Recovery Strategies After Simulated 400-meter Sprint in University AthletesARFRNCT07439523
Effect of Combined Active Recovery and Foam Rolling Enhance Lactate Clearance and Reduce Muscle Soreness Following a Simulated Running Competition
A study testing Active Recovery + Foam Rolling and Active Recovery Only in people with Recovery Strategies After Simulated 400-meter Sprint in University Athletes, run by Surabaya State University at 1 site in Indonesia.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 23 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Recovery Strategies After Simulated 400-meter Sprint in University Athletes
- What is being tested?
- Active Recovery + Foam Rolling and Active Recovery Only
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteIndonesia
- Study dates
- 18 Feb 2026to 19 Feb 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 23 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- 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
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country.
Indonesia1 site
Universitas Negeri Surabaya - Athletics Track
Surabaya, East Java
About this study
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.
Read more
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).
Read the 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.
- Being tested
- Active Recovery + Foam Rolling, Active Recovery Only
- Keywords
- Active Recovery, Foam Rolling, Blood Lactate, combination, Heart Rate, Muscle Soreness, Athletics, Quadriceps, Hamstring, Gastrocnemius, Track and Field
- Medical subject headings
- Myalgia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Active Recovery + Foam RollingBehavioural
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 OnlyBehavioural
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.
| Study group | Role | What they receive |
|---|---|---|
| Active Recovery + Foam Rolling | Experimental | Participants perform a 400-meter sprint followed by 5 minutes of active recovery (light jogging). Subsequently, participants in this group perform 10 minutes of foam rolling focusing 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. Receives: Behavioral: Active Recovery + Foam Rolling |
| Active Recovery Only | Active comparator | 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. Receives: Behavioral: Active Recovery Only |
What is being measured
The primary outcome is the main question the study is designed to answer.
Blood Lactate Concentration
Blood lactate will be measured using a finger-prick lactate analyzer immediately before and after the recovery protocol following a 400-meter sprint.
Measured: Pre-recovery and post-recovery (15 minutes)
Heart Rate
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.
Measured: Baseline, pre-exercise, and post-recovery (15 minutes after completion of recovery protocol)
Muscle Soreness VAS (Quadriceps, Hamstring, Gastrocnemius)
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.
Measured: Baseline, pre-exercise, post-recovery (15 minutes after completion of recovery protocol), 1 hour, 24 hours post-exercise
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Feb 2026
- Study start18 Feb 2026
- Primary completion19 Feb 2026
- Study completion19 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (6)Papers the sponsor has linked to this study.
- Other trials for Recovery Strategies After Simulated 400-meter Sprint in University AthletesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- 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.
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Surabaya State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Waristra Tyo Nirwansyah, Surabaya State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07439523
- Sponsor's protocol ID
- UNESA-ARFR-2026
- Acronym
- ARFR
- Status last verified
- May 2026
- First submitted
- 17 Feb 2026
- Last updated
- 7 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared due to the small sample size (n=20) and the sensitive nature of physiological and subjective measures, including blood lactate, heart rate, and muscle soreness scores. Data confidentiality and participant privacy will be strictly maintained
Publications
Konrad A, Nakamura M, Bernsteiner D, Tilp M. The Accumulated Effects of Foam Rolling Combined with Stretching on Range of Motion and Physical Performance: A Systematic Review and Meta-Analysis. J Sports Sci Med. 2021 Jul 1;20(3):535-545. doi: 10.52082/jssm.2021.535. eCollection 2021 Sep.
PubMed 34267594Pearcey GE, Bradbury-Squires DJ, Kawamoto JE, Drinkwater EJ, Behm DG, Button DC. Foam rolling for delayed-onset muscle soreness and recovery of dynamic performance measures. J Athl Train. 2015 Jan;50(1):5-13. doi: 10.4085/1062-6050-50.1.01. Epub 2014 Nov 21.
PubMed 25415413Hendricks S, Hill H, Hollander SD, Lombard W, Parker R. Effects of foam rolling on performance and recovery: A systematic review of the literature to guide practitioners on the use of foam rolling. J Bodyw Mov Ther. 2020 Apr;24(2):151-174. doi: 10.1016/j.jbmt.2019.10.019. Epub 2019 Nov 2.
PubMed 32507141D'Amico A, Paolone V. The Effect of Foam Rolling on Recovery Between two Eight Hundred Metre Runs. J Hum Kinet. 2017 Jun 22;57:97-105. doi: 10.1515/hukin-2017-0051. eCollection 2017 Jun.
PubMed 28713462Bibic E, Barisic V, Katanic B, Chernozub A, Trajkovic N. Acute Effects of Foam Rolling and Stretching on Physical Performance and Self-Perceived Fatigue in Young Football Players. J Funct Morphol Kinesiol. 2025 Jan 17;10(1):36. doi: 10.3390/jfmk10010036.
