<?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>IRCT20180917041052N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-10-29</date_registration>
      <primary_sponsor>Tehran University of Medical Science</primary_sponsor>
      <public_title>The effect of sexual health discharge planning on the sexual function of patients undergoing transurethral resection of prostate (TURP)</public_title>
      <acronym></acronym>
      <scientific_title>The effect of sexual health discharge planning on the sexual function of patients undergoing transurethral resection of prostate (TURP)</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2018-10-07</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>80</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/34014</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Treatment, Randomization description: the samples  will randomly assign to the control and intervention groups by quadruple block method.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Benign Prostate Hyperplasia and TURP Surgery.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group:in the design of discharge planning, focus was placed on an educational program based on sexual health. its content was based on evidence (from literature review). The program focuses on the role of mental status and beliefs in sexual functioning, the role of fatigue on sexual function, the role of pelvic floor muscle exercises in improving function and sexual activity by controlling urinary incontinence and other mechanisms, the role of physical activity and exercise in sexual performance recovery , And the importance of managing the symptoms of the lower urinary system and urinary incontinence on sexual satisfaction and willingness to do.This program will accomplish in three sessions from 30 to 45 minutes from admission until to discharge. At the end, the booklet will give to the patient or companion patient, and the researcher's telephone number will give to the client for answer the patient questions. Intervention 2: Control group: For the control group, training will be performed Based on the standard of the Urology Department.</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 abstract, the title of the statement, the method of submission and discussion, and the conclusions will be published.
Content available for statistical analysis will be published.
In the case of samples, the process is not coded or run.
In case of customer satisfaction, proprietary information will be quoted with encoding.

When:
After completing the study, its contents will be published in prestigious journals

To whom:
All people

Conditions:
In order to improve the sexual function of patients under turp

Where to obtain:
Related magazine site

How to obtain:
Available data can be submitted to applicants after request

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ramin Bayat</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Plaque 39. Shahid Hami Ebrahim Khani Alley. 17 Shahrivar Street</address>
        <city>Zanjan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>45196-44491</zip>
        <telephone>+98 24 3355 3313</telephone>
        <email>baiatramin@gmail.com</email>
        <affiliation>Faculty of Nursing and Midwifery</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Ramin Bayat</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Plaque 39. Shahid Hami Ebrahim Khani Alley. 17 Shahrivar Street</address>
        <city>Zanjan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4519644491</zip>
        <telephone>+98 24 3355 3313</telephone>
        <email>baiatramin@gmail.com</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Men under the age of 85 under TURP surgery.
not Consumption of antidepressants or anti-psychotic drugs.
Lack of addictive substances such as opium, alcohol and cocaine compounds.
Not participating in previous sexual health programs.
Having patient satisfaction to participate in the study.
Married men.
Not having untreated psychological problems.
Have not history of pelvic floor muscle surgery.
No use of phosphodiesterase inhibitors (PDE).
Having no history of CABG.
Lack of atherosclerotic diseases, skeletal and muscular disorders that prevent excessive mobility of the patient.
Lack of diseases affecting the nervous system, such as multiple sclerosis, hypogonadism, hyperprolactinemia, dementia, Parkinson's disease, and spinal cord injury.</inclusion_criteria>
      <agemin>no limit</agemin>
      <agemax>85 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>Not being educated of client</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>N40</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Benign prostatic hyperplasia</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:in the design of discharge planning, focus was placed on an educational program based on sexual health. its content was based on evidence (from literature review). The program focuses on the role of mental status and beliefs in sexual functioning, the role of fatigue on sexual function, the role of pelvic floor muscle exercises in improving function and sexual activity by controlling urinary incontinence and other mechanisms, the role of physical activity and exercise in sexual performance recovery , And the importance of managing the symptoms of the lower urinary system and urinary incontinence on sexual satisfaction and willingness to do.This program will accomplish in three sessions from 30 to 45 minutes from admission until to discharge. At the end, the booklet will give to the patient or companion patient, and the researcher's telephone number will give to the client for answer the patient questions.</i_keyword>
      <i_keyword>Control group: For the control group, training will be performed Based on the standard of the Urology Department</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Sexuall function. Timepoint: Before the intervention. One and three months after the intervention. Method of measurement: based on the IIEF-15 questionnare.</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 Science</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2017-06-06</approval_date>
        <contact_name>The Ethics Committee of the Nursing and Rehabilitation  faculty of Tehran</contact_name>
        <contact_address>Faculty of Nursing and Midwifery. East Nusrat Street. Tohid Street. Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
