AzTrials
AzTrials

Sport InjuriesSUPERGirlNCT07913451

Integrating Sport-Specific Comprehensive Training to Upscale Performance in Women and Girls

A study testing Typical training and SUPERGirl training in people with Sport Injuries and Performance in Sport, run by Sport Injury Prevention Research Centre.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

To date, sport training methodologies have focused primarily on male/men/boy (MMB) athletes, with much less emphasis on female/women/girl (FWG) athletes. Relatively little research has been conducted to identify how to enhance FWG performance in sport and there is a lack of understanding of how training delivery… Read more about this study

Who is it for?
Ages 11 to 26 years, women onlyHealthy volunteers can take part
Conditions the study is for
Sport Injuries, Performance in Sport
What is being tested?
Typical training and SUPERGirl training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
250 participants
Where
No sites listed yet
Study dates
15 Oct 2026to 31 Oct 2027
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 11 to 26 years
  • Women only
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • The population to be included in this study are 11-26 year old female women and girl ice hockey players and skeleton athletes.
  • For the survey portion of the study, additional participants will be recruited to gain an understanding of the perceptions and needs of female, women and girl athletes across sports. These additional participants will be recruited through INS Quebec (cheerleading, artistic swimming and synchronized skating), Calgary and area dance studios, and volleyball clubs.

Who cannot join

  • Individuals who are not members of the teams being approached

About this study

Official title: SUPERGIRLS: Integrating Sport-Specific Comprehensive Training to Upscale Performance in Women and Girls

To date, sport training methodologies have focused primarily on male/men/boy (MMB) athletes, with much less emphasis on female/women/girl (FWG) athletes. Relatively little research has been conducted to identify how to enhance FWG performance in sport and there is a lack of understanding of how training delivery models should be modified to optimize performance for FWG athletes. Typical physical training focuses on strength and fitness to improve power and endurance, depending on the sport. Evidence highlights the importance of combining Mental Performance (MP) competencies with physical training to achieve peak performance. Programs that interweave psychological and rehabilitation principles (including sensorimotor (SM) training) have demonstrated efficacy in individuals with pain and dizziness disorders. In addition, high-performance athletes have self-reported performance improvements and achieved record-breaking outcomes in their sport performance with SM training. Furthermore, these domains are shaped by broader sport and societal structures that are barriers to FWG athletes' equitable participation in sport. An integrated approach across pillars/domains has not yet been applied, nor in FWG sport specifically. Therefore, this new area of inquiry for the newly created SUPERGirl team will challenge current paradigms of sport development and specifically focus on elite FWG athlete training and performance requirements. With the combined transdisciplinary expertise in the SUPERGirl team, an integrated FWG athlete development program that goes beyond historical physical training and addresses FWG-specific needs will be co-created with coaches and sport partners. This innovative transdisciplinary model, integrating physical, SM, MP, and mental health training, could redefine the long-term FWG athlete development pathways and enhance sport experiences and performance for FWG athletes.

This study will recruit a total of 250 female, women and girl ice hockey players and skeleton athletes ages 11-26 years old.

Read the detailed description

The overarching objective of the SUPERGirl program is to understand FWG perspectives, develop outcomes and integrated training strategies to optimize performance in FWG athletes. The primary aims of the SUPERGirl program are to:

  1. Understand FWG perspectives on sport performance
  2. co-design FWG sport-specific performance measures and SUPERGirl training programs
  3. Evaluate the association between FWG multidomain outcomes and performance
  4. Evaluate the feasibility of and effects of SUPERGirl training on performance
  5. Refine the SUPERGirl training program in 11-26 year old FWG athletes.

FWG athletes will complete questionnaires and a cross-sectional survey, multisystem outcomes and performance-based outcomes. These outcomes will be completed following 6 weeks of typical training, after SUPERGirl training and again at the end of the season. At the start of the study, participants will also complete a survey to understand perspectives on performance and at the end of the study, participants will complete a survey to share their experiences with the SUPERGirl program and their recommendations for future iterations of the program. A subset of participants will be purposively sampled to participate in semi-structured interviews.

