<?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>IRCT2016043027676N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2016-05-29</date_registration>
      <primary_sponsor>Yasouj University of Medical Sciences and Health Services</primary_sponsor>
      <public_title>The effect of proprioceptive neuromuscular facilitation on cerebrovascular accident.</public_title>
      <acronym></acronym>
      <scientific_title>The effect of proprioceptive neuromuscular facilitation on muscle strength and activities of daily living of client with cerebrovascular accident .</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2016-05-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>60</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/22616</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Other design features: Does not.</study_design>
      <phase>2-3</phase>
      <hc_freetext>Cerebrovascular Accident.</hc_freetext>
      <i_freetext>Intervention 1: Control group:&#13;
 First, while the experimental group, muscle strength and activities of daily living will be measured using the relevant protocol. Next any specific action on the control, proprioceptive neuromuscular facilitation exercise will be done in experimental group.Immediately and four weeks after the intervention in the experimental group, muscle strength and activity of daily living in both groups was measured using the relevant protocol. Intervention 2: The intervention groups: &#13;
First samples are available as a convenient choice then randomly allocated to two groups of test and control blocks would be allocated. Then the patients eligible for inclusion in the control groups, before exercise, muscle strength and activities of daily living will be measured. Then proprioceptive neuromuscular facilitation  exercise program for 8 weeks, each session lasting 30 to 45 minutes (16 sessions during 2 months) based on the protocol will be implemented following the intervention group. In this study, the pattern of motion of the arm (Upper Extremity ) and hip movement patterns (lower Extremity) is used.&#13;
Patterns of the arm joint (upper extremity):&#13;
D1 flexion pattern: Flexion, abduction, External rotation (elbow flexed and elbow extended).&#13;
D1 extension pattern: Extension, adduction, internal rotation (elbow flexed and elbow extended).&#13;
D2 flexion pattern: flexion, adduction, external rotation (elbow flexed and elbow extended).&#13;
D2 extension pattern: extension, abduction,  internal rotation (elbow flexed and elbow extended).&#13;
Patterns of knee joint(lower extremity):&#13;
D1 flexion pattern:&#13;
Flexion, abduction, internal rotation (knee flexed and knee extended).&#13;
D1 extension pattern: Extension, adduction, external rotation (knee flexed and knee extended).&#13;
D2 flexion pattern: Flexion, adduction, external rotation (knee flexed and knee extended).&#13;
D2 extension pattern: Extension, abduction, internal rotation (knee flexed and knee extended).&#13;
 The therapist first member to be balanced with respect to the three axes of motion in the desired position and in this case the muscles as much as possible not to limit your range of motion dragged.&#13;
The first step: A passive stretching or active within 10 to 20 seconds actions and target muscle or muscles gently used gradually the end range of motion.This situation is maintained for a while.&#13;
Second stage: Immediately or after a break of about 2 to 3 seconds of contraction unlike the therapist takes place. The contract period is typically 3 to 6 seconds. &#13;
Third stage: Immediately or after a pause of about 2 to 3 seconds again to reach the target muscle or muscle twitching find a new point of range of motion.&#13;
Immediately and 4 weeks after the last training session, muscle strength and activities of daily   living of the patient is measured (post test) will be.</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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Parandvar Yaghoub</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Department of General Surgery, Martyr Dr.Beheshti hospital , Martyr  mohammad montazeri street, Yasuj</address>
        <city>Yasuj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7591794857</zip>
        <telephone>+98 74 3322 4721</telephone>
        <email>yaghoub.parandvar@yums.ac.ir ; y.parandvar@gmail.com</email>
        <affiliation>Martyr Dr.Beheshti hospital, Yasouj University of Medical Sciences and Health Services</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Najafi Dolatabad Shahla</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Martyr Dr.Jalil stree, Yasuj</address>
        <city>Yasuj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7591794857</zip>
        <telephone>+98 74 3323 4115</telephone>
        <email>shahlaiss@yahoo.com ; yaghoub.parandvar@yums.ac.ir</email>
        <affiliation>School of Nursing and Midwifery, yasuj university of medical sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria:&#13;
