Acute bout of High Intensity Interval Training for Healthy Aging

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
University of Virginia; Kinesiology Labs, Charlottesville, VAHealthy AgingAcute bout of High Intensity Interval Training - Other
Eligibility
65+
All Sexes
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Study Summary

This trialwill study the effect of different exercise intensities on brain blood flow and cognition in elderly people. It will help find the best exercise for seniors to protect against age-related mental decline.

Treatment Effectiveness

Effectiveness Progress

1 of 3

Study Objectives

1 Primary · 6 Secondary · Reporting Duration: 4 individual measurements taken during each experimental session with each session lasting up to about 3 hours. 1 pre-intervention measurement and 3 post-intervention measurements spaced at least 15min apart

Hour 3
Vascular Endothelial Growth Factor (VEGF)
Hour 3
Brain-Derived Neurotrophic Factor (BDNF)
Hour 3
Augmentation Index (AI)
Internal Carotid Artery (ICA) Diameter
Internal Carotid Artery (ICA) Distensibility
Internal Carotid Artery (ICA) Pulse Velocity
Pulse Wave Velocity (Brachial-Femoral)
Working Memory
Hour 3
End Tidal CO2 (ETCO2)
Heart Rate
Mean Arterial Pressure (MAP)
Middle Cerebral Artery Velocity (MCAv)
Pre-frontal Hemoglobin Oxygen Saturation

Trial Safety

Trial Design

3 Treatment Groups

Control
1 of 3
Acute bout of Continuous Moderate Intensity Exercise
1 of 3
Acute bout of High Intensity Interval Training (HIIT)
1 of 3

Experimental Treatment

16 Total Participants · 3 Treatment Groups

Primary Treatment: Acute bout of High Intensity Interval Training · No Placebo Group · N/A

Control
Other
Experimental Group · 1 Intervention: Control · Intervention Types: Other
Acute bout of Continuous Moderate Intensity Exercise
Other
Experimental Group · 1 Intervention: Acute bout of Continuous Moderate Intensity Exercise · Intervention Types: Other
Acute bout of High Intensity Interval Training (HIIT)
Other
Experimental Group · 1 Intervention: Acute bout of High Intensity Interval Training · Intervention Types: Other

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 4 individual measurements taken during each experimental session with each session lasting up to about 3 hours. 1 pre-intervention measurement and 3 post-intervention measurements spaced at least 15min apart

Who is running the clinical trial?

University of VirginiaLead Sponsor
694 Previous Clinical Trials
1,467,446 Total Patients Enrolled
Jason Allen, PhDPrincipal InvestigatorUniversity of Virginia
2 Previous Clinical Trials
124 Total Patients Enrolled

Eligibility Criteria

Age 65+ · All Participants · 5 Total Inclusion Criteria

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References

Frequently Asked Questions

How extensive is the participant pool in this clinical trial?

"Affirmative. According to clinicaltrials.gov, this investigation was first posted on the 14th of January 2022 and is still actively recruiting participants. This trial requires 16 volunteers from a single medical centre." - Anonymous Online Contributor

Unverified Answer

Are there any opportunities for new participants to join this experiment?

"Affirmative. According to the data accessible on clinicaltrials.gov, this research endeavour is actively recruiting participants. It was initially posted on January 14th 2022 and subsequently modified November 4th of that same year. 16 individuals are being sought from a single medical centre for participation in the study." - Anonymous Online Contributor

Unverified Answer
Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.