocols, BMI measurements, and CRF protocols were published before the start of the pandemic ( 36 , 37 ) and did not change over the course of the pandemic. All participants provided written informed consent (or assent in the case of children) in accordance with the Institutional Review Board at their testing site.…”
Section: Methodsmentioning
confidence: 99%
“…This cross-sectional investigation was a secondary analysis of a larger clinical trial ( ClinicalTrials.gov Identifier: NCT03592238). The inclusion criteria for participants included: parental/guardian consent and participant assent, between the 9–10 years of age, capable of performing exercise, normal/average intelligence quotient (IQ) or above (i.e., >85), classified as pre-pubescent or in the earliest stages of puberty ( 37 ), no prior diagnosis of cognitive or physical disability, not taking any anti-psychotic, anti-depressant, anti-anxiety, or attention deficit disorder (ADD)/ attention deficit hyperactivity disorder (ADHD) medications, normal or corrected-to-normal vision, and able to speak and read English ( 38 ). The detailed methodology is provided in a recent publication ( 38 ).…”
Section: Methodsmentioning
confidence: 99%
“…Twenty-one healthy children aged 9 to 13 years old (mean age 11.5 ± 1.1 years, 9 female) were recruited from an ongoing randomized crossover trial (Raine et al, 2021). Participants came from the Greater Boston area and included racial and ethnic diversity.…”
Section: Participantsmentioning
confidence: 99%
“…In addition, they completed the Kaufman Brief Intelligence Test-2 (KBIT-2) to assess IQ. Exclusion criteria included non-consent from guardian or non-assent from participant, being unable to exercise due to physical disability, an IQ less than 85, diagnosis of physical or cognitive disability, use of psychiatric medication, poor vision, and not being fluent in English (Raine et al, 2021). Participant demographics are depicted in Table 1.…”
Section: Participantsmentioning
confidence: 99%
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