Recovery Following Acute Endurance Training (ETRec)

January 21, 2024 updated by: Chariklia K. Deli, University of Thessaly

Recovery Following Different Endurance Training Protocols in Middle- and Long-Distance Runners

Aerobic capacity is critical for many athletes, especially for endurance athletes. Althgough several training methods are implemented by coaches to improve endurance performance, recovery following acute endurance training is not adequately studied. However, such information is crucial for coaches to effectively design the most favorable training program, to avoid muscle injuries and overtraining, and ultimately to improve performance of their athletes. This study aims to examine the acute effect of different continuous and HIIT training protocols on indices of metabolism, EIMD, neuromuscular fatigue and performance in middle- and long-distance runners.

Study Overview

Detailed Description

Aerobic capacity is critical for many athletes, especially for endurance athletes. Endurance training leads to cardiopulmonary and musculoskeletal adaptations, which in turn lead to improvement of endurance performance. Several training methods have been established for the improvement of aerobic capacity and performance, including long distance and low speed training, and high intensity interval training (HIIT). Training methods are used depending on the kind of endurance that aim to improve, and the specific characteristics and energy demands of the event. Especially regarding middle- and long-distance runners, the energy comes mainly from the oxidative system, however, the contribution of the glycolytic pathway is equally important. Thus, improvement mainly of the low-intensity endurance, but also high-intensity endurance is important for these athletes. Additionally, both continuous endurance and HIIT are effective training methods for improving cardiorespiratory and metabolic function, and athletic performance, while evidence also exists in favor of HIIT being more effective. Thus both training methods are used by coaches to improve aerobic capacity and performance of their athletes.

Coaches should be careful regarding the frequency of HIIT training during a microcycle, to provide adequate recovery between training sessions to avoid muscle injuries and overtraining. Existing evidence suggests that endurance exercise (continuous or HIIT) may result in exercise-induced muscle damage (EIMD), inflammatory responses, oxidative stress, and performance deterioration, yet, the timeframe of recovery of physiological and biochemical indices following different endurance training protocols has not been adequately studied. However, such information is crucial for coaches to effectively design the most favorable training program for their athletes.

This study aims to examine the acute effect of different continuous and HIIT training protocols on indices of metabolism, EIMD, neuromuscular fatigue and performance in middle- and long-distance runners.

According to a preliminary power analysis (a probability error of 0.05, and a statistical power of 80%), a sample size of 8 subjects per group was considered appropriate in order to detect statistically meaningful changes between groups. Thus, 10 men and female middle- and long-distance runners, will participate in the study.

The study will be performed in a randomized, cross over, repeated measures design. During their first 1st and 2nd visit, all participants will sign an informed consent form after they will be informed about all the benefits and risks of the study and they will fill in and sign a medical history questionnaire. Fasting blood samples will be collected in order to estimate muscle damage concentration markers. Participants will be instructed by a dietitian how to record a 7-days diet recalls to ensure that they do not consume to greater extent nutrients that may affect EIMD and fatigue (e.g. antioxidants, amino acids, etc.) and to ensure that the energy intake during the trials will be the same. Assessment of body mass and body height, body composition, and aerobic capacity (VO2max), will be performed. Using a photocells system, countermovement jump will be performed to assess jump height, and 30 sec Bosco test to assess mean jump height, peak power, mean power, and fatigue index. The peak concentric, eccentric and isometric isokinetic torque of the knee flexors and extensors, in both limbs will be evaluated on an isokinetic dynamometer at 60°/sec. Maximal voluntary isometric contraction (MVIC) of the knee extensors at 65o in both limbs, as well as the fatigue rate during MVIC through the percent drop of peak torque between the first and the last three seconds of a 10-sec MVIC, will also be evaluated. Afterwards, participants will be randomly assigned into, and perform one of the three different conditions of the study design: a) Continuous running (CT) for 40 min at lactic threshold, b) High intensity interval training (HIIT): 10x2min running at vVO2max with active recovery at 40% της VO2max (interval:recovery 1:1) with a load of 10% of body weight (BW), and c) control condition, no training (measurements only). The training protocols will be matched for mean power and total duration (Tschakert and Hofmann 2013). Prior and immediately after each experimental trial, delayed onset of muscle soreness (DOMS) in the knee flexors (KF) and extensors (KE) of both limbs, as well as blood lactate will be assessed. Additionally, DOMS of KF and KE, peak concentric, eccentric and isometric isokinetic torque, CMJ height, as well as mean jump height, peak power, mean power, and fatigue index during a 30 sec Bosco test, will be assessed 24h, 48h and 72h after the end of the trial. MVIC of the knee extensors of both limbs, as well as the fatigue rate during MVIC will also be assessed at 1h, 2h and 3h, as well as 24h, 48h, and 72h after the end of the trial. Creatine kinase will be assessed at 24h, 48h, and 72h after the end of the trial. The exact above procedures will be repeated by the participants during the remaining two experimental trials. A 2-weeks wash-out period will be implemented between trials.

