<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE trials [
<!ELEMENT trials (trial+)>

<!ELEMENT trial (main,contacts,countries,criteria,health_condition_code,health_condition_keyword,intervention_code,
          intervention_keyword,primary_outcome,secondary_outcome,secondary_sponsor,secondary_ids,source_support,ethics_reviews)>

<!ELEMENT main (trial_id,utrn?,reg_name,date_registration,primary_sponsor,public_title,acronym?,scientific_title,scientific_acronym?,
          date_enrolment,type_enrolment,target_size,recruitment_status,url?,study_type,study_design,phase,hc_freetext?,i_freetext?,results_actual_enrolment,results_date_completed,results_url_link,results_summary,           results_date_posted,results_date_first_publication,results_baseline_char,results_participant_flow,results_adverse_events,results_outcome_measures,results_url_protocol,results_IPD_plan, results_IPD_description)>
<!ELEMENT trial_id (#PCDATA)>
<!ELEMENT utrn (#PCDATA)>
<!ELEMENT reg_name (#PCDATA)>
<!ELEMENT date_registration (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT primary_sponsor (#PCDATA)>
<!ELEMENT public_title (#PCDATA)>
<!ELEMENT acronym (#PCDATA)>
<!ELEMENT scientific_title (#PCDATA)>
<!ELEMENT scientific_acronym (#PCDATA)>
<!ELEMENT date_enrolment (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT type_enrolment (#PCDATA)>
<!ELEMENT target_size (#PCDATA)>
<!ELEMENT recruitment_status (#PCDATA)><!-- Pending,Recruiting,Suspended,Complete,Other -->
<!ELEMENT url (#PCDATA)>
<!ELEMENT study_type (#PCDATA)><!-- interventional,observational -->
<!ELEMENT study_design (#PCDATA)>
<!ELEMENT phase (#PCDATA)>
<!ELEMENT hc_freetext (#PCDATA)>
<!ELEMENT i_freetext (#PCDATA)>
<!ELEMENT results_actual_enrolment (#PCDATA)>
<!ELEMENT results_date_completed (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_url_link (#PCDATA)>
<!ELEMENT results_summary (#PCDATA)>
<!ELEMENT results_date_posted (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_date_first_publication (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_baseline_char (#PCDATA)>
<!ELEMENT results_participant_flow (#PCDATA)>
<!ELEMENT results_adverse_events (#PCDATA)>
<!ELEMENT results_outcome_measures (#PCDATA)>
<!ELEMENT results_url_protocol (#PCDATA)>
<!ELEMENT results_IPD_plan (#PCDATA)>
<!ELEMENT results_IPD_description (#PCDATA)>


<!ELEMENT contacts (contact+)>
<!ELEMENT contact (type,firstname,middlename,lastname,address,city,country1,zip,telephone,email,affiliation)>
<!ELEMENT type (#PCDATA)><!-- Public,Scientific -->
<!ELEMENT firstname (#PCDATA)>
<!ELEMENT middlename (#PCDATA)>
<!ELEMENT lastname (#PCDATA)>
<!ELEMENT address (#PCDATA)>
<!ELEMENT city (#PCDATA)>
<!ELEMENT country1 (#PCDATA)>
<!ELEMENT zip (#PCDATA)>
<!ELEMENT telephone (#PCDATA)>
<!ELEMENT email (#PCDATA)>
<!ELEMENT affiliation (#PCDATA)>

<!ELEMENT countries (country2+)>
<!ELEMENT country2 (#PCDATA)>

<!ELEMENT criteria (inclusion_criteria,agemin,agemax,gender,exclusion_criteria)>
<!ELEMENT inclusion_criteria (#PCDATA)>
<!ELEMENT agemin (#PCDATA)>
<!ELEMENT agemax (#PCDATA)>
<!ELEMENT gender (#PCDATA)>
<!ELEMENT exclusion_criteria (#PCDATA)>

