- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07127211
- Original Trial
Angle-Specific Upper and Lower Body Muscle Activation in Suspension Training
August 15, 2025 updated by: TSUNG-LIN CHIANG
Angle-Specific Upper and Lower Body Muscle Activation in Suspension Push-Ups: An Electromyographic Analysis Across Different Body Angles
The study aims to compare differences in muscle activation during push-ups performed at five body angles using different suspension methods.
The investigators will recruit 20 healthy men with resistance-training experience.
Each participant will perform push-ups under three suspension conditions (no suspension, hands suspended, and feet suspended) at +30°, +15°, 0°, -15°, and -30°.
For each angle, participants will complete five repetitions with 3-5 minutes of rest between angles; at least 48 hours will separate suspension conditions.
Surface electromyography (EMG) will record activity of the pectoralis major, anterior deltoid, triceps brachii, upper trapezius, and serratus anterior.
EMG amplitudes will be normalized to maximal voluntary isometric contraction (%MVIC).
Data will be analyzed using a repeated-measures two-way ANOVA to test the effects of suspension type and angle on muscle activation.
The a priori hypothesis is that feet-suspended push-ups will elicit greater activation than other conditions, and that lower body angles will be associated with higher activation levels.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
26
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Taipei City, Taiwan, 11114
- Chinese Culture University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Healthy male adults with at least 3 months of regular resistance-training experience, capable of independently performing a standard push-up with proper form.
Participants will be recruited from university sports facilities and local fitness centers through flyers, online announcements, and word of mouth.
Description
Inclusion Criteria:
- Healthy male adults with ≥3 months of regular resistance-training experience.
- Able to independently perform a standard push-up with proper form.
- Willing to follow pre-session restrictions (e.g., avoid strenuous exercise within 24 h) and provide written informed consent.
Exclusion Criteria:
- Physician-diagnosed cardiovascular disease, musculoskeletal disorders, chronic pulmonary disease, or arthritis.
- Major surgery or severe injury within the past 12 months that affects physical activity.
- Current pain, injury, or functional limitation of the upper or lower limbs or trunk that would interfere with push-up performance.
- Any medical condition judged by the investigators to make participation unsafe.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Activation (%MVIC) of Upper Body Muscles During Suspension and Stable Push-Ups at Different Angles
Time Frame: Baseline measurement during each exercise condition within 4 weeks of study start
|
Surface electromyography (EMG) will measure the root mean square (RMS) activity of the pectoralis major, anterior deltoid, triceps brachii, upper trapezius, and serratus anterior during push-ups performed under three suspension conditions (no suspension, hands suspended, feet suspended) at five body angles (+30°, +15°, 0°, -15°, -30°).
RMS values will be normalized to maximal voluntary isometric contraction (%MVIC).
Comparisons will be made using repeated-measures two-way ANOVA to determine the effects of suspension condition and angle on muscle activation.
|
Baseline measurement during each exercise condition within 4 weeks of study start
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 3, 2019
Primary Completion (Actual)
November 22, 2019
Study Completion (Actual)
November 22, 2019
Study Registration Dates
First Submitted
August 11, 2025
First Submitted That Met QC Criteria
August 11, 2025
First Posted (Actual)
August 17, 2025
Study Record Updates
Last Update Posted (Actual)
August 20, 2025
Last Update Submitted That Met QC Criteria
August 15, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- No. 10711HS080
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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