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Lower-Limb Explosive PerformanceNCT07776808

French Contrast Training in Male Collegiate Basketball Players

A study testing French Contrast Training and Resistance Training in people with Lower-Limb Explosive Performance, run by Ziren Zhao at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This randomized controlled trial evaluated the effects of 12 weeks of French Contrast Training (FCT) compared with traditional resistance training (RT) on lower-limb explosive performance in male collegiate basketball players. Read more about this study

Who is it for?
Ages 18 to 24 years, men onlyHealthy volunteers can take part
Conditions the study is for
Lower-Limb Explosive Performance
What is being tested?
French Contrast Training and Resistance Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteChina
Study dates
1 Mar 2026to 7 Jun 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 24 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male collegiate basketball players aged 18-24 years.
  • At least 7 years of systematic basketball training experience.
  • At least 2 years of resistance training experience.
  • Competitive classification of Chinese National Second-Class Athlete or higher in basketball.
  • Regular participation in basketball-specific technical training three times per week under the same training program.
  • Physically healthy and able to participate in resistance and jumping training.
  • Willing to participate in the study and provide written informed consent.

Who cannot join

  • Lower-limb injury within the 3 months prior to enrollment.
  • Severe musculoskeletal or joint disorders that could interfere with resistance or jumping exercise.
  • Cardiovascular disease or other medical conditions that could prevent safe participation in high-intensity resistance or plyometric exercise.
  • Previous experience with structured French Contrast Training.
  • Unable to safely complete the prescribed training or performance testing procedures.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Stadium

    Chongqing

Other trials in China

About this study

Official title: Effects of 12 Weeks of French Contrast Training on Lower-Limb Explosive Performance in Male Collegiate Basketball Players

This randomized controlled trial evaluated the effects of 12 weeks of French Contrast Training (FCT) compared with traditional resistance training (RT) on lower-limb explosive performance in male collegiate basketball players. Forty participants were randomly assigned in a 1:1 ratio to either the FCT group or the RT group. Both groups trained twice per week for 12 weeks, with at least 48 hours between sessions. Lower-limb performance was assessed before and after the intervention using countermovement jump height, drop jump height, ground contact time, reactive strength index, 10-m sprint time, and isometric mid-thigh pull peak force. The study aimed to determine whether FCT produces greater improvements in jumping performance, reactive strength, short-distance acceleration, and maximal force than traditional resistance training.

Being tested
French Contrast Training, Resistance Training

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • French Contrast TrainingBehavioural

    Participants performed French Contrast Training (FCT) twice per week for 12 weeks, with at least 48 hours between sessions. Each FCT sequence consisted of four exercises performed in the following order: back squat at 85% of 1RM, 30-cm hurdle jumps, squat jumps at 25% of 1RM, and band-assisted jumps. A 20-second recovery period was provided between consecutive exercises. Participants completed 4 sets of 8 repetitions for each exercise, with 3 minutes of rest between sets. Training loads were prescribed according to baseline 1RM values and remained unchanged throughout the 12-week intervention. All training sessions were supervised by certified strength and conditioning coaches.

  • Resistance TrainingBehavioural

    Participants performed a 12-week traditional resistance training program, with two sessions per week and at least 48 hours between sessions. The program consisted of back squat at 85% of 1RM, Romanian deadlift at 85% of 1RM, leg press at 85% of 1RM, and walking lunge at 30% of 1RM. Participants completed 4 sets of 8 repetitions for each exercise, with 3 minutes of rest between sets. Training loads were prescribed according to baseline 1RM values and remained unchanged throughout the 12-week intervention. All training sessions were supervised by certified strength and conditioning coaches.

