<?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>IRCT20191030045287N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-03-11</date_registration>
      <primary_sponsor>The University of Faisalabad</primary_sponsor>
      <public_title>Effects of two exercises for bad head posture in Desk Workers</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of Upper Thoracic and Cervical Spine Mobilization for Forward Head Posture in Desk Workers</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-01-10</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>45</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/53528</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: A convenient sampling technique will be used for the selection of a sample from the populations and then the sample will be allocated to groups A, B, and C using the lottery method of randomization in which the researcher will randomly pick numbers, with each number corresponding to a subject, in order to create the sample. Allocation concealment will not be carried out.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Forward Head Posture.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group 1: Thoracic mobilization group: Subjects will be in the prone position. Mobilization will be performed for 30-second bout of grade I, II and III, according to clinical indication, mobilization at the T1 spinous process. After 30-sec the technique will proceed to T2 with the same protocol. This process will be sequentially continued in a caudal direction towards T6, for an overall interventional time of approximately &lt;5 min with a 10-sec break between the mobilizations of each joint. Intervention 2: Intervention group 2: Cervical mobilization group: Cervical mobilization will be conducted for 30 sec, three times for each segment. The mobilization will last for a total of &lt;5 mins, with a 10-sec break between the mobilizations of each joint. The total time of inter-segmental movement and break intervals will be 30 sec. This process will be continued from C3-C7. Intervention 3: Intervention group 3: Cervico-thoracic mobilization group: Cervical mobilization will be performed for 30 sec, three repetitions for each segment for a total of &lt;5 min. there was a 10-sec break between each mobilization for each joint according to tissue resistance. The total time of inter-segmental movement, as well as break intervals, will be the 30s. This mobilization for the cervical region will be continued from C3 to C7 and then continued towards mobilization at the T1 spinous process. After the 30-sec treatment in the cervical region, the same technique will be applied to T2. The same process will be sequentially continued in a caudal direction from C7 to T6. The interventional time at the thoracic region will be &lt;5 min with a break of 10 sec between the mobilizations of each joint. An overall interventional time of mobilization treatment at the cervicothoracic region will be approximately &lt;10 min with a 10-sec break between the mobilizations of each joint.</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>Undecided - It is not yet known if there will be a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for indecision in sharing IPD is There is no further information.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Nimra Arshad</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>House no 91,street no 4,Muslim town no 3,Sargodha road Faisalabad,Pakistan</address>
        <city>Faisalabad</city>
        <country1>Pakistan</country1>
        <zip>38000</zip>
        <telephone>+92 41 8811692</telephone>
        <email>nimraarshad70@yahoo.com</email>
        <affiliation>The University of Faisalabad</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Nimra Arshad</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>House no 91,street no 4,Muslim town no 3,Sargodha road Faisalabad,Pakistan</address>
        <city>Faisalabad</city>
        <country1>Pakistan</country1>
        <zip>38000</zip>
        <telephone>+92 41 8811692</telephone>
        <email>nimraarshad70@yahoo.com</email>
        <affiliation>The University of Faisalabad</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Pakistan</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age between 20-40 years.
Sings and symptoms of FHP last for one month like general soreness, intense pain, muscle tightness.
Pain greater than 3 on NPRS.
Office workers who engage in their work with computer for minimum 3 hours continuously.
Only female participants.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>40 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Any history of neck trauma or accident
Degenerative condition
Prior history of surgery to the cervical or thoracic spine at least before 6 months ago
Diagnosed/known psychiatric illness
Signs of nerve root compression
Systemic disease e.g. hyper/hypotension, diabetes and hypo/hyperthyroidism
Inflammatory arthritis
Any known malignancy / neoplasm
Any medication for current condition
Any known vascular condition</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>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group 1: Thoracic mobilization group: Subjects will be in the prone position. Mobilization will be performed for 30-second bout of grade I, II and III, according to clinical indication, mobilization at the T1 spinous process. After 30-sec the technique will proceed to T2 with the same protocol. This process will be sequentially continued in a caudal direction towards T6, for an overall interventional time of approximately &lt;5 min with a 10-sec break between the mobilizations of each joint.</i_keyword>
      <i_keyword>Intervention group 2: Cervical mobilization group: Cervical mobilization will be conducted for 30 sec, three times for each segment. The mobilization will last for a total of &lt;5 mins, with a 10-sec break between the mobilizations of each joint. The total time of inter-segmental movement and break intervals will be 30 sec. This process will be continued from C3-C7.</i_keyword>
      <i_keyword>Intervention group 3: Cervico-thoracic mobilization group: Cervical mobilization will be performed for 30 sec, three repetitions for each segment for a total of &lt;5 min. there was a 10-sec break between each mobilization for each joint according to tissue resistance. The total time of inter-segmental movement, as well as break intervals, will be the 30s. This mobilization for the cervical region will be continued from C3 to C7 and then continued towards mobilization at the T1 spinous process. After the 30-sec treatment in the cervical region, the same technique will be applied to T2. The same process will be sequentially continued in a caudal direction from C7 to T6. The interventional time at the thoracic region will be &lt;5 min with a break of 10 sec between the mobilizations of each joint. An overall interventional time of mobilization treatment at the cervicothoracic region will be approximately &lt;10 min with a 10-sec break between the mobilizations of each joint.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Craniovertebral angle (CVA). Timepoint: Cranio-Vertebral Angle will be measured before treatment at the baseline 1st week and at the end  of treatment of last session at 4th week. Method of measurement: Will be Measured by taking photograph of each participant.</prim_outcome>
      <prim_outcome>Neck Range of Motion. Timepoint: ROM measurements will only be filled at baseline 1st week, mid-session 2nd week and after the last session 4th week. Method of measurement: Goniometer.</prim_outcome>
      <prim_outcome>Neck Disability. Timepoint: NDI score will be measured before at 1st week and at the end of session at 4th week. Method of measurement: Neck Disability Index.</prim_outcome>
      <prim_outcome>Neck Pain. Timepoint: Pain measurements will be taken after each week till 4 weeks. Method of measurement: Numeric Pain Rating Scale (NPRS).</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>The University of Faisalabad</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2020-10-22</approval_date>
        <contact_name>Ethics committee of The University of Faisalabad,Pakistan</contact_name>
        <contact_address>Sargodha Road, University Town, Faisalabad, Pakistan Faisalabad Punjab Pakistan</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
