<?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>IRCT20241004063260N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-04-02</date_registration>
      <primary_sponsor>Shiraz University of Medical Sciences</primary_sponsor>
      <public_title>The effects of adding subscapularis muscle dry needling to exercise therapy on symptoms of individuals with forward head posture</public_title>
      <acronym></acronym>
      <scientific_title>Investigating the added effects of subscapularis muscle dry needling to exercise therapy on pain, kinematics, and cervical position sense in individuals with forward head posture</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-04-09</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>32</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/82387</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: The random allocation method in this study is permutation (block) randomization. Considering 8 blocks of 4 in two groups and adding individuals with an allocation ratio of 1:1 in each group, 32 patients are studied in two groups of 16. Randomization is performed using a random number table, Blinding description: In this study, assessment and treatment are performed separately by two physiotherapists, with the assessing physiotherapist blinded to the participants' treatment. Also statistical analysis is performed by a statistician who is blinded to the participants' allocation to groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Forward head posture.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Dry needling of the subscapularis muscle combined with exercise therapy. Individuals in this group will undergo 10 sessions of treatment, 3 sessions per week. The exercises will include stretching and strengthening exercises, and at the end of sessions one, three, five, seven, and nine, individuals will undergo dry needling of the subscapularis muscle. To perform dry needling, the participant is asked to lie supine, with the shoulder in 90 degrees of abduction and 90 degrees of external rotation. The therapist uses one hand to pull the participant's shoulder further outward, palpating the outer edge of the scapula. The latissimus dorsi tendon is identified and lifted using a pincer grip to provide better access to the muscle. The needle is then inserted parallel to the chest and perpendicular to the anterior surface of the scapula. The needle entry site is cleaned with alcohol and cotton. Dry needling is performed on the muscle at three points, each point for 1 minute using a fast in-fast out method. A Chinese-made Huan Qiu needle, 30 mm in diameter and 50 mm in height, is used. Assessments will be conducted before treatment, immediately after treatment, and two weeks later. Intervention 2: Control group: Exercise therapy. Individuals in this group will undergo 10 sessions of therapy, 3 sessions per week. The exercises in this group are exactly the same as those in the intervention group and include stretching and strengthening exercises. Assessments will be conducted before treatment, immediately after treatment, and two weeks later.</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:
Data collection form including primary and secondary outcomes, informed consent form, and SPSS file

When:
After the publication of the study results

To whom:
Researchers working in academic and scientific institutions

Conditions:
Only for recording information in scientific databases

Where to obtain:
Correspondence with the project manager via email yazdani_far@sums.ac.ir

How to obtain:
Maximum one month after sending the request via email

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Farzaneh Yazdani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Rehabilitation Sciences, Shahid Doran Campus, after Amir-al-momenin Burn Hospital, Sadra Town Road</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7198754361</zip>
        <telephone>+98 71 3212 2600</telephone>
        <email>yazdani_far@sums.ac.ir</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Farzaneh Yazdani</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>School of Rehabilitation Sciences, Shahid Doran Campus, after Amir-al-momenin Burn Hospital, Sadra Town Road</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>7198754361</zip>
        <telephone>+98 71 3212 2600</telephone>
        <email>yazdani_far@sums.ac.ir</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Women and men between the ages of 18 and 50
Craniovertebral angle less than 50 degrees
Shoulder angle less than 52 degrees</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having central nervous system problems
Having musculoskeletal problems
Having congenital neck problems
Having spondylolisthesis
Taking any pharmacological or non-pharmacological treatment for neck pain and postural disorders
Having any mental disorder such as anxiety and depression
Cancer
Pregnancy
The patient's fear of needles
The patient's reluctance and negative beliefs about this method
The patient's inability to obtain consent (cognitive problems and advanced age)
The patient has a medical emergency or acute medical condition
The patient has lymphedema in a region or an organ
The patient has severe neutropenia or thrombocytopenia</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>R29.3</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Abnormal posture</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Other</i_code>
      <i_code>Treatment - Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Dry needling of the subscapularis muscle combined with exercise therapy. Individuals in this group will undergo 10 sessions of treatment, 3 sessions per week. The exercises will include stretching and strengthening exercises, and at the end of sessions one, three, five, seven, and nine, individuals will undergo dry needling of the subscapularis muscle. To perform dry needling, the participant is asked to lie supine, with the shoulder in 90 degrees of abduction and 90 degrees of external rotation. The therapist uses one hand to pull the participant's shoulder further outward, palpating the outer edge of the scapula. The latissimus dorsi tendon is identified and lifted using a pincer grip to provide better access to the muscle. The needle is then inserted parallel to the chest and perpendicular to the anterior surface of the scapula. The needle entry site is cleaned with alcohol and cotton. Dry needling is performed on the muscle at three points, each point for 1 minute using a fast in-fast out method. A Chinese-made Huan Qiu needle, 30 mm in diameter and 50 mm in height, is used. Assessments will be conducted before treatment, immediately after treatment, and two weeks later.</i_keyword>
      <i_keyword>Control group: Exercise therapy. Individuals in this group will undergo 10 sessions of therapy, 3 sessions per week. The exercises in this group are exactly the same as those in the intervention group and include stretching and strengthening exercises. Assessments will be conducted before treatment, immediately after treatment, and two weeks later.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Craniovertebral angle. Timepoint: Before the start of the intervention, after the intervention and two weeks after the intervention. Method of measurement: The craniovertebral angle is the angle between two anatomical landmarks (the spinous process of the seventh cervical vertebra and the outer part of the tragus of the ear) that is examined with the Kinovea software.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Shoulder angle. Timepoint: Before the intervention, after the intervention, and two weeks after the intervention. Method of measurement: The shoulder angle is the angle formed by the intersection between the horizontal line passing through the acromion and the line connecting the spinous process of the seventh cervical vertebra to the acromion, and is measured with the Kinovea software.</sec_outcome>
      <sec_outcome>Pain. Timepoint: Before the intervention, after the intervention, and two weeks after the intervention. Method of measurement: Visual Analogue Scale.</sec_outcome>
      <sec_outcome>Cervical positioning sense. Timepoint: Before the intervention, after the intervention, and two weeks after the intervention. Method of measurement: Joint position error test.</sec_outcome>
      <sec_outcome>Cervical range of motion. Timepoint: Before the intervention, after the intervention, and two weeks after the intervention. Method of measurement: Goniometry.</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>2025-02-05</approval_date>
        <contact_name>Research Ethics Committees of Shiraz School of Rehabilitation Sciences</contact_name>
        <contact_address>Ethics Committee, Vice President for Research, School of Rehabilitation Sciences, Shahid Doran Campus, after Amir-al-momenin Burn Hospital, Sadra Town Road Shiraz Fars Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
