<?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>IRCT20210725051976N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-09-08</date_registration>
      <primary_sponsor>Zahedan University of Medical Sciences</primary_sponsor>
      <public_title>The comparison of Effects of stabilization exercises and proprioceptive neuromuscular facilitationon balance in patients with chronic non-specific neck pain</public_title>
      <acronym></acronym>
      <scientific_title>The comparison of Effects of stabilization exercises and proprioceptive neuromuscular facilitationon balance in patients with chronic non-specific neck pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-08-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>34</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/57865</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: In the present study of the Biodex balance device, which is a more accurate and objective tool, the assessments are by standing on the platform and moving the degree and precise center of mass of the body on the screen, which is more accurate information with higher sensitivity than movements. The center of mass of the body, separately in the anterior-posterior, internal and external directions, provides general stability index and information related to equilibrium reactions on different pages and can be used in different static, dynamic and displacement conditions. Provides individual assessments to the assessor in a quantified and accurate manner, Randomization description: Patients in both groups will be selected using the easy (available) sampling method. As soon as patients arrive, permutation blocks will be assigned to one of the two groups by stratified randomization (Figure below)
B: Stability Exercises Group
A: Neuromuscular facilitation exercises group
In this method, after determining the age and then gender, the following table enters the groups, so that for example, the first person under 40 years old enters group B, the second B and the third and fourth person under 40 years old enter group A. . This method makes the groups the same in terms of age and gender, Blinding description: . The subjects will not be aware of the existence of two exercise groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Chronic nonspecific neck pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Stability exercises. Intervention 2: Intervention group: Neuromuscular facilitation exercises.</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:
Part of the data, such as information about the main outcome, can be shared.

When:
Access period starts from 1401 "

To whom:
Real people working in academic and scientific institutions

Conditions:
Study

Where to obtain:
mz.mohammady@yahoo.com

How to obtain:
Request by email and review and consult with the tutor and announce the result

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>marzieh mohammadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Zibashahr, Alborz 4, sixth door on the left</address>
        <city>zahedan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9817943473</zip>
        <telephone>+98 54 3328 5627</telephone>
        <email>mz.mohammadi@zaums.ac.ir</email>
        <affiliation>Zahedan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Marzieh Mohammadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No.4,alborz alley.alborz ave</address>
        <city>Zahedan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9817943473</zip>
        <telephone>+98 54 3327 5628</telephone>
        <email>MZ.MOHAMMADI@zaums.ac.ir</email>
        <affiliation>Zahedan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Of both sexes, men and women between the ages of 20 and 50Have neck pain that lasts 12 weeks or more.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Referral and radicular pain to the distal upper limb
History of musculoskeletal disorders
No history of head trauma
No history of visual or hearing or speech impairment
Having treatment in the last three months in the neck or shoulder area
Pregnancy
Take painkillers, sedatives and alcohol 48 hours before the test</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>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Stability exercises</i_keyword>
      <i_keyword>Intervention group: Neuromuscular facilitation exercises</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The overall static balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>The overall static balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Overall dynamic balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Overall dynamic balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Internal and external static balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Internal and external static balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Internal and external dynamic balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Internal and external dynamic balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Anterior and posterior static balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Anterior and posterior static balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Anterior and posterior dynamic balance with my eyes open. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Anterior and posterior dynamic balance with my eyes closed. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Based on the deviation of the Biodex device.</prim_outcome>
      <prim_outcome>Cranial cervical flexion test. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Compression biofeedback.</prim_outcome>
      <prim_outcome>Pain. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Visual Analogue Scale.</prim_outcome>
      <prim_outcome>The degree of functional disability. Timepoint: At the beginning of the study and 8 weeks after the start of training. Method of measurement: Neck Disability Index.</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>Zahedan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-05-25</approval_date>
        <contact_name>Ethics Committee of Zahedan University of Medical Sciences</contact_name>
        <contact_address>Zibashahr, Alborz 4, sixth door on the left zahedan Sistan-va-Balouchestan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
