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Exercise Induced Changes in Fat Metabolism (BC)

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University of Michigan

Status

Completed

Conditions

Healthy Volunteers

Treatments

Other: Exercise session

Study type

Interventional

Funder types

Other

Identifiers

NCT02581306
HUM00103937

Details and patient eligibility

About

If eligible to participate in the research study after completing the physical screening procedures, participants will be asked to return to the Substrate Metabolism Laboratory on another occasion after a short fast (no food or beverages - besides water) for at least 6 hours. After participants arrive, participants will rest quietly for approximately 30 min. The investigators will then collect a blood sample from a vein in participants hand, or forearm. After obtaining a baseline blood sample, participants will exercise at a moderate intensity (on a treadmill or a stationary bike) for one hour. This one hour moderate exercise session will feel like a slow jog during which participants would be able to carry a conversation. In order for the investigators to measure energy expended and the amount of fat participants are burning during exercise, the investigators will periodically ask participants to breathe through a mouthpiece so the investigators can collect participants expired breath. After the exercise session the investigators will collect another blood sample from a vein in participants hand, or forearm.

Full description

General study design

  • Subjects who exercise regularly will be instructed to exercise exactly 3 days before the experimental trial, and then abstain from their exercise training program until after the experiment is complete.

  • Subjects will arrive to the Substrate Metabolism Laboratory (1210 CCRB) after at least a 6h fast.

  • After resting quietly in the laboratory for approximately 30min, Dr. Horowitz will collect a resting blood sample by venipuncture, as he has done in our other IRB approved protocols (e.g., HUM00029179). Briefly, Dr. Horowitz will wash his hands and put on gloves. The participant's skin will be disinfected at the venipuncture site with isopropyl alcohol. Single-use needles will be used for each participant and immediately discarded into a biohazard sharps container after use. After the blood draw, direct pressure will be applied to the site of needle insertion to avoid/reduce bruising and discomfort.

  • Subjects will exercise (bike or treadmill) for 1h at a moderate exercise intensity (approximately 65% of their predicted VO2peak). This moderate exercise intensity has been used extensively by Dr. Horowitz's laboratory in previous exercise testing and training studies in both lean and obese individuals, and is well tolerated by both populations.

    • During the exercise session, subjects will wear a heart rate monitor to ensure participants are exercising at the correct exercise intensity.
    • Subjects will also use the mouthpiece and nose clip (described above) for ~5min at the beginning, middle, and end of exercise to verify they are exercising at approximately 65% of their predicted VO2peak.
    • A study team member will be present with the participant at all times during exercise to ensure the comfort and safety.
  • Immediately after exercise another blood sample will be collected.

Enrollment

29 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: 18-40
  • Body Mass Index: 20-35 kg/m2
  • Women must have regularly occurring menses and must be premenopausal

Exclusion criteria

  • Pregnant or lactating
  • Evidence/history of cardiovascular or metabolic disease
  • Medications known to affect lipid or glucose metabolism

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

29 participants in 1 patient group

Exercise session
Other group
Description:
All subjects will exercise for 1 hour at a moderate intensity. There are no different arms in this study
Treatment:
Other: Exercise session

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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