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Completed

NCT Number: NCT07439523

Effect of Combined Active Recovery and Foam Rolling Enhance Lactate Clearance and Reduce Muscle Soreness Following a Simulated Running Competition

This study investigates the effects of combining Active Recovery (AR) and Foam Rolling (FR) on blood lactate, heart rate, and muscle soreness in competitive 400-meter sprint athletes. Twenty healthy athletes will be randomly assigned to one of two groups:

Experimental group: Active Recovery + Foam Rolling Control group: Active Recovery only All participants will perform a simulated 400-meter sprint. Following the sprint, both groups perform 5 minutes of light jogging (Active Recovery). Subsequently, participants in the experimental group will perform 10 minutes of foam rolling on the quadriceps, hamstring, and gastrocnemius muscles.

Measurements include:

Blood lactate: pre- and post-recovery Heart rate: baseline, pre-exercise, post-recovery Muscle soreness (VAS 0-10): quadriceps, hamstring, gastrocnemius at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours post-exercise The study aims to determine whether adding foam rolling to active recovery improves post-exercise physiological and perceptual recovery markers. Participants will not be informed of their group assignment to reduce bias; only the investigators will know.

All procedures will take place at the Athletics Track, Surabaya State University, Indonesia.

Ethical approval has been obtained from Komite Etik Penelitian Kesehatan STIKES Guna Bangsa Yogyakarta (Ethical Approval No: 009/KEPK/II/2026).

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Key information

Age range

18 year–23 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Universitas Negeri Surabaya - Athletics Track

Surabaya, East Java, Indonesia

About this study

Background:

Recovery strategies are crucial in sprinting to restore physiological homeostasis, reduce muscle fatigue, and prevent injury. Active recovery (AR) through light jogging has been shown to facilitate lactate clearance and maintain cardiovascular stability. Foam rolling (FR) has recently gained popularity as a self-myofascial release technique, potentially enhancing recovery by improving blood flow, reducing muscle stiffness, and decreasing perceived soreness. However, evidence in competitive 400-meter sprint athletes remains limited.

Study Design:

This study is a randomized controlled trial with two parallel arms. Twenty competitive 400-meter sprint athletes will be recruited and randomized into:

Experimental group: AR + FR Control group: AR only Randomization will occur prior to the study day. Participants will remain blinded to their group allocation, ensuring unbiased outcome assessment. On the study day, participants perform a 400-meter sprint. Afterward, both groups perform 5 minutes of light jogging (AR). Then, participants in the experimental group continue with 10 minutes of foam rolling on key lower limb muscles (quadriceps, hamstring, gastrocnemius).

Outcome Measures:

Primary Outcomes:

Blood lactate (mmol/L), pre- and post-recovery Heart rate (bpm), baseline, pre-exercise, post-recovery

Secondary Outcomes:

Muscle soreness (VAS 0-10), assessed in quadriceps, hamstring, and gastrocnemius at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours

Procedures:

Lactate measured via finger-prick using a lactate analyzer Heart rate recorded using Polar H-10 chest strap monitor Muscle soreness assessed using standardized VAS

Study Location:

All procedures will take place at Athletics Track, Surabaya State University, Indonesia.

Ethical Considerations:

This study has received ethical approval from Komite Etik Penelitian Kesehatan STIKES Guna Bangsa Yogyakarta (009/KEPK/II/2026). Participants will provide written informed consent prior to enrollment.

Significance:

This study will provide evidence on whether adding foam rolling to active recovery enhances physiological and perceptual recovery markers in sprint athletes, potentially informing best practices in sprint training and competition recovery protocols.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male university athletes specializing in 400-meter sprint.
  • Age between 18 and 23 years.
  • Currently training regularly and free from musculoskeletal injuries.
  • Willing to provide written informed consent

Exclusion criteria

  • History of cardiovascular, metabolic, or musculoskeletal disorders.
  • Use of performance-enhancing drugs or supplements in the past 3 months.
  • Inability to perform maximal sprint due to injury or other medical conditions.
  • Refusal or inability to provide written informed consent.

Treatment and study plan

Active Recovery + Foam Rolling

Behavioral

Participants perform a 400-meter sprint followed by 5 minutes of active recovery (light jogging). Subsequently, participants perform 10 minutes of foam rolling on quadriceps, hamstring, and gastrocnemius muscles. Blood lactate is measured pre- and post-recovery. Heart rate is recorded at baseline, pre-exercise, and post-recovery using a chest strap monitor. Muscle soreness is assessed using a visual analog scale (0-10) at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours post-exercise.

Active Recovery Only

Behavioral

Participants perform a 400-meter sprint followed by 5 minutes of active recovery (light jogging) only. Blood lactate is measured pre- and post-recovery. Heart rate is recorded at baseline, pre-exercise, and post-recovery using a chest strap monitor. Muscle soreness is assessed using a visual analog scale (0-10) at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours post-exercise.

Primary outcomes

  1. Blood Lactate Concentration

    Time frame: Pre-recovery and post-recovery (15 minutes)

    Blood lactate will be measured using a finger-prick lactate analyzer immediately before and after the recovery protocol following a 400-meter sprint.

  2. Heart Rate

    Time frame: Baseline, pre-exercise, and post-recovery (15 minutes after completion of recovery protocol)

    Heart rate will be recorded using a Polar H-10 chest strap monitor at baseline, immediately before the sprint, and immediately after the recovery protocol.

  3. Muscle Soreness VAS (Quadriceps, Hamstring, Gastrocnemius)

    Time frame: Baseline, pre-exercise, post-recovery (15 minutes after completion of recovery protocol), 1 hour, 24 hours post-exercise

    Muscle soreness will be assessed using a visual analog scale (0-10) for quadriceps, hamstring, and gastrocnemius muscles at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours post-exercise.

Sponsors and collaborators

Lead sponsor

Surabaya State University

Other

Registry information

Acronym: ARFR

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 27, 2026
Registry last updated
May 7, 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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