<?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>IRCT20160821029446N11</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-03-07</date_registration>
      <primary_sponsor>Tehran University of Medical Sciences</primary_sponsor>
      <public_title>the effect of spiritual therapy on resilience</public_title>
      <acronym></acronym>
      <scientific_title>The effect of spiritual therapy on resilience of mothers following abortion</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-04-04</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>68</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/60600</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: Assignment of samples to intervention (A) and control (B) groups (34 people in each group) will be done using blocks with size of 4. In this way, 6 possible modes will be considered using a table of random numbers. These 6 modes are written on 6 separate cards and the cards will be placed in a black bag (for concealment) . A card will be issued for 17 times to finally get 68 letters written as the sample size. The intervention group will be the group that will receive spiritual therapy sessions, and the control group will be the group that will receive only the routine cares.</study_design>
      <phase>N/A</phase>
      <hc_freetext>abortion.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: individuals are trained in spiritual therapy in 8 sessions (twice a week) for 4 weeks for 60 minutes. Once before the intervention   and once after the training sessions,  the reliance questionnaire will be filled out by the intervention group,. spiritual therapy training will be provided based on the package of kajbaf et al. the content of the meetings is as follows.session1: in this session, hope and empathetic relationship are discussed. Session 2: In this session, the first premise (spiritual human being) and the second premise that pleasant and unpleasant feelings are not dependent on phenomena but on inner feelings will be discussed. In this session, the promotion of intentions and purposeful behaviors and positive mental imagery towards God will be taught. Session 3: Includes the third premise which is the principle of action. This principle is based on the attributes of God's mercy and generosity. That is, God always provides the opportunity for human growth, and the fourth premise (divisibility: means that worldly affairs can be divided into changeable and immutable affairs). Session 4: In this session, the fifth premise (the moral world is created and always moving in the direction of happiness) will be taught. The strategy of prayer and its place in human life and increasing women's resilience following abortion and reducing anxiety and stress will be taught. Session 5: It is based on the principle that the future is not entirely in our hands. In this session, the strategies of remembrance, trust and hope in God will be discussed. Session 6: It is based on the principle that man is constantly in touch with God. In this session, the position of patience as a strategy to increase women's resilience following abortion, increase the quality of married life and deal with anxiety will be taught.Session 7: It is based on this principle that the eighth premise (spiritual man lives with his attributes, not with his property and possessions) and the ninth premise (achieving spiritual life requires charity, forgiveness, forgiveness and love). Session 8: Default (understanding the meaning of hardships and responsibilities to God, self, others and the universe). Intervention 2: Control group:  No action is taken for members of the control group. These people receive hospital routine  care. Once before the intervention in the intervention group and once after the training sessions in the intervention group, the reliance questionnaire will be filled out by the control group.</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 main outcome can be shared
the protocol used in this intervention

When:
6 months after printing the resuits

To whom:
Researchers working in academic and scientific institutions

Conditions:
for use in articles

Where to obtain:
Dr.Maryam Damghanian
maryamdamghanian@gmail.com

How to obtain:
the applicant must notify the e-mail of the request for use and after review,their request will be answered

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Maryam Damghanian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Tohid Square, Dr. Mirkhani St (Eastern Nusrat</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1419733171</zip>
        <telephone>+98 21 6692 7171</telephone>
        <email>fnm@tums.ac.ir</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Maryam Damghanian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Tohid Square, Dr. Mirkhani St. (Eastern nusrat)</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1419733171</zip>
        <telephone>021669271171</telephone>
        <email>fnm@tums.ac.ir</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Abortion before 20 weeks
Minimum literacy
No physical or psycholigical illness based on the patient's statement and no medication associated with the illness
Willingness to participate in the study</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>no limit</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Having a physical and psychological illness based on the patients statement
selective abortion</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>O03</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Spontaneous abortion</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: individuals are trained in spiritual therapy in 8 sessions (twice a week) for 4 weeks for 60 minutes. Once before the intervention   and once after the training sessions,  the reliance questionnaire will be filled out by the intervention group,. spiritual therapy training will be provided based on the package of kajbaf et al. the content of the meetings is as follows.session1: in this session, hope and empathetic relationship are discussed. Session 2: In this session, the first premise (spiritual human being) and the second premise that pleasant and unpleasant feelings are not dependent on phenomena but on inner feelings will be discussed. In this session, the promotion of intentions and purposeful behaviors and positive mental imagery towards God will be taught. Session 3: Includes the third premise which is the principle of action. This principle is based on the attributes of God's mercy and generosity. That is, God always provides the opportunity for human growth, and the fourth premise (divisibility: means that worldly affairs can be divided into changeable and immutable affairs). Session 4: In this session, the fifth premise (the moral world is created and always moving in the direction of happiness) will be taught. The strategy of prayer and its place in human life and increasing women's resilience following abortion and reducing anxiety and stress will be taught. Session 5: It is based on the principle that the future is not entirely in our hands. In this session, the strategies of remembrance, trust and hope in God will be discussed. Session 6: It is based on the principle that man is constantly in touch with God. In this session, the position of patience as a strategy to increase women's resilience following abortion, increase the quality of married life and deal with anxiety will be taught.Session 7: It is based on this principle that the eighth premise (spiritual man lives with his attributes, not with his property and possessions) and the ninth premise (achieving spiritual life requires charity, forgiveness, forgiveness and love). Session 8: Default (understanding the meaning of hardships and responsibilities to God, self, others and the universe).</i_keyword>
      <i_keyword>Control group:  No action is taken for members of the control group. These people receive hospital routine  care. Once before the intervention in the intervention group and once after the training sessions in the intervention group, the reliance questionnaire will be filled out by the control group.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>THe resilience score that individuals obtain from the Connor and Davidson Resilience Questionnaire. Timepoint: Before the intervention and at the end of the eighth session. Method of measurement: Connor and Davidson Resilience 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>Tehran University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-01-13</approval_date>
        <contact_name>Ethics Committee of the School of Nursing and Midwifery and the School of Rehabilitation of Tehran U</contact_name>
        <contact_address>Tohid Square,Dr. Mir Khani St.(Eastern Nursat) Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
