<?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>IRCT2014100119358N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2014-12-08</date_registration>
      <primary_sponsor>Shiraz University of Medical Sciences</primary_sponsor>
      <public_title>The effect of scapulothorasic joint mobilization on treatment of patients with neck pain</public_title>
      <acronym></acronym>
      <scientific_title>Evaluation of the effect of scapulothorasic joint mobilization on pain intensity, pinch strength and upper limb function in patients with mechanical neck pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2014-09-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>46</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/17320</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Mechanical neck pain.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: In the intervention group patients receive routine physical therapy treatment protocol for neck pain for 5 sessions over a week. The routine physical therapy treatment protocol contained: Transcutaneous electrical nerve stimulation: conventional mode, frequency 100 Hz, tolerable intensity for 20 min over the pain site; Hot pack: for 20 minutes on the neck; exercise therapy: - the patient place both hands on the forehead and press the forehead into the palms while not moving. - The patient press the back of the head into both hands. - the patient press one hand against the side of the head and attempt to side-bend, as if trying to bring the ear toward the shoulder but not allowing motion, this exercise done for both left and right side. Each patient does exercises 20 times in a day and holds contraction to 6 seconds. The intensity of the contraction must be maximum; scapulothorasic joint mobilization: In intervention group, mobilization techniques applied in the direction of the limited movements of scapula (Retraction, Depression, Elevation, Upward Rotation and Downward Rotation). Patient sleeps on the sound side, close to the edge of the bed. Her head is on the pillow and hips and knees are bent. The therapist stands in front of the patient's hip and bends on it, so that the patient's ileum taken by therapist's axilla. Then each of the techniques done on the intervention group. These techniques applied Sustained with grade 4. Each technique consists of 10 sets of 10 repetitions with 30 seconds rest between each set. Each movement hold 5 seconds and there are 3 seconds rest between each movement in each set. Patients in intervention group receive 5 sessions scapulothorasic joint mobilization in a week. Intervention 2: Control group: In the control group patients receive routine physical therapy treatment protocol for neck pain for 10 sessions over a week. The routine physical therapy treatment protocol contained: Transcutaneous electrical nerve stimulation: conventional mode, frequency 100 Hz, tolerable intensity for 20 min over the pain site; Hot pack: for 20 minutes on the neck; exercise therapy: - the patient place both hands on the forehead and press the forehead into the palms while not moving. - The patient press the back of the head into both hands. - the patient press one hand against the side of the head and attempt to side-bend, as if trying to bring the ear toward the shoulder but not allowing motion, this exercise done for both left and right side. Each patient does exercises 20 times in a day and holds contraction to 6 seconds. The intensity of the contraction must be maximum. Control group receive 5 treatment sessions in a week.</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>Zeinab Shirzadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Rehabilitation Sciences, Abiverdi 1 Avenue, Chamran Blvd, Shiraz</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 71 3627 1552</telephone>
        <email>shirzadi.zeinab@gmail.com</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Dr. Zahra Rojhani Shirazi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Rehabilitation Sciences, Abiverdi 1 Avenue, Chamran Blvd, Shiraz</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 71 3627 1552</telephone>
        <email>rojhaniz@sums.ac.ir</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Inclusion criteria: Complaint of mechanical neck pain (general pain in the neck that induced with movement or constant holding of neck and palpation of the neck muscles); age between 20-50 years; neck disability index between 10 to 45 percent; duration of the involvement more than three months; incorrect position of scapula and scapular dyskinesia. Exclusion criteria: History of whiplash injury; Surgery in the neck or upper limb; serious pathology (eg malignant tumor, infection, inflammatory disorders or fracture); any disease or disorder of the central nervous system including: stroke, MS and ...; any disease of peripheral nervous system which may affect the study results such as: neuropathies, carpal tunnel syndrome, Guyan tunnel syndrome and cervical radiculopathy.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M95.3</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Acquired deformity of neck</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: In the intervention group patients receive routine physical therapy treatment protocol for neck pain for 5 sessions over a week. The routine physical therapy treatment protocol contained: Transcutaneous electrical nerve stimulation: conventional mode, frequency 100 Hz, tolerable intensity for 20 min over the pain site; Hot pack: for 20 minutes on the neck; exercise therapy: - the patient place both hands on the forehead and press the forehead into the palms while not moving. - The patient press the back of the head into both hands. - the patient press one hand against the side of the head and attempt to side-bend, as if trying to bring the ear toward the shoulder but not allowing motion, this exercise done for both left and right side. Each patient does exercises 20 times in a day and holds contraction to 6 seconds. The intensity of the contraction must be maximum; scapulothorasic joint mobilization: In intervention group, mobilization techniques applied in the direction of the limited movements of scapula (Retraction, Depression, Elevation, Upward Rotation and Downward Rotation). Patient sleeps on the sound side, close to the edge of the bed. Her head is on the pillow and hips and knees are bent. The therapist stands in front of the patient's hip and bends on it, so that the patient's ileum taken by therapist's axilla. Then each of the techniques done on the intervention group. These techniques applied Sustained with grade 4. Each technique consists of 10 sets of 10 repetitions with 30 seconds rest between each set. Each movement hold 5 seconds and there are 3 seconds rest between each movement in each set. Patients in intervention group receive 5 sessions scapulothorasic joint mobilization in a week.</i_keyword>
      <i_keyword>Control group: In the control group patients receive routine physical therapy treatment protocol for neck pain for 10 sessions over a week. The routine physical therapy treatment protocol contained: Transcutaneous electrical nerve stimulation: conventional mode, frequency 100 Hz, tolerable intensity for 20 min over the pain site; Hot pack: for 20 minutes on the neck; exercise therapy: - the patient place both hands on the forehead and press the forehead into the palms while not moving. - The patient press the back of the head into both hands. - the patient press one hand against the side of the head and attempt to side-bend, as if trying to bring the ear toward the shoulder but not allowing motion, this exercise done for both left and right side. Each patient does exercises 20 times in a day and holds contraction to 6 seconds. The intensity of the contraction must be maximum. Control group receive 5 treatment sessions in a week.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain intensity. Timepoint: before and immediately after the first session and at the end of the course of treatment. Method of measurement: Pain Numeric Rating Scale.</prim_outcome>
      <prim_outcome>Maximum grip strength. Timepoint: before and immediately after the first session and at the end of the course of treatment. Method of measurement: Newton scale with digital dynamometer.</prim_outcome>
      <prim_outcome>Pinch strength. Timepoint: before and immediately after the first session and at the end of the course of treatment. Method of measurement: Newton scale with Pinch Gage.</prim_outcome>
      <prim_outcome>Disability of upper limb. Timepoint: before and after intervention. Method of measurement: Disabilities of Arm, Shoulder and Hand questionnaire.</prim_outcome>
      <prim_outcome>Disability of neck. Timepoint: before and after intervention. 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>Shiraz University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2014-08-26</approval_date>
        <contact_name>Shiraz University of Medical Sciences</contact_name>
        <contact_address>Central building of Shiraz University of Medical Sciences, Zand avenue, Shiraz Shiraz  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
