Elastic Band Exercise to Improve Hip Strength and Agility in Young Basketball Players

February 12, 2026 updated by: Nebojša Trajković

Does Short-Term Eccentric Strengthening With Elastic Bands Improve Hip Adductor Strength in Young Basketball Players?

Here is the complete Brief Summary entry in a single paragraph, written in plain language, and excluding the study results (as requested), but maintaining academic rigor in describing the study design:

The purpose of this study is to evaluate the effect of a 4-week short-term eccentric strengthening program using elastic bands on both hip adductor muscle strength and agility performance in young male basketball players. For this randomized controlled trial, twenty-one healthy young male athletes were separated by chance into two conditions: a training group, which performed the 4-week elastic band protocol in addition to their regular basketball training, and a control group, which engaged exclusively in their routine training. The primary measurements for comparison were maximal eccentric and isometric hip adduction strength (using a hand-held dynamometer) and the agility T-test. It is hypothesized that this targeted eccentric strengthening will lead to a significant enhancement of both hip adduction strength and overall athletic performance in the intervention group

Study Overview

Detailed Description

The incidence of lower-limb and groin injuries in professional basketball is significant, with weak hip adductor strength identified as a major risk factor. While eccentric strengthening programs have shown promise in athletic populations, there is a clear gap in the literature regarding the effectiveness of short-term hip-adduction strengthening using available tools like elastic bands in young basketball players. This study was thus designed as a rigorous randomized controlled trial to investigate this specific intervention.

This study was a 4-week Interventional Randomized Controlled Trial (RCT) involving 21 healthy young male basketball players. Participants were recruited from a single sub-elite team and were excluded if they had any history of lower-limb injury (knee, hip, groin, lower back) in the preceding six months, or if they had performed any systematic hip adductor exercises during that period. Participants were randomized into two groups, paired based on their initial isometric hip adduction force. The Training Group (TG) conducted a supervised hip adduction protocol using Tuber-Band elastic bands. This program was performed 2-3 times per week for 4 weeks, in addition to their regular basketball training. The exercise involved a full range of motion in a standing position, incorporating three distinct contraction phases: a 3-second concentric contraction, a 2-second isometric hold, and a 3-second eccentric return phase. The load was individually adjusted to the 8-15 Repetition Maximum (RM) target to ensure progressive resistance throughout the program.

All measurements were performed pre- and post-intervention by an experienced rater. Primary outcome measures included maximal eccentric hip adduction strength (EHAD) and agility T-test time. Secondary outcome measures included maximal isometric hip adduction strength (IHAD) and isometric hip abduction strength (IHAB).

Strength was quantified using a hand-held dynamometer (HHD), performing a make test for isometric strength and a break test for eccentric strength. Agility was assessed objectively using photocell gates for the T-test. Data were analyzed using a 2×2 Analysis of Variance (ANOVA) with repeated measures (group × time) to assess training-related effects. Effect sizes (Cohen's d) were also calculated and reported.

Study Type

Interventional

Enrollment (Actual)

21

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

      • Niš, Serbia, 18000
        • Faculty of Sport and Physical Education

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy young male basketball players.
  • Must be a participant in a sub-elite basketball team.
  • Age: 15-18 years

Exclusion Criteria:

  • Injury and/or pain in the knee, hip, groin, and/or lower back within the last six months
  • Previous history of hip-adductor exercises performed in the preceding six months

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Training group, Elastic Band Training Group, Eccentric Strengthening Group
Four-week eccentric and isometric hip-adduction training using elastic bands. Training sessions were supervised group sessions performed 2-3 times per week (2x/week in week 1; 3x/week in weeks 2-4) prior to regular basketball training. The exercise was performed in a standing position using elastic bands. Each repetition involved a 3-second concentric contraction, a 2-second isometric contraction, and a 3-second eccentric (hip-adduction) movement until full hip-abduction. The training load progressed from 3 sets of 15 RM in week 1, to 3 sets of 10 RM in weeks 2-3, and finally 3 sets of 8 RM in week 4. Both legs were trained
The training was performed in a standing position, focusing on eccentric hip adduction. The participant started from full hip-abduction. A single repetition consisted of a 3-second concentric contraction (adduction), followed by a 2-second isometric contraction, and then a 3-second eccentric movement (abduction) back to full hip-abduction, with a 2-second pause before the next repetition. The intervention spanned 4 weeks, with the training frequency and intensity progressively increasing. Load (elastic band resistance and fixation distance) was individually determined one week prior to the intervention based on repetition maximum (RM) sets. During Week 1, participants trained 2 times per week, performing 3 sets per leg at 15 RM. This progressed to 3 sessions per week for Weeks 2 and 3, with the load increasing to 10 RM (3 sets per leg). Finally, in Week 4, the frequency remained at 3 sessions per week, and the intensity was further increased to 8 RM (3 sets per leg).
No Intervention: Contro group (CG), Regular Training Control
The Control Group (CG) continued with their regular basketball training. This included five basketball training sessions and one competitive game per week, which was the same frequency as the training group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximal Eccentric Hip Adduction Strength (EHAD)
Time Frame: Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Maximum force (in kilograms) produced during an eccentric contraction of the hip adductor muscles, measured using a hand-held dynamometer (HHD) in a side-lying position on the dominant leg.
Baseline (Pre-intervention) and 4 Weeks (Post-intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximal Isometric Hip Adduction Strength (IHAD)
Time Frame: Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Maximum force (in kilograms) produced during an isometric contraction of the hip adductor muscles, measured using a hand-held dynamometer (HHD) in a supine lying position on the dominant leg.
Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Isometric Hip Abduction Strength (IHAB)
Time Frame: Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Maximum force (in kilograms) produced during an isometric contraction of the hip abductor muscles, measured using a hand-held dynamometer (HHD) in a supine lying position on the dominant leg.
Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Agility T-test Time
Time Frame: Baseline (Pre-intervention) and 4 Weeks (Post-intervention)
Time (in seconds) required to complete the Agility T-test, measured using photocell gates. The test involves a straight run, lateral shuffling, and hand-touching of cones.
Baseline (Pre-intervention) and 4 Weeks (Post-intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

January 10, 2024

Primary Completion (Actual)

February 10, 2024

Study Completion (Actual)

March 1, 2024

Study Registration Dates

First Submitted

February 12, 2026

First Submitted That Met QC Criteria

February 12, 2026

First Posted (Actual)

February 19, 2026

Study Record Updates

Last Update Posted (Actual)

February 19, 2026

Last Update Submitted That Met QC Criteria

February 12, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 04-2059/3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data (IPD) will not be shared with other researchers. All data used to generate the findings is already provided within the published manuscript and supplementary information files.

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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