Aim 1: The researchers will implement a concurrent mixed methods approach using a cross-sectional survey to understand FWG perspectives on sport performance. The survey will include a series of questions related to the participants' perception of contributors to sport performance as well as open-ended questions that inquire about barriers and facilitators to optimal performance guided by the FUEL model.

Aim 2: Co-design FWG sport-specific performance measures and the SUPERGirl training program: The researchers will use a community based participatory research (CBPR) approach guided by a knowledge to action framework. The researcher's pilot work, previous literature, existing sport training, together with the survey output will inform co-design of:

  1. meaningful team and individual sport-specific performance measures (e.g. win/loss/tie records, individual technical and/or tactical skills)
  2. the SUPERGirl training program. Survey and co-design partners will include interested end-point sport knowledge users with different areas of expertise (e.g. athletes, parents, coaches, technical leads, sport administrators, health care professionals) Potential components of the training protocol include sensorimotor training (SM), mental performance training (MP), mental health (MH), and typical physical training. Additional factors such as growth and development, diet, and sleep, will also be considered and informed from the outputs of the survey.

Performance outcomes: Feasibility, reliability, and validity will be evaluated in a subset of participants.

Training strategies: Based on current literature and the research team's pilot work, it is anticipated that multiple components of sport- and FWG-specific SM training, MP, mental health strategies, nutrition, sleep, etc. will be interwoven into the current physical training programs to co-design the initial SUPERGirl training program.

This co-design process will incorporate the collective local knowledge and guidance of the CAB. We anticipate some aspects will be common to all sports (which will be included as multisport outcomes/training as a basis for other sports to build upon), while other aspects will be sport-specific. Given the pilot nature of this study, the researchers will include an initial convenience sample of 200 ice hockey and 25-50 skeleton athletes (depending on the size of the local Calgary team).

Aim 3: Evaluate the association between FWG multidomain outcomes and performance: A cross-sectional design will be used to evaluate the association between multimodal measures (exposures) and performance (outcome), assessed at the initial timepoint and following the SUPERGirl training in an inclusive sample of participating FWG ice hockey teams and skeleton athletes. Physical, SM, MP, sociocultural, nutrition, mental health, and sport experience will be included as exposures. The initial timepoint will use team/time performance outcomes. Secondary outcomes will include mental health, injury, concussion, and participation rates.

Aim 4: Evaluate the feasibility and efficacy of SUPERGirl training on performance: A quasi-experimental design will be used to evaluate the SUPERGirl training program (intervention) compared to standard training (control season prior to SUPERGirl training) from a feasibility and efficacy standpoint (exploratory outcome). An estimated 6 weeks of SUPERGirl training to be adequate based on current literature, however program parameters (e.g. frequency, duration, intensity) will be adapted based on the needs of the community partners and feedback from the CAB. Weekly coach, trainer and athlete feedback during training will be sought to inform adaptations to training. Components of training will be recorded. The efficacy of SUPERGirl training on multidomain outcomes, mental health, concussion and injury risk will be explored. Injury will be defined as any injury that results in time loss or medical attention. Concussion will be defined as per the Amsterdam International Consensus in Sport.

Aim 5: Refine the SUPERGirl training program: Following SUPERGirl training, a survey will be shared with participants to understand their experience in the SUPERGirl training program. Additionally, results of the first year of the SUPERGirl cohort will be used to refine the initial SUPERGirl training program. Following completion of the SUPERGirl training program, FWG athlete, coach and sport parties will be invited to participate in semi-structured interviews (one-on-one or focus group) to better understand their perspectives on the SUPERGirl training program and the FWG sport experience, particularly performance and specific training factors. A descriptive qualitative approach will be used to inductively analyze the data from the interviews and provide recommendations for future SUPERGirl training.

