- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06094075
Dynamic Strength Index-based Intervention in Basketball.
December 4, 2024 updated by: Žiga Kozinc, University of Primorska
Effectiveness of an Individualized Training Based on Dynamic Strength Index on Sprinting, Jumping and Change of Direction Performance in Basketball Players: a Randomized Controlled Trial.
The goal of this randomized controlled trial will be to determine the effectiveness of the dynamic strength index (DSI) in optimizing training programs to improve physical performance proxies (sprinting, jumping, and CoD) in basketball players.
Subjects will be randomly allocated to one of two groups: the intervention group and the control group.
Measurement and intervention will occur during a 7-week in-season period, right before the play off starts.
Throughout this period, all participants will engage in an average of 10 hours of basketball training per week, which will comprise 5 basketball sessions and 2 strength training sessions.
In addition, they are anticipated to play 2 games weekly.
A pre-test will be performed one week before the first training session, and post-tests will be performed in the week after the training sessions have finished.
Athletes will perform both testing sessions at the same time of the day (± 2 hours).
Each athlete will perform a 20-m sprint test, with timing gates positioned at every 5 m distance, a 505 CoD test, countermovement jump (CMJ), and isometric mid-thigh pull (IMTP).
Based on CMJ peak force and IMTP peak force data, we will calculate DSI.
Based on the average DSI value, the participants in the intervention group will be divided into two groups - strength group and ballistic group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
46
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Izola, Slovenia, 6310
- University of Primorska, Faculty of Health Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Perform basketball training for at least 5 years
- Plays in professional regional, national or international league
Exclusion Criteria:
- Any musculoskeletal injury in the past 6 months
- Any neurological issues
- Any chronic non-communicable diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: DSI-based training group
This group will perform resistance exercises based in their DSI values.
|
The intervention consist of modifying the ongoing resistance exercises.
Those with low DSI values will perform ballistics, explosive exercises.
Those with high DSI will perform heavy-load training.
The resistance training program will consist of 2 sessions per week for 5 weeks (10 sessions in total).
The sessions will be separated by a minimum of 48 hours.
The strength training group will consist mostly of exercises with high load, whereas the ballistic training group will perform ballistic exercises with low load or without any additional load.
The training principle will be the same for both subgroups, consisting of 3 exercises per training session and a total of 6 exercises per week, with four of the exercises being bilateral, one unilateral, and one quasi-unilateral (Bulgarian split squat and scissor jumps).
|
|
Active Comparator: Normal training group
This group will perform a normal, typical resistance exercise program
|
The participants will do a general training program (not based on DSI values).
The resistance training program will consist of 2 sessions per week for 5 weeks (10 sessions in total).
The sessions will be separated by a minimum of 48 hours.
The strength training group will consist mostly of exercises with high load, whereas the ballistic training group will perform ballistic exercises with low load or without any additional load.
The training principle will be the same for both subgroups, consisting of 3 exercises per training session and a total of 6 exercises per week, with four of the exercises being bilateral, one unilateral, and one quasi-unilateral (Bulgarian split squat and scissor jumps).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
20 m Sprint performance
Time Frame: Baseline and after 5 weeks.
|
20 m sprint test in seconds
|
Baseline and after 5 weeks.
|
|
Change of direction performance
Time Frame: Baseline and after 5 weeks.
|
Standardized 505-agility test
|
Baseline and after 5 weeks.
|
|
Jumping ability
Time Frame: Baseline and after 5 weeks.
|
Jump height during jumps with countermovement
|
Baseline and after 5 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2023
Primary Completion (Actual)
October 25, 2023
Study Completion (Actual)
May 1, 2024
Study Registration Dates
First Submitted
October 12, 2023
First Submitted That Met QC Criteria
October 18, 2023
First Posted (Actual)
October 23, 2023
Study Record Updates
Last Update Posted (Estimated)
December 9, 2024
Last Update Submitted That Met QC Criteria
December 4, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- DSI_Intervention_FVZ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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