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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07439523
Acronym
ARFR
Enrollment
20
Registered
2026-02-27
Start date
2026-02-18
Completion date
2026-02-19
Last updated
2026-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recovery Strategies After Simulated 400-meter Sprint in University Athletes

Keywords

Active Recovery, Foam Rolling, Blood Lactate, combination, Heart Rate, Muscle Soreness, Athletics, Quadriceps, Hamstring, Gastrocnemius, Track and Field

Brief summary

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).

Detailed description

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.

Interventions

BEHAVIORALActive Recovery + Foam Rolling

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.

BEHAVIORALActive Recovery Only

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.

Sponsors

Surabaya State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants were blinded to group allocation; only investigators were aware. Randomization was performed prior to the study day. On the day of testing, participants completed a 400-meter sprint followed by 5 minutes of active recovery. Subsequently, participants in the experimental group were called to perform foam rolling, while control participants continued active recovery only.

Intervention model description

Participants will be randomly assigned to one of two groups: Experimental group (Active Recovery + Foam Rolling) or Control group (Active Recovery only). Each participant will perform a simulated 400-meter sprint. Blood lactate will be measured pre- and post-recovery using a finger-prick lactate analyzer. Heart rate will be recorded at baseline, pre-exercise, and post-recovery using a Polar H-10. Muscle soreness of the quadriceps, hamstring, and gastrocnemius will be assessed using a visual analog scale (0-10) at baseline, pre-exercise, post-recovery, 1 hour, and 24 hours post-exercise. All procedures will be conducted at the Athletics Track, State University of Surabaya, Indonesia.

Eligibility

Sex/Gender
MALE
Age
18 Years to 23 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Blood Lactate ConcentrationPre-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.
Heart RateBaseline, 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.
Muscle Soreness VAS (Quadriceps, Hamstring, Gastrocnemius)Baseline, pre-exercise, post-recovery (15 minutes after completion of recovery protocol), 1 hour, 24 hours post-exerciseMuscle 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.

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026