BasketballNCT07899619
Recovery Modalities and Application Sequence in Elite Female Basketball Players
A study testing Intermittent Pneumatic Compression (IPC), Local Heat and Mechanical Vibration (Venom 2 Leg) and Passive Rest in people with Basketball and Basketball Performance, run by Medipol University at 1 site in Turkey (Türkiye).
Trial summary
The purpose of this study is to compare the effects of intermittent pneumatic compression, local heat, and mechanical vibration applications on recovery following high-intensity anaerobic exercise in elite female basketball players. Read more about this study
- Who is it for?
- Ages 18 to 35 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Basketball, Basketball Performance, Recovery
- What is being tested?
- Intermittent Pneumatic Compression (IPC), Local Heat and Mechanical Vibration (Venom 2 Leg) and Passive Rest
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 45 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Aug 2026to 1 Nov 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 35 years
- Women only
- Healthy volunteers accepted
- Adult
Inclusion Criteria Female athletes aged 18-30 years. Being an active, licensed elite or professional female basketball player. Having played basketball regularly for at least 3 years. Being in the early follicular phase (days 2-5) of the menstrual cycle on the day of evaluation.
No history of severe lower extremity musculoskeletal injury or surgical operation in the last 6 months.
No regular use of medications that may affect physical performance or cardiometabolic responses.
Volunteering to participate in the study. Exclusion Criteria History of cardiovascular, neurological, or metabolic disease. Having experienced a lower extremity injury or undergone any surgical operation in the last 6 months.
Failure to comply with the pre-test restrictions (exercise, caffeine, alcohol, etc.) prior to the testing day.
Use of anticoagulant (blood thinner) medications or pregnancy. Presence of acute infection or delayed onset muscle soreness (DOMS) on the test day.
Occurrence of an injury during the study or emergence of any health problem that prevents continued participation.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Turkey (Türkiye)1 site
Istanbul Medipol University
Istanbul, Kavacık, 34810
About this study
Official title: The Effect of Application Sequence of Recovery Modalities on Blood Lactate and Acute Recovery in Elite Female Basketball Players
The purpose of this study is to compare the effects of intermittent pneumatic compression, local heat, and mechanical vibration applications on recovery following high-intensity anaerobic exercise in elite female basketball players. Recovery levels of the athletes will be evaluated through blood lactate concentration, countermovement jump performance, perceived recovery status, and perceived muscle soreness. The study will compare the effects of different recovery application sequences on post-exercise recovery indicators.
Read the detailed description
High-intensity anaerobic exercise, especially in sports such as basketball involving repetitive sprints, jumps, and high-intensity efforts, can cause temporary fatigue and performance decrements following exercise. Accelerating post-exercise recovery is crucial for enabling athletes to become physically prepared for subsequent training sessions or competitions. Various physical recovery modalities are utilized to support recovery in athletes. Intermittent pneumatic compression is a method aimed at supporting circulation by applying controlled pressure to the extremities, contributing to the clearance of metabolic load accumulated after exercise. Local heat and mechanical vibration application aims to facilitate the recovery process by generating thermal and mechanical stimulation in the targeted region. However, further research is required to compare the effects of these two distinct modalities on recovery indicators following high-intensity anaerobic exercise. This study aims to examine the responses of elite female basketball players to different recovery applications following high-intensity anaerobic exercise. Changes during the recovery process will be monitored using biochemical, performance-based, and subjective evaluation measures. Thus, the potential effects of different physical recovery methods during post-exercise recovery will be evaluated comparatively. The findings obtained from this study are expected to contribute to the evaluation of recovery strategies applicable to elite female basketball players following high-intensity exercise, as well as to practices supporting athlete health and performance.
- Conditions
- Basketball, Basketball Performance, Recovery, Recovery After Exercise
- Being tested
- Intermittent Pneumatic Compression (IPC), Local Heat and Mechanical Vibration (Venom 2 Leg), Passive Rest
- Keywords
- Recovery, Basketball, Exercise, Sports
- Medical subject headings
- Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Intermittent Pneumatic Compression (IPC)Device
Intermittent pneumatic compression will be applied following high-intensity anaerobic exercise using the Jobst compression device. The application will be performed on the lower extremities at a pressure of 80 mmHg for a total duration of 15 minutes. The standard intermittent pneumatic compression program of the device will be utilized during the procedure.
Local Heat and Mechanical Vibration (Venom 2 Leg)Device
Local heat and mechanical vibration will be applied to both lower extremities following high-intensity anaerobic exercise using the Venom device. The application will last for a total duration of 15 minutes. Local heat will be administered at a medium level, and mechanical vibration will be applied using Mode 1 of the device.
