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Change-of-Direction Repeated Sprints in Adolescent Female Basketball Players

Effects of Changes of Direction on Repeated-Sprint Performance, Perceived Exertion, and Acute Cardiovascular Responses in Adolescent Female Basketball Players: A Randomized Crossover Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07727850
Enrollment
20
Registered
2026-07-27
Start date
2026-05-02
Completion date
2026-05-21
Last updated
2026-07-30

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

Conditions

Athletic Performance

Keywords

Repeated-Sprint Ability, Change of Direction, Female Basketball Players, Adolescent Athletes, Perceived Exertion, Cardiovascular Responses, Crossover Study

Brief summary

The purpose of this randomized crossover study was to compare the acute effects of repeated-sprint protocols incorporating different numbers of 180-degree changes of direction in adolescent female basketball players. Twenty participants completed three exercise conditions in a randomized, counterbalanced order: 10 × 15-m linear sprints, 10 × 15-m sprints incorporating one 180-degree change of direction, and 10 × 15-m sprints incorporating two 180-degree changes of direction. Each sprint was followed by 30 seconds of passive recovery. Sprint performance, perceived exertion, heart rate, peripheral oxygen saturation, and systolic and diastolic blood pressure were assessed. The study examined whether increasing the number of changes of direction affected repeated-sprint performance and acute perceptual and cardiovascular responses.

Detailed description

This was an acute, randomized, counterbalanced, three-condition crossover study in which each participant completed all experimental conditions and served as her own control. Following a standardized warm-up, participants completed one of three repeated-sprint protocols during each experimental condition: 10 × 15-m linear sprints without a change of direction, 10 × 15-m sprints incorporating one 180-degree change of direction, or 10 × 15-m sprints incorporating two 180-degree changes of direction. A 30-second passive recovery period was provided between repetitions. Total sprint distance, number of repetitions, and recovery duration were standardized across the three conditions; only the number of changes of direction differed. Sprint times were recorded using electronic timing gates. Best, average, and worst sprint times were determined, and sprint decrement and the change from best to worst performance were calculated. Rating of perceived exertion was recorded after each protocol. Heart rate, peripheral oxygen saturation, and systolic and diastolic blood pressure were assessed immediately before and after each condition. The experimental conditions were compared to determine whether increasing the number of 180-degree changes of direction altered absolute repeated-sprint performance, performance maintenance, perceived exertion, or immediate cardiovascular responses.

Interventions

BEHAVIORALLinear Repeated-Sprint Protocol

Following a standardized 20-minute dynamic warm-up, participants performed 10 maximal 15-m linear sprints without a change of direction. Each sprint began from a standing position 0.5 m behind the starting line and was recorded using electronic timing gates. A 30-second passive recovery period was provided between repetitions, during which participants remained standing.

BEHAVIORALOne-COD Repeated-Sprint Protocol

Following a standardized 20-minute dynamic warm-up, participants performed 10 maximal 15-m repeated sprints. Each repetition consisted of 7.5 m of forward sprinting followed by one 180-degree change of direction and a 7.5-m return sprint. Each sprint began from a standing position 0.5 m behind the starting line and was recorded using electronic timing gates. A 30-second passive recovery period was provided between repetitions, during which participants remained standing.

BEHAVIORALTwo-COD Repeated-Sprint Protocol

Following a standardized 20-minute dynamic warm-up, participants performed 10 maximal 15-m repeated sprints. Each repetition consisted of three consecutive 5-m sections and incorporated two 180-degree changes of direction. Each sprint began from a standing position 0.5 m behind the starting line and was recorded using electronic timing gates. A 30-second passive recovery period was provided between repetitions, during which participants remained standing.

Sponsors

Pamukkale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Intervention model description

Participants were randomized to one of three counterbalanced testing sequences. Each participant completed the linear, one-COD, and two-COD repeated-sprint conditions, with at least 48 hours between consecutive sessions. The sequences were linear-one-COD-two-COD, one-COD-two-COD-linear, and two-COD-linear-one-COD.

Eligibility

Sex/Gender
FEMALE
Age
16 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Female basketball players aged 16-18 years. * Currently competing in the U16 or U18 basketball leagues in Denizli, Türkiye. * At least two years of structured basketball training experience. * Regular participation in at least three training sessions and one official match per week. * No injury or illness that could prevent maximal sprint performance.

Exclusion criteria

* Reporting an injury before testing that could prevent maximal sprint performance. * Failure to attend all testing sessions or complete all three experimental conditions.

Design outcomes

Primary

MeasureTime frameDescription
Average Sprint TimeDuring the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.The mean completion time of the 10 maximal 15-m sprint repetitions, recorded using Witty electronic timing gates and expressed in seconds. The outcome was calculated separately for the linear, one-COD, and two-COD repeated-sprint conditions.
Best Sprint TimeDuring the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.The fastest completion time (lowest value) among the 10 maximal 15-m sprint repetitions, recorded using Witty electronic timing gates and expressed in seconds. The outcome was determined separately for the linear, one-COD, and two-COD repeated-sprint conditions.
Worst Sprint TimeDuring the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.The slowest completion time (highest value) among the 10 maximal 15-m sprint repetitions, recorded using Witty electronic timing gates and expressed in seconds. The outcome was determined separately for the linear, one-COD, and two-COD repeated-sprint conditions.

Secondary

MeasureTime frameDescription
Sprint DecrementCalculated from the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.The percentage reduction in performance across the 10 maximal sprint repetitions. Sprint decrement was calculated separately for each experimental condition using the following formula: Sdec (%) = (\[sum of the 10 sprint times / (best sprint time × 10)\] - 1) × 100. Higher values indicate a greater decline in repeated-sprint performance.
Worst-to-Best DecrementCalculated from the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.The percentage difference between the fastest and slowest sprint repetitions, calculated separately for each experimental condition using the following formula: \[(worst sprint time - best sprint time) / best sprint time\] × 100. Higher values indicate a greater decline from the best to the worst performance.
Rating of Perceived ExertionImmediately after completion of the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.Perceived exertion was assessed using the Borg category-ratio scale ranging from 0 to 10, where 0 represents rest and 10 represents maximal exertion. Participants rated the overall difficulty of each completed repeated-sprint condition.
Heart RateImmediately before and immediately after the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.Heart rate was measured using a Soulfix fingertip pulse oximeter placed on the index finger of the left hand. Values were recorded in beats per minute before and immediately after each repeated-sprint condition.
Peripheral Oxygen SaturationImmediately before and immediately after the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.Peripheral oxygen saturation (SpO2) was measured using a Soulfix fingertip pulse oximeter placed on the index finger of the left hand. Values were recorded as a percentage before and immediately after each repeated-sprint condition.
Systolic Blood PressureImmediately before and immediately after the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.Systolic blood pressure was measured on the left upper arm using an Omron M2 Essential automated digital blood-pressure monitor. Values were recorded in millimeters of mercury (mmHg) before and immediately after each repeated-sprint condition.
Diastolic Blood PressureImmediately before and immediately after the repeated-sprint protocol in Sessions 1, 2, and 3 on Study Days 1, 3, and 5, respectively.Diastolic blood pressure was measured on the left upper arm using an Omron M2 Essential automated digital blood-pressure monitor. Values were recorded in millimeters of mercury (mmHg) before and immediately after each repeated-sprint condition.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATOREngin Güneş Atabaş, PhD

Pamukkale Üniversitesi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026