- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07475078
Reactive Strength and Dynamic Rebound: A Drop Jump Index Comparison
Which Index Tells the Full Story? Comparing Reactive Strength and Dynamic Rebound Index in Drop Jump Performance
The stretch-shortening cycle (SSC) is a fundamental mechanism in explosive human movement, enabling musculotendinous units to store and release elastic energy, thereby allowing the body to produce higher forces and velocities with greater mechanical efficiency. Movements such as sprinting, jumping, hopping, and sudden changes of direction, which depend on rapid force application, are supported by an effective SSC. Because of this, identifying a simple and interpretable index of SSC function has long been a priority in both research and applied sport settings.
The Reactive Strength Index (RSI), most commonly defined as the ratio of jump height to ground contact time, has become the most widely used metric for quantifying SSC performance. However, this ratio presents notable methodological limitations: it combines variables of incompatible dimensions and is insensitive to drop height, thereby ignoring the eccentric load imposed on the musculotendinous system. The Dynamic Rebound Index (DRI), recently proposed as a dimensionless and mechanically grounded alternative, is calculated as DRI = (box height + jump height) / (9.8 × ground contact time²). Despite its theoretical advantages, a direct comparison between the RSI and DRI remains unexplored in the literature, which justifies the relevance of the present study.
This study aims to compare the RSI and the DRI in physically active adults of both sexes during the execution of the Drop Jump at four different drop heights (20, 30, 40, and 50 cm). The specific objectives are: (a) to characterize performance across the four height conditions; (b) to analyze differences between sexes in both indices; (c) to examine the effect of drop height on both indices; and (d) to explore the informative complementarity between the two indices.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Porto District
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Maia, Porto District, Portugal, 4475-690 Maia
- University of Maia
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Contact:
- Henrique S Sousa, MSc
- Phone Number: +351 22 986 6000
- Email: hsousa.dcd@umaia.pt
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 18 years or older.
- Physically active (engaging in regular physical activity at least 3 times per week - minimum of 180 min of physical activity).
Exclusion Criteria:
- Any musculoskeletal injuries at the time of data collection.
- Any medical condition that could compromise physical performance or safety during testing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Drop Jump 20 cm
Participants perform 3 valid Drop Jump trials from a 20 cm drop height
|
Participants perform 3 valid Drop Jump trials at each of four drop heights (20, 30, 40, and 50 cm) in a randomized order, with 1 minute of rest between trials and 5 minutes between conditions.
Jump height and ground contact time are recorded using a contact mat (ChronoJump, Boscosystem, Spain) for subsequent calculation of the RSI and DRI.
Other Names:
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|
Experimental: Drop Jump 30 cm
Participants perform 3 valid Drop Jump trials from a 30 cm drop height
|
Participants perform 3 valid Drop Jump trials at each of four drop heights (20, 30, 40, and 50 cm) in a randomized order, with 1 minute of rest between trials and 5 minutes between conditions.
Jump height and ground contact time are recorded using a contact mat (ChronoJump, Boscosystem, Spain) for subsequent calculation of the RSI and DRI.
Other Names:
|
|
Experimental: Drop Jump 40 cm
Participants perform 3 valid Drop Jump trials from a 40 cm drop height
|
Participants perform 3 valid Drop Jump trials at each of four drop heights (20, 30, 40, and 50 cm) in a randomized order, with 1 minute of rest between trials and 5 minutes between conditions.
Jump height and ground contact time are recorded using a contact mat (ChronoJump, Boscosystem, Spain) for subsequent calculation of the RSI and DRI.
Other Names:
|
|
Experimental: Drop Jump 50 cm
Participants perform 3 valid Drop Jump trials from a 50 cm drop height
|
Participants perform 3 valid Drop Jump trials at each of four drop heights (20, 30, 40, and 50 cm) in a randomized order, with 1 minute of rest between trials and 5 minutes between conditions.
Jump height and ground contact time are recorded using a contact mat (ChronoJump, Boscosystem, Spain) for subsequent calculation of the RSI and DRI.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reactive Strength Index (RSI)
Time Frame: Baseline
|
Calculated as RSI = jump height (m) / ground contact time (s), measured during the Drop Jump at four drop heights (20, 30, 40, and 50 cm).
|
Baseline
|
|
Dynamic Rebound Index (DRI)
Time Frame: Baseline
|
Calculated as DRI = (box height (m) + jump height (m)) / (9.8 × ground contact time² (s)), measured during the Drop Jump at four drop heights (20, 30, 40, and 50 cm)
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Jump Height
Time Frame: Baseline
|
Vertical jump height (m) recorded via contact mat during the Drop Jump.
|
Baseline
|
|
Ground Contact Time
Time Frame: Baseline
|
Time (s) spent in contact with the ground during the Drop Jump, recorded via contact mat.
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- DRI_HS_01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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