Passive RestOther
Participants will rest in a supine position for 30 minutes.
| Study group | Role | What they receive |
|---|---|---|
| Jobst-Venom Group | Experimental | Athletes in this group will undergo two consecutive recovery applications following the high-intensity anaerobic exercise protocol. First, intermittent pneumatic compression will be applied for 15 minutes, after which blood lactate concentration will be measured. This will be immediately followed by 15 minutes of local heat and mechanical vibration application. All procedures will be performed in accordance with the durations and standardized conditions specified in the study protocol. Recovery indicators will be evaluated at predetermined measurement time points before and after the applications. Receives: Device: Intermittent Pneumatic Compression (IPC); Device: Local Heat and Mechanical Vibration (Venom 2 Leg) |
| Venom-Jobst Group | Experimental | Athletes in this group will undergo two consecutive recovery applications following the high-intensity anaerobic exercise protocol. First, local heat and mechanical vibration will be applied for 15 minutes, after which blood lactate concentration will be measured. This will be immediately followed by 15 minutes of intermittent pneumatic compression application. All procedures will be performed in accordance with the durations and standardized conditions specified in the study protocol. Recovery indicators will be evaluated at predetermined measurement time points before and after the applications. Receives: Device: Intermittent Pneumatic Compression (IPC); Device: Local Heat and Mechanical Vibration (Venom 2 Leg) |
| Passive Rest | Placebo comparator | Participants in this group will rest passively in a supine position for 30 minutes instead of receiving intervention applications. No recovery modality will be applied during the passive rest period. Receives: Other: Passive Rest |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Post-Exercise Blood Lactate Concentration
Blood lactate measurement performed using a portable blood lactate analyzer from capillary blood samples obtained via fingertip puncture to evaluate the metabolic efficacy of recovery modalities following high-intensity anaerobic exercise (RAST). Measurement results are expressed in mmol/L.
Measured: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Secondary outcomes (3)
Lower Extremity Neuromuscular Performance (CMJ)
A vertical jump test conducted to evaluate lower extremity neuromuscular performance. Participants are asked to perform a maximum vertical jump with their hands on their hips. The average jump height of three trials is recorded in centimeters (cm).
Measured: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Perceived Recovery Status (PRS)
A single-item 0-10 point scale evaluating the subjective recovery level of athletes (0 = Very poorly recovered / Extremely tired, 10 = Completely recovered / Very well rested). Higher scores indicate better recovery status.
Measured: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Perceived Muscle Soreness (VAS)
A 10-cm visual analog scale evaluating the level of perceived lower extremity muscle soreness following exercise. 0 cm indicates 'no pain' and 10 cm indicates 'unbearable pain.
Measured: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Oct 2026
- Study start1 Aug 2026
- Primary completion30 Oct 2026 (estimated)
- Study completion1 Nov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for BasketballStudies of the same condition, open and under way.
- More trials run by Medipol UniversityThe sponsor's other registered studies.
- 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
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 45 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Medipol University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Gülay Aras Bayram, Medipol University
- Investigators
- Gülay A Bayram, 1, Study director, Medipol University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07899619
- Sponsor's protocol ID
- E-10840098-50.04-5380
- Status last verified
- Oct 2026
- First submitted
- 12 Oct 2026
- Last updated
- 27 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be shared to protect participant privacy and maintain confidentiality in accordance with institutional review board (IRB) and data protection guidelines.
Study at a glance
From the registry record, last updated by the sponsor on 27 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Application Sequence of Recovery Modalities on Blood Lactate and Acute Recovery in Elite Female Basketball Players
- ClinicalTrials.gov ID
- NCT07899619
- Acronym / sponsor ID
- E-10840098-50.04-5380
- Conditions
- Basketball, Basketball Performance, Recovery, Recovery After Exercise
- Keywords
- Recovery, Basketball, Exercise, Sports
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 45 participants (estimated)
- Lead sponsor
- Medipol UniversityUniversity, hospital or other
- Study start
- 1 Aug 2026 (actual)
- Primary completion
- 30 Oct 2026 (estimated)
- Study completion
- 1 Nov 2026 (estimated)
- First posted
- 27 Oct 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.
The purpose of this study is to compare the effects of intermittent pneumatic compression, local heat, and mechanical vibration applications on recovery following high-intensity anaerobic exercise in elite female basketball players. Recovery levels of the athletes will be evaluated through blood lactate concentration, countermovement jump performance, perceived recovery status, and perceived muscle soreness. The study will compare the effects of different recovery application sequences on post-exercise recovery indicators.
