- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06992271
- Original Trial
Comparing Two Eccentric Protocols on Muscle Damage
A Novel Eccentric Resistance Training Strategy to Maximize Exercise Induced Muscle Damage in Young Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants will come to the lab for 3 sessions, plus two email follow-up questionnaires.
Session 1 (45 minutes)
- Complete a demographic questionnaire
- Self-assess muscle soreness
- Walk on the treadmill to warm-up
- Maximal voluntary contraction on the chest press
- Two sets of eccentric (lowering) bench press at 75% of max
Session 2 (45 minutes)
- Walk on the treadmill to warm up
- Maximal voluntary contraction on the chest press
- Three sets of 10 eccentric contractions at 75% of max
- Repeat the maximal voluntary contraction on the chest press
Session 2 Follow-up Rate muscle soreness for each of the three days following Session 2 Answer open-ended questions about perceptions of the muscle soreness
Session 3 (45 minutes) Walk on the treadmill to warm up Maximal voluntary contraction on the chest press Three sets of 10 eccentric contractions at 75% of max Repeat the maximal voluntary contraction on the chest press
Session 3 Follow-up Rate muscle soreness for each of the three days following Session 2 Answer open-ended questions about perceptions of the muscle soreness
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Amerigo Rossi, Ed.D
- Phone Number: 516 686-3884
- Email: arossi01@nyit.edu
Study Locations
-
-
New York
-
Old Westbury, New York, United States, 11568
- Recruiting
- NYIT
-
Contact:
- Amerigo Rossi, EdD
- Phone Number: 516-686-3884
- Email: arossi01@nyit.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Sixteen young adults (ages 18-35) will be enrolled in this study.
- In order to be enrolled, they must have completed at least three months of resistance training in the past five years in order to minimize the learning effect and chance of injury.
Exclusion Criteria:
- Since regular resistance training reduces the primary outcomes, muscle damage and soreness, individuals who currently participate in chest press resistance training at least once per week will be excluded.
- Individuals who have musculoskeletal injuries in the shoulder, elbow or wrist that preclude pain-free resistance training, or who have underlying uncontrolled cardiovascular complications will also be excluded.
- Women who are pregnant, or may consider becoming pregnant over the subsequent 2 months, will be excluded
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Fast Eccentric
Participants will perform fast eccentric resistance training
|
Resistance training done quickly
|
|
Active Comparator: Slow eccentric
Participants will perform slow eccentric resistance training
|
Resistance training done slowly
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle soreness 1
Time Frame: 1 day
|
Visual analog scale as indirect indicator of muscle damage.
Scale of 1-5.
Higher score = more soreness
|
1 day
|
|
Muscle soreness 2
Time Frame: 2 days
|
Visual analog scale as indirect indicator of muscle damage.
Scale of 1-5.
Higher score = more soreness
|
2 days
|
|
Muscle soreness 3
Time Frame: 3 days
|
Visual analog scale as indirect indicator of muscle damage.
Scale of 1-5.
Higher score = more soreness
|
3 days
|
|
Maximal Voluntary Isometric Contraction Change
Time Frame: pre-intervention, immediately after the intervention
|
Change in MVIC will be used to indicated muscle damage.
|
pre-intervention, immediately after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amerigo Rossi, Ed.D, New York Institute of Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BHS-1835
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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