<?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>IRCT20260812070631N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-08-19</date_registration>
      <primary_sponsor>Research Vice-Chancellery of the University of Birjand</primary_sponsor>
      <public_title>Effects of Jump Rope and Trampoline Exercises on Static and Dynamic Plantar Pressure, Static and Dynamic Balance, Center of Pressure Sway, Time to Stabilization, Somatic Anxiety, Loneliness, Depression, Life Satisfaction, and Aggression</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of the Effects of Jump Rope and Trampoline Training with a Control Group on Selected Biomechanical and Psychological Variables in Overweight Boys Aged 9–12 Years</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-08-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/92556</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: Participants are randomly allocated to the study groups in an equal allocation ratio. The individual participant serves as the unit of randomization, and after eligibility is confirmed and informed consent is obtained, participants are randomly assigned to one of three groups: jump rope exercise, trampoline exercise, or control. During the random allocation process, baseline characteristics, including age and body mass index (BMI), are taken into consideration to ensure that these characteristics are as balanced as possible across the three groups. The randomization sequence is generated and participant allocation is performed by an independent statistician. The researchers have no involvement in generating the randomization sequence, allocating participants to groups, or accessing the allocation sequence, and they remain unaware of each participant’s group assignment before the allocation process is completed. Thus, allocation is fully concealed from the researchers, Blinding description: This study will be conducted using a double-blind design. The principal investigator and researchers involved in the conduct of the study will be unaware of the randomization sequence and the participants’ group assignments. In addition, the data collectors and outcome assessors will be blinded to the participants’ group assignments. Participants’ data will be recorded and maintained using unique identification codes throughout all stages of the study. Data analysis will also be performed by an independent data analyst who will be blinded to the identities of the study groups. Therefore, the outcome assessors, data collectors, principal investigator, researchers, and data analyst will be blinded to the participants’ group assignments. A Data Safety and Monitoring Committee (DSMC) will not be established in this study.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Overweight.</hc_freetext>
      <i_freetext>Intervention 1: first Intervention group: Jump Rope Exercise Group. Students will participate in jump rope training for 8 weeks, with 3 sessions per week. The exercises will be performed in an indoor sports hall with a 6-mm-thick polyurethane sports flooring. Each session will begin with 5 minutes of organization, attendance, and positioning of the students, followed by 10 minutes of warm-up exercises, including dynamic stretching, walking, running, and marching in place. Subsequently, the students will perform 30 minutes of the main jump rope exercises using the TanZib Magic fitness jump rope, also known as a beaded rope. The exercise program will include two-foot hops, jogging, heel taps, twists, cross legs, lateral jogging, jumping jacks, zigzag hops, crisscross jumps, backward jumps, half jacks, high-knee jump rope, and double single-foot jumps. At least two types of these exercises will be performed during each session. Each session will conclude with 5 minutes of cool-down exercises, including slow movements, low-intensity static stretching, and deep breathing. Students will be required to wear appropriate sports shoes and sportswear during the sessions and will be allowed to drink water during the activity. A minimum distance of 2 meters between students on all sides will be maintained, and the researcher will be present throughout all training sessions to supervise the correct execution of the exercises and adherence to the study protocol. Intervention 2: second Intervention group: Trampoline Exercise Group. Students will participate in trampoline training for 8 weeks, with 3 sessions per week. The exercises will be performed on a park trampoline located in Azadegan Park in Birjand. Each session will consist of 5 minutes of organization, attendance, positioning of the students, and safety instructions; 10 minutes of warm-up including jogging, light jogging in place, dynamic stretching, and low-impact aerobic activities; 30 minutes of main trampoline exercises; and 5 minutes of cool-down.The main exercises will include two-foot jumps, jumping jacks, front-and-back single-leg jumps, two-foot lateral jumps, scissors, butterfly jumps, tuck jumps, butt landings, and jumps combined with various arm movements. At least two types of these exercises will be performed during each session. As the students' skills improve, the height and speed of the jumps will gradually increase. During the first four weeks, a 30-second rest period will be provided after every 2 minutes and 30 seconds of exercise, while during the second four weeks, a 1-minute rest period will be provided after every 3 minutes of exercise. The exercises will be performed barefoot, and students will be required to wear appropriate and comfortable sportswear. Drinking water will be permitted during the activity. Dangerous and complex movements, double-person jumps, and movements that may increase the risk of injury will be prohibited. The researcher will supervise the correct execution of the exercises, the students' physical condition, and compliance with safety instructions throughout all training sessions. Each session will conclude with 5 minutes of cool-down, including walking, light dynamic and stretching exercises, and deep breathing. Intervention 3: Control group: Overweight boys in the control group will participate in the study for 8 weeks; however, they will not receive any specific exercise training or structured physical activity during this period and will continue their usual daily activities. The boys will be asked not to participate in regular or organized sports activities outside the study during the intervention period. The researcher will maintain regular contact with the boys and their parents throughout the study period and monitor compliance with the study conditions and any potential changes in their physical activity levels. After the 8-week intervention period, the post-test assessments will be conducted for all overweight boys in the control group under the same conditions and procedures as the pre-test assessments.</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>Yes - There is a plan to make this available</results_IPD_plan>
      <results_IPD_description>What will be shared:
The study protocol includes information on the study design, participant inclusion and exclusion criteria, participant selection and group allocation procedures, characteristics and implementation of the jump rope and trampoline exercise protocols, pre-test and post-test procedures, and methods used to assess the study variables. Individual and identifiable participant data will not be shared as part of this document.