Detailed description
High-intensity anaerobic exercise, especially in sports such as basketball involving repetitive sprints, jumps, and high-intensity efforts, can cause temporary fatigue and performance decrements following exercise. Accelerating post-exercise recovery is crucial for enabling athletes to become physically prepared for subsequent training sessions or competitions. Various physical recovery modalities are utilized to support recovery in athletes. Intermittent pneumatic compression is a method aimed at supporting circulation by applying controlled pressure to the extremities, contributing to the clearance of metabolic load accumulated after exercise. Local heat and mechanical vibration application aims to facilitate the recovery process by generating thermal and mechanical stimulation in the targeted region. However, further research is required to compare the effects of these two distinct modalities on recovery indicators following high-intensity anaerobic exercise. This study aims to examine the responses of elite female basketball players to different recovery applications following high-intensity anaerobic exercise. Changes during the recovery process will be monitored using biochemical, performance-based, and subjective evaluation measures. Thus, the potential effects of different physical recovery methods during post-exercise recovery will be evaluated comparatively. The findings obtained from this study are expected to contribute to the evaluation of recovery strategies applicable to elite female basketball players following high-intensity exercise, as well as to practices supporting athlete health and performance.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Jobst-Venom Group | Experimental | Device: Intermittent Pneumatic Compression (IPC), Device: Local Heat and Mechanical Vibration (Venom 2 Leg)Athletes in this group will undergo two consecutive recovery applications following the high-intensity anaerobic exercise protocol. First, intermittent pneumatic compression will be applied for 15 minutes, after which blood lactate concentration will be measured. This will be immediately followed by 15 minutes of local heat and mechanical vibration application. All procedures will be performed in accordance with the durations and standardized conditions specified in the study protocol. Recovery indicators will be evaluated at predetermined measurement time points before and after the applications. |
| Venom-Jobst Group | Experimental | Device: Intermittent Pneumatic Compression (IPC), Device: Local Heat and Mechanical Vibration (Venom 2 Leg)Athletes in this group will undergo two consecutive recovery applications following the high-intensity anaerobic exercise protocol. First, local heat and mechanical vibration will be applied for 15 minutes, after which blood lactate concentration will be measured. This will be immediately followed by 15 minutes of intermittent pneumatic compression application. All procedures will be performed in accordance with the durations and standardized conditions specified in the study protocol. Recovery indicators will be evaluated at predetermined measurement time points before and after the applications. |
| Passive Rest | Placebo comparator | Other: Passive RestParticipants in this group will rest passively in a supine position for 30 minutes instead of receiving intervention applications. No recovery modality will be applied during the passive rest period. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
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 |
|---|---|---|
| Intermittent Pneumatic Compression (IPC)Intermittent pneumatic compression will be applied following high-intensity anaerobic exercise using the Jobst compression device. The application will be performed on the lower extremities at a pressure of 80 mmHg for a total duration of 15 minutes. The standard intermittent pneumatic compression program of the device will be utilized during the procedure. | Device | Jobst-Venom Group, Venom-Jobst Group |
| Local Heat and Mechanical Vibration (Venom 2 Leg)Local heat and mechanical vibration will be applied to both lower extremities following high-intensity anaerobic exercise using the Venom device. The application will last for a total duration of 15 minutes. Local heat will be administered at a medium level, and mechanical vibration will be applied using Mode 1 of the device. | Device | Jobst-Venom Group, Venom-Jobst Group |
| Passive RestParticipants will rest in a supine position for 30 minutes. | Other | Passive Rest |
Primary outcome
Change in Post-Exercise Blood Lactate Concentration
Time frame: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Blood lactate measurement performed using a portable blood lactate analyzer from capillary blood samples obtained via fingertip puncture to evaluate the metabolic efficacy of recovery modalities following high-intensity anaerobic exercise (RAST). Measurement results are expressed in mmol/L.
3 secondary outcomes
Lower Extremity Neuromuscular Performance (CMJ)
Time frame: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Perceived Recovery Status (PRS)
Time frame: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Perceived Muscle Soreness (VAS)
Time frame: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Oct 2026.
- Individual participant dataSharing planned: No. Individual participant data will not be shared to protect participant privacy and maintain confidentiality in accordance with institutional review board (IRB) and data protection guidelines.
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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.
Gülay A Bayram, 1 study director
Medipol University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intermittent Pneumatic Compression (IPC), Local Heat and Mechanical Vibration (Venom 2 Leg) and Passive Rest in people with Basketball and Basketball Performance, run by Medipol University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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: enrolling by invitation, as of the sponsor's last update on 27 Oct 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 Turkey (Türkiye). 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. Some participants in this study may receive a placebo. 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?
This study is still under way. Results are not available in the source record yet.
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?
Change in Post-Exercise Blood Lactate Concentration (time frame: At baseline, 3 minutes post-RAST, immediately post-first intervention, and at the end of the second intervention or passive recovery period.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 27 Oct 2026.