Outcomes:

Physical:

Knee Extensor Explosive Strength: Knee extensor explosive strength will be assessed using a rigid custom-built dynamometer mounted with a load cell sampling at 1000 Hz. Participants will be positioned in the seat with the centre of the knee joint aligned with the axis of rotation. The backplate will be adjusted to maintain a hip flexion angle of 80° relative to full extension, and the load cell connected to a shank plate will be adjusted to the same position for all participants, approximately 2.5 cm above the lateral malleolus. Testing will be conducted at 80° of knee flexion relative to full extension, verified using a goniometer. Velcro straps will be secured across the shoulders, waist, and thigh to minimize participant movement. The participant's shank will be strapped to an ankle attachment with a Velcro strap. The moment arm, defined as the distance from the knee joint centre to the contact point with the ankle attachment, will be measured using a measuring tape. The seat position and moment arm from the centre of the knee joint to the load cell will be recorded for each participant to ensure that the setup is identical across testing sessions.

Participants will be instructed to hold the sides of the chair for additional stability and to avoid any countermovement action before contraction. Contractions showing a countermovement will be discarded and repeated.

Participants will first complete three maximal voluntary isometric contraction repetitions of knee extension using the right limb. Each contraction will be held for 3 seconds, with a 20-second rest interval between repetitions. Participants will be instructed to achieve maximal voluntary torque "as fast and as hard as possible," with strong verbal encouragement during testing. A computer monitor will provide continuous visual feedback of knee extensor force. Following a 5-minute rest interval, burst contractions will be performed for the right knee extensors. A knee extensor torque target, calculated as 80% of the MVIC knee extensor torque, will be visually displayed on the monitor. Participants will perform 10 burst contraction repetitions lasting 1 second with the aim of reaching the torque target. Participants will be instructed to "create torque as fast as possible," with strong verbal encouragement during testing. Each repetition will be separated by a 15-second rest interval. Participants will then be given a 10-minute rest before performing the same protocol using the left limb.

Lower Limb Explosive Strength: Lower-limb force-velocity testing will be assessed using loaded countermovement jump testing and robotic servomotor leg press maximal voluntary contraction testing. Participants will complete a standardized 10-minute warm-up protocol at a self-selected moderate intensity on a cycle ergometer, followed by four 10-second maximal cycling sprints interspersed with 50 seconds of rest. After warming up, participants will perform five maximal-effort repetitions of countermovement jump testing with no external load, followed by three maximal-effort repetitions with 30% of body mass loaded on a hexagonal trap bar and three maximal-effort repetitions with 60% of body mass loaded on a hexagonal trap bar. Each loading condition will be separated by a 3-5-minute rest period, and each countermovement jump repetition will be separated by 20 seconds of rest.

Participants will then perform three MVCs of isometric, concentric, and eccentric leg press force testing using a robotic servomotor leg press. This will include three MVCs of isokinetic eccentric and concentric leg press actions performed at a constant speed of 0.2 m·s-¹. Each strength test will be separated by a 3-5-minute rest period, and each repetition will be separated by a 10-second rest interval. Strong verbal encouragement will be provided throughout the testing session by a certified exercise physiologist.

MVC leg extensor strength will be measured using a robotic servomotor leg press device sampling at 200 Hz. Three repetitions of MVC eccentric and concentric leg press movements will be performed between 100° and 10° of knee flexion at a constant speed of 0.2 m·s-¹, with a 0.5-second pause between the concentric and eccentric movement phases. Servomotor torque will be converted into force and low-pass filtered using a fourth-order recursive zero-lag Butterworth filter with a 6 Hz cut-off frequency. The acceleration phase of the isokinetic MVCs will be removed using the manufacturer's software to define a stable isokinetic phase across the leg press range of motion. Each force-time curve will be visually inspected to exclude erroneous trials. The repetitions with the highest peak eccentric MVC force, peak concentric MVC force, and maximal isometric MVC force will be used for analysis.

The force-velocity models will be built using vertical take-off velocity from countermovement jump testing and external load normalized to maximal unilateral concentric MVC force converted to kilograms. The countermovement jump repetition with the highest take-off velocity at each loading condition will be plotted with a best-fit least-squares linear regression function to obtain the maximum velocity intercept, Vmax, and the slope of the velocity-load relationship.

