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NCT Number: NCT07547566

Recovery After Fatigue in Young Athletes: Comparison Between TECAR Therapy and Cycle Ergometer"

The goal of this clinical trial is to compare two recovery methods after fatigue in young athletes. It aims to find out if tecar therapy (TECAR) or cycle ergometer exercise can improve recovery after intense physical activity and help athletes return to their normal performance more quickly.

The main questions it aims to answer are:

Does TECAR or cycle ergometer improve physical performance after fatigue?

Do these methods reduce muscle pain and soreness after fatigue?

Researchers will compare TECAR with active recovery using a cycle ergometer to see which method is more effective.

Participants will:

Perform a series of jumps to induce fatigue

Be randomly assigned to one of the recovery methods

Complete physical tests before and after fatigue

Undergo simple measurements of muscle condition and pain

Report their level of effort and muscle soreness

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physiobalance

Córdoba, 14011, Spain

Location status: Recruiting

Location contact

Lourdes García Luque, PhD PT

CONTACT

[email protected]

+34627366324

Lourdes García Luque, PhD PT

SUB_INVESTIGATOR

Sandra Alcaraz Clariana, PhD PT

CONTACT

[email protected]

+34625434043

Sandra Alcaraz Clariana, PhD PT

PRINCIPAL_INVESTIGATOR

About this study

This study is a randomized controlled trial designed to evaluate and compare the effectiveness of two recovery strategies following exercise-induced fatigue in young athletes: tecar therapy (TECAR) and active recovery (usual care) using a cycle ergometer.

Exercise-induced fatigue can reduce physical performance and increase muscle soreness, which may negatively affect athletic performance and increase injury risk. This study aims to compare the effects of two commonly used recovery strategies on physical performance, muscle mechanical properties, and perceived recovery.

Participants will be physically active young athletes over 18 years of age, familiar with plyometric or jump-based activities. They will be recruited through convenience sampling. Individuals with recent musculoskeletal injuries or those who have performed intense physical exercise within 24 hours prior to testing will be excluded.

All procedures will be conducted in a controlled environment by trained personnel following a standardized protocol. After providing informed consent, participants will undergo baseline assessments, including physical performance tests, measurements of muscle mechanical properties, and subjective perception of effort and muscle soreness.

A standardized warm-up will be performed prior to testing, consisting of low-intensity aerobic activity for approximately five minutes, aiming to reach a moderate level of perceived exertion.

Participants will then complete a fatigue protocol consisting of repeated drop jumps from a fixed height of approximately 0.6 meters. The protocol will be organized into multiple sets with controlled rest intervals between repetitions and sets in order to induce acute neuromuscular fatigue in a standardized manner.

Immediately after the fatigue protocol, the same assessments will be repeated to evaluate the acute effects of fatigue.

Participants will then be randomly assigned to one of the two recovery interventions:

TECAR: application of capacitive and resistive electric transfer using radiofrequency energy for 20 minutes

Active recovery (usual care): continuous cycling on a cycle ergometer at low-to-moderate intensity for 20 minutes, reflecting standard recovery practices commonly used in athletic settings

Following the assigned recovery intervention, all assessments will be repeated to evaluate recovery effects.

In addition, subjective measures of muscle soreness and perceived effort will be collected at 12 and 24 hours after the intervention to assess short-term recovery.

Outcome measures will include objective indicators of physical performance and muscle mechanical properties, assessed using a handheld myotonometer, as well as pressure pain threshold (a measure of sensitivity to pressure), and subjective measures related to perceived effort and muscle soreness.

Statistical analysis will include descriptive statistics and inferential analysis to compare differences between groups and over time. A two-way analysis of variance (group × time) will be used to evaluate the effects of the recovery intervention and measurement time points, including potential interaction effects. Statistical significance will be set at p < 0.05.

This study aims to provide evidence on the comparative effectiveness of TECAR and active recovery strategies, contributing to the optimization of recovery protocols in athletic populations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18 years or older
  • Engaging in regular physical activity
  • Experience with sports involving jumping or plyometric exercises

Exclusion criteria

  • Performed intense physical exercise within 24 hours before the study
  • Planned to perform intense physical exercise within 24 hours after the study
  • Presence of muscle soreness at the beginning of the study
  • Musculoskeletal injury in the previous 6 months

Treatment and study plan

Tecar therapy (capacitive mode)

Device

TECAR is applied using capacitive radiofrequency energy for 20 minutes following a standardized fatigue protocol. The intervention is delivered using capacitive mode only, combining manual mobile application and fixed automatic application over the quadriceps region to promote recovery after exercise-induced fatigue.

Other names: Capacitive and resistive electric transfer therapy. Radiofrequency therapy

Active recovery using cycle ergometer

Behavioral

Active recovery consists of continuous cycling on a cycle ergometer for 20 minutes at low intensity, not exceeding 2-3 on a 0-10 rating of perceived exertion scale. This intervention is performed after a standardized fatigue protocol and reflects common recovery practices in athletic settings.

Other names: Low-intensity cycling exercise

Primary outcomes

  1. Countermovement jump height

    Time frame: Baseline (after warm-up), immediately after fatigue protocol, and immediately after intervention (20 minutes).

    Vertical jump performance will be assessed using a countermovement jump test. Jump height will be measured using a validated mobile application after three attempts, and the mean value will be recorded.

Secondary outcomes

  1. Muscle mechanical properties

    Time frame: Baseline (after warm-up), immediately after fatigue protocol, and immediately after intervention (20 minutes).

    Muscle mechanical properties will be assessed using a handheld myotonometer. Parameters will include muscle tone and stiffness measured at standardized anatomical locations of the rectus femoris, vastus lateralis, medial gastrocnemius, and lateral gastrocnemius.

  2. Pressure pain threshold

    Time frame: Baseline (after warm-up), immediately after fatigue protocol, and immediately after intervention (20 minutes).

    Pressure pain threshold will be assessed using a handheld algometer. Measurements will be performed at standardized anatomical locations of the rectus femoris, vastus lateralis, and medial gastrocnemius, and the mean of repeated measurements will be recorded.

  3. Rating of perceived exertion

    Time frame: Baseline (after warm-up), immediately after fatigue protocol, immediately after intervention (20 minutes), 12 hours, and 24 hours.

    Perceived exertion will be assessed using a 0-10 rating scale, where higher values indicate greater perceived effort.

  4. Delayed-onset muscle soreness.

    Time frame: Baseline (after warm-up), 12 hours, and 24 hours.

    Delayed-onset muscle soreness (DOMS) will be assessed using a 0-10 numeric rating scale, where 0 indicates no muscle soreness and 10 indicates the worst possible muscle soreness.

Study contacts

Contact information is provided by the study sponsor or research team.

Lourdes García Luque, PhD PT

CONTACT

[email protected]

+34627366324

Sandra Alcaraz Clariana, PhD PT

CONTACT

[email protected]

+34625434043

Sponsors and collaborators

Lead sponsor

Maimónides Biomedical Research Institute of Córdoba

Other

Registry information

Official study title

Immediate and Short-term Effects of TECAR Therapy and Cycle Ergometer on Recovery After Fatigue in Young Athletes: a Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 23, 2026
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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