Personal and informed consent to participate in the study; Residence in Yasouj; Over 4 months to 2 years after stroke; The definitive diagnosis of stroke by neurologist; Age over 60 years; One catching of stroke; No active phase of the disease; The absence of spinal cord injury; Lack of PNF techniques from six months ago; No other chronic diseases such as neurological disorders and orthopedic and rheumatology; Ability to communicate and answer questions Persian; The third and less muscle strength; Daily life activities less than 60 .&#13;
Exclusion criteria:&#13;
The unwillingness or inability of the Company to continue reading; Exacerbation or re CVA; The need for hospitalization; Physiotherapy at the same time; The occurrence of other diseases; Leave practice over two sessions; Death; Impairment of cognitive function; Mental alertness and presence of cognitive impairment during the study.</inclusion_criteria>
      <agemin>60 years</agemin>
      <agemax>100 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>sequelae o</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Stroke, not specified as haemorrhage or infarction</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Control group:&#13;
 First, while the experimental group, muscle strength and activities of daily living will be measured using the relevant protocol. Next any specific action on the control, proprioceptive neuromuscular facilitation exercise will be done in experimental group.Immediately and four weeks after the intervention in the experimental group, muscle strength and activity of daily living in both groups was measured using the relevant protocol.</i_keyword>
      <i_keyword>The intervention groups: &#13;
First samples are available as a convenient choice then randomly allocated to two groups of test and control blocks would be allocated. Then the patients eligible for inclusion in the control groups, before exercise, muscle strength and activities of daily living will be measured. Then proprioceptive neuromuscular facilitation  exercise program for 8 weeks, each session lasting 30 to 45 minutes (16 sessions during 2 months) based on the protocol will be implemented following the intervention group. In this study, the pattern of motion of the arm (Upper Extremity ) and hip movement patterns (lower Extremity) is used.&#13;
Patterns of the arm joint (upper extremity):&#13;
D1 flexion pattern: Flexion, abduction, External rotation (elbow flexed and elbow extended).&#13;
D1 extension pattern: Extension, adduction, internal rotation (elbow flexed and elbow extended).&#13;
D2 flexion pattern: flexion, adduction, external rotation (elbow flexed and elbow extended).&#13;
D2 extension pattern: extension, abduction,  internal rotation (elbow flexed and elbow extended).&#13;
Patterns of knee joint(lower extremity):&#13;
D1 flexion pattern:&#13;
Flexion, abduction, internal rotation (knee flexed and knee extended).&#13;
D1 extension pattern: Extension, adduction, external rotation (knee flexed and knee extended).&#13;
D2 flexion pattern: Flexion, adduction, external rotation (knee flexed and knee extended).&#13;
D2 extension pattern: Extension, abduction, internal rotation (knee flexed and knee extended).&#13;
 The therapist first member to be balanced with respect to the three axes of motion in the desired position and in this case the muscles as much as possible not to limit your range of motion dragged.&#13;
The first step: A passive stretching or active within 10 to 20 seconds actions and target muscle or muscles gently used gradually the end range of motion.This situation is maintained for a while.&#13;
Second stage: Immediately or after a break of about 2 to 3 seconds of contraction unlike the therapist takes place. The contract period is typically 3 to 6 seconds. &#13;
Third stage: Immediately or after a pause of about 2 to 3 seconds again to reach the target muscle or muscle twitching find a new point of range of motion.&#13;
Immediately and 4 weeks after the last training session, muscle strength and activities of daily   living of the patient is measured (post test) will be.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Muscle strength. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Manual Muscle Testing grading scale.</prim_outcome>
      <prim_outcome>Activities of Daily living. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Activities of Daily living Questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Quality of Life. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: The World Health Organization Quality of Life Questionnaire of 26 questions.</sec_outcome>
      <sec_outcome>Muscle Strength. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Digital Balance/Kg.</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>Yasouj University of Medical Sciences and Health Services</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2016-04-16</approval_date>
        <contact_name>Ethics Committee Yasuj University of Medical Sciences and Health Services</contact_name>
        <contact_address>Yasuj University of Medical Sciences and Health Services, Mottahari BLvd, Yasuj Yasuj  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
