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Exercise-Induced Muscle DamageNCT07352319

DOES LOWER BODY PLYOMETRICS CAUSE RHABDOMYOLYSIS IN FEMALE VOLLEYBALL PLAYERS-AN EXPERIMENTAL STUDY

A study testing plyometric program in people with Exercise-Induced Muscle Damage and Rhabdomyolysis, run by Cairo University at 1 site in Saudi Arabia.

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

Eight-week interventional study to evaluate whether lower-body plyometric training alters serum creatine phosphokinase (CPK) and creatinine levels in female collegiate volleyball players. Sixty participants were randomized to experimental (plyometrics twice weekly) or control (routine volleyball) groups. Read more about this study

Who is it for?
Ages 18 to 25 years, women onlyHealthy volunteers can take part
What is being tested?
plyometric program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteSaudi Arabia
Study dates
12 Jan 2022to 25 Oct 2022
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 25 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Active collegiate female volleyball players
  • consent to participate
  • no prior plyometric training program.

Who cannot join

  • Neuromuscular impairments
  • recent injuries.

Trial locations and contacts

1 site in 1 country.

Saudi Arabia1 site
  • Dr. Mariam Salem

    Jeddah, 32143

Other trials in Saudi Arabia

About this study

Official title: Effects of Lower Body Plyometric Training on Serum CPK and Creatinine Levels in Collegiate Female Volleyball Players: An Experimental Study

Eight-week interventional study to evaluate whether lower-body plyometric training alters serum creatine phosphokinase (CPK) and creatinine levels in female collegiate volleyball players. Sixty participants were randomized to experimental (plyometrics twice weekly) or control (routine volleyball) groups. Blood sampling occurred at baseline; days 2, 4, and 6; and weeks 1, 2, 4, 6, and 8.

Read the detailed description

Intervention adapted from James \& Robert (2015). Experimental group completed progressive lower-body plyometrics twice weekly (Monday/Wednesday) over eight weeks with warm-up and cool-down. Exercises included squat jump; jump to box (30 cm); tuck jump; split squat jump; lateral hurdle jump (50 cm); zigzag jump; single-leg tuck jump; and depth jump (80 cm). Control group continued routine volleyball activities and did not perform low/medium/high-intensity plyometrics. Primary biomarker (serum CPK) assessed via CK-NAC optimized IFCC method; serum creatinine by modified Jaffe's method. Two-way ANOVA with Bonferroni post hoc used. Findings: CPK increased from day 2, peaked day 4, stabilized to week 2, then declined toward baseline by week 8; creatinine remained stable.

Being tested
plyometric program
Medical subject headings
Rhabdomyolysis

What participants receive

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

  • plyometric programOther

    Also called Lower-body plyometric training

    Twice-weekly sessions (Mon/Wed) for 8 weeks; exercise menu and dosing per Table 1 (intensity, rest, and jumps/set).

Study groups in NCT07352319
Study groupRoleWhat they receive
Lower-body plyometric trainingExperimentalProgressive plyometric program, twice weekly for eight weeks.
Receives: Other: plyometric program
ControlActive comparatorRoutine volleyball practice; no plyometric exercises.
Receives: Other: plyometric program

What is being measured

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

  1. Serum CPK (U/L)

    change from baseline at day 2, day 4, week 1, week 2, week 4, week 6, week 8

    Measured: Baseline; 2, 4, 6 days; 1, 2, 4, 6, 8 weeks

Secondary outcomes (1)
  1. Serum creatinine (mg/dL)

    change from baseline over same time points

    Measured: Baseline; 2, 4, 6 days; 1, 2, 4, 6, 8 weeks

Timeline

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

  1. First posted20 Jan 2026
  2. Study start12 Jan 2022
  3. Primary completion15 May 2022
  4. Study completion25 Oct 2022

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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07352319
Sponsor's protocol ID
BMC VP
Status last verified
Jan 2026
First submitted
11 Jan 2026
Last updated
20 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared because this study does not include a data-sharing plan and is limited to internal analysis only.

Questions about this trial

What is this clinical trial studying?

A study testing plyometric program in people with Exercise-Induced Muscle Damage and Rhabdomyolysis, run by Cairo University at 1 site in Saudi Arabia.

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 3 inclusion and 2 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 Jan 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 Saudi Arabia. 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?

Serum CPK (U/L) (time frame: Baseline; 2, 4, 6 days; 1, 2, 4, 6, 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 Jan 2026.

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