PubMed 39846677Wiewelhove T, Doweling A, Schneider C, Hottenrott L, Meyer T, Kellmann M, Pfeiffer M, Ferrauti A. A Meta-Analysis of the Effects of Foam Rolling on Performance and Recovery. Front Physiol. 2019 Apr 9;10:376. doi: 10.3389/fphys.2019.00376. eCollection 2019.
PubMed 31024339
Study at a glance
From the registry record, last updated by the sponsor on 7 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Combined Active Recovery and Foam Rolling Enhance Lactate Clearance and Reduce Muscle Soreness Following a Simulated Running Competition
- ClinicalTrials.gov ID
- NCT07439523
- Acronym / sponsor ID
- ARFR / UNESA-ARFR-2026
- Keywords
- Active Recovery, Foam Rolling, Blood Lactate, combination, Heart Rate, Muscle Soreness, Athletics, Quadriceps
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Surabaya State UniversityUniversity, hospital or other
- Study start
- 18 Feb 2026 (actual)
- Primary completion
- 19 Feb 2026 (actual)
- Study completion
- 19 Feb 2026 (actual)
- First posted
- 27 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- 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.
| Arm | Type | Receives |
|---|---|---|
| Active Recovery + Foam Rolling | Experimental | Behavioral: Active Recovery + Foam RollingParticipants perform a 400-meter sprint followed by 5 minutes of active recovery (light jogging). Subsequently, participants in this group perform 10 minutes of foam rolling focusing 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 | Active comparator | Behavioral: Active Recovery OnlyParticipants 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. |
Who may qualify
- Ages
- 18 to 23 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Active Recovery + Foam RollingParticipants 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. | Behavioural | Active Recovery + Foam Rolling |
| Active Recovery OnlyParticipants 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. | Behavioural | Active Recovery Only |
Primary outcome
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.
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.
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 May 2026.
- Background: PubMed 34267594Konrad A, Nakamura M, Bernsteiner D, Tilp M. The Accumulated Effects of Foam Rolling Combined with Stretching on Range of Motion and Physical Performance: A Systematic Review and Meta-Analysis. J Sports Sci Med. 2021 Jul 1;20(3):535-545. doi: 10.52082/jssm.2021.535. eCollection 2021 Sep.
- Background: PubMed 25415413Pearcey GE, Bradbury-Squires DJ, Kawamoto JE, Drinkwater EJ, Behm DG, Button DC. Foam rolling for delayed-onset muscle soreness and recovery of dynamic performance measures. J Athl Train. 2015 Jan;50(1):5-13. doi: 10.4085/1062-6050-50.1.01. Epub 2014 Nov 21.
- Background: PubMed 32507141Hendricks S, Hill H, Hollander SD, Lombard W, Parker R. Effects of foam rolling on performance and recovery: A systematic review of the literature to guide practitioners on the use of foam rolling. J Bodyw Mov Ther. 2020 Apr;24(2):151-174. doi: 10.1016/j.jbmt.2019.10.019. Epub 2019 Nov 2.
- Background: PubMed 28713462D'Amico A, Paolone V. The Effect of Foam Rolling on Recovery Between two Eight Hundred Metre Runs. J Hum Kinet. 2017 Jun 22;57:97-105. doi: 10.1515/hukin-2017-0051. eCollection 2017 Jun.
- Background: PubMed 39846677Bibic E, Barisic V, Katanic B, Chernozub A, Trajkovic N. Acute Effects of Foam Rolling and Stretching on Physical Performance and Self-Perceived Fatigue in Young Football Players. J Funct Morphol Kinesiol. 2025 Jan 17;10(1):36. doi: 10.3390/jfmk10010036.
- Background: PubMed 31024339Wiewelhove T, Doweling A, Schneider C, Hottenrott L, Meyer T, Kellmann M, Pfeiffer M, Ferrauti A. A Meta-Analysis of the Effects of Foam Rolling on Performance and Recovery. Front Physiol. 2019 Apr 9;10:376. doi: 10.3389/fphys.2019.00376. eCollection 2019.
- Individual participant dataSharing planned: No. Individual participant data will not be shared due to the small sample size (n=20) and the sensitive nature of physiological and subjective measures, including blood lactate, heart rate, and muscle soreness scores. Data confidentiality and participant privacy will be strictly maintained
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Active Recovery + Foam Rolling and Active Recovery Only in people with Recovery Strategies After Simulated 400-meter Sprint in University Athletes, run by Surabaya State University at 1 site in Indonesia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 7 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Indonesia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Blood Lactate Concentration (time frame: Pre-recovery and post-recovery (15 minutes)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07439523, which also lists 6 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 May 2026.