<!ELEMENT health_condition_code (hc_code+)>
<!ELEMENT hc_code (#PCDATA)>

<!ELEMENT health_condition_keyword (hc_keyword+)>
<!ELEMENT hc_keyword (#PCDATA)>

<!ELEMENT intervention_code (i_code+)>
<!ELEMENT i_code (#PCDATA)>

<!ELEMENT intervention_keyword (i_keyword+)>
<!ELEMENT i_keyword (#PCDATA)>

<!ELEMENT primary_outcome (prim_outcome+)>
<!ELEMENT prim_outcome (#PCDATA)>

<!ELEMENT secondary_outcome (sec_outcome+)>
<!ELEMENT sec_outcome (#PCDATA)>

<!ELEMENT secondary_sponsor (sponsor_name+)>
<!ELEMENT sponsor_name (#PCDATA)>

<!ELEMENT secondary_ids (secondary_id+)>
<!ELEMENT secondary_id (sec_id,issuing_authority)>
<!ELEMENT sec_id (#PCDATA)>
<!ELEMENT issuing_authority (#PCDATA)>

<!ELEMENT source_support (source_name+)>
<!ELEMENT source_name (#PCDATA)>

<!ELEMENT ethics_reviews (ethics_review+)>
<!ELEMENT ethics_review (status,approval_date,contact_name,contact_address,contact_phone,contact_email)>
<!ELEMENT status (#PCDATA)><!-- Not approved,Approved,NA -->
<!ELEMENT approval_date (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT contact_name (#PCDATA)>
<!ELEMENT contact_address (#PCDATA)>
<!ELEMENT contact_phone (#PCDATA)>
<!ELEMENT contact_email (#PCDATA)>
]>
<trials>
  <trial>
    <main>
      <trial_id>IRCT20250905067129N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-04-21</date_registration>
      <primary_sponsor>National Defense University (Center for Elites and Top Talents of the Armed Forces)</primary_sponsor>
      <public_title>Unstable Loaded Plyometric Training</public_title>
      <acronym>ULPT=Unstable Loaded Plyometric Training</acronym>
      <scientific_title>Comparison of the Effects of Unstable and Stable Loaded Plyometric Training on Some Physical Fitness Factors in Pas Gorgan Volleyball Team Players</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-05-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>21</target_size>
      <recruitment_status>Recruiting</recruitment_status>
      <url>https://irct.ir/trial/89035</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: In this study, the process of assigning participants to groups will be carried out with a combined approach of initial pairing (pair-matching) and simple randomization to reduce initial heterogeneity between groups on the one hand and ensure true randomization on the other.
First, all participants will be grouped into pairs of equal jumping ability based on the results of the vertical jump test (Jump-and-Reach) at the beginning of the study. This pairing method will be used to initially balance the jumping ability in the groups. Then, in each pair, assignment to study groups will be done randomly. Microsoft Excel software and the (RAND) function will be used to generate the random sequence. A random number will be generated for each individual and based on the ascending sorting of these numbers, participants will be divided into three study groups including: 1. Unstable Loaded Plyometric Training (ULPT) group, 2. Stable Loaded Plyometric Training (SLPT) group, and 3. The active control group (CON) will be allocated.
The randomization unit in this study will be individual-based. The randomization sequence will be generated and maintained by one of the researchers who is not involved in data collection and analysis. To maintain confidentiality and prevent any possible bias in the allocation process, the randomization sequence will be placed in opaque, sealed, and numbered envelopes and will only be returned at the time of allocation of each participant.
Thus, the randomization process in this study will both reduce the initial heterogeneity between groups and fully respect the random nature of the allocation of participants, Blinding description: In this study, blinding will be performed in a single-blind manner. Participants will be unaware of their group assignment and the exact purpose of the intervention. In addition, data analysis will be performed by a consulting statistician who is unaware of the group assignment. However, the intervention and functional test administrator will be aware of the group assignment due to the nature of the research and the need to monitor the correct implementation of the exercises. Thus, in this study, blinding will be observed at the level of participants and data analyst, but there will be no possibility of blinding the test administrator.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Volleyball players' performance.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group 1: Participants in this group performed unstable loaded plyometric exercises equivalent to 10% of body weight over a 12-week period (three sessions per week, a total of 36 sessions). The unstable load was provided by a barbell and two water-filled gimbal balls. The exercises were performed on the gym floor and included countermovement jumps. The intensity and volume of the exercise gradually increased, such that the number of jumps increased from 72 repetitions in the first session to 140 repetitions in the final sessions. Each session lasted 15 to 25 minutes, with a work-to-rest ratio of 1:7 and a two-minute rest interval between exercises. All sessions began with a RAMP warm-up protocol (light jogging, dynamic stretching, and submaximal jumps). Intervention 2: Intervention Group 2: Participants in this group performed 10% of their body weight of sustained loading plyometric exercises over a 12-week period (three sessions per week, a total of 36 sessions). The unstable load was provided by a barbell and weights. The exercises were performed on the gym floor and included countermovement jumps. The intensity and volume of the exercise gradually increased, such that the number of jumps increased from 72 repetitions in the first session to 140 repetitions in the final sessions. Each session lasted 15 to 25 minutes, with a work-to-rest ratio of 1:7 and a two-minute rest interval between exercises. All sessions began with a RAMP warm-up protocol (light jogging, dynamic stretching, and submaximal jumps). Intervention 3: Control group: Participants in the control group continued their normal volleyball training during the 12-week period. Their training consisted of typical team technical and tactical activities and did not receive any additional plyometric training or specific intervention. This group served as a comparison to determine the net effect of the plyometric interventions on the other two groups.</i_freetext>
      <results_actual_enrolment></results_actual_enrolment>
      <results_date_completed></results_date_completed>
      <results_url_link></results_url_link>
      <results_summary></results_summary>
      <results_date_posted></results_date_posted>
      <results_date_first_publication></results_date_first_publication>
      <results_baseline_char></results_baseline_char>
      <results_participant_flow></results_participant_flow>
      <results_adverse_events></results_adverse_events>
      <results_outcome_measures></results_outcome_measures>
      <results_url_protocol></results_url_protocol>
      <results_IPD_plan>No - There is not a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for not sharing IPD is To adhere to ethical principles and protect participants' personal and confidential information, the raw data (individual participant data) from this study will not be shared for public use or secondary research. However, if required, and solely to assure journal reviewers or editors of the accuracy of statistical analyses, the data will be provided confidentially.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Parsa Soltani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 182, Shahid Beheshti Governance School, Corner of Shohada St. (Opposite Indonesian Embassy), Qaem Maqam Farahani St., Shahid Beheshti St.</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۱۵۸۶۷۵۵۴۱۴</zip>
        <telephone>+98 21 8872 8937</telephone>
        <email>par.soltani@mail.sbu.ac.ir</email>
        <affiliation>National Elite Foundation</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Amir Falahnezhad Mojarad</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Amin University of Law Enforcement Sciences - Shahid Kharrazi Highway - End of Shahid Hemmat Gharb Highway - Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۱۴۳۹۹۱۴۱۵۳</zip>
        <telephone>+98 21 4893 1289</telephone>
        <email>amirfalh.sport@gmail.com</email>
        <affiliation>Amin University of Police Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age range: 18-28 years
sports history of participating in league competitions for at least 2 years,
ability to jump vertically at least 45 cm
be completely medically healthy and have no problems performing sports related to the research
have no cardiovascular problems
Avoid using stimulants and certain medications (steroids).
Player of the Gorgan Pas volleyball team</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>28 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>History of acute or chronic musculoskeletal injuries/disorders of the ankles, knees, or back
History of cardiovascular disease and problems in the participant.
Taking steroid medications.
Tobacco and alcohol consumption</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword></hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group 1: Participants in this group performed unstable loaded plyometric exercises equivalent to 10% of body weight over a 12-week period (three sessions per week, a total of 36 sessions). The unstable load was provided by a barbell and two water-filled gimbal balls. The exercises were performed on the gym floor and included countermovement jumps. The intensity and volume of the exercise gradually increased, such that the number of jumps increased from 72 repetitions in the first session to 140 repetitions in the final sessions. Each session lasted 15 to 25 minutes, with a work-to-rest ratio of 1:7 and a two-minute rest interval between exercises. All sessions began with a RAMP warm-up protocol (light jogging, dynamic stretching, and submaximal jumps).</i_keyword>
