- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06254963
The Effect of 6 Weeks Jump Training on Sand Versus Hard Surfaces on Jump Landing and Performance in Young Females
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
Study Overview
Status
Intervention / Treatment
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Tees Valley
-
Middlesbrough, Tees Valley, United Kingdom, TS1 3BA
- Teesside University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sand jump training
Participants will conduct 6 weeks (twice weekly) supplemental jump training on a sand surface (within their warm ups) in addition to their regular training.
|
A series of progressive jumping activities on sand increasing in difficulty over the 6 week period
|
|
Active Comparator: Land jump training
Participants will conduct 6 weeks (twice weekly) supplemental jump training on a land surface (within their warm ups) in addition to their regular training.
|
A series of progressive jumping activities on land increasing in difficulty over the 6 week period
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Frontal Plane Projection Angle
Time Frame: 1 week pre intervention and 1 week post intervention
|
The angle of knee valgus or varus upon landing
|
1 week pre intervention and 1 week post intervention
|
|
Maximal Countermovement Jump
Time Frame: 1 week pre intervention and 1 week post intervention
|
Measure of jump height
|
1 week pre intervention and 1 week post intervention
|
|
10/5 Repeated Jump Test
Time Frame: 1 week pre intervention and 1 week post intervention
|
Measures Reactive Strength Index
|
1 week pre intervention and 1 week post intervention
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Mark C Richardson, MSc, Teesside University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Jan24 18946
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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