<?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>IRCT20220710055428N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-08-04</date_registration>
      <primary_sponsor>Oroumia University of Medical Sciences</primary_sponsor>
      <public_title>Study survey of The effect on positive psychology intervention on health-promoting lifestyle</public_title>
      <acronym></acronym>
      <scientific_title>Study survey of The effect on positive psychology intervention on health-promoting lifestyle in postmenopausal women</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-08-11</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>70</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/64697</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Other design features: The first group is the intervention group, which will be subjected to positive psychology intervention for six weeks and one ninety-minute session per week.The second group is the control group and no special intervention is done on them and they receive routine care from the Comprehensive Health Center and at the end of the study an educational text will be prepared and will be available to them, Randomization description: In this experimental study, the research population includes 70 postmenopausal women who refer to the comprehensive health centers of Urmia city, who have health records registered in the Sib system, and they were contacted using the telephone numbers of the selected people and given explanations of The reasons and methods of conducting the research are given to them and they are invited to participate in the research.70 menopausal women willing to participate in the research will be selected as the research sample in a targeted manner and will be randomly assigned(The choice is such that we will have 70 sealed envelopes, 35 envelopes will contain A and 35 envelopes will contain B).The envelopes will be shuffled and will not be in any particular order.When the reference is contacted and after checking the criteria for entering the study and obtaining the consent form to conduct the study, a staff member at the comprehensive health centers is asked to choose an envelope from among 70 envelopes, and in this way it is determined in which group this person will be placed.If a sample did not meet the inclusion criteria, or was unwilling to participate in the study or unavailable, the next person would be randomly replaced.



نماد «مورد تأیید انجمن»

نماد «مورد تأیید انجمن».</study_design>
      <phase>N/A</phase>
      <hc_freetext>Health-promoting lifestyle in postmenopausal women.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group:35 menopausal women who have passed 12 months since their last menstrual period will be subjected to positive psychotherapy protocol (Parks-Shiner, 2009) which includes 6 sessions of 90 minutes, one session per week for 6 weeks.35 people in the intervention group will be divided into five groups of 7 people If the restrictions related to the covid disease continue, psychotherapy protocol sessions will be held virtually (by forming groups of five people in the Whats App application and providing training in the form of video calls, sending short animation videos, uploading brochures and homework forms in the application Whats App and getting feedback from subjects) will be provided.The content of this program is as follows:The first session: Getting to know and using the abilities: knowing the top 5 abilities and using them in daily life. Getting to know the training course, enjoyment of life, happiness and cheerfulness and its role in a good life and ways to achieve a satisfying life, measuring the level of cheerfulness, depression and enjoyment of the participants' life. Personal capabilities, getting to know the classification of capabilities and moral virtues, using personal capabilities in a new way.Second session: Appreciation meeting: Appreciation of people who have done important work for you. Emphasis on good memories, moving towards creating appropriate interpersonal communication, training in the technique of appreciation and gratitude (thankful letter and meeting).The third session: Active/constructive response: Active and constructive response to the good news of others. Familiarity with positive social relationships, the role of positive relationships in a happy life, training and application of the technique of constructive and active response.Fourth session: Counting the blessings: paying attention to the small blessings of life and remembering three of them every day. Examining the effects of writing three blessings or good things in life, intention and meaning in life.The fifth session: sense of taste: enjoying the small pleasures of life, such as drinking a cup of tea, getting to know positive emotions, the role of positive emotions in happiness and joy, using the mention of blessings and good things in life as positive things.The sixth session: maintaining the therapeutic effects: receiving feedback from the subjects and providing exercises for use in the future. Feedback from the training course, holding a celebration, coordinating the way to follow up.Tools: use of PowerPoint, animation, short film and brochure.نماد «مورد تأیید انجمن».نماد «مورد تأیید انجمن». Intervention 2: Control group: 35 menopausal women who have passed 12 months since their last menstrual period and meet the conditions to enter the study.No special intervention is done on them and they receive routine care from the Comprehensive Health Center and an educational text will be prepared and provided to them at the end of the study.نماد «مورد تأیید انجمن».</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:
in the form of an article

When:
6 months after the publication of the article

To whom:
Researchers working in academic and scientific institutions and research students in this field

Conditions:
Using the results in articles and comparing them in new works is not prohibited

Where to obtain:
saramehrpooya1359@gmail.com

How to obtain:
After the applicant's request via email, the necessary checks will be done and the information will be available shortly after the confirmation.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Sara Mehrpooya</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Emergency room,Resalat Blvd</address>
        <city>Urmia</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5714783734</zip>
        <telephone>+98 44 3223 4897</telephone>
        <email>saramehrpooya1359@gmail.com</email>
        <affiliation>Oroumia University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Soheila Rabiepoor</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Emergency room,Resalat Blvd</address>
        <city>Urmia</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5714783734</zip>
        <telephone>+98 44 3223 4897</telephone>
        <email>soheila80@yahoo.com</email>
        <affiliation>Oroumia University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age 45-60 years (at least 12 full months have passed since their last period)
Not using sleeping pills and antidepressants, tobacco and alcohol
Willingness to participate in the study
Being literate in reading and writing
Not suffering from mental illnesses that require hospitalization (such as psychosis)
Not receiving medication or any treatment for menopause symptoms</inclusion_criteria>
      <agemin>45 years</agemin>
      <agemax>60 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Traveling or changing the place of residence during the intervention
Having more than two absences in meetings
Participation in other psychological treatments at the same time.</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>Lifestyle</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group:35 menopausal women who have passed 12 months since their last menstrual period will be subjected to positive psychotherapy protocol (Parks-Shiner, 2009) which includes 6 sessions of 90 minutes, one session per week for 6 weeks.35 people in the intervention group will be divided into five groups of 7 people If the restrictions related to the covid disease continue, psychotherapy protocol sessions will be held virtually (by forming groups of five people in the Whats App application and providing training in the form of video calls, sending short animation videos, uploading brochures and homework forms in the application Whats App and getting feedback from subjects) will be provided.The content of this program is as follows:The first session: Getting to know and using the abilities: knowing the top 5 abilities and using them in daily life. Getting to know the training course, enjoyment of life, happiness and cheerfulness and its role in a good life and ways to achieve a satisfying life, measuring the level of cheerfulness, depression and enjoyment of the participants' life. Personal capabilities, getting to know the classification of capabilities and moral virtues, using personal capabilities in a new way.Second session: Appreciation meeting: Appreciation of people who have done important work for you. Emphasis on good memories, moving towards creating appropriate interpersonal communication, training in the technique of appreciation and gratitude (thankful letter and meeting).The third session: Active/constructive response: Active and constructive response to the good news of others. Familiarity with positive social relationships, the role of positive relationships in a happy life, training and application of the technique of constructive and active response.Fourth session: Counting the blessings: paying attention to the small blessings of life and remembering three of them every day. Examining the effects of writing three blessings or good things in life, intention and meaning in life.The fifth session: sense of taste: enjoying the small pleasures of life, such as drinking a cup of tea, getting to know positive emotions, the role of positive emotions in happiness and joy, using the mention of blessings and good things in life as positive things.The sixth session: maintaining the therapeutic effects: receiving feedback from the subjects and providing exercises for use in the future. Feedback from the training course, holding a celebration, coordinating the way to follow up.Tools: use of PowerPoint, animation, short film and brochure.نماد «مورد تأیید انجمن».نماد «مورد تأیید انجمن»</i_keyword>
      <i_keyword>Control group: 35 menopausal women who have passed 12 months since their last menstrual period and meet the conditions to enter the study.No special intervention is done on them and they receive routine care from the Comprehensive Health Center and an educational text will be prepared and provided to them at the end of the study.نماد «مورد تأیید انجمن»</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Health promoting lifestyle. Timepoint: Before and after the six-week intervention. Method of measurement: Walker's standard health promoting lifestyle 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>Oroumia University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-06-29</approval_date>
        <contact_name>Ethics Committee of Urmia University of Medical Sciences</contact_name>
        <contact_address>Emergency room, Resalat Blvd Urmia West Azarbaijan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