When:
Access to the study protocol will begin 6 months after publication of the main study results and will remain available for as long as the protocol is considered scientifically and academically relevant.

To whom:
Researchers, faculty members, and postgraduate students affiliated with academic and research institutions may submit a request to access the study protocol.

Conditions:
The study protocol may be used solely for scientific, research, and educational purposes. Permitted uses include conducting scientific research, designing similar studies, comparing exercise protocols, and developing research protocols. Commercial use of the document and any use that could violate the rights of the researchers or participants will not be permitted. The requester must specify the intended purpose of use and their academic or institutional affiliation.

Where to obtain:
Requests for access to the study protocol may be submitted by contacting the principal investigator at the University of Birjand. The request should include the applicant’s full name, institutional or academic affiliation, email address, and intended purpose of access.

How to obtain:
The request will be reviewed by the principal investigator. Following assessment of the purpose of the request, the applicant’s academic or research affiliation, and the proposed conditions of use, the study protocol will be provided by email if the request is approved. Requests will be reviewed and a decision will be communicated to the applicant within a maximum of 30 business days.

Comments:
Sharing of the study protocol will not include any identifying information or individual participant data. Access to the document will be subject to confidentiality requirements, intellectual property rights, and use solely for scientific and research purposes.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Saeed Ilbeigi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Behavioral Sciences Campus, University of Birjand, End of University Boulevard, Shokatabad, Birjand, South Khorasan Province, Iran</address>
        <city>Birjand</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9717434765</zip>
        <telephone>+98 56 3102 6901</telephone>
        <email>silbeigi@birjand.ac.ir</email>
        <affiliation>University of Birjand</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Saeed Ilbeigi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Behavioral Sciences Campus, University of Birjand, End of University Boulevard, Shokatabad, Birjand, South Khorasan Province, Iran</address>
        <city>Birjand</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9717434765</zip>
        <telephone>+98 56 3102 6901</telephone>
        <email>silbeigi@birjand.ac.ir</email>
        <affiliation>University of Birjand</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Being male and aged 9–12 years
Being classified as overweight based on the body composition analyzer results
Residing in Birjand
Being physically inactive and having no history of professional or regular sports participation
Not taking any medications, including pharmaceutical drugs or herbal products
Having no acute or chronic disease that could affect the study outcomes
Having no history of burns, surgery, injury, or pain involving the spine, wrist, knee, or ankle
Having no generalized joint hypermobility, as determined by a Beighton score of less than 4
Obtaining written informed consent from the parent or legal guardian and the child's willingness to participate in the study</inclusion_criteria>
      <agemin>9 years</agemin>
      <agemax>12 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>Having an acute or chronic disease that may affect balance, motor performance, or the psychological variables under investigation.
Taking medications that may affect balance, motor performance, or the psychological variables under investigation
Having a history of regular or professional sports participation
Having a history of surgery, injury, or pain involving the spine, wrist, knee, or ankle
Having visual or hearing impairments that may interfere with the performance of the study assessments
Having generalized joint hypermobility, as indicated by a Beighton score of 4 or higher
Being unable to safely perform the study assessments or exercise program
Failure to obtain written informed consent from the parent or legal guardian</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>E66</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Overweight and obesity</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>first Intervention group: Jump Rope Exercise Group. Students will participate in jump rope training for 8 weeks, with 3 sessions per week. The exercises will be performed in an indoor sports hall with a 6-mm-thick polyurethane sports flooring. Each session will begin with 5 minutes of organization, attendance, and positioning of the students, followed by 10 minutes of warm-up exercises, including dynamic stretching, walking, running, and marching in place. Subsequently, the students will perform 30 minutes of the main jump rope exercises using the TanZib Magic fitness jump rope, also known as a beaded rope. The exercise program will include two-foot hops, jogging, heel taps, twists, cross legs, lateral jogging, jumping jacks, zigzag hops, crisscross jumps, backward jumps, half jacks, high-knee jump rope, and double single-foot jumps. At least two types of these exercises will be performed during each session. Each session will conclude with 5 minutes of cool-down exercises, including slow movements, low-intensity static stretching, and deep breathing. Students will be required to wear appropriate sports shoes and sportswear during the sessions and will be allowed to drink water during the activity. A minimum distance of 2 meters between students on all sides will be maintained, and the researcher will be present throughout all training sessions to supervise the correct execution of the exercises and adherence to the study protocol.</i_keyword>
