<?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>IRCT20260421069127N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-04-30</date_registration>
      <primary_sponsor>Urmia University</primary_sponsor>
      <public_title>Effectiveness of corrective exercise with and without the Alexander technique on forward head, round shoulder and function in violin players</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of corrective exercise with and without the Alexander technique on forward head, round shoulder and function in violin players: a randomized control trial</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-04-28</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>66</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/89639</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: A total of 66 eligible violinists participated in the study. Participants were allocated to the study groups using a computer‑based randomization procedure. A random sequence generator available at https://www.randomizer.org was used to generate the allocation sequence, according to which participants were randomly assigned to one of three groups: a corrective exercise group, a corrective exercise plus Alexander Technique group, and a control group. The randomization list was stored on a password‑protected computer and was accessible only to the researcher responsible for participant allocation. Recruitment personnel and others involved in the enrollment process did not have access to this information, Blinding description: Single‑blind design

Participants: blinded to group allocation.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Forward head posture (forward head angle abnormality).</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Participants assigned to the Corrective Exercise Group will perform an 8‑week corrective exercise program designed to address forward head posture and rounded shoulder posture. Each training session will last approximately 60 minutes and will include 5–10 minutes of general warm‑up, 20–40 minutes of corrective stretching and strengthening exercises targeting cervical, thoracic, and scapular muscles, and 5–10 minutes of cool‑down.The program will be performed three times per week throughout the 8‑week period.The progressive protocol consists of a series of ten corrective exercises, including deep cervical flexor activation, pectoralis minor stretching, scapular retraction strengthening, thoracic extension mobility, and shoulder girdle stabilization tasks. Exercise sets and repetitions are adjusted based on weekly progression while ensuring proper technique and postural alignment under researcher supervision. Intervention 2: Intervention group: Participants assigned to this group will receive both the corrective exercise program and the Alexander Technique instructional protocol.Each training session will last 60 minutes and will be structured as follows:5–10 minutes of general warm‑up5–10 minutes of Alexander Technique instruction focusing on inhibition, primary control (head–neck–spine coordination), and conscious direction of movements, based on a 19‑item standardized protocol20–40 minutes of corrective stretching and strengthening exercises (identical to those in the corrective exercise group)5–10 minutes of cool‑downThe intervention will be performed three times per week for 8 weeks. Throughout the Alexander Technique component, participants are guided to maintain optimal head–neck alignment, reduce unnecessary muscular tension, and perform movements with improved postural awareness. Intervention 3: Control group: Participants in the control group will not receive any structured training or therapeutic intervention during the 8‑week study period. They will be instructed to continue their routine daily activities without initiating new 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>Yes - There is a plan to make this available</results_IPD_plan>
      <results_IPD_description>What will be shared:
Some of the images used in the study will be corrupted.