Study Type

Interventional

Enrollment (Actual)

10

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

    • Thessaly
      • Trikala, Thessaly, Greece, 42100
        • Department of Physical Education and Sport Science, Uninersity of Thessaly

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:

  • Middle- and long-distance runners
  • Absence of musculoskeletal injuries (≥ 6 months)
  • No use of drugs or ergogenic supplements (≥ 1 month)
  • Absense from eccentric exercise (≥ 3 days)
  • No alcohol or ergogenic drinks consumption before each training protocol

Exclusion Criteria:

  • Musculoskeletal injury (< 6 months)
  • Use of drugs or ergogenic supplements (< 1 month)
  • Participation in eccentric exercise (< 3 days)
  • Alcohol or ergogenic drinks consumption before the training protocol

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: Screening
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High Intensity Interval Training
The participants will perform an acute bout of high intensity interval training
10 x 2 min running at vVO2max, interspersed by 2 min recovery at 40% VO2max
Experimental: Coninuous Running
The participants will perform an acute bout of continuous running
40 min continuous running at lactate threshold
Other: Control Trial
The participants will not perform any endurance exercise protocol
The participants will perform only the baseline and post acute-training evaluations, without performing exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in blood lactate
Time Frame: Baseline (pre), 4 minutes post-trial
Lactate will be measured in capillary blood with a hand-portable analyzer.
Baseline (pre), 4 minutes post-trial
Changes in Creatine kinase (CK)
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
CK will be measured in plasma using a Clinical Chemistry Analyzer with commercially available kits.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in DOMS
Time Frame: Baseline (pre), post-, 24 hours post-, 48 hours post-, 72 hours post-trial
DOMS of knee extensors and knee flexors of both lower extremities will be measured during palpation of the muscle belly and the distal region after performing three repetitions of a full squat.
Baseline (pre), post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in squat jump height
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Squat jump height will be measured with a photocells system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean jump height during a 30 sec Bosco test
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Mean jump height will be measured with a photocells system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak power during a 30 sec Bosco test
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Peak power will be measured with a photocells system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in mean power during a 30 sec Bosco test
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Mean power will be measured with a photocells system.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in fatigue rate during a 30 sec Bosco test
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Fatigue rate will be estimated through the persent drop in mean jump height between the first 5 jumps and the last 5 jumps.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in maximal voluntary isometric contraction (MVIC)
Time Frame: Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial
MVIC of the knee extensors and knee flexors will be measured on an isokinetic dynamometer.
Baseline (pre), 1 hour post-, 2 hours post-, 3 hours post-, 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak concentric torque
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Concentric torque of the knee extensors and knee flexors will be measured on an isokinetic dynamometer.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Changes in peak eccentric torque
Time Frame: Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial
Eccentric torque of the knee extensors and knee flexors will be measured on an isokinetic dynamometer.
Baseline (pre), 24 hours post-, 48 hours post-, 72 hours post-trial

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body weight
Time Frame: Baseline
Body weight will be measured on a beam balance with stadiometer.
Baseline
Body height
Time Frame: Baseline
Body height will be measured on a beam balance with stadiometer.
Baseline
Body mass index (BMI)
Time Frame: Baseline
BMI will be calculated from the ratio of body mass/ body height squared.
Baseline
Body fat
Time Frame: Baseline
Body fat will be measured by using Dual-emission X-ray absorptiometry.
Baseline
Lean body mass
Time Frame: Baseline
Lean body mass will be measured by using Dual-emission X-ray absorptiometry.
Baseline
Dietary intake
Time Frame: Baseline
Dietary intake will be assessed using 7-day diet recalls.
Baseline
Maximal oxygen consumption (VO2max)
Time Frame: Baseline
VO2max will be measured by open circuit spirometry via breath by breath method during a graded treadmill running protocol.
Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Chariklia K Deli, PhD, University of Thessaly

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

September 30, 2023

Primary Completion (Actual)

December 15, 2023

Study Completion (Actual)

December 15, 2023

Study Registration Dates

First Submitted

September 17, 2023

First Submitted That Met QC Criteria

September 18, 2023

First Posted (Actual)

September 21, 2023

Study Record Updates

Last Update Posted (Actual)

January 23, 2024

Last Update Submitted That Met QC Criteria

January 21, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Endurance Training - Recovery

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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