<?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>IRCT2016102630516N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2016-11-26</date_registration>
      <primary_sponsor>vice chancellor for research,Tehran university of Medical science</primary_sponsor>
      <public_title>Effects of corrective exercise on cognitive and muscular factor</public_title>
      <acronym></acronym>
      <scientific_title>Effects of postural corrective exercise on neurocognitive and musculoskeletal parameters in forward head posture women</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2016-12-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>20</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/24225</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Treatment.</study_design>
      <phase>2-3</phase>
      <hc_freetext>forward head posture.</hc_freetext>
      <i_freetext>The intervention of this study is postural corrective exercise in the form of of two strengthening (deep cervical flexors and shoulder retractors)and two stretching (pectoral muscles and sternocleidomastoid)exercises. The participants are asked to perform 3 sets of 12 repetitions of strengthening exercises and 2 stretching exercises held for 30 seconds each. 30 seconds as a rest time is considered between each exercise. the intervention protocol lasts for 4 weeks and is repeated 4 times per week. this intervention program takes an average of 15 min..</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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Zahra Abdollahzade</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>between Sadi ST and Darvaze shemiran.Enqelab ST,Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>11489-65111</zip>
        <telephone>+98 51 4464 0577</telephone>
        <email>Rehabilitation@tums.ac.irzabdollahzade1990@gmail.com</email>
        <affiliation>rehabilitation school of Tehran university of medical science</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr.Azade Shadmehr</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>between Sadi ST and Darvaze shemiran,Enqelab ST,Tehran</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>11489-65111</zip>
        <telephone>+98 21 7752 8468</telephone>
        <email>Rehabilitation@tums.ac.irshadmehr@tums.ac.ir</email>
        <affiliation>rehabilitation school of tums</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>INCLIUSION CRITERIA:  CVA&lt;50 Women. at the age of 20-30. Not having vision or hearing problems and eyeglasses, contact lenses and hearing aids do not use. No history of acute or chronic diseases such as neurological,  cardiovascular or metabolic &#13;
. VAS&lt;2(lumbar and cervical).  BMI&lt;30. Not having musculoskeletal injury during one years ago.  Having associate degree at least.  Avoid taking any medication affecting the motor function and cognition.  Avoid taking stimulants like coffee and alcohol drink.  Not having head injury.  Not having impairment of balance.  Not having fracture or surgery of shoulder &amp; spine.  Not having mental illness.  EXCLUSION CRITERIA:  Not wanting people to test.  be tired, headache, disturbed individual and the inability to continue testing.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>30 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Xlll(M62.4</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Disorders of muscles  </hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>The intervention of this study is postural corrective exercise in the form of of two strengthening (deep cervical flexors and shoulder retractors)and two stretching (pectoral muscles and sternocleidomastoid)exercises. The participants are asked to perform 3 sets of 12 repetitions of strengthening exercises and 2 stretching exercises held for 30 seconds each. 30 seconds as a rest time is considered between each exercise. the intervention protocol lasts for 4 weeks and is repeated 4 times per week. this intervention program takes an average of 15 min.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Craniovertebral angle. Timepoint: before intervention.after 1month. Method of measurement: lmage J software.</prim_outcome>
      <prim_outcome>Visual choice reaction time. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
      <prim_outcome>Visual complex choice reaction time. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
      <prim_outcome>Auditory choice reaction time. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
      <prim_outcome>Auditorycomplex choice reaction time. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
      <prim_outcome>Low speed anticipation. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
      <prim_outcome>High speed anticipation. Timepoint: before intervention.after 1month. Method of measurement: SART software.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Range of motion neck flexion. Timepoint: before intervention,after one month. Method of measurement: goniometer.</sec_outcome>
      <sec_outcome>Middle trapezius muscles strength. Timepoint: before intervention,after one month. Method of measurement: dynamometer.</sec_outcome>
      <sec_outcome>Lower trapezius muscles strength. Timepoint: before intervention,after one month. Method of measurement: dynamometer.</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>vice chancellor for research,Tehran university of Medical science</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2016-08-20</approval_date>
        <contact_name>Ethics Committee of Tehran university of medical science</contact_name>
        <contact_address>central office of TUMS,corner of Ghods St,Keshavarz BLvd,Tehran Tehran  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
