- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07617831
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
Status
Completed
Intervention / Treatment
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
Additional Relevant MeSH Terms
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Therapeutics
- Physical Therapy Modalities
- Patient Care
- Exercise Therapy
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Physical Conditioning, Human
- Exercise
- Resistance Training
- Plyometric Exercise
Other Study ID Numbers
- BSU-2026029H
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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