<?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>IRCT20200124046237N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2020-02-01</date_registration>
      <primary_sponsor>University of social welfare and rehabilitation sciences</primary_sponsor>
      <public_title>The effect of t-DCS on proprioception</public_title>
      <acronym></acronym>
      <scientific_title>The effect of transcranial direct current stimulation over posterior parietal cortex and premotor cortex on upper limb joint position sense in healthy adults</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2020-02-19</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/45334</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Basic scienece, Randomization description: Regarding participants sexuality, they will choose one paper among two sealed pockets to get into study groups.Also in order to randomize the priority of assessing joints and ipsilateral or controlateral limb, participants will choose 2 paper out of isolated sealed pockets, Blinding description: All the participants will be blind about the study groups. Analyzor of the results will be blind to participants and study groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Healthy people.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: After assessing the active  joint position sense of shoulder,elbow and wrist from both sides, t-DCS will be used on right posterior parietal cortex with 1mA , 20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed. Intervention 2: Intervention group:  After assessing the active  joint position sense of shoulder,elbow and wrist from both sides, t-DCS will be used on right premotor cortex with 1mA , 20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed. Intervention 3: Control group:  After assessing the active  joint position sense of shoulder,elbow and wrist from both sides,sham t-DCS will be used on right posterior parietal cortex or premotor cortexs with  20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed.</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 statistical analyses of the data is published upon the request of the publishing journal.

When:
Once the resultant paper was published, We will share the statistical analyses upon the journal request.

To whom:
According the journal policy

Conditions:
We will not publish participants identification codes, but we publish the statistical analyses to let the reader and researcher make sure about the validity of the results.

Where to obtain:
The journal in which the resultant paper will be published.

How to obtain:
The request sent by the journal editor reviewers

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Elnaz Allahverdlo</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 38,Aghaghia blvd.Shahrake Golestan</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1494913176</zip>
        <telephone>+98 21 4473 6165</telephone>
        <email>Elnazallahverdlo@gmail.com</email>
        <affiliation>University of social welfare and rehabilitation sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Iraj Abdollahi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Kodakyar Dd End., Daneshjo Blvd., Velenjak</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985713834</zip>
        <telephone>+98 21 2218 0039</telephone>
        <email>irajabdollahi@USWR.ac.ir</email>
        <affiliation>University of social welfare and rehabilitation sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age under 40 years
Right handedness
No history of neurological diseases
No history of convulsion
No history of psychological disorders
No pace maker and implant
No history of pain,discomfort and injury on upper limb during 6 months ago</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>40 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>No cooperation of participants
Dispensing and not willing to follow study
Sensitivity of the skin of the participants head</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>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: After assessing the active  joint position sense of shoulder,elbow and wrist from both sides, t-DCS will be used on right posterior parietal cortex with 1mA , 20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed.</i_keyword>
      <i_keyword>Intervention group:  After assessing the active  joint position sense of shoulder,elbow and wrist from both sides, t-DCS will be used on right premotor cortex with 1mA , 20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed.</i_keyword>
      <i_keyword>Control group:  After assessing the active  joint position sense of shoulder,elbow and wrist from both sides,sham t-DCS will be used on right posterior parietal cortex or premotor cortexs with  20 minutes for 5 consecutive days and at the end of the 5 session, the active joint position sense for both upper limbs will be reassessed.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Active  left shoulder joint reposition sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</prim_outcome>
      <prim_outcome>Active left elbow joint reposition sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</prim_outcome>
      <prim_outcome>Active left wrist reposition  sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Active right shoulder reposition sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</sec_outcome>
      <sec_outcome>Active right elbow joint reposition sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</sec_outcome>
      <sec_outcome>Active right wrist reposition sense. Timepoint: Before and immediately after intervention. Method of measurement: Photography technique.</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>University of social welfare and rehabilitation sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-07-07</approval_date>
        <contact_name>Ethics committee of University of Social welfare and Rehabilitation Sciences</contact_name>
        <contact_address>Kodak yar Dead end , Daneshjoo Blvd , velenjak Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
