TRX Training Intensity in Male Adolescent Basketball Players
TRX-INT
Comparing Low-, Moderate-, and High-Intensity TRX Suspension Training in Male Adolescent Basketball Players
1 other identifier
interventional
45
1 country
1
Brief Summary
This randomized interventional study aims to compare the effects of low-, moderate-, and high-intensity TRX suspension training on physical performance in male adolescent basketball players. Forty-two athletes aged 15 to 17 years are assigned to one of three TRX training intensity groups and complete an 8-week supervised training program in addition to their regular basketball practice. Outcomes are assessed before and after the intervention and include agility, dual-task agility, balance, upper-extremity muscular endurance, and rating of perceived exertion (RPE). The study seeks to determine whether different TRX training intensities produce distinct adaptations in these performance outcomes and to provide evidence for optimizing suspension-training prescription in youth basketball players.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2024
CompletedFirst Submitted
Initial submission to the registry
August 25, 2026
CompletedFirst Posted
Study publicly available on registry
September 2, 2026
CompletedSeptember 28, 2026
August 1, 2026
3 months
August 25, 2026
September 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Agility Performance
Agility performance assessed using the Illinois Agility Test. Completion time was recorded in seconds using electronic timing gates. Lower values indicate better performance.
Baseline and immediately after the 8-week intervention
Secondary Outcomes (4)
Dual-task Agility Performance
Baseline and immediately after the 8-week intervention
Balance Performance
Baseline and immediately after the 8-week intervention
Upper-extremity Muscular Endurance
Baseline and immediately after the 8-week intervention
Rating of Perceived Exertion (RPE)
Baseline and immediately after the 8-week intervention
Study Arms (3)
LI-TRX
EXPERIMENTALParticipants performed an 8-week supervised TRX suspension training program at 45-60% heart rate reserve (HRR), three sessions per week, in addition to regular basketball training.
MI-TRX
EXPERIMENTALParticipants performed an 8-week supervised TRX suspension training program at 65-75% heart rate reserve (HRR), three sessions per week, in addition to regular basketball training.
HI-TRX
EXPERIMENTALParticipants performed an 8-week supervised TRX suspension training program at 80-95% heart rate reserve (HRR), three sessions per week, in addition to regular basketball training.
Interventions
Participants completed an 8-week supervised TRX suspension training program performed three times per week in addition to their regular basketball training. All groups completed the same exercises, session frequency, session duration, training volume, and supervision. The intervention included TRX Side Bend, Knee Pull, T-Jump, Squat Jump, Mountain Climber, Superman, Sumo Squat Jump, Single-Leg Squat, Side Squat, and Hamstring Curl. The only difference between groups was the prescribed internal training intensity based on heart rate reserve (HRR): 45-60% (LI-TRX), 65-75% (MI-TRX), or 80-95% (HI-TRX).
Eligibility Criteria
You may qualify if:
- Male basketball players aged 15 to 17 years.
- Active participation in organized basketball training and competition.
- At least 6 years of regular basketball training experience.
- Participation in basketball training at least 5 days per week.
- Written informed consent from a parent or legal guardian and assent from the participant.
You may not qualify if:
- Serious lower-extremity injury within the previous 6 months.
- Diagnosed neurological or orthopedic condition limiting training or testing.
- Failure to complete the intervention protocol.
- Missing required pre- or post-intervention assessments.
- Incomplete testing records.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bursa Uludag University
Bursa, 16000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Sadettin Erol, PhD
Uludag University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MsC
Study Record Dates
First Submitted
August 25, 2026
First Posted
September 2, 2026
Study Start
July 15, 2024
Primary Completion
September 30, 2024
Study Completion
September 30, 2024
Last Updated
September 28, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
De-identified individual participant data (IPD) underlying the results reported in this study, including participant characteristics and outcome measure data, will be made available to qualified researchers upon reasonable request to the corresponding author. Data sharing will be subject to institutional policies, ethical approval, and applicable data protection regulations.