      <i_keyword>Intervention Group 2: Participants in this group performed 10% of their body weight of sustained loading plyometric exercises over a 12-week period (three sessions per week, a total of 36 sessions). The unstable load was provided by a barbell and weights. The exercises were performed on the gym floor and included countermovement jumps. The intensity and volume of the exercise gradually increased, such that the number of jumps increased from 72 repetitions in the first session to 140 repetitions in the final sessions. Each session lasted 15 to 25 minutes, with a work-to-rest ratio of 1:7 and a two-minute rest interval between exercises. All sessions began with a RAMP warm-up protocol (light jogging, dynamic stretching, and submaximal jumps).</i_keyword>
      <i_keyword>Control group: Participants in the control group continued their normal volleyball training during the 12-week period. Their training consisted of typical team technical and tactical activities and did not receive any additional plyometric training or specific intervention. This group served as a comparison to determine the net effect of the plyometric interventions on the other two groups.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Sargent's jump height. Timepoint: 1. Initial measurement (pre-test) of Sargent jump height in week 0, before the start of training 2; Intermediate measurement at the end of week 4, 48 hours after the last training session, 3. Intermediate measurement at the end of week 8, 48 hours after the last training session, 4. Final measurement (post-test) at the end of week 12, 48 hours after the last training session. Method of measurement: For the Sargent jump height, hand height is initially assessed in a straight standing position with both feet in a lateral position close to the wall, the arm of the dominant hand fully extended in a vertical direction, and the fingers touching a wall-mounted tactile sensor connected to a digital display (Sargent Jumping Device, Danesh Salar Iranian, Iran). After that, participants perform a reverse movement (i.e., knee and hip flexion) with an arm swing immediately after a rapid and powerful vertical jump. The participants’ task is to touch the scale mounted on the wall with their middle finger while flying at the highest position.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Depth jump. Timepoint: 1. Initial measurement (pre-test) of Sargent jump height in week 0, before the start of training 2; Intermediate measurement at the end of week 4, 48 hours after the last training session, 3. Intermediate measurement at the end of week 8, 48 hours after the last training session, 4. Final measurement (post-test) at the end of week 12, 48 hours after the last training session. Method of measurement: The depth jump is performed by landing from a 40 cm box on firm ground and immediately jumping as high as possible. Participants are instructed to touch a scale mounted on the wall during the flight at the highest point. The jump height is defined as the difference between the height of the hand in the standing position and the height of the hand in the jumping position.</sec_outcome>
      <sec_outcome>Standing long jump. Timepoint: 1. Initial measurement (pre-test) of standing long jump in week 0, before the start of training; 2. Intermediate measurement at the end of week 4, 48 hours after the last training session; 3. Intermediate measurement at the end of week 8, 48 hours after the last training session; 4. Final measurement (post-test) at the end of week 12, 48 hours after the last training session. Method of measurement: To measure horizontal explosive power of the lower limbs, the subject will stand on the ground behind a designated starting line with both feet together. After a warm-up movement involving bending the knees and swinging the arms, the subject will jump forward with maximum force and attempt to cover as much distance as possible. The landing must be done with both feet simultaneously within the landing area. The distance from the front edge of the starting line to the heel of the foot closest to the landing area will be measured in centimeters using an accurate tape measure. Each subject will make three valid attempts and the best record will be recorded as the final result. A 2-minute rest period will be given between each attempt. Attempts in which the subject stands further than the permitted distance on the starting line or loses balance during landing will be considered invalid and will be repeated.</sec_outcome>
      <sec_outcome>Linear speed 10 meters. Timepoint: 1. Initial measurement (pre-test) of 10-meter linear speed in week 0, before the start of training; 2. Intermediate measurement at the end of week 4, 48 hours after the last training session; 3. Intermediate measurement at the end of week 8, 48 hours after the last training session; 4. Final measurement (post-test) at the end of week 12, 48 hours after the last training session. Method of measurement: To assess short-term linear acceleration and speed, subjects will perform a 10-meter sprint test. The subject will stand in a ready position behind the designated starting line and, upon the examiner's command, will begin an explosive run. The running time will be recorded using an accurate hand-held stopwatch from the moment of crossing the starting line to reaching the finish line at a distance of 10 meters. Each subject will make two valid attempts and the best record (the shortest time in seconds) will be recorded as the final result. A 3-minute rest period will be considered between attempts to prevent fatigue. Subjects will be required to run at maximum power in each attempt and not deviate from a straight line along the way.</sec_outcome>
      <sec_outcome>Agility T. Timepoint: 1. Initial measurement (pre-test) of T agility in week 0, before the start of training; 2. Intermediate measurement at the end of the fourth week, 48 hours after the last training session; 3. Intermediate measurement at the end of the eighth week, 48 hours after the last training session; 4. Final measurement (post-test) at the end of the twelfth week, 48 hours after the last training session. Method of measurement: The test route consists of four cones arranged in the shape of the letter T: one cone at the starting line, one 9.14 m in front of it, and two other cones each 4.57 m apart on either side of the middle cone. The subject will stand behind the starting line in a ready position and, at the command of the examiner, will begin an explosive run. First, he will run forward to the middle cone, then quickly shuffle to the right and touch the side cone, immediately move sideways to the left and touch the other cone, then move sideways again to the center, and finally run backwards to the starting line. The test time from the moment of departure until the complete crossing of the finish line will be recorded with a hand stopwatch. Each subject will have two valid attempts and the best time (the shortest time in seconds) will be recorded as the final record. A minimum of 3 minutes of rest will be given between each attempt.</sec_outcome>
      <sec_outcome>Dynamic balance Y. Timepoint: 1. Initial measurement (pre-test) of dynamic balance Y in week 0, before the start of training 2; Intermediate measurement at the end of the fourth week, 48 hours after the last training session, 3. Intermediate measurement at the end of the eighth week, 48 hours after the last training session, 4. Final measurement (post-test) at the end of the twelfth week, 48 hours after the last training session. Method of measurement: In this test, after a standard warm-up (light jogging and dynamic stretching), subjects will stand on the supporting (dominant) leg and touch the opposite leg as far as possible in three directions: anterior, posterior-medial, and posterolateral. The order of execution will consist of three attempts in each direction, and the best valid record will be recorded. During the execution, the supporting leg must remain completely fixed on the ground and the hands must be placed on the pelvis. Attempts in which the subject loses balance, the standing leg is moved, or the hands are used for assistance will be considered invalid and will be repeated. To prevent fatigue, a minimum of 30 seconds of rest will be given between each attempt. The test will be performed for the dominant leg.</sec_outcome>
    </secondary_outcome>
    <secondary_sponsor>
      <sponsor_name></sponsor_name>
    </secondary_sponsor>
    <secondary_ids>
      <secondary_id>
        <sec_id></sec_id>
        <issuing_authority></issuing_authority>
      </secondary_id>
    </secondary_ids>
    <source_support>
      <source_name>Police Command of the Islamic Republic of Iran</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-02-09</approval_date>
        <contact_name>Deputy of Health, Relief and Treatment, Police Command of the Islamic Republic of Iran - Shahid Behe</contact_name>
        <contact_address>Tehran, Valiasr St., above Vanak Square, opposite Zafar, Hazrat Valiasr Hospital, Applied Research Center of the Deputy of Health Services of NAJA Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