Study groups in NCT07776808
Study groupRoleWhat they receive
French Contrast Training GroupExperimentalParticipants assigned to this arm completed a 12-week French Contrast Training program, with two training sessions per week and at least 48 hours between sessions. Each training sequence consisted of four exercises performed in order: back squat at 85% of 1RM, 30-cm hurdle jumps, squat jumps at 25% of 1RM, and band-assisted jumps. A 20-second recovery period was provided between consecutive exercises. Participants completed 4 sets of 8 repetitions for each exercise, with 3 minutes of rest between sets. Training loads were prescribed based on baseline 1RM values and remained unchanged throughout the 12-week intervention. All sessions were supervised by certified strength and conditioning coaches.
Receives: Behavioral: French Contrast Training
Resistance Training GroupActive comparatorParticipants assigned to this arm completed a 12-week traditional resistance training program, with two training sessions per week and at least 48 hours between sessions. The program consisted of back squat at 85% of 1RM, Romanian deadlift at 85% of 1RM, leg press at 85% of 1RM, and walking lunge at 30% of 1RM. Participants completed 4 sets of 8 repetitions for each exercise, with 3 minutes of rest between sets. Training loads were prescribed based on baseline 1RM values and remained unchanged throughout the 12-week intervention. All sessions were supervised by certified strength and conditioning coaches.
Receives: Behavioral: Resistance Training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Countermovement Jump Height

    Countermovement jump (CMJ) height was assessed using a force platform system (Kistler, Winterthur, Switzerland; sampling frequency: 1000 Hz). Participants performed three maximal countermovement jumps with their hands placed on the iliac crests to minimize arm-swing contribution. A 1-minute rest interval was provided between attempts. The highest jump height, expressed in centimeters (cm), was used for analysis.

    Measured: Baseline and immediately after the 12-week intervention

Secondary outcomes (5)
  1. Drop Jump Height

    Drop jump (DJ) height was assessed using a force platform system (Kistler, Winterthur, Switzerland; sampling frequency: 1000 Hz). Participants stepped from a 30-cm box onto the force platform and immediately performed a maximal vertical jump while attempting to minimize ground contact time. Three maximal attempts were performed with 1-minute rest intervals. The trial with the highest reactive strength index was selected, and DJ height from the same trial was recorded in centimeters (cm).

    Measured: Baseline and immediately after the 12-week intervention

  2. Ground Contact Time

    Ground contact time (GCT) was obtained during the drop jump test using a force platform system (Kistler, Winterthur, Switzerland; sampling frequency: 1000 Hz). The trial with the highest reactive strength index was selected, and GCT from the same trial was recorded in milliseconds (ms).

    Measured: Baseline and immediately after the 12-week intervention

  3. Reactive Strength Index

    Reactive strength index (RSI) was assessed during the 30-cm drop jump test using force-platform data. Participants completed three maximal attempts, and the trial producing the highest RSI was used for analysis. RSI was calculated from drop jump performance and ground contact time.

    Measured: Baseline and immediately after the 12-week intervention

  4. 10-Meter Sprint Time

    Sprint performance was assessed using electronic timing gates (Brower Timing Systems, Draper, UT, USA). Participants started from a split-stance position 0.5 m behind the first timing gate and sprinted maximally through 15 m. Three maximal trials were completed with 2-3 minutes of rest between trials. The fastest 10-m sprint time, expressed in seconds (s), was used for analysis.

    Measured: Baseline and immediately after the 12-week intervention

  5. Isometric Mid-Thigh Pull Peak Force

    Isometric mid-thigh pull (IMTP) peak force was assessed using a force platform system (Kistler, Winterthur, Switzerland; sampling frequency: 1000 Hz). Knee and hip angles were standardized at approximately 130° and 145°, respectively. Participants pulled maximally against a fixed bar for 3-5 seconds. Three maximal attempts were completed with 2-minute rest intervals, and the highest absolute peak force value, expressed in Newtons (N), was used for analysis.

    Measured: Baseline and immediately after the 12-week intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Aug 2026
  2. Study start1 Mar 2026
  3. Primary completion7 Jun 2026
  4. Study completion7 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07776808
Sponsor's protocol ID
CQUE-LL20260331009
Status last verified
Aug 2026
First submitted
18 Aug 2026
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Ding X. Effects of 12 weeks of French contrast training on lower-limb explosive performance in male collegiate basketball players. BMC Sports Sci Med Rehabil. 2026 Aug 28;18(1):551. doi: 10.1186/s13102-026-02021-z.

    PubMed 42983572

Questions about this trial

What is this clinical trial studying?

A study testing French Contrast Training and Resistance Training in people with Lower-Limb Explosive Performance, run by Ziren Zhao at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Countermovement Jump Height (time frame: Baseline and immediately after the 12-week intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07776808, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2026.

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