Resisted Training in Runners

February 19, 2026 updated by: Pablo Góngora Rodríguez, University of Cadiz

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

Completed

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Not Applicable

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

    • Andalusia
      • Cadiz, Andalusia, Spain, 11012
        • CD Atletismo Bahía de Cádiz

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

  • Adult

Accepts Healthy Volunteers

Yes

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

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

  • 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.
Experimental: Resisted Sprint
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.

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

This is where you will find people and organizations involved with this study.

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)

April 10, 2025

Primary Completion (Actual)

June 30, 2025

Study Completion (Actual)

August 31, 2025

Study Registration Dates

First Submitted

November 24, 2024

First Submitted That Met QC Criteria

December 6, 2024

First Posted (Actual)

December 11, 2024

Study Record Updates

Last Update Posted (Actual)

February 23, 2026

Last Update Submitted That Met QC Criteria

February 19, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All data about the study will be shared, while maintaining the confidentiality of the participants.

IPD Sharing Time Frame

All data will be available from the end of the study. And thereafter for a period of 10 years.

IPD Sharing Access Criteria

Access to the data will be granted to all researchers who request it by the appropriate means and always respecting the confidentiality of the participants' data.

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

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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