<?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>IRCT20200622047888N3</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2023-11-14</date_registration>
      <primary_sponsor>Razi University, Kermanshah</primary_sponsor>
      <public_title>neck stabilization and dynamic neuromuscular stabilization exercises and muscle activity</public_title>
      <acronym></acronym>
      <scientific_title>Comparison the effect of  neck stabilization exercise and  dynamic neuromuscular stabilization on pain intensity, forward head angle and muscle activity of employees with chronic non-specific neck pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2023-05-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/72416</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The participants were randomly assigned to two intervention groups (intervention group one: dynamic neuromuscular stabilization and intervention group two: neck stabilization exercise), and control group by drawing a number from 1 to 54, prepared in advance by the trainer and placed in sealed envelopes in a box. The number envelopes were placed inside a box. The trainer was asked to pick 15 envelopes from the numbers inside the box for each group. The randomization sequence was not disclosed until participants had completed their baseline assessments. The assessor was blinded to group allocation, Blinding description: The randomization sequence was not disclosed until patients completed their baseline assessments. The statistician and the assessor were blind to group allocation. Patients were not blind to the interventions (intervention group one: dynamic neuromuscular stabilization and intervention group two: neck stabilization exercise), but did not  know which group was the treatment therapy.</study_design>
      <phase>N/A</phase>
      <hc_freetext>chronic non-specific neck pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group1: Intervention group 1: In this group the electrical activity of muscles, pain intensity and forward head angle  is respectively measured by electromyography device, the numeric pain rating scale (NPRS), camera respectively. Then Subjects receive  neck stabilization exercise for six weeks, and then at the end of the  six weeks the electrical activity of muscles is measured again. Training sessions consist of six weeks with three training sessions per week for one hour. Intervention 2: Intervention group2: Intervention group 2: In this group the electrical activity of muscles, pain intensity and forward head angle  is respectively measured by electromyography device, the numeric pain rating scale (NPRS), camera respectively. Then Subjects receive  dynamic neuromuscular stabilization  exercise for six weeks, and then at the end of the six weeks the electrical activity of muscles is measured again. Training sessions consist of six weeks with three training sessions per week for one hour. Intervention 3: Control group: The control group was asked to maintain their ordinary daily activities and not to participate in any exercise programs.</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>No - There is not a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for not sharing IPD is There is no more information</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ainollah Sakinepoor</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>HOR Street</address>
        <city>Eslam Abad Garb</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6761753164</zip>
        <telephone>+98 83 4522 6103</telephone>
        <email>asakenapoor@yahoo.com</email>
        <affiliation>The Razi University, Kermanshah</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Ainollah Sakinepoor</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>HOR Street</address>
        <city>Eslam Abad Garb</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6761753164</zip>
        <telephone>+98 83 4522 6103</telephone>
        <email>asakenapoor@yahoo.com</email>
        <affiliation>The Razi University, Kermanshah</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Subjects who had persistent neck pain (more than three months).
Subjects who used the computer for at least four hours a day
Subjects who  got score three  from the visual analog scale one week before the pre-test.
Subjects who got score between 3 and 7 in the visual pain grading system (scale 0=10 cm).
Neck pain for which the specialist doctor did not mention a specific cause
Subjects who were female.</inclusion_criteria>
      <agemin>32 years</agemin>
      <agemax>50 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Neck pain for which a specialist doctor has mentioned a specific cause.
Specific structural damage in the neck, neck disc
Spine surgery</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>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group1: Intervention group 1: In this group the electrical activity of muscles, pain intensity and forward head angle  is respectively measured by electromyography device, the numeric pain rating scale (NPRS), camera respectively. Then Subjects receive  neck stabilization exercise for six weeks, and then at the end of the  six weeks the electrical activity of muscles is measured again. Training sessions consist of six weeks with three training sessions per week for one hour.</i_keyword>
      <i_keyword>Intervention group2: Intervention group 2: In this group the electrical activity of muscles, pain intensity and forward head angle  is respectively measured by electromyography device, the numeric pain rating scale (NPRS), camera respectively. Then Subjects receive  dynamic neuromuscular stabilization  exercise for six weeks, and then at the end of the six weeks the electrical activity of muscles is measured again. Training sessions consist of six weeks with three training sessions per week for one hour.</i_keyword>
      <i_keyword>Control group: The control group was asked to maintain their ordinary daily activities and not to participate in any exercise programs</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Electrical activity of muscles. Timepoint: The electrical activity of muscles were measured before and six weeks after the stabilization exercise and  dynamic neuromuscular stabilization exercises. Method of measurement: The ground reaction forces is measured by sixteen channel electromyography device.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Forward head angle. Timepoint: Forward head angle  was measured before and after the six the neck stabilization exercise and  dynamic neuromuscular stabilization exercises. Method of measurement: Forward head was measured by photogrammetric method.</sec_outcome>
      <sec_outcome>Pain intensity. Timepoint: pain intensity was measured before and after the six the neck stabilization exercise and dynamic neuromuscular. Method of measurement: Pain intensity was measured by the numeric pain rating scale method.</sec_outcome>
      <sec_outcome>Electrical activity of muscles. Timepoint: Electrical activity of muscles  was measured before and after the six the neck stabilization exercise and  dynamic neuromuscular. Method of measurement: Electrical activity of muscles was measured by electromyography device.</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>It is a personal financial source</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2023-08-04</approval_date>
        <contact_name>Research Ethics Committees of Hormozgan University of Medical Sciences</contact_name>
        <contact_address>Imam Hossein Street Bandar Abas Hormozgan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
