<?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>IRCT20171205037757N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2018-01-17</date_registration>
      <primary_sponsor>The University of Bu-Ali Sina</primary_sponsor>
      <public_title>Water therapy to improve patellofemoral pain syndrome</public_title>
      <acronym>PFPS</acronym>
      <scientific_title>The effect of hip and knee muscles strength exercises in the water with or without use of kinesiotapes) as instant and long term (in improvement  of pain, dynamic performance, Disability and the balance in women patients Patellofemoral pain syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2016-11-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/27977</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: Use kinesiotape the water, Blinding description: The researcher has by no means interfered in test neither in pre-test before exercise or post-test after exercise as the tests were given by individuals who had no clue about the plan.the participants were not alert of test application as well and just acted to instruction.The person who analyzed the data did not know about the study and generally looked at the data.</study_design>
      <phase>2</phase>
      <hc_freetext>Patellofemoral pain syndrome.</hc_freetext>
      <i_freetext>Intervention 1: First Intervention group: water therapy without kinesiotape (n=15),A two-month-long therapeutic exercise without the use of a kinesiotape. Intervention 2: Second Intervention group: water therapy with temporary kinesiotaping (n=15), A two-month-long therapeutic exercise using short-term kinesiotap. Intervention 3: Third Intervention group: water therapy with permanent kinesiotaping (n=15), A two-month-long exercise therapy using long-term  kinesiotap.</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:
Data and documentation can be shared, but with unidentifiable individuals and private information for subjects

When:
Starting data access 1 year after printing results

To whom:
Researchers in this field are allowed to act for documentation

Conditions:
Only the type of analysis that can be done in the research can be redefined

Where to obtain:
mokhtari.marzieh.1371@gmail.com

How to obtain:
When the applicant submits a document for his / her work area in relation to the subject matter of the thesis, and if the request is reasonable and the commitment not to misuse the data of this research, the data will be sent to him within 1 week of work.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Marzieh Mokhtari Karchegani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No.76, Deadend Ershad., Nastoh Street.</address>
        <city>Esfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8174784986</zip>
        <telephone>+98 31 3775 8601</telephone>
        <email>Mokhtari.Marzieh.1371@Gmail.com</email>
        <affiliation>The University of Bu-Ali Sina</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Marzieh Mokhtari Karchegani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No.76, Deadend Ershad., Nastoh Street.</address>
        <city>Esfahan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>8174784986</zip>
        <telephone>+98 31 3775 8601</telephone>
        <email>Mokhtari.Marzieh.1371@Gmail.com</email>
        <affiliation>The University of Bu-Ali Sina</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Diagnosis and confirmation of the presence of patellofemoral pain syndrome by a specialist
Positive Clark's test and Patellar Apprehension
Womens aged 18 to 45 years
Not participating in other sports activities</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>45 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Diseases like osteoarthritis, joint diseases
Having an artificial joints in the leg
Performing knee surgery in the past
Use of pain medications for knee pain in the present
Affected by diseases that affect the variables of balance such as: Having no proper vision or any visual impairment, having an internal ear venereal disease</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M00-M99</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Diseases of the musculoskeletal system and connective tissue</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>First Intervention group: water therapy without kinesiotape (n=15),A two-month-long therapeutic exercise without the use of a kinesiotape</i_keyword>
      <i_keyword>Second Intervention group: water therapy with temporary kinesiotaping (n=15), A two-month-long therapeutic exercise using short-term kinesiotap</i_keyword>
      <i_keyword>Third Intervention group: water therapy with permanent kinesiotaping (n=15), A two-month-long exercise therapy using long-term  kinesiotap</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The amount of Visual pain. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Use the Visual Analogue Scale ruler.</prim_outcome>
      <prim_outcome>The amount of pain. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Using the McGill Pain Questionnaire.</prim_outcome>
      <prim_outcome>Motor function. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Use the Kujala questionnaire.</prim_outcome>
      <prim_outcome>Disability. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Van Kurf et al. Disability questionnaire.</prim_outcome>
      <prim_outcome>Dynamic balance. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Biodegrade System balance.</prim_outcome>
      <prim_outcome>Static balance. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Biodegrade System balance.</prim_outcome>
      <prim_outcome>Quality of Life. Timepoint: At the beginning of the study before the intervention and 60 days after the exercises. Method of measurement: Sherbourne SF36 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>The University of Bu-Ali Sina</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2017-01-14</approval_date>
        <contact_name>Ethics committee of Hamedan University of Medical Sciences</contact_name>
        <contact_address>Pajohesh Intersection ., Mahdieh Street Hamedan Hamadan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