Countermovement Jump Stretch-Shortening Cycle Mechanics: Countermovement jump stretch-shortening cycle mechanics will be assessed using a dual force plate system sampling at 1000 Hz. Participants will be instructed to keep their hands firmly placed on their hips during unloaded countermovement jump testing to isolate the contributions of the lower limbs to vertical jump height and body centre of mass power and work production. During loaded countermovement jump testing, participants will hold the hexagonal trap bar and will be instructed to keep their arms straight throughout the entire jumping procedure. Participants will freely determine all other aspects of jump strategy, including their preferred depth, defined as downward body centre of mass displacement. The vertical ground reaction forces of the right and left leg will be measured synchronously and stored for later offline analysis.

Body centre of mass vertical velocity will be obtained by time integration of the instantaneous acceleration signal from the sum of the left and right vertical ground reaction force signals.

Maximal Sprint Speed: Maximal sprint speed (vMax) will be assessed using a 40 m linear sprint with electronic timing gates positioned perpendicular to a flat, non-slip sprinting surface at 10, 20, 30, and 40 m. Over-ground sprint testing across distances of 5-40 m is commonly used to assess sprint ability in youth athletes. Timing gates will be set at a standardized height of 1.0 m from the ground and positioned 1.22 m apart, corresponding to the approximate width of a standard track lane.

Participants will begin from a stationary two-point standing start with the front foot positioned at the 0 m start line. Participants will start when ready and will be instructed to sprint maximally through the 40 m finish line without decelerating before the final timing gate. Each athlete will complete three maximal sprint trials, with 3-5 min of passive recovery between trials. Split times will be recorded at 10, 20, 30, and 40 m. vMax will be calculated from the fastest 10 m split recorded between timing gates, using the 10-20 m, 20-30 m, and 30-40 m intervals. The fastest valid trial will be retained for analysis.

Maximal Aerobic Speed: Maximal aerobic speed (vMAS) was estimated using a 5-minute maximal running time trial performed on an indoor track. Athletes were instructed to cover the greatest possible distance in 5 minutes using an even maximal pacing strategy. Total distance covered was recorded to the nearest meter. The 5-minute running field test was selected because it provides a practical group-administered estimate of vMAS and has demonstrated strong agreement with treadmill-derived vMAS, and the test has also demonstrated strong test-retest reliability in trained men and women.

5-10-5 Change of Direction Test: Change-of-direction speed will be assessed using the standardized 5-10-5 shuttle test. The course consisted of three parallel lines positioned in a straight line, with the centre line serving as the start/finish line and two turn lines positioned 5 yards (4.57 m) to the left and right of centre on a flat, dry, non-slip surface with sufficient space beyond each turn line. This produced a total running distance of 20 yards (18.28 m): 5 yards to the first turn line, 10 yards (9.14 m) to the opposite turn line, and 5 yards back through the finish. Electronic timing gates were positioned at the centre start/finish line, perpendicular to the running direction. Timing gates were set at a standardized height of 1.0 m and positioned consistently for all athletes and across all testing sessions.

Athletes begin in a three-point stance straddling the centre line, with feet placed on either side of the line. The hand in contact with the floor corresponded to the initial direction of travel. Athletes started when ready and were instructed to accelerate maximally to the first turn line, touch the line with the lead foot and hand, change direction and sprint 10 yards to the opposite turn line, touch the line with the lead foot and hand, then change direction again and sprint 5 yards back through the centre finish line.

Each athlete completed trials in both starting directions. Athletes completed 3 maximal trials per direction, with 2-3 minutes of passive recovery between trials. Trials were considered invalid if the athlete failed to touch either turn line with the foot and hand, slipped, fell, deviated from the required path, or failed to sprint maximally through the finish line. The fastest valid trial was retained for analysis. If directional performance was being examined, the fastest valid trial in each starting direction was retained separately.

Sensorimotor: Please see documents section for detail. Cervical Spine outcomes: Cervical Spine range of motion (full/reduced), Cervical Flexor Endurance (CFE), Cervical Flexion Rotation Test (CFRT), Manual Spinal Exam (MSE), Cervical anterolateral flexion strength; Joint Position Sense, Head Perturbation Test (HPT) Vestibulo-ocular reflex (VOR) outcomes: Head thrust test (HTT), dynamic visual acuity, functional video head impulse test (f-vHIT) Quantified Vestibular Ocular Motor Screen (qVOMS): The VOMS with a clinician observed rating of performance on each of the 7 tests.

