CClinicalTrials.gg
CompletedNCT02802462Updated Jun 16, 2016

High-intensity Interval Training Enhances Mobilization/Functionality of Endothelial Progenitor Cells and Depressed Shedding of Vascular Endothelial Cells Undergoing Hypoxia

An interventional study of HIT and MCT in Hypoxia, sponsored by Chang Gung Memorial Hospital. Completed. Open to male participants aged 20 Years to 28 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-06-16.

Sponsored by Chang Gung Memorial Hospital · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
20 Years to 28 Years
Sex
Male
01

Study summary

Exercise training improves endothelium-dependent vasodilation, whereas hypoxic stress causes vascular endothelial dysfunction. Monocyte- derived endothelial progenitor cells (Mon-EPCs) contribute to vascular repair process by differentiating into endothelial cells. This study investigates how high-intensity interval (HIT) and moderate intensity-continuous (MCT) exercise training affect circulating Mon-EPC levels and EPC functionality under hypoxic condition. Sixty healthy sedentary males were randomized to engage either HIT (3-minute intervals at 40% and 80%VO2max , n=20) or MCT (sustained 60%VO2max , n=20) for 30 minutes/day, 5 days/week for 6 weeks, or to a control group that did not received exercise intervention (n=20). Mon-EPC characteristics and EPC functionality under hypoxic exercise (HE, 100W under 12%O 2 ) were determined before and after various interventions.

02

Conditions studied

  • Hypoxia

Browse trials for

Keywords

  • endothelial progenitor cell
  • hemodynamic
  • Exercise
  • HIIT
03

In context

Hypoxia

1,231 studies on the registry are indexed under Hypoxia; 241 are open to participants now.

This study's enrollment of 60 is above the median of 45 across 853 interventional studies indexed under Hypoxia.

Browse Hypoxia studies →

Lead sponsor

Chang Gung Memorial Hospital is the lead sponsor of 1,064 studies on the registry; 235 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 28 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Sedentary life
  • Age 20\~28

Exclusion criteria

Exclusion Criteria:

  • Smokers
  • Users of medication/vitamins
  • Any cardiopulmonary/hematological risk
  • Regular exercise habits at least 1 year
  • Exposed to high altitudes (>3000 m) for at least 1 year
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    High intensity-interval (HIT)

    Behavioral: HIT

  • Experimental
    moderate intensity-continuous (MCT)

    Behavioral: MCT

  • No intervention
    control (CTL)

Interventions

  • BehavioralHIT

    3-minute intervals at 40% and 80%VO 2max

  • BehavioralMCT

    sustained 60%VO 2max

06

What researchers measure

Primary outcomes

  1. Circulating progenitor cells conten

    by flow cytometry before and after rehabilitation circulating progenitor cells conten before and after hypoxic exercise test

    Time frame: 6 weeks

Secondary outcomes

  1. Cardiopulmonary fitness

    Time frame: 6 weeks

Other outcomes

  1. Cardiac hemodynamic measurement

    evaluate cardiac hemodynamic response to exercise by noninvasive continuous cardiac output monitoring system

    Time frame: 6 weeks

  2. Cerebral hemodynamic measurement

    Two pairs of near infrared probes were attached to each subject to monitor the absorption of near infrared light across left frontal cortex during graded exercise test

    Time frame: 6 weeks

  3. Muscular hemodynamic measurement

    Two pairs of near infrared probes were attached to each subject to monitor the absorption of near infrared light across left vastus lateralis muscle during graded exercise test

    Time frame: 6 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 16, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02802462
Lead sponsor
Chang Gung Memorial Hospital
Responsible party
Jong-Shyan Wang (PhD, Rehabilitation Science, Chang Gung Memorial Hospital) — Principal investigator
First posted
Jun 16, 2016
Start date
Dec 2012
Primary completion
Dec 2013
Completion
Dec 2013
Last update
Jun 16, 2016

Study contacts

Jong-Shyan Wang, PhD
principal investigator · Chang Gung Memorial Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion