<?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>IRCT20210308050629N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-04-29</date_registration>
      <primary_sponsor>Kermanshah University of Medical Sciences</primary_sponsor>
      <public_title>Investigating the effect of counseling based on positive psychology on body image</public_title>
      <acronym></acronym>
      <scientific_title>The effect of counseling based positive psychology on the body image of burn patient</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-05-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/55560</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Eligible samples, after obtaining informed consent, will be randomly assigned to the intervention and control groups by simple random sampling. For each of the two intervention and control groups, 30 people will be considered (60 people in total). In this study, a simple randomization method was used to perform random allocation (allocation concealment).In this way, 60 cards that were identical in appearance were prepared and on 30 of them, the number or code 1, which identifies the test group, ie counseling based on positive psychology, and on the other 30 of them, the number or code 2, which identifies The control group was included. Then, each eligible person randomly selected one of these cards with the codes written on it. In this way, the random allocation of patients to each group was determined.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Body image.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: After obtaining informed consent, eligible samples are divided into two groups of intervention A and control B (each group includes 30 people) by simple random sampling method. Patients with grade 2 or higher burns who also need follow-up care for at least one month are selected. The purpose and method of conducting the research is explained to them by the researcher. At first, both groups are given a body image pre-test questionnaire (this questionnaire is a 46-item test.The six-dimensional test questions measure body-self relations, including face evaluation, face orientation, fitness evaluation, fitness orientation, mental weight, and physical satisfaction on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). . To complete it, and then Group A, which includes 30 randomly selected patients, according to the patients' condition, counseling sessions based on positive psychology by the researcher with the approval of the relevant professors in a quiet environment located in the examination room of the burn clinic, at the time Patients are expected to visit a doctor and undergo treatment according to the agreement with the patients and will be done with their companions for 60 minutes, in order not to meet groups A and B, the time of group A meetings is even days and the time of group B meetings are considered individual days. The content of training sessions after extracting from reliable sources The concept of positivity, teaching happiness skills, the concept of appreciation and hope, the meaning of life, as well as consulting with professors is designed in 6 sessions.In the last session, closing and thanking the members, presenting a summary of the topics of the sessions to the members, completing the post-test questionnaires. Intervention 2: Control group: Group B or the control group, which includes 30 randomly selected patients, is first given a body image pre-test questionnaire (this questionnaire is a 46-item test. The body measures fitness orientation, mental weight, and physical satisfaction on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree).In order not to meet in groups A and B, the time of group A meetings is considered as even days and the time of group B meetings is considered as individual days. However, training and counseling sessions based on positive psychology are not provided for the control group, and they only receive their usual treatment,After the allotted time, the post-test physical image questionnaire, which was completed at the beginning of the study, was completed by the control group to examine the effectiveness of counseling sessions based on positive psychology.</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:
Information about the content of counseling sessions, questionnaire information at the beginning and end of the study without the names of the participants, data analysis.

When:
6 months after publishing the results

To whom:
Researchers working in  universities and prestigious scientific centers

Conditions:
In order to view and as a model with permission

Where to obtain:
To the people in charge of the study, including Zahra Moradi and Dr. Rostam Jalali, call 00989183892861, and send an email to zahra59.moradi@gmail.com

How to obtain:
Request from the relevant officials and correspond with them by phone and email and provide valid documents

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Zahra Moradi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No 10, Aram building, Ruhollah Akbari Alley,  Khayyam St</address>
        <city>Kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6718895617</zip>
        <telephone>+98 83 3726 8030</telephone>
        <email>zahra59.moradi@gmail.com</email>
        <affiliation>Kermanshah University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Rostam Jalali</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Nursing and Midwifery-Isar Square - Dolatabad</address>
        <city>Kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6718895617</zip>
        <telephone>+98 83 3816 2532</telephone>
        <email>rjalali@kums.ac.ir</email>
        <affiliation>Kermanshah University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Grade 2 and higher burns
No mental problems and mental disorders
Being 18 to 50 years old
Acceptable listening and speaking ability
Requires follow-up for at least a month or more
Interest in cooperation
No drug addiction and sedatives</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Grade 1 burns
Drug addiction and sedatives
Having mental problems and mental disorder
Age less than 18 years
The duration of follow-up treatment is less than one month</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>F88</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Other disorders of psychological development</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: After obtaining informed consent, eligible samples are divided into two groups of intervention A and control B (each group includes 30 people) by simple random sampling method. Patients with grade 2 or higher burns who also need follow-up care for at least one month are selected. The purpose and method of conducting the research is explained to them by the researcher. At first, both groups are given a body image pre-test questionnaire (this questionnaire is a 46-item test.The six-dimensional test questions measure body-self relations, including face evaluation, face orientation, fitness evaluation, fitness orientation, mental weight, and physical satisfaction on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree). . To complete it, and then Group A, which includes 30 randomly selected patients, according to the patients' condition, counseling sessions based on positive psychology by the researcher with the approval of the relevant professors in a quiet environment located in the examination room of the burn clinic, at the time Patients are expected to visit a doctor and undergo treatment according to the agreement with the patients and will be done with their companions for 60 minutes, in order not to meet groups A and B, the time of group A meetings is even days and the time of group B meetings are considered individual days. The content of training sessions after extracting from reliable sources The concept of positivity, teaching happiness skills, the concept of appreciation and hope, the meaning of life, as well as consulting with professors is designed in 6 sessions.In the last session, closing and thanking the members, presenting a summary of the topics of the sessions to the members, completing the post-test questionnaires.</i_keyword>
      <i_keyword>Control group: Group B or the control group, which includes 30 randomly selected patients, is first given a body image pre-test questionnaire (this questionnaire is a 46-item test. The body measures fitness orientation, mental weight, and physical satisfaction on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree).In order not to meet in groups A and B, the time of group A meetings is considered as even days and the time of group B meetings is considered as individual days. However, training and counseling sessions based on positive psychology are not provided for the control group, and they only receive their usual treatment,After the allotted time, the post-test physical image questionnaire, which was completed at the beginning of the study, was completed by the control group to examine the effectiveness of counseling sessions based on positive psychology.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Body image. Timepoint: At the beginning of the study (before the intervention) and at the end of the study (counseling based on positive psychology). Method of measurement: Multidimensional body-self relations questionnaire.</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>Kermanshah University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-03-09</approval_date>
        <contact_name>Ethics Committee of Kermanshah University of Medical Sciences</contact_name>
        <contact_address>Burn unit, Imam Khomeini Hospital- Naghlieh Street Kermanshah Kermanshah Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
