<?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>IRCT20220216054033N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-02-18</date_registration>
      <primary_sponsor>Riphah International University</primary_sponsor>
      <public_title>EFFECTS OF RESISTANCE EXERCISES WITH AND WITHOUT PLYOMETRIC TRAINING ON ARM AND LEG DYNAMIC STRENGTH OF AMATEUR BODYBUILDERS.</public_title>
      <acronym></acronym>
      <scientific_title>EFFECTS OF RESISTANCE EXERCISES WITH AND WITHOUT PLYOMETRIC TRAINING ON ARM AND LEG DYNAMIC STRENGTH OF AMATEUR BODYBUILDERS.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-03-15</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>34</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/61961</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Health service research, Randomization description: After selecting the subjects using Purposive sampling the included cases will randomly allocated into two groups by simple random sampling using Gold Fish bowl method. Participants will be informed about their registration Number. The participants group will be masked as A &amp; B by the Trainer/Assessor.  Pre and post Data will be collected and analyzed by the data analyst. After analysis the Groups will be unmasked, Blinding description: 34 Participants will be involved in my study using Purposive Sampling Technique.
2 groups of 17 participants each will be made and will be randomized using systematic sampling. 
Participants will be blinded by not knowing the outcome of the exercises and about participants of control and experimental group.
Care Giver Fitness coach will be blinded by the not knowing on the initial performance of participants and outcome of the exercises.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Arm and Leg Dynamic Strength.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Interventional Group will receive Plyometric Training along with Resistance training for upper and lower limbs. Plyometric training for Arms and Legs involve Bounds, Side to Side Ankle Hops, Lateral Cone Hops, Medicine Ball Chest Pass, Push-ups with one Clap. The resistance training program included seven to 10 exercises that activated all of the main muscle groups. Every training session included two exercises for the leg extensors (leg press and knee extension), one exercise for knee flexors (leg curl) and one to two other exercises for the lower extremities (seated calf raise, hip abduction or adduction). For the upper body, each session included three to four exercises (bench press, biceps curl, triceps pushdown, lateral pull-down), and one to two exercises for the trunk (abdominal crunch, seated back extension). The overall intensity and amount of training increased progressively throughout the 6-week training period. Intervention 2: Control group: Control Group will only receive Resistance Training for upper and lower limbs. The resistance training program included seven to 10 exercises that activated all of the main muscle groups. Every training session included two exercises for the leg extensors (leg press and knee extension), one exercise for knee flexors (leg curl) and one to two other exercises for the lower extremities (seated calf raise, hip abduction or adduction). For the upper body, each session included three to four exercises (bench press, biceps curl, triceps pushdown, lateral pull-down), and one to two exercises for the trunk (abdominal crunch, seated back extension).</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 There is no further information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Sufian Ahmed</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Shalamar Medical and Dental college</address>
        <city>Gujranwala</city>
        <country1>Pakistan</country1>
        <zip>52250</zip>
        <telephone>+92 321 8835085</telephone>
        <email>sufianahmedghuman@gmail.com</email>
        <affiliation>Shalamar Medical and Dental College</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Muhammad Hashim</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Quaid e azam industrial estate Lahore</address>
        <city>Lahore</city>
        <country1>Pakistan</country1>
        <zip>40050</zip>
        <telephone>+92 323 4071564</telephone>
        <email>muhammad.hashim@riphah.edu.pk</email>
        <affiliation>Riphah International University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age 20-40 years Male.
Participants involved in Resistance Training Program for at least 6 months.
Resistance training athletes volunteer to participate in the study.
No use of medication which would help improves the performance of the athlete.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>40 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>Any physical injury, pathology during last 6 months.
Any surgical history during last 6 months.
Involved in other sports activity that could affect the performance of the athlete.</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>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Interventional Group will receive Plyometric Training along with Resistance training for upper and lower limbs. Plyometric training for Arms and Legs involve Bounds, Side to Side Ankle Hops, Lateral Cone Hops, Medicine Ball Chest Pass, Push-ups with one Clap. The resistance training program included seven to 10 exercises that activated all of the main muscle groups. Every training session included two exercises for the leg extensors (leg press and knee extension), one exercise for knee flexors (leg curl) and one to two other exercises for the lower extremities (seated calf raise, hip abduction or adduction). For the upper body, each session included three to four exercises (bench press, biceps curl, triceps pushdown, lateral pull-down), and one to two exercises for the trunk (abdominal crunch, seated back extension). The overall intensity and amount of training increased progressively throughout the 6-week training period.</i_keyword>
      <i_keyword>Control group: Control Group will only receive Resistance Training for upper and lower limbs. The resistance training program included seven to 10 exercises that activated all of the main muscle groups. Every training session included two exercises for the leg extensors (leg press and knee extension), one exercise for knee flexors (leg curl) and one to two other exercises for the lower extremities (seated calf raise, hip abduction or adduction). For the upper body, each session included three to four exercises (bench press, biceps curl, triceps pushdown, lateral pull-down), and one to two exercises for the trunk (abdominal crunch, seated back extension).</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Dynamic Strength. Timepoint: Before Intervention And 6 weeks After Intervention. Method of measurement: Pull Ups, Push Ups, Vertical Jump Test, 1 RM Bench Press and Leg Press.</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>Riphah International University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-12-27</approval_date>
        <contact_name>Riphah International University</contact_name>
        <contact_address>Quaid e Azam Industrial Estate Lahore. Lahore Punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