Additional Vision outcomes: accommodation, Frisby test Dynamic balance: Advanced Functional Gait Assessment (/48) Divided Attention: walking while talking test and timed dual task tandem gait

Ottawa Mental Skills Assessment Tool-3:12 mental skills measure: goal setting, self-confidence, commitment, stress reactions, relaxation, fear control, activation, focusing, imagery, competition planning, mental practice, and refocusing;

Mental health:

Sport Mental Health Assessment Tool (SMHAT) PHQ9, GAD7

Sport Specific Performance:

Ice hockey: Hockey Canada Skills Test: The Transition-Agility Skate course will be set up using four pylons arranged in a square measuring 24 ft × 24 ft (7.32 m × 7.32 m), measured from the centre of each pylon base. The start/finish line will be positioned at the bottom of the circle on the near side of the course, and the designated stop line will be positioned on the opposite side of the course, as shown in Figure 2. Pylon locations, the start/finish line, and the stop line will be measured before testing and marked on the ice using spray paint or tape to ensure consistent placement across athletes and trials. If a pylon is displaced, it will be returned to the marked location before the next trial.

Each player will begin from a stationary hockey-ready T-start position 0.5 m behind the start/finish photocell beam. The lead skate will be oriented toward the first pylon, with the rear skate positioned approximately perpendicular to the lead skate. Athletes may use their preferred lead foot; however, the same lead foot and starting stance must be used across all trials. Right and left directions will be defined from the athlete's perspective at the start position.

The player will skate forward to the far-right side pylon, pivot, and skate backward to the lower-right side pylon. The player will then pivot and skate forward to the far-left side pylon, pivot, and skate backward to the lower-left side pylon. The player will then pivot, skate forward to the designated line, stop completely, and skate back through the start/finish line. Players will complete the test first without a puck and then with a puck.

Timing will be recorded using paired laser photocell timing gates positioned at the start/finish line. The transmitter and receiver will be placed 2.0 m apart, centred on the athlete's intended skating path, with the beam set at 1.0 m above the ice surface. Timing will begin automatically when the athlete crosses the start/finish photocell beam and will stop when the athlete crosses back through the same beam at the end of the trial. The 0.5 m starting distance, photocell height, gate width, and gate location will be kept consistent across all athletes and trials.

For puck trials, the puck will be positioned on the ice directly in front of the athlete's stick blade and fully behind the photocell beam. The athlete, stick blade, and puck will not be permitted to cross or obstruct the beam before trial initiation. Athletes must begin with the puck under control and avoid extending the stick or puck through the timing gate before starting.

Each athlete will complete two valid trials without a puck and two valid trials with a puck. A passive recovery period of 2-3 minutes will be provided between trials. The fastest valid trial from each condition will be retained for analysis.

Athletes will be instructed to complete the course as quickly as possible while following the prescribed skating pattern and maintaining control. A trial will be considered valid only if the player completes the full course in the correct order, skates around the required side of each pylon, performs the required stop at the designated line, maintains the required skating pattern, and crosses the finish line under control.

A trial will be considered invalid and repeated if the athlete misses a pylon, completes the course in the wrong order, skates on the wrong side of a pylon, fails to complete the required stop, falls, stops unintentionally, triggers the timing system early, or fails to skate through the finish line. For puck trials, the trial will also be invalid if the athlete loses control of the puck such that the intended skating pattern or forward progression is disrupted, if the athlete finishes the trial without the puck, or if the athlete, stick, or puck prematurely triggers the photocell beam before trial initiation.

Incidental pylon contact will be permitted if the athlete maintains the correct skating path, retains control, and does not gain an advantage. Knocking over, displacing, or bypassing a pylon will invalidate the trial.

Skeleton: Gold Medal Profile (GMP), National Ranking System (NRS), Individual Race Performances (Percent-Back Calculations): Skeleton sport-specific performance will be assessed using percent back from the race winner. Official race results will be used to extract each athlete's total race time and the winning race time. All race times will be converted to seconds before analysis. Percent back will be calculated as the athlete's race time minus the winning race time, divided by the winning race time, multiplied by 100. This produces a relative race-performance outcome where the race winner receives a value of 0.00%, and higher values represent a greater time deficit from the race winner. Lower percent-back values will therefore indicate better skeleton race performance. Percent back from the leader is used by Bobsleigh Canada Skeleton as a competition performance variable within National Skeleton Program performance evaluation and ranking procedures.

