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Frontal Plane Projection AngleNCT06254963

The Effect of 6 Weeks Jump Training on Sand Versus Hard Surfaces on Jump Landing and Performance in Young Females

A study testing sand jump training and land jump training in people with Frontal Plane Projection Angle and Maximal Countermovement Jump, run by Teesside University at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this study is to investigate the effect of a supplemental jump training program (added to a warm up) conducted on either sand or hard surfaces on the landing and jumping ability of young female football players. Read more about this study

Who is it for?
Ages 10 to 15 years, women only
What is being tested?
sand jump training and land jump training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
56 participants
Where
1 siteUnited Kingdom
Study dates
14 Feb 2024to 19 Apr 2024
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 10 to 15 years
  • Women only
  • No healthy volunteers
  • Child

Who may be able to join

  • female under the age of 16 and have been deemed medically fit to train and play football by the Emerging Talent Centre
  • parental consent and child assent gained
  • no history of anterior cruciate ligament (ACL) injury or previous lower limb fracture or surgery
  • no lower limb injury in the last 3 months.
  • no allergy to hypoallergenic adhesive tape.

Who cannot join

  • male
  • 16 or over
  • no parental consent and/or no child assent given
  • not deemed medically fit to train and play football by the Emerging Talent Centre
  • history of anterior cruciate ligament (ACL) injury or previous lower limb fracture or surgery
  • lower limb injury in the last 3 months
  • allergy to hypoallergenic adhesive tape

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Teesside University

    Middlesbrough, Tees Valley, TS1 3BA

Other trials in United Kingdom

About this study

Official title: The Effect of 6 Weeks Supplemental Jump Training on Sand Versus Hard Surfaces on Landing Knee Valgus and Jump Performance in Adolescent Female Football Players

The aim of this study is to investigate the effect of a supplemental jump training program (added to a warm up) conducted on either sand or hard surfaces on the landing and jumping ability of young female football players. The jump training program (intervention) will be carried out twice weekly for a period of 6 weeks. Participants will be randomised (computer package will decide) into one of 2 groups (either sand training or land training). The landing ability and jumping performance of all participants will be measured both before and after the 6 week jump training intervention. It is hypothesised that supplemental training on both sand and hard surfaces will improve landing ability and jumping performance. It is also hypothesised that sand will be equally as effective as a hard surface for improving jump landing ability but may be less effective than a hard surface for improving jumping performance.

Read the detailed description

Participants will be under 16 females currently training and playing for the football Emerging Talent Centre (ETC) at Teesside University.

The testing will take place at Teesside University. Participants will attend on 2 occasions (Pre and post intervention). During the first session participants age, height, and weight, will be collected. Participants will then perform a warmup consisting of fundamental movements like squatting, lunging, running, skipping and jumping.

Participants will then be asked to perform 5 practice trials of a single leg step landing task from a 30cm box. This will be demonstrated to them initially and then the practice trials will allow participants a chance to orient themselves to the task before data collection. For the step down task participants will be instructed to stand on the box and then step off the box and land and hold the position on their dominant leg (which is decided by the leg they prefer to kick a ball with).

Throughout testing participants will be required to wear reflective markers (14mm) over dark coloured shorts and top. The markers will be attached with double sided adhesive tape to the participants lower extremities over the following landmarks: anterior superior iliac spine (left and right), mid tibiofemoral joint (left and right) and mid talocrural joint (left and right). The same individual (MR) will place the markers on all participants. Midpoint will be determined using a standard tape measure. These markers will be used to calculate a knee angle on landing (specific outcome measure detailed elsewhere), measured using a high speed digital video camera (Quintic GigE 1mp; Quintic Consultancy Ltd, West Midlands, United Kingdom) recording at 200 frames per second, positioned 2 m anterior to the subjects' landing target at the height of the participant's knee and aligned perpendicular to the frontal plane. Images captured will be imported into a digitizing software program (Quintic 29; Quintic Consultancy Ltd) ready for analysis. The average landing value from 5 trials during the task will be used for analysis.

