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NCT Number: NCT06243016

Breaking Sitting with High-intensity Interval Training for Brain Health

This trial will examine whether interrupting 3.5 hours of sitting every 30 min with 6 min high intensity interval training (HIIT) breaks compared to light intensity interval training (LIIT) will improve brain health in cognitively normal older adults. This trial will test the feasibility of HIIT breaks to sitting. It will also address several important but unanswered questions: (1) Does interrupting sitting with short HIIT breaks improve frontoparietal function? (2) Can interrupting sitting with HIIT breaks improve cognitive functions?

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Key information

Conditions

Age range

40 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Illinois at Urbana-Champaign

Urbana, Illinois, 61801, United States

Location status: Recruiting

Location contact

Dominika M Pindus, PhD

CONTACT

[email protected]

2173007317

About this study

The investigators are conducting an acute, single site randomized crossover trial testing two conditions lasting 3.5 hours each with a one to four-weeks washout period: (1) Interrupting sitting with 6 min of high-intensity interval training (HIIT) every 30 min, and (2) interrupting sitting with 6-min light-intensity interval training (LIIT) every 30 min. Investigators will administer the conditions in a counterbalanced order to 54 older adults (40-75 years). Brain function will be assessed using event-related brain potentials and measures of functional connectivity derived from electroencephalography. Cognitive functions will be assessed using a modified Eriksen flanker task and an antisaccade task. Investigators will measure episodic memory using a mnemonic discrimination task.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 40-75 years
  • BMI <40 kg/m2
  • Sedentary (≥ 6 h/day sitting by a survey question)
  • Physically inactive adults based on the CSEP-PATH: Physical Activity and Sedentayr Behaviour Questionnaire (PASB-Q) Adult (low or medium physical activity range equivalent to less than 300 min of moderate intensity physical activity per week)
  • Capable of exercising vigorously based on the Physical Activity Readiness Questionnaire (PARQ+)
  • Has a medical clearance for maximal exercise and HIIT from a physician
  • Normotensive or participant's blood pressure is controlled
  • Intelligence quotient (IQ) ≥85
  • Fasting plasma glucose <126 mg/dL
  • Good or corrected vision and hearing
  • Right-handed
  • No significant abnormalities on the ECG during the maximal exercise test
  • No signs and symptoms that suggest an underlying cardiovascular disease as recorded during the maximal exercise test by a study physician.
  • No indications to prematurely stop the maximal exercise test as outlined by the ACSM's Guidelines for Exercise Testing and Prescription
  • Concussion if more than 12 months before the study screening.
  • History of cancer but in full remission for at least 12 months and no history of chemotherapy, signed off by the physician or an oncologist

Exclusion criteria

  • Physical disability or musculoskeletal disease prohibitive to vigorous exercise
  • Learning disabilities
  • Cognitive impairment (MoCA <26)
  • Type 1 or 2 diabetes
  • Neurological condition (e.g., Multiple Sclerosis, Parkinson, Dementia, Mild Cognitive Impairment)
  • Color blindness
  • Brain injury (e.g., traumatic brain injury, stroke, concussion)
  • Migraine headaches
  • Presence of other health conditions that may be exacerbated by exercise
  • History of heart disease
  • High cholesterol not controlled by medication
  • Signs and symptoms indicative of underlying cardiovascular disease
  • A chronic pulmonary disease
  • Emphysema
  • Pulmonary embolus
  • Asthma
  • History of renal disease
  • History of seizures
  • A neuropsychiatric disorder
  • Osteoporosis if it interferes with an individual's ability to exercise
  • Severe back problems
  • Severe arthritis if it interferes with an individual's ability to exercise
  • Thyroid disorder not controlled by medication
  • Polyneuropathy
  • Sleep disorders
  • Acquired immunodeficiency syndrome (AIDS)
  • Hepatitis C
  • History of long Coronavirus Disease 2019 (COVID-19)
  • History of cancer if not in full remission for at least 12 months and if a participant had the history of chemotherapy
  • Current or past smoking <12 months
  • Corticosteroid intake < 31 days before screening
  • Opioids taken < 6 months from screening
  • Anabolic androgens taken < 31 days before screening
  • A serious illness or hospitalization in the last six months
  • Currently taking medications that can affect the central nervous system (except for anxiolytics)
  • Current participation in an ongoing trial likely to influence exercise ability or cognitive function

Treatment and study plan

High-Intensity Interval Training (HIIT) Breaks to Sitting

Behavioral

HIIT Breaks: a 3.5-hour sitting will be interrupted every 30 min with 6-min HIIT Breaks. During sitting participants will engage in standardized sedentary activities. Each 6-min HIIT break comprises a one-minute warm-up, followed by a 2-minute high-intensity interval, one minute rest (sitting on a cycle ergometer) followed by another 2 minutes at high intensity.

Light-Intensity Interval Training (LIIT) Breaks to Sitting

Behavioral

LIIT Breaks: a 3.5-hour sitting will be interrupted every 30 min with 6-min LIIT Breaks. Each 6-min LIIT break comprises a one-minute warm-up, followed by a 2-minute light-intensity interval, one minute rest (sitting on a cycle ergometer) followed by another 2-minute light-intensity interval.

Primary outcomes

  1. Change in task-evoked brain activity

    Time frame: Immediately before intervention, 2 x during the intervention (50 min and 120 min into the intervention), and immediately after the intervention

    EEG will be used to measure event-related brain potentials including the P3b-component during an inhibitory control task.

Secondary outcomes

  1. Change in cognitive functions

    Time frame: Immediately before intervention, 2 x during the intervention (50 min and 120 min into the intervention), and immediately after the intervention

    A modified Eriksen flanker task will be used to measure inhibitory control.

  2. Change in cognitive functions

    Time frame: Immediately before intervention and immediately after the intervention

    An antisaccade tasks will be used to measure inhibitory control. A mnemonic discrimination task will be used to measure episodic memory.

  3. Change in resting stated and task evoked brain activity

    Time frame: Immediately before intervention and immediately after the intervention

    EEG will be used to measure functional connectivity at rest and during engagement in inhibitory control and episodic memory tasks.

Study contacts

Contact information is provided by the study sponsor or research team.

Dominika M Pindus, Ph.D.

CONTACT

[email protected]

217-300-7317

Sponsors and collaborators

Lead sponsor

University of Illinois at Urbana-Champaign

Other

Collaborators

  • National Institute on Aging (NIA)
  • Northeastern University

Registry information

Official study title

Breaking Prolonged Sitting with High-intensity Interval Training to Improve Cognitive and Brain Health in Older Adults: a Pilot Feasibility Trial.

Acronym: HIIT2SITLess

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 5, 2024
Registry last updated
Feb 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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