Percent back will be calculated separately for each race before any aggregation across races or competitions. When multiple races are included, each athlete's mean percent-back value will be calculated from their valid race results.

When qualification or cut procedures prevent some athletes from completing additional runs, percent back will be calculated using stage-matched cumulative times. Athletes who do not qualify for subsequent runs will be assigned a percent-back value relative to the leader at the same completed stage of competition. For example, athletes eliminated after Run 1 will be compared with the Run 1 leader, and athletes eliminated after Run 2 will be compared with the leader's cumulative time after Runs 1-2. Final-race percent back will only be calculated for athletes who complete all runs included in the final race classification.

Athletes with no valid official finish time because of "Did not start" (DNS), "Did not finish" (DNF), or "Disqualified" (DSQ) will be excluded from percent-back calculation for that race.

Being tested
Typical training, SUPERGirl training
Keywords
Performance, Sensorimotor, hockey, physical fitness, Mental performance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Typical trainingOther

    Typical training including dryland, strength and conditioning, technical training, practices will be recorded

  • SUPERGirl trainingOther

    SUPERGirl training is an integrated training that includes sensorimotor training (i.e. training the vestibulo-ocular, oculomotor, cervico-ocular, cervical neuromuscular control, and balance), mental performance training and physical training.

Study groups in NCT07913451
Study groupRoleWhat they receive
Initial trainingActive comparatorTypical training
Receives: Other: Typical training
SUPERGirl trainingExperimentalSUPERGirl training that includes an integrated combination of sensorimotor, mental performance and physical training
Receives: Other: SUPERGirl training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Knee Extensor Explosive Strength

    Knee extensor explosive strength will be assessed using a rigid custom-built dynamometer mounted with a load cell sampling at 1000 Hz. Participants will be positioned in the seat with the centre of the knee joint aligned with the axis of rotation. The backplate will be adjusted to maintain a hip flexion angle of 80° relative to full extension, and the load cell connected to a shank plate will be adjusted to the same position for all participants, approximately 2.5 cm above the lateral malleolus. Testing will be conducted at 80° of knee flexion relative to full extension, verified using a goniometer. Velcro straps will be secured across the shoulders, waist, and thigh to minimize participant movement. The participant's shank will be strapped to an ankle attachment with a Velcro strap. The moment arm, defined as the distance from the knee joint centre to the contact point with the ankle attachment, will be measured using a measuring tape. The seat position and moment arm from the centre

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  2. Lower Limb Explosive Strength

    Leg Press Testing: Lower-limb strength will be assessed using robotic servomotor leg press maximal voluntary contraction testing. Participants will complete three MVCs of isometric, concentric, and eccentric leg press force testing using a robotic servomotor leg press. This will include three MVCs of isokinetic eccentric and concentric leg press actions performed at a constant speed of 0.2 m·s-¹. Each strength test will be separated by a 3-5-minute rest period, and each repetition will be separated by a 10-second rest interval. Strong verbal encouragement will be provided throughout the testing session by a certified exercise physiologist.

    MVC leg extensor strength will be measured using a robotic servomotor leg press device sampling at 200 Hz. Three repetitions of MVC eccentric and concentric leg press movements will be performed between 100° and 10° of knee flexion at a constant speed of 0.2 m·s-¹, with a 0.5-second pause between the concentric and eccentric movement phases. Servomo

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  3. Countermovement Jump Stretch-Shortening Cycle Mechanics

    Countermovement jump stretch-shortening cycle mechanics will be assessed using a dual force plate system sampling at 1000 Hz. Participants will be instructed to keep their hands firmly placed on their hips during unloaded countermovement jump testing to isolate the contributions of the lower limbs to vertical jump height and body centre of mass power and work production. During loaded countermovement jump testing, participants will hold the hexagonal trap bar and will be instructed to keep their arms straight throughout the entire jumping procedure. Participants will freely determine all other aspects of jump strategy, including their preferred depth, defined as downward body centre of mass displacement. The vertical ground reaction forces of the right and left leg will be measured synchronously and stored for later offline analysis.

