Combined Strength and Plyometric Training in Sanda Athletes

May 25, 2026 updated by: Mingjie Hu

Effects of Combined Strength and Plyometric Training on Lower-Limb Performance and Neuromuscular Function in Sanda Athletes: A Randomized Controlled Trial

This randomized controlled trial evaluated the effects of an 8-week combined strength and plyometric training program on lower-limb performance and neuromuscular function in male Sanda athletes. Thirty male Sanda athletes were randomly assigned to a strength training group or a combined strength and plyometric training group. Both groups trained three times per week for 8 weeks. Outcomes were assessed before and after the intervention and included standing long jump, countermovement jump, hexagon test, reactive strength index, lower-limb vertical stiffness, and lead-leg Sanda roundhouse kick attack time.

Study Overview

Study Type

Interventional

Enrollment (Actual)

30

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

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100084
        • Beijing Sport University, Beijing, China

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:

Male Sanda athletes aged 18-25 years. Holders of National Second-Class Athlete certification or above. Provided written informed consent before participation.

Exclusion Criteria:

Recent musculoskeletal injury, particularly of the lower limbs. Any contraindication to high-intensity training. Participation in additional structured strength or plyometric training during the previous 8 weeks.

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
Active Comparator: Strength Training
The strength training intervention consisted of periodized resistance training over 8 weeks, with progressive increases in intensity based on one-repetition maximum. Exercises included lower-limb resistance exercises such as squat, deadlift, and lunge variations.
Experimental: Combined Strength and Plyometric Training
The combined training intervention consisted of the same periodized strength training program as the strength training group plus a plyometric training component. Plyometric exercises were performed on non-slip rubber flooring, and jump height was monitored before each session.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Standing Long Jump Performance
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Standing long jump distance was assessed using standardized procedures. Participants completed three maximal trials, and the best distance in centimeters was recorded.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Change in Countermovement Jump Height
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Countermovement jump height was assessed using a force platform. Participants completed three trials with hands on hips, and jump height was derived from the equipment.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Change in Hexagon Test Performance
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Change-of-direction performance was evaluated using the hexagon test. Participants completed three timed trials, and the fastest time in seconds was retained.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Change in Reactive Strength Index
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Reactive strength index was derived from force-platform data during repeated bilateral maximal vertical hops.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Change in Lower-Limb Vertical Stiffness
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Lower-limb vertical stiffness was calculated from force-platform data during repeated hopping trials using peak ground reaction force, center-of-mass vertical displacement, body mass, contact time, and gravitational acceleration.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Lead-Leg Sanda Roundhouse Kick Attack Time
Time Frame: Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks
Lead-leg Sanda roundhouse kick attack time was assessed as a sport-specific outcome using high-speed video recording. Attack time was defined as the interval from movement onset to first target contact, and the mean of three valid trials was used for analysis.
Baseline and post-intervention within 48 hours after the final training session, approximately 8 weeks

Collaborators and Investigators

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

Sponsor

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 20, 2026

Primary Completion (Actual)

April 15, 2026

Study Completion (Actual)

April 20, 2026

Study Registration Dates

First Submitted

May 25, 2026

First Submitted That Met QC Criteria

May 25, 2026

First Posted (Actual)

June 1, 2026

Study Record Updates

Last Update Posted (Actual)

June 1, 2026

Last Update Submitted That Met QC Criteria

May 25, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

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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