- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06729138
Resisted Training in Runners
Resisted Training in Runners. A Randomized Controlled Trial.
INTRODUCTION: Sprint training and resisted sprint training with sled has generated interest in the scientific literature due to its potential to improve performance, different studies have shown that incorporating strength training and sprints into studies have shown that the incorporation of strength and sprint training into the training programmes of long-distance runners can have significant training programmes for long-distance runners can have significant effects on running economy, anaerobic capacity of the runners and the anaerobic capacity of athletes, along with various neuromuscular adaptations. Despite these findings, the application of sprint and resisted sprint training with dragging in middle-distance and long-distance runners has been and long-distance runners has been scarcely studied, with most studies focusing on sprinters and athletes from team sports and sprinters, leaving a gap in the understanding of how these methods can influence distance runners. Along with how the intensity of external external loads affect this type of work and the influence on key kinetic variables such as vertical oscillation, contact time with the oscillation, ground contact time and muscle stiffness in this specific population.
PURPOSE: Analyse the effects that sprint training and resisted sprint training can have on running economy, force production, speed and various kinetics variables such as vertical oscillation, contact time, speed and vertical oscillation, ground contact time and muscle stiffness. MATERIAL AND METHODS: A randomised, longitudinal, prospective, blinded, assessor-blinded clinical trial will be conducted. Different variables related to sports performance will be evaluated, such as maximum oxygen consumption, critical power, heart rate variability or kinetic variables, among others.
kinetic variables among others. The evaluation will be carried out before the application of the training intervention and after two months. The study will be conducted with runners recruited through athletics clubs in the region of Cadiz, being randomly assigned a system of numerical tables using a computer programme between the sprint group (n=40) and the resisted sprint group (n=40). Both groups will perform two training sessions training sessions for eight weeks, consisting of sprint or resisted sprint repetitions based on the assigned group.
KEY WORDS: athletics, runners, resisted training, sprint.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Andalusia
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Cadiz, Andalusia, Spain, 11012
- CD Atletismo Bahía de Cádiz
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- At least 2 years of training experience as a runner.
- Do more than 30 kilometres per week.
- Perform at least 3 training sessions per week.
- Have competed in a 10km race or longer distance in the last 6 months.
- Be between 18 and 35 years old.
- Availability to attend the proposed training sessions.
Exclusion Criteria:
- Have a musculoskeletal injury or have had a musculoskeletal injury in the 6 months prior to the start of the study.
- Have chronic diseases.
- Have a BMI over 24.9.
- Combine training and competition in other disciplines other than running.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Sprint training
|
In this intervention, participants will perform 16 sessions of sprint training over eight weeks.
In these 16 sessions the intensity will vary in the distance.
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|
Experimental: Resisted Sprint
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In this intervention, participants will perform 16 sessions of resisted sprint training with external loads using a sled over eight weeks.
In these 16 sessions the intensity will vary in both the distance to be covered and the load to be moved.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
V02 max
Time Frame: Through study completion, an average of 10 weeks
|
VO2 Max (Maximum Oxygen Consumption) is the maximum amount of oxygen that an individual can utilize during intense or maximal exercise.
It is a key indicator of cardiovascular and aerobic fitness, reflecting the capacity of the heart, lungs, and muscles to deliver and use oxygen efficiently.
VO2 Max is typically measured in milliliters of oxygen consumed per kilogram of body weight per minute (ml/kg/min).
A higher VO2 Max value generally indicates better endurance performance.
|
Through study completion, an average of 10 weeks
|
|
Critical Power
Time Frame: Through study completion, an average of 10 weeks
|
Critical power (CP) is the maximum work intensity that an athlete can maintain consistently over a prolonged period of time.
|
Through study completion, an average of 10 weeks
|
|
Jump Height
Time Frame: Through study completion, an average of 10 weeks. In each training sesion.
|
This is the height reached in centimetres during the performance of the countermovement jump and the box jump. countermovement jump and jump from the box. Both tests and their respective jumping heights provide valuable information on the explosive and reactive strength capacity of the leg muscles. |
Through study completion, an average of 10 weeks. In each training sesion.
|
|
Heart Rate
Time Frame: Through study completion, an average of 10 weeks
|
Heart rate is measured in beats per minute (bpm) and is an important indicator of cardiovascular function and exercise intensity.
The maximum heart rate is the maximum number of heartbeats the heart can achieve per minute during maximum physical exertion.
It is an individual value, although there are different formulas for its calculation, it can vary significantly between trained and untrained individuals or by trained or untrained individuals or for other reasons.
|
Through study completion, an average of 10 weeks
|
|
Heart Rate Variability
Time Frame: Through study completion, an average of 10 weeks
|
Heart Rate Variability (HRV) is the variation in the time intervals between consecutive heartbeats, measured in milliseconds.
It reflects the ability of the autonomic nervous system (ANS) to adapt to changing physiological demands by balancing sympathetic ("fight or flight") and parasympathetic ("rest and digest") activity.
A higher HRV typically indicates greater cardiovascular and nervous system adaptability, resilience, and recovery, while a lower HRV may signal stress, fatigue, or decreased fitness.
HRV is often used as a marker for overall health, recovery, and readiness in both clinical and athletic contexts.
|
Through study completion, an average of 10 weeks
|
|
Stride Length
Time Frame: Through study completion, an average of 10 weeks
|
Stride length is the distance a runner covers with each step during a run.
It is measured from the point of contact of one foot to the point of contact of the same foot in the next step.
It is a key metric in the biomechanics of running and can significantly influence a runner's performance and efficiency.
|
Through study completion, an average of 10 weeks
|
|
Vertical oscillation
Time Frame: Through study completion, an average of 10 weeks
|
Vertical oscillation in the context of running biomechanics refers to the upward and downward movement of the body's centre of mass during the running cycle.
This vertical motion is a natural component of the running movement pattern and It occurs as a result of the complex interaction between momentum forces and gait dynamics.
|
Through study completion, an average of 10 weeks
|
|
Contact time
Time Frame: Through study completion, an average of 10 weeks
|
Contact time in biomechanical running terms refers to the period of time a runner's foot is in contact with the ground during each stride cycle.
|
Through study completion, an average of 10 weeks
|
|
Perceived exertion
Time Frame: In each training session through study completion, an average of 10 weeks
|
Perceived exertion refers to an individual's subjective perception of the intensity or difficulty of a physical activity.
|
In each training session through study completion, an average of 10 weeks
|
|
Body Mass Index (BMI)
Time Frame: Through study completion, an average of 10 weeks
|
Body Mass Index (BMI) is a numerical value calculated by dividing a person's weight in kilograms by the square of their height in meters (kg/m²).
It is a widely used screening tool to categorize individuals into weight categories such as underweight, normal weight, overweight, or obese, based on their body composition.
Although BMI does not directly measure body fat percentage, it provides a general indication of whether a person's weight is appropriate for their height and is commonly used in public health and clinical settings.
|
Through study completion, an average of 10 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PGR0001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
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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