When:
from 29/06/2026 to 6 months later

To whom:
Researcher

Conditions:
An official email should be used to contact the corresponding author

Where to obtain:
corresponding author

How to obtain:
official email

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ebrahim Mohammad ali nasab firouzjah</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Urmia University, Kilometer 11 Serow Road</address>
        <city>Urmia</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5756151818</zip>
        <telephone>+98 44 3275 2741</telephone>
        <email>Ebrahim.mzb@gmail.com</email>
        <affiliation>Urmia University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Faeze Mehdipour</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Urmia University, Kilometer 11 Serow Road</address>
        <city>Urmia</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>5756151818</zip>
        <telephone>+98 44 3275 2741</telephone>
        <email>faezemehdipour8@gmail.com</email>
        <affiliation>Urmia University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Forward head angle greater than 46° and rounded shoulder angle greater than 52°
At least three years of playing experience
No concurrent use of other corrective or therapeutic interventions
Not engaged in occupations involving prolonged postures or repetitive movements
No history of fractures, surgery, or joint disorders affecting the spine or shoulder girdle
No structural or functional shortening greater than 2 cm in either upper limb
No participation in regular exercise programs</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>35 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Failure to complete the training program in accordance with the study objectives or unwillingness of the participant to continue the program
Observation of any pathological symptoms during the training sessions
Absence from more than three training sessions</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M40.0</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Postural kyphosis</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Participants assigned to the Corrective Exercise Group will perform an 8‑week corrective exercise program designed to address forward head posture and rounded shoulder posture. Each training session will last approximately 60 minutes and will include 5–10 minutes of general warm‑up, 20–40 minutes of corrective stretching and strengthening exercises targeting cervical, thoracic, and scapular muscles, and 5–10 minutes of cool‑down.The program will be performed three times per week throughout the 8‑week period.The progressive protocol consists of a series of ten corrective exercises, including deep cervical flexor activation, pectoralis minor stretching, scapular retraction strengthening, thoracic extension mobility, and shoulder girdle stabilization tasks. Exercise sets and repetitions are adjusted based on weekly progression while ensuring proper technique and postural alignment under researcher supervision.</i_keyword>
      <i_keyword>Intervention group: Participants assigned to this group will receive both the corrective exercise program and the Alexander Technique instructional protocol.Each training session will last 60 minutes and will be structured as follows:5–10 minutes of general warm‑up5–10 minutes of Alexander Technique instruction focusing on inhibition, primary control (head–neck–spine coordination), and conscious direction of movements, based on a 19‑item standardized protocol20–40 minutes of corrective stretching and strengthening exercises (identical to those in the corrective exercise group)5–10 minutes of cool‑downThe intervention will be performed three times per week for 8 weeks. Throughout the Alexander Technique component, participants are guided to maintain optimal head–neck alignment, reduce unnecessary muscular tension, and perform movements with improved postural awareness.</i_keyword>
      <i_keyword>Control group: Participants in the control group will not receive any structured training or therapeutic intervention during the 8‑week study period. They will be instructed to continue their routine daily activities without initiating new exercise programs.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>The primary outcome in this record is the forward head angle. This variable represents the alignment of the head in the sagittal plane and indicates the degree of anterior displacement of the head relative to the trunk. It is selected as a primary outcome to evaluate the postural alignment of violin players and to determine whether the eight‑week intervention leads to measurable changes in head posture. Timepoint: The forward head angle will be measured at two time points: at baseline before the beginning of the intervention, and after completion of the eight‑week intervention period. Method of measurement: The forward head angle will be measured using digital photogrammetry in the sagittal plane. Standardized lateral photographs will be obtained from each participant, and the images will be analyzed using Kinovea motion analysis software to calculate the two‑dimensional forward head angle.</prim_outcome>
      <prim_outcome>The primary outcome in this record is the rounded shoulder angle. This variable reflects the anterior displacement and protraction of the shoulder girdle in the sagittal plane. It has been selected as a primary outcome to evaluate postural alignment of the shoulder girdle in violin players and to determine whether the eight‑week intervention leads to improvement in shoulder posture. Timepoint: The rounded shoulder angle will be measured at two time points: at baseline before the beginning of the intervention, and after completion of the eight‑week intervention period. Method of measurement: The rounded shoulder angle will be measured using digital photogrammetry in the sagittal plane. Standardized lateral photographs will be taken from each participant, and the images will be analyzed using Kinovea motion analysis software to calculate the two‑dimensional rounded shoulder angle.</prim_outcome>
      <prim_outcome>The primary outcome in this record is upper extremity function. This variable reflects the functional status of the arm, shoulder, and hand during daily and instrumental activities. It has been selected as a primary outcome to evaluate whether the eight‑week intervention leads to improvements in upper limb functional capacity in violin players. Timepoint: Upper extremity function will be evaluated at two time points: at baseline before the beginning of the intervention, and after completion of the eight‑week intervention period. Method of measurement: Upper extremity function will be assessed using the full Persian version of the Disabilities of the Arm, Shoulder and Hand questionnaire. This validated questionnaire will be completed by participants to determine their level of functional limitation in the upper limb.</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>Urmia University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-04-20</approval_date>
        <contact_name>Research Ethics Committees of Sport Sciences Research Institute (SSRI)</contact_name>
        <contact_address>Tehran Province, Tehran, District 7, 5th Dead End Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
