Adana Olympic Preparation Center
Adana, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT07715786
This crossover experimental study aims to compare acute hamstring muscle oxygenation responses during Nordic Hamstring Exercise (NHE) and Blood Flow Restriction Nordic Hamstring Exercise (BFR-NHE) in elite adolescent athletes. Participants will complete both exercise conditions in a randomized order separated by a 7-day washout period. Muscle oxygen saturation will be assessed using near-infrared spectroscopy (MOXY), together with total hemoglobin responses, blood lactate concentration, perceived exertion, and exercise performance variables. The findings may improve understanding of the physiological effects of blood flow restriction during eccentric hamstring exercise in adolescent athletes.
Interested in participating?
Request Info14 year–18 year
All sexes
Interventional
Not applicable
Adana, Turkey (Türkiye)
Location status: Recruiting
Hamstring muscles play a crucial role in sprinting, jumping, change-of-direction movements, and other high-intensity athletic activities. Nordic Hamstring Exercise (NHE) is one of the most effective eccentric strengthening exercises for improving hamstring function and reducing the risk of hamstring strain injuries. Recently, blood flow restriction (BFR) training has gained increasing attention because it may enhance metabolic stress and alter muscle oxygenation responses during exercise. However, evidence regarding the acute physiological effects of combining BFR with Nordic Hamstring Exercise in elite adolescent athletes remains limited.
This study aims to compare hamstring muscle oxygenation responses during conventional Nordic Hamstring Exercise and Blood Flow Restriction Nordic Hamstring Exercise in elite adolescent athletes. A prospective crossover experimental design will be used, allowing each participant to complete both exercise conditions and serve as his or her own control. The order of the interventions will be randomized, and the two testing sessions will be separated by a 7-day washout period to minimize potential carryover effects.
Elite adolescent athletes aged 14-18 years who have participated in regular training for at least three years will be recruited. During each testing session, hamstring muscle oxygen saturation (SmO₂) and total hemoglobin (tHb) responses will be continuously monitored using wearable near-infrared spectroscopy (MOXY). Measurements will include baseline SmO₂, minimum SmO₂, delta SmO₂, recovery SmO₂, baseline total hemoglobin, peak total hemoglobin, and delta total hemoglobin. Blood lactate concentration, rating of perceived exertion using the Borg Rating of Perceived Exertion Scale, exercise performance variables, and post-exercise symptoms such as muscle soreness and fatigue will also be recorded.
Nordic Hamstring Exercise will be performed according to a standardized protocol under physiotherapist supervision. During the Blood Flow Restriction Nordic Hamstring Exercise condition, the same exercise protocol will be performed while individualized blood flow restriction is applied to the proximal lower extremity using a pneumatic cuff. The cuff pressure will be individualized based on participant tolerance and safety, and the intervention will be discontinued immediately if any adverse symptoms occur.
The primary objective is to determine whether blood flow restriction alters acute hamstring muscle oxygenation responses during Nordic Hamstring Exercise. Secondary objectives include comparing total hemoglobin responses, blood lactate concentration, perceived exertion, exercise performance, and post-exercise recovery between the two exercise conditions. The findings of this study are expected to improve understanding of the physiological mechanisms of blood flow restriction during eccentric hamstring exercise and provide evidence for its safe and effective use in adolescent athletic populations.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will perform a standardized Nordic Hamstring Exercise protocol under physiotherapist supervision. From a kneeling position with the ankles stabilized, participants will lower the trunk forward in a controlled manner while maintaining alignment of the trunk and hips.
Participants will perform the same standardized Nordic Hamstring Exercise protocol while individualized blood flow restriction is applied using a pneumatic cuff positioned on the proximal lower extremity.
Time frame: During each exercise session, with the two sessions separated by a 7-day washout period
Hamstring muscle oxygen saturation will be continuously measured using a wearable near-infrared spectroscopy device (MOXY) during conventional Nordic Hamstring Exercise and Blood Flow Restriction Nordic Hamstring Exercise. Delta SmO₂ will be calculated as the difference between baseline SmO₂ and the minimum SmO₂ recorded during each exercise condition. Greater negative change indicates greater muscle deoxygenation.
Time frame: During each exercise session, with the two sessions separated by a 7-day washout period
The minimum hamstring muscle oxygen saturation value (SmO₂, %) recorded during each exercise condition will be obtained using the MOXY near-infrared spectroscopy device. Lower values indicate greater muscle deoxygenation.
Time frame: Immediately after each exercise session during the recovery period, with sessions separated by a 7-day washout period
Hamstring muscle oxygen saturation (SmO₂, %) will be recorded during the post-exercise recovery period following each exercise condition using the MOXY device.
Time frame: During each exercise session, with the two sessions separated by a 7-day washout period.
Peak total hemoglobin concentration in the hamstring muscle will be recorded during each exercise condition using the MOXY near-infrared spectroscopy device.
Time frame: During each exercise session, with the two sessions separated by a 7-day washout period.
Change in total hemoglobin will be calculated as the difference between baseline total hemoglobin and peak total hemoglobin recorded during each exercise condition using the MOXY device.
Time frame: Immediately after each exercise session, with the two sessions separated by a 7-day washout period
Blood lactate concentration will be measured using a portable lactate analyzer following each exercise condition and reported in mmol/L. Higher values indicate a greater acute metabolic response.
Time frame: Immediately after each exercise session, with the two sessions separated by a 7-day washout period
Perceived exertion will be assessed using the Borg Rating of Perceived Exertion Scale following each exercise condition. Higher scores indicate greater perceived exertion.
Time frame: During each exercise session, with the two sessions separated by a 7-day washout period
The number of Nordic Hamstring Exercise repetitions completed with the required technique will be recorded during each exercise condition. A higher number indicates better acute exercise performance.
Time frame: 24 hours after each exercise session
Hamstring muscle soreness will be assessed using an 11-point Numerical Rating Scale ranging from 0, indicating no soreness, to 10, indicating the worst imaginable soreness.
Contact information is provided by the study sponsor or research team.
Toros University
Other
Comparison of Hamstring Muscle Oxygenation Responses During Nordic Hamstring Exercise and Blood Flow Restriction Nordic Hamstring Exercise in Elite Adolescent Athletes: A Crossover Experimental Study
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.
Published trials that share one or more normalized conditions with this study.
NCT07673601
Healthy Volunteer, Healthy Volunteers (HV)
Montreal, Canada
View Trial DetailsNCT07658274
Healthy Volunteers (HV)
Xi'an, Shaanxi, China
View Trial DetailsNCT07525947
Healthy Volunteers (HV)
Glendale, California, United States
View Trial DetailsNCT07449741
Healthy Volunteers (HV)
Bayswater, Victoria, Australia
View Trial Details