Following completion of the step-down task participants will then be asked to complete two performance tests (with a standardised 3 minute rest period between them). As within the step landing task they will be given practice trials to help familiarise themselves with the tests prior to data collection. The first test with be a countermovement jump (CMJ), where participants will stand on a force platform (built into the laboratory floor). Each foot will be on an individual force plate. Participants will then be asked to squat down, keeping their hands on their hips and subsequently jump as high as they can. Whilst in flight they must keep their hands on their hips and keep their leg straight. Participants will be instructed to land in the same position they took off from (i.e. not forward or backwards). Tape will be stuck on the floor as a marker to help guide the participants towards achieving this. The participant will perform 3 efforts with the average height being used for analysis. The second test is the 10/5 repeated jump test to evaluate the participants reactive strength index. The test requires the participant to execute 10 maximal rebound jumps (attempting to minimise ground contact time between jumps). Of the 10 jumps, the 5 that display the greatest jump height are used for analysis. The 10/5 test will be measured using the same in-ground force plate noted for the CMJ test. As with the CMJ test participants will be instructed to keep their hands on their hips throughout the jump phase and each of the 10 repeated jumps. One trial of the test is all that is required for data analysis purposes.

The testing protocol will be performed by all participants (pre and post an intervention time period of 6 weeks). There will be 2 groups (see below). Participants will be randomised into one of two groups. Both groups will perform a jump training protocol (on either a firm or sand surface) which involves a series of exercises that will be added to their usual warm up routine pre training. All participants will continue to train and play as normal during the intervention time period. They will then be invited back in at the end of the 6 week period for a second and final testing session.

The jump training protocol will involve a series of jumping tasks, which will be increased in difficulty level over the 6 week intervention period. The supplemental jump training protocol should take approximately 5-10 minutes to complete and will be incorporated into the participants warm up routine for their regularly training sessions x 2 weekly. Participants will continue with the rest of their football training as normal across the 6-week period.

Being tested
sand jump training, land jump training
Keywords
sand, jump training, knee valgus, jump height

What participants receive

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

  • sand jump trainingOther

    A series of progressive jumping activities on sand increasing in difficulty over the 6 week period

  • land jump trainingOther

    A series of progressive jumping activities on land increasing in difficulty over the 6 week period

Study groups in NCT06254963
Study groupRoleWhat they receive
Sand jump trainingExperimentalParticipants will conduct 6 weeks (twice weekly) supplemental jump training on a sand surface (within their warm ups) in addition to their regular training.
Receives: Other: sand jump training
Land jump trainingActive comparatorParticipants will conduct 6 weeks (twice weekly) supplemental jump training on a land surface (within their warm ups) in addition to their regular training.
Receives: Other: land jump training

What is being measured

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

  1. Frontal Plane Projection Angle

    The angle of knee valgus or varus upon landing

    Measured: 1 week pre intervention and 1 week post intervention

  2. Maximal Countermovement Jump

    Measure of jump height

    Measured: 1 week pre intervention and 1 week post intervention

  3. 10/5 Repeated Jump Test

    Measures Reactive Strength Index

    Measured: 1 week pre intervention and 1 week post intervention

Timeline

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

  1. First posted12 Feb 2024
  2. Study start14 Feb 2024
  3. Primary completion19 Apr 2024
  4. Study completion19 Apr 2024

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be randomised into one of 2 groups, either supplemental sand jump training or land jump training.
Masking
None (open label)
Enrolment
56 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06254963
Sponsor's protocol ID
Jan24 18946
Status last verified
Nov 2024
First submitted
2 Feb 2024
Last updated
22 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: There is no specific plan to make IPD available at present but relevant data can be made available to other researchers following publication at reasonable request

Questions about this trial

What is this clinical trial studying?

A study testing sand jump training and land jump training in people with Frontal Plane Projection Angle and Maximal Countermovement Jump, run by Teesside University at 1 site in United Kingdom.

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 5 inclusion and 7 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 22 Nov 2024. 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 United Kingdom. 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?

Frontal Plane Projection Angle (time frame: 1 week pre intervention and 1 week post intervention). 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?
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 22 Nov 2024.

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