<?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>IRCT20171022036932N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-11-30</date_registration>
      <primary_sponsor>Iranian academic center for education culture and research</primary_sponsor>
      <public_title>The Impact of Transcranial Stimulation on Positive Emotions and Working Memory</public_title>
      <acronym></acronym>
      <scientific_title>The Impact of Transcranial Direct Current Stimulation on Positive Emotions and Working Memory  in Healthy People</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-11-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>40</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/27460</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Blinding description: Subjects are unaware of which of the two experimental or control groups are assigned. Measurement is done by one of the research colleagues who is completely unaware of the placement of the subjects. In other words, it will be done blindly.</study_design>
      <phase>3</phase>
      <hc_freetext>working memory, positive emotion.</hc_freetext>
      <i_freetext>Intervention 1: The intervention group will be assessed before the intervention using the positive and negative affect scale (PANAS) and n-back task due to computer. Measurement is accomplished by one of the research partners who are completely unaware of the placement of the subjects in the two groups of intervention and control. This test will be carried out in a laboratory environment. Variables such as temperature, light and sound are controlled in all sessions. During the test, first, the performance of the tDCS device will be explained to the subjects, and the Consent letter will be signed by the subjects with the possible side effects of the test. Subjects will be given further details on the test process. A direct electric current is received from an electric current-generator device and transmitted to a pair of electrodes. The electrodes are carbon-based and placed inside the sponge coating that has been contained with serum. The intervention group will receive an electrical stimulus from the brain. In such a way that a certain intensity will pass through his brain in 20 minutes. After a short break, the subjects will again perform the Positive and Negative affective questionnaire (PANAS) and the n-back task due to computer. Then the money will be paid as a fee and subjects will be discharged at the end. Intervention 2: Control group: The control group will be assessed before the intervention using the positive and negative affect scale (PANAS) and n-back task due to computer. Measurement is accomplished by one of the research partners who are completely unaware of the placement of the subjects in the two groups of intervention and control. This test will be carried out in a laboratory environment. Variables such as temperature, light and sound are controlled in all sessions. During the test, first, the performance of the tDCS device will be explained to the subjects, and the Consent letter will be signed by the subjects with the possible side effects of the test. Subjects will be given further details on the test process. Then, the control group receives artificial brain electric stimulation from the skull. To artificially stimulate the location of anode and cathode electrodes, it will be the actual stimulation. While the flow generator outputs the current to 2 mA for 30 seconds, then it gradually returns to zero for 30 seconds, and the device turns off. But the electrodes will be on the subject for 20 minutes, and he will not be aware of the power off. After a short break, the subjects will again perform the Positive and Negative Affective Questionnaire (PANAS) and the n-back task due to computer. Then the money will be paid as a fee and subjects will be discharged at the end.</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 total potential data includes the scores that subjects have received from positive emotional questionnaire and working memory task after unidentifing can be shared.

When:
Start the access period 6 months after sharing the results

To whom:
Researchers working in academic and research institutes

Conditions:
The publication, or presentation or analysis of data should be done with the research author's permission

Where to obtain:
Department of Cognitive Science, Jahad Alborz University, Dara Building,  Poone Street, Golshahr
telephon:  02634574607
E-mail: cognitivescience.acecr@gmail.com
Responsive person: Dr.Nima Gangi

How to obtain:
If people want to ask for documents by e-mail, they must email the email address mentioned in the previous option. A response will be sent about a week to ten days later. In case of needing a personal appointment, the contact person will be contacted first by phone and appointment will be sent to the Office of the Department of Cognitive Science.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Nima Gangi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Department of Cognitive Science, Jahad Alborz University, Dara Building, Poone Street, Golshahr</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3138744746</zip>
        <telephone>+98 262634574607</telephone>
        <email>nimaganji.psy@gmail.com</email>
        <affiliation>Iranian academic center for education culture and research</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Nima Gangi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Department of Cognitive Science, Jahad Alborz University, Dara Building, Poone Street, Golshahr</address>
        <city>Karaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>3138744746</zip>
        <telephone>+98 262634574607</telephone>
        <email>nimaganji.psy@gmail.com</email>
        <affiliation>Iranian academic center for education culture and research</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Absence of any type of mental illness
right-handedness
age between 20-45 years
signing the consent form of the company in the study</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>45 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>The presence of a current neurological disorder or its positive history (especially seizure attacks)
Any psychiatric disorder based on DSM-IV-TR axis 1 and 2
Using of drugs affecting the central nervous system
Epileptic seizures
brain surgery
The presence of a tumor
A hit on the head that has led to anesthesia</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>The intervention group will be assessed before the intervention using the positive and negative affect scale (PANAS) and n-back task due to computer. Measurement is accomplished by one of the research partners who are completely unaware of the placement of the subjects in the two groups of intervention and control. This test will be carried out in a laboratory environment. Variables such as temperature, light and sound are controlled in all sessions. During the test, first, the performance of the tDCS device will be explained to the subjects, and the Consent letter will be signed by the subjects with the possible side effects of the test. Subjects will be given further details on the test process. A direct electric current is received from an electric current-generator device and transmitted to a pair of electrodes. The electrodes are carbon-based and placed inside the sponge coating that has been contained with serum. The intervention group will receive an electrical stimulus from the brain. In such a way that a certain intensity will pass through his brain in 20 minutes. After a short break, the subjects will again perform the Positive and Negative affective questionnaire (PANAS) and the n-back task due to computer. Then the money will be paid as a fee and subjects will be discharged at the end.</i_keyword>
      <i_keyword>Control group: The control group will be assessed before the intervention using the positive and negative affect scale (PANAS) and n-back task due to computer. Measurement is accomplished by one of the research partners who are completely unaware of the placement of the subjects in the two groups of intervention and control. This test will be carried out in a laboratory environment. Variables such as temperature, light and sound are controlled in all sessions. During the test, first, the performance of the tDCS device will be explained to the subjects, and the Consent letter will be signed by the subjects with the possible side effects of the test. Subjects will be given further details on the test process. Then, the control group receives artificial brain electric stimulation from the skull. To artificially stimulate the location of anode and cathode electrodes, it will be the actual stimulation. While the flow generator outputs the current to 2 mA for 30 seconds, then it gradually returns to zero for 30 seconds, and the device turns off. But the electrodes will be on the subject for 20 minutes, and he will not be aware of the power off. After a short break, the subjects will again perform the Positive and Negative Affective Questionnaire (PANAS) and the n-back task due to computer. Then the money will be paid as a fee and subjects will be discharged at the end.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The Positive and Negative Affect Schedule (PANAS) - N Back Test. Timepoint: At the beginning of the study (before the study began) and one day after the intervention. Method of measurement: The Positive and Negative Affect Schedule (PANAS) - N Back Test.</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>Iranian academic center for education culture and research</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2017-10-21</approval_date>
        <contact_name>Avicenna Research Institute of the Ethics Committee on Biomedical Research</contact_name>
        <contact_address>Department of Cognitive Science, Jahad Alborz University, Dara Building, Poone Street, Golshahr Karaj Alborz Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
