<?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>IRCT20180813040787N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2019-05-28</date_registration>
      <primary_sponsor>kharazmi University</primary_sponsor>
      <public_title>Comparison of the effect of corrective exercises with and without Cognitive Functional exercises on pain, Kinesiophobia, disability, electromyography and alignment of scapula in people with chronic neck pain</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of the effect of corrective exercises with and without Cognitive Functional exercises on pain, Kinesiophobia, disability, electromyography and alignment of scapula in people with chronic neck pain Along with scapular downward rotation syndrome</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2019-05-31</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>36</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/39712</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: -, Randomization description: Samples are selected according to the criteria for entering the research and are randomly divided into three groups, Blinding description: Outcome evaluator and data analyzer are kept blind. The assessor was blinded to the group allocation.</study_design>
      <phase>N/A</phase>
      <hc_freetext>non-specific Chronic  neck pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: CORRECTIVE exercise;scapula  stabilization exercises were performed with and without resistance. In non-resistance exercises, body weight was used to perform the exercises, and in the exercises with resistance, free weights and elastic bands were used as resistance exercises. . . The CFT aimed at altering the perception of pain consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback  . Rest time between each set was 30 seconds and between each exercise one minute. Intervention 2: Intervention group: CORRECTIVE exercise whit Cognitive Functional exercises;The CFT  consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback. The CFT aimed at altering the perception of pain consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback. Intervention 3: Control group: The control group attended a single session where they were instructed in a home exercise program  mainly focused on posture during daily task as well as demonstrations of lifting, pushing, pulling tasks as well as office ergonomics (computer placement, chair and desk adjustments etc.).</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:
Only part of the data, such as dependent variables,The average of all samples, can be shared in scientific articles.

When:
The date of access is September 2019.

To whom:
Personal information is confidential and General outcomes in paper form Available to everyone..

Conditions:
Information is not available to anyone.General outcomes in paper form Available to everyone.

Where to obtain:
Noorollah javdaneh
Phone: 09176616415
Email: njavdaneg68@gmail.com

How to obtain:
-

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>noorollah javdaneh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>tehran</address>
        <city>tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9575153714</zip>
        <telephone>+98 21 4471 8356</telephone>
        <email>njavdaneh68@gmail.com</email>
        <affiliation>kharazmi University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>noorollah javdaneh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>tehran</address>
        <city>tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7595153714</zip>
        <telephone>+98 21 4471 8356</telephone>
        <email>njavdaneh68@gmail.com</email>
        <affiliation>kharazmi University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>- People with neck pain for at least three months
- Pain amount, gaining a rating between 3 -7 in the visual grading system of pain
- Having a disability score score of between 15 and 30 from a functional disability questionnaire
- A neck pain that the doctor has not mentioned for a specific reason
People with scapular downward rotation syndrome</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>45 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria>- Having any history of fracture and surgery in the shoulder joint
- Shoulder instability
- The presence of any shoulder injury such as shoulder dislocation, tendonitis and frozen shoulder
- The kyphosis angle is greater than 50 and less than 20 degrees
- The cranio angle is less than 45 degrees and more than 60 degrees
- lack of regular participation in training programs for two consecutive sessions and three non-consecutive sessions
prolapsed disk with nerve symptoms.
- Spinal surgery.
- There is a definite structural damage in the neck.
- severe mental illnesses.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>xiii</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>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: CORRECTIVE exercise;scapula  stabilization exercises were performed with and without resistance. In non-resistance exercises, body weight was used to perform the exercises, and in the exercises with resistance, free weights and elastic bands were used as resistance exercises. . . The CFT aimed at altering the perception of pain consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback  . Rest time between each set was 30 seconds and between each exercise one minute.</i_keyword>
      <i_keyword>Intervention group: CORRECTIVE exercise whit Cognitive Functional exercises;The CFT  consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback. The CFT aimed at altering the perception of pain consisted of patient education regarding the multidimensional nature of ongoing pain, management of flair-ups, visual and kinesthetic motor imagery , functional training, and mirror feedback</i_keyword>
      <i_keyword>Control group: The control group attended a single session where they were instructed in a home exercise program  mainly focused on posture during daily task as well as demonstrations of lifting, pushing, pulling tasks as well as office ergonomics (computer placement, chair and desk adjustments etc.).</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain rate. Timepoint: pre and post test. Method of measurement: Pain Visual Scale.</prim_outcome>
      <prim_outcome>Disability. Timepoint: pre and post test. Method of measurement: Neck Disability Questionnaire.</prim_outcome>
      <prim_outcome>Electromyography. Timepoint: pre and post test. Method of measurement: Electromyographic Device.</prim_outcome>
      <prim_outcome>Alignment of scapula. Timepoint: pre and post test. Method of measurement: caliper.</prim_outcome>
      <prim_outcome>Kinesiophobia. Timepoint: pre and post. Method of measurement: Tampa Scale for Kinesiophobia.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Scapular kinematics-. Timepoint: pre and post tesr. Method of measurement: IMU Sensor,.</sec_outcome>
      <sec_outcome>Flexion relaxation phenomenon. Timepoint: pre and post test. Method of measurement: Electromyographic Device.</sec_outcome>
      <sec_outcome>Self-efficacy. Timepoint: pre and post test. Method of measurement: Self-efficacy Questionnaire.</sec_outcome>
      <sec_outcome>Quality of life. Timepoint: pre and post test. Method of measurement: SF-36 Questionnaire.</sec_outcome>
      <sec_outcome>Pain catastrophizing. Timepoint: pre and post. Method of measurement: Pain catastrophizing Scale.</sec_outcome>
      <sec_outcome>Self-efficacy for pain management. Timepoint: pre and post. Method of measurement: Self-efficacy for pain management.</sec_outcome>
      <sec_outcome>Self-efficacy for physical function. Timepoint: pre and post. Method of measurement: Self-efficacy for physical function.</sec_outcome>
      <sec_outcome>Fear-Avoidance Beliefs. Timepoint: pre and post. Method of measurement: Fear-Avoidance Beliefs Questionnaire (FABQ).</sec_outcome>
      <sec_outcome>Depression. Timepoint: pre and post. Method of measurement: Depression  Questionnaire.</sec_outcome>
      <sec_outcome>Anxiety. Timepoint: pre and post. Method of measurement: Anxiety Questionnaire.</sec_outcome>
      <sec_outcome>Range of motion of neck. Timepoint: pre and post test. Method of measurement: IMU Sensor.</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>kharazmi University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2019-05-12</approval_date>
        <contact_name>KHARAZMI UNIVERSITY</contact_name>
        <contact_address>TEHRAN TEHRAN Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
