Skip to content

The Body's Response to Aerobic Versus Resistance Exercise

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00761163
Enrollment
25
Registered
2008-09-29
Start date
2007-02-28
Completion date
2008-11-30
Last updated
2013-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise

Keywords

The purpose of this study is to identify the body's response to aerobic vs. resistance exercise

Brief summary

The purpose of this study is to identify the body's response to aerobic vs. resistance exercise. Throughout this study, we will examine food intake, appetite, and physical and mental well-being before, during, and after aerobic and resistance exercise.

Interventions

OTHERResistance Exercise

The subjects will complete 2 resistive exercise sessions on non-consecutive days that will be supervised by our laboratory staff. The following exercises will be performed using the Keiser Sports Health equipment in Ismail Health, Exercise, and Nutrition Center: seated row, double leg press, seated leg curl, chest press, and leg extension. The subjects will individually perform 3 sets of 8-10 repetitions at an exercise intensity of 70% of pre-determined maximal strength for these exercises. Each repetition will be performed in a slow (six to eight seconds) uniform fashion, giving equal time to the concentric (muscle shortening) and eccentric (muscle lengthening) portions. One minute of rest will be allowed between sets. The last repetition of the third set of each exercise will be done to voluntary fatigue or the performance of 12 repetitions.

OTHERAerobic Exercise

The subjects will complete 2 aerobic exercise sessions on non-consecutive days that will also be supervised by our laboratory staff. The subjects will perform 45 minutes of aerobic exercise on a stationary bike at an exercise intensity of 70% of their heart-rate reserve.

The subjects will also complete 2 non-exercise sessions on non-consecutive days that will also be supervised by our laboratory staff. These sessions will consist of incorporating diversionary tasks throughout a 45 minute period consisting of a variety of motor and psychological tasks (tests of hand steadiness, alertness, optical illusions, mental acuity, etc.)

Sponsors

Purdue University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Body mass index between 18-29 kg/m2 * Weight stable (\< 4.5 kg weight change within last 6 months) * Non-smoking * Constant habitual activity patterns within last 3 months * Non-diabetic * Resistive exercise training (≥ 2 times a week) based on reported physical activity levels (questionnaire) * Aerobic exercise training (≥ 2 times a week, 30-min sessions) based on reported physical activity levels (questionnaire) * Confirmation of acceptability of eating the study test foods (macaroni casserole) * Approved to participate in this study by our study physician and principle investigator The older subjects must also meet the following eligibility criteria: * Age range: 65 years and older * Body fat (women: \<38%; men: \<28%) * Normal resting EKG as assessed by a Cardiologist The younger subjects must also meet the following eligibility criteria: * Age range: 18-29 years * Body fat (women: \<28%; men: \<18%)

Exclusion criteria

* Body mass index: outside of the 18-29 kg/m2 range * Gained or lost \> 4.5 kg within the last 6 months * Smoker (currently or within the last year) * Intermittently been involved in a diet and/or exercise program within the last 3 months * Clinically diagnosed as diabetic * Did not perform resistive exercise training (currently or within the last 3 months) based on reported physical activity levels (questionnaire) * Did not perform adequate aerobic exercise (currently or within the last 3 months) based on physical activity levels (questionnaire) * Study food is found to be unacceptable for consumption by the subject * Unapproved to participate in this study by our study physician and principle investigator The older subjects: * Age range: \<65 yrs * Body fat (women: \>38%; men: \>28%) * Abnormal resting EKG (interpreted by a cardiologist) and assessed (for study exclusion) by our study physician, Arthur Rosen, MD The younger subjects: * Age range: outside the \>29 yrs or \<18 yrs * Body fat (women: \>28%; men: \>18%)

Design outcomes

Primary

MeasureTime frame
Physical well being via electrocardiogram and body composition5-6 weeks
Mental well being via questionnaires5-6 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026