    Body centre of mass vertical velocity will be obtained by time integration of the instantaneous acceleration signal from the sum of the left and right ve

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  4. Maximal Sprint Speed

    Maximal sprint speed (vMax) will be assessed using a 40 m linear sprint with electronic timing gates positioned perpendicular to a flat, non-slip sprinting surface at 10, 20, 30, and 40 m. Over-ground sprint testing across distances of 5-40 m is commonly used to assess sprint ability in youth athletes. Timing gates will be set at a standardized height of 1.0 m from the ground and positioned 1.22 m apart, corresponding to the approximate width of a standard track lane.

    Participants will begin from a stationary two-point standing start with the front foot positioned at the 0 m start line. Participants will start when ready and will be instructed to sprint maximally through the 40 m finish line without decelerating before the final timing gate. Each athlete will complete three maximal sprint trials, with 3-5 min of passive recovery between trials. Split times will be recorded at 10, 20, 30, and 40 m. vMax will be calculated from the fastest 10 m split recorded between timing gates, using

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  5. Maximal Aerobic Speed

    Maximal aerobic speed (vMAS) was estimated using a 5-minute maximal running time trial performed on an indoor track. Athletes were instructed to cover the greatest possible distance in 5 minutes using an even maximal pacing strategy. Total distance covered was recorded to the nearest meter. The 5-minute running field test was selected because it provides a practical group-administered estimate of vMAS and has demonstrated strong agreement with treadmill-derived vMAS, and the test has also demonstrated strong test-retest reliability in trained men and women.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  6. 5-10-5 Change of Direction Test

    Change-of-direction speed will be assessed using the standardized 5-10-5 shuttle test. The course consisted of three parallel lines positioned in a straight line, with the centre line serving as the start/finish line and two turn lines positioned 5 yards (4.57 m) to the left and right of centre on a flat, dry, non-slip surface with sufficient space beyond each turn line. This produced a total running distance of 20 yards (18.28 m): 5 yards to the first turn line, 10 yards (9.14 m) to the opposite turn line, and 5 yards back through the finish. Electronic timing gates were positioned at the centre start/finish line, perpendicular to the running direction. Timing gates were set at a standardized height of 1.0 m and positioned consistently for all athletes and across all testing sessions.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  7. Feasibility - recruitment

    Number of participants recruited

    Measured: From enrolment to the end of the stud (approx 24 weeks)

  8. Feasibility - retention rate

    Number of participants completing the trial divided by the total number of participants recruited

    Measured: From enrolment to the end of the stud (approx 24 weeks)

  9. Feasibility - adverse events

    Number of adverse events

    Measured: From enrolment to the end of the stud (approx 24 weeks)

  10. Feasibility - barriers and facilitators

    Barriers and facilitators to the protocol as described by the participants and physiotherapists

    Measured: From enrolment to the end of the stud (approx 24 weeks)

Secondary outcomes (21)
  1. Cervical Spine range of motion

    Cervical spine range of motion full/reduced in each motion tested for flexion, extension, rotation right and left, side flexion right and left

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  2. Cervical Flexor Endurance (CFE)

    Cervical spine range of motion full/reduced in each motion tested for flexion, extension, rotation right and left, side flexion right and left; measured in seconds where longer is better

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  3. Cervical Flexion Rotation Test (CFRT)

    Limitation of cervical spine range of rotation by greater than 20 decrease in a fully flexed position - has been demonstrated to have excellent diagnostic accuracy for cervicogenic headache. positive/negative

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  4. Manual Spinal Exam (MSE)

    Evaluation of segmental pain rated as positive if >3/10 pain is reproduced and limited motion

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  5. Cervical anterolateral flexion strength

    Cervical spine strength in full rotation and side flexion, measured with a handheld dynamometer (kg)

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  6. Joint Position Sense

    Observational test measuring the ability to relocate the head to a neutral position following rotation, measured with a head lamp in degrees from centre. A lower score is a better score.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  7. Head Perturbation Test (HPT)

