- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06378762
Interference of Endurance Training on Strength Development and Neuromuscular Adaptations
This study aims to find out if performing combined strength and endurance exercise in the same program (called concurrent training-CT) leads to similar long-term improvements in neuromuscular function as doing each type of exercise separately. The main questions it seeks to answer are:
Does performing CT result in similar improvements in strength and power as doing just strength training? Does performing CT result in similar improvements in cardiorespiratory fitness as doing just endurance training? Are neuromuscular adaptations similar between CT and just strength training? Researchers will compare the results between three groups: the CT group, the endurance training group (E), and the strength training group (S) to answer these questions.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study looks at how different types of exercise affect neuromuscular and cardiorespiratory improvements over time. It aims to see how combining strength and endurance training (concurrent training - CT) affects neuromuscular and cardiorespiratory adaptations compared to doing just strength or endurance training. Participants who regularly do both types of exercise will be split into three groups: Concurrent training (CT), endurance training (E), or strength training (S) and will be involved in 11 weeks of supervised training, three days a week:
Endurance training involves 30 minutes of continuous running, three days a week, at an intensity corresponding to the heavy domain (between the first and second ventilatory threshold) Strength training includes weightlifting three days a week, focusing on building both strength and power.
Concurrent training incorporates both strength and endurance exercises in the same session, three days a week, with strength training being executed prior to endurance training.
Researchers will collect data at three time-points during the 11 weeks: before starting the program (Baseline), at the end of week 5 (Week 5), and at the end of the program (Week 11). Measurements include lower-body strength and power, aerobic capacity, nerve evoked responses, and muscle structure if the quadriceps femoris.
Researchers will then compare the CT, E, and S groups at each measurement point to see which type of training elicited the best adaptations for the different neuromuscular and cardiorespiratory outcomes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Cruz Quebrada - Dafundo
-
Lisboa, Cruz Quebrada - Dafundo, Portugal, 1499-002
- Faculdade de Motricidade Humana - Universidade de Lisboa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Active training status (strength and endurance (running) exercise at least 2 times per week over the last three months prior to inclusion in the study)
Exclusion Criteria:
- Active smoking status
- Orthopedic injuries
- On medication
- Known cardiovascular or respiratory disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Endurance
|
30 minutes of running at an intensity corresponding to the heavy-domain (between the first and second ventilatory thresholds)
|
|
Experimental: Strength
|
Combination of strength and power exercises Weeks 1-5 focus on building maximal strength Weeks 6-11 focus on maintaining maximal strength and improve muscle power
|
|
Experimental: Concurrent
|
Combining both strength and endurance training programs, with strength preceding endurance, incorporating a 20-min rest period between each modality
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Surface EMG
Time Frame: Baseline, Week 5, Week 11
|
Using surface electromyography (EMG), the muscle activation of the plantarflexors muscles will me assessed, as well as the quadriceps femoris during the leg press and back squat exercise
|
Baseline, Week 5, Week 11
|
|
H-reflex excitability
Time Frame: Baseline, Week 5, Week 11
|
Using percutaneous electrostimulation of the tibial nerve, spinal reflex excitability will be explored by assessing H-reflex evoked responses
|
Baseline, Week 5, Week 11
|
|
V-wave
Time Frame: Baseline, Week 5, Week 11
|
Using percutaneous electrostimulation of the tibial nerve, neural drive to the active muscle will be assessed by measuring V-wave amplitudes
|
Baseline, Week 5, Week 11
|
|
Maximal Isometric Strength
Time Frame: Baseline, Week 5, Week 11
|
Maximal voluntary isometric strength of the plantarflexors and leg press exercise in Newtons
|
Baseline, Week 5, Week 11
|
|
Maximal Dynamic Strength
Time Frame: Baseline, Week 5, Week 11
|
Maximal dynamic strength on the back squat exercise in kilograms lifted
|
Baseline, Week 5, Week 11
|
|
Lower Body Muscle Power
Time Frame: Baseline, Week 5, Week 11
|
Lower body muscle power in watts will be assessed during countermovement jumps
|
Baseline, Week 5, Week 11
|
|
Muscle fascicle length
Time Frame: Baseline, Week 5, Week 11
|
Fascicle length of the vastus lateralis muscles in centimeters
|
Baseline, Week 5, Week 11
|
|
Muscle fascicle pennation angle
Time Frame: Baseline, Week 5, Week 11
|
Pennation angle of the vastus laterais fascicles, in degrees
|
Baseline, Week 5, Week 11
|
|
Muscle thickenss
Time Frame: Baseline, Week 5, Week 11
|
Muscle thickenss of the vastus lateralis, in centimeters
|
Baseline, Week 5, Week 11
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
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
Other Study ID Numbers
- 6/2021
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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