<?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>IRCT2014060117937N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2014-09-03</date_registration>
      <primary_sponsor>Qazvin university of Medical Sciences</primary_sponsor>
      <public_title>anxiety of pain</public_title>
      <acronym>eye movement Desensitization and reprocessing</acronym>
      <scientific_title>Assessment the effect of desensitization method with eye movements and reprocessing  on anxiety induced by dressing pain in burn patients</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2014-03-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/16384</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Burn patients.</hc_freetext>
      <i_freetext>Intervention 1: Patients in intervention group should do the followings with the guidance and cooperation of therapist.&#13;
The visual embodiment of an image most prominent of the traumatic scene.&#13;
Focusing on the negative cognition of the scene that is expressed as a brief description to explain the traumatic event before, for example I’m guilty or that scene was really heartbreaking and horrible for me. &#13;
Focus on emotions and physical conditions related to stress and anxiety, and expressing the location of stress or anxiety on body parts. Visual following of therapist finger motions in the state of continuing imaging the traumatic scene by patient, patient should follow the rapid therapist finger motions which are in across of his/her vision sight with rapid eye movements. The finger of therapist should be away from patient’s eyes approximately 30 cm and it should be moved from right to left and vice versa in patient vision sight. This movement involves two went and back to the sides within one second that is one cycle and each 12 to 24 cycles are one series. After each series, the therapist says to the patient that stops the imaging of the scene and sits back on seat and takes a deep breath. &#13;
Then therapist who earlier rated the levels of anxiety units or mental discomfort and cognitive credibility with cooperation of patient, attempting to rate and re-evaluation of these two variables by the patient, and will record them. This process will repeated several times according to the patient’s needs and level of motivation and if possible it will repeated so extent till the levels of mental discomfort units meets the zero and minimized. Session lasts up to 90 minutes. Intervention 2: Control group: the group that will receive the standard treatment ordered by the physician according to the hospital protocol by staff and the interventions will not be performed by the researcher.</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>Mostafa chatrrooz</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Nursing Faculty, Qazvin University of Medical Sciences, Bahonar Blv, Qazvin</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 28 3333 8127</telephone>
        <email>mchatrrooz@qums.ac.ir</email>
        <affiliation>Qazvin University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mostafa chatrrooz</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Nursing Faculty, Qazvin University of Medical Sciences, Bahonar Blv, Qazvin</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 28 3333 8127</telephone>
        <email>mchatrrooz@qums.ac.ir</email>
        <affiliation>Qazvin University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: &#13;
Grade 2 burn which diagnosed by specialist physician؛ Patients have passed the acute phase of illness؛ Patients didn’t have a history of seizures؛ The level of education should be higher than fifth grade؛ Patients didn’t have a history of mental illness؛ Patients who dont have drug addiction؛ Patients were between 18 and 60 years old؛ Patients shouldn’t have strabismus or vision problems؛ Patients should be able to speak and understand Persian language؛ Patients shouldn’t have burns on head, face and respiratory system؛ Patients experienced dressing change at least once after their admission.&#13;
&#13;
Exclusion criteria:&#13;
Patients are not able to tolerate the treatment method؛ Patients don’t cooperate with the therapist؛ Patients who candidate for skin graft surgery after choose.</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>60 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>T20-T32</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Burns and corrosions</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Other</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Patients in intervention group should do the followings with the guidance and cooperation of therapist.&#13;
The visual embodiment of an image most prominent of the traumatic scene.&#13;
Focusing on the negative cognition of the scene that is expressed as a brief description to explain the traumatic event before, for example I’m guilty or that scene was really heartbreaking and horrible for me. &#13;
Focus on emotions and physical conditions related to stress and anxiety, and expressing the location of stress or anxiety on body parts. Visual following of therapist finger motions in the state of continuing imaging the traumatic scene by patient, patient should follow the rapid therapist finger motions which are in across of his/her vision sight with rapid eye movements. The finger of therapist should be away from patient’s eyes approximately 30 cm and it should be moved from right to left and vice versa in patient vision sight. This movement involves two went and back to the sides within one second that is one cycle and each 12 to 24 cycles are one series. After each series, the therapist says to the patient that stops the imaging of the scene and sits back on seat and takes a deep breath. &#13;
Then therapist who earlier rated the levels of anxiety units or mental discomfort and cognitive credibility with cooperation of patient, attempting to rate and re-evaluation of these two variables by the patient, and will record them. This process will repeated several times according to the patient’s needs and level of motivation and if possible it will repeated so extent till the levels of mental discomfort units meets the zero and minimized. Session lasts up to 90 minutes.</i_keyword>
      <i_keyword>Control group: the group that will receive the standard treatment ordered by the physician according to the hospital protocol by staff and the interventions will not be performed by the researcher.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Anxiety of burn  pain. Timepoint: Ninety-six days simultaneously in the intervention and control groups. Method of measurement: Burns Specific Pain Anxiety Scale.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Outcome of patient care. Timepoint: Ninety-six days simultaneously in the intervention and control groups. Method of measurement: Burns Specific Pain Anxiety Scale.</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>Qazvin university of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2014-02-26</approval_date>
        <contact_name>Qazvin university of Medical Sciences Ethics Committee</contact_name>
        <contact_address>Nursing Faculty,Qazvin University of Medical Sciences, Bahonar Blv, Qazvin Qazvin  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