    Ability of the participant to maintain a still head position when an unanticipated external force is applied, score /8 and a higher score is a better score

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  8. Head thrust test (HTT)

    Ability to maintain eyes focused on a target with a quick head motion, measured to the right and left. positive/negative.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  9. Clinical test of dynamic visual acuity (DVA)

    Behavioural representation of the vestibule-ocular reflex reflecting the ability to maintain eyes on a target with head motion, measured in LogMAR where a lower score is a better score

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  10. functional video head impulse test (f-vHIT)

    Functional version of the vHIT; measures gain of the vestibulo-ocular reflex; score is percent of correct answers where higher is better

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  11. Quantified Vestibular Ocular Motor Screen (qVOMS)

    Test that evaluates both symptom reproduction (headache, dizziness, nausea, fogginess) and clinical performance on 7 tests that include both eye and head motion. normal/abnormal for clinical performance and 0-10 for symptoms where a lower number for symptoms is a better score.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  12. Accommodation

    Maximal point at which the participant can see clearly as a target moves toward the face, measured for right and left eye separately, cm and a lower score is a better score

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  13. Frisby test

    Ability to see depth, yes/no

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  14. Advanced Functional Gait Assessment

    Dynamic balance test that includes 16 different tests with higher scores representing better performance 0-48 and a higher score is a better performance

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  15. walking while talking test

    20 foot walking test that evaluates the ability to divide attention while walking, outcome is measured in seconds to complete the task. measured in seconds, a lower score is a better score

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  16. timed dual task tandem gait

    Heel to toe gait with a cognitive task. seconds and a lower score is a better score

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  17. Ottawa Mental Skills Assessment Tool-3

    12 mental skills measure: goal setting, self-confidence, commitment, stress reactions, relaxation, fear control, activation, focusing, imagery, competition planning, mental practice, and refocusing; each item scored on a scale from 1 totally disagree to 7 totally agree; mean score per scale for each individual skill.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  18. Sport Mental Health Assessment Tool (SMHAT)

    Tool that screens for mental health conditions in athletes; multistage screening using a step by step process to evaluate specific mental health domains.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  19. Patient Health Questionnaire (PHQ9)

    Patient Health Questionnaire - 9 to screen for depression, 0-27 with higher scores representing greater depression severity

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  20. Generalized Anxiety Disorder 7 (GAD7)

    Self report measure for generalized anxiety disorder; scored from 0-21 with over 10 is typically a clinical cutoff suggesting probably Generalized anxiety disorder

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

  21. The Transition-Agility Skate

    The Transition-Agility Skate course will be set up using four pylons arranged in a square measuring 24 ft × 24 ft (7.32 m × 7.32 m), measured from the centre of each pylon base. The start/finish line will be positioned 12 feet (3.65 m) from the centre of horizontal line between the 2 nearest cones. , and the designated stop line will be positioned on the opposite side of the course, as shown in Figure 2. Pylon locations, the start/finish line, and the stop line will be measured before testing and marked on the ice using spray paint or tape to ensure consistent placement across athletes and trials. If a pylon is displaced, it will be returned to the marked location before the next trial. Measured in seconds, a shorter score is considered to be a better score.

    Measured: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Nov 2026
  2. Study start15 Oct 2026 (estimated)
  3. Primary completion31 Oct 2027 (estimated)
  4. Study completion31 Oct 2027 (estimated)

Resources

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
Other
Allocation
Non-randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07913451
Sponsor's protocol ID
SUPERGirl
Acronym
SUPERGirl
Status last verified
Oct 2026
First submitted
5 Oct 2026
Last updated
3 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Typical training and SUPERGirl training in people with Sport Injuries and Performance in Sport, run by Sport Injury Prevention Research Centre.

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 2 inclusion and 1 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: opening soon, as of the sponsor's last update on 3 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

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?

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?

Knee Extensor Explosive Strength (time frame: Day 1, 6 weeks, 12 weeks, end of season (approximately 24 weeks)). The study lists 10 primary outcomes in all. 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 3 Nov 2026; AzTrials last refreshed its copy on 6 Nov 2026.

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