      <i_keyword>second Intervention group: Trampoline Exercise Group. Students will participate in trampoline training for 8 weeks, with 3 sessions per week. The exercises will be performed on a park trampoline located in Azadegan Park in Birjand. Each session will consist of 5 minutes of organization, attendance, positioning of the students, and safety instructions; 10 minutes of warm-up including jogging, light jogging in place, dynamic stretching, and low-impact aerobic activities; 30 minutes of main trampoline exercises; and 5 minutes of cool-down.The main exercises will include two-foot jumps, jumping jacks, front-and-back single-leg jumps, two-foot lateral jumps, scissors, butterfly jumps, tuck jumps, butt landings, and jumps combined with various arm movements. At least two types of these exercises will be performed during each session. As the students' skills improve, the height and speed of the jumps will gradually increase. During the first four weeks, a 30-second rest period will be provided after every 2 minutes and 30 seconds of exercise, while during the second four weeks, a 1-minute rest period will be provided after every 3 minutes of exercise. The exercises will be performed barefoot, and students will be required to wear appropriate and comfortable sportswear. Drinking water will be permitted during the activity. Dangerous and complex movements, double-person jumps, and movements that may increase the risk of injury will be prohibited. The researcher will supervise the correct execution of the exercises, the students' physical condition, and compliance with safety instructions throughout all training sessions. Each session will conclude with 5 minutes of cool-down, including walking, light dynamic and stretching exercises, and deep breathing.</i_keyword>
      <i_keyword>Control group: Overweight boys in the control group will participate in the study for 8 weeks; however, they will not receive any specific exercise training or structured physical activity during this period and will continue their usual daily activities. The boys will be asked not to participate in regular or organized sports activities outside the study during the intervention period. The researcher will maintain regular contact with the boys and their parents throughout the study period and monitor compliance with the study conditions and any potential changes in their physical activity levels. After the 8-week intervention period, the post-test assessments will be conducted for all overweight boys in the control group under the same conditions and procedures as the pre-test assessments.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Changes in the magnitude and distribution of static plantar pressure during standing, measured using a plantar pressure measurement device. Timepoint: Static plantar pressure will be measured at baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Foot Medisense (Foot pressure).</prim_outcome>
      <prim_outcome>Changes in the magnitude and distribution of dynamic plantar pressure during walking, measured using a plantar pressure measurement device. Timepoint: Dynamic plantar pressure will be measured during walking at baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Foot Medisense (Foot pressure).</prim_outcome>
      <prim_outcome>Changes in static balance performance during double-leg and single-leg standing under eyes-open and eyes-closed conditionsپ. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using a force plate by assessing center-of-pressure sway parameters during standing.</prim_outcome>
      <prim_outcome>Changes in dynamic balance performance during a dynamic balance test. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: force plate.</prim_outcome>
      <prim_outcome>Changes in center-of-pressure oscillations during standing. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: force plate.</prim_outcome>
      <prim_outcome>Changes in the time required to achieve post-landing stabilization. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using a force plate by assessing the time required to achieve post-landing stabilization.</prim_outcome>
      <prim_outcome>Changes in students’ life satisfaction are measured using the Brief Multidimensional Students’ Life Satisfaction Scale. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using Huebner’s BMSLSS, consisting of 6 items rated on a 7-point Likert scale.</prim_outcome>
      <prim_outcome>Changes in loneliness and social dissatisfaction are measured using the Social and Emotional Loneliness Scale (SLFS). Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using the Social and Emotional Loneliness Scale (SLFS) developed by Asher et al., consisting of 24 items rated on a 5-point Likert scale.</prim_outcome>
      <prim_outcome>Changes in the severity of depressive symptoms are measured using the Depression Self-Rating Scale (DSRS). Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using Birleson’s Depression Self-Rating Scale (DSRS), consisting of 18 items rated on a 5-point Likert scale.</prim_outcome>
      <prim_outcome>Changes in social physique anxiety related to body appearance are measured using the Social Physique Anxiety Scale. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: Measured using the Social Physique Anxiety Scale developed by Motl and Conroy, consisting of 7 items rated on a 5-point Likert scale.</prim_outcome>
      <prim_outcome>Changes in aggression levels are measured using the Aggression Scale. Timepoint: At baseline, before the intervention, and immediately after completion of the 8-week training program. Method of measurement: At baseline, before the intervention, and immediately after completion of the 8-week training program.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome></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>Research Vice-Chancellery of the University of Birjand</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-01-27</approval_date>
        <contact_name>Ethics Committee of the University of Birjand</contact_name>
        <contact_address>Birjand, Shahid Avini Blvd., University Blvd., Shokatabad Campus, University of Birjand, Behavioral Sciences Campus. Birjand South Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
