<?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>IRCT20251223068421N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-04-26</date_registration>
      <primary_sponsor>Hamedan University of Medical Sciences</primary_sponsor>
      <public_title>Ergonomics and Stretching Training for Dentists’ Musculoskeletal Pain</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of Ergonomic Principles Training and Workplace Stretching Exercises on Reducing Upper Limb Musculoskeletal Disorders in Dentists</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-01-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>19</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/88501</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Education/Guidance, Other design features: A quasi-experimental pretest–posttest study on 19 dentists. Upper-extremity musculoskeletal disability will be assessed using the QuickDASH questionnaire. Ergonomics and workplace stretching trainings will be delivered via educational contents and videos on online platforms.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Upper limb work-related musculoskeletal disorders in dentists.</hc_freetext>
      <i_freetext>Intervention group: The level of upper limb disability among participants who meet the study’s inclusion criteria will be measured using the DASH (Disabilities of the Arm, Shoulder, and Hand) instrument. Subsequently, participants will undergo a "two‑month ergonomics educational intervention" comprised of the following components: Part I – Classroom‑based Instruction Based on scientific content and published research articles, two virtual training sessions will be held on the Skyroom platform during the fourth and sixth weeks of the intervention. 1) First session (approximately one hour): This session will address ergonomic risk factors such as improper posture, prolonged working hours, repetitive movements, vibration, and unsuitable hand tools in clinical environments. The aim is to ensure that dentists become familiar with the causes of musculoskeletal disorders and are able to recognize them effectively in their workplaces. 2) Second session (approximately one hour): This session will focus on strategies for mitigating the identified ergonomic risk factors. Participants will be introduced to appropriate workstation designs, healthy behavioral habits, ergonomic hand tools, and related topics. They will be expected to select and implement suitable solutions according to the risk factors identified in their own work settings.Part II – Social network‑based TrainingDrawing upon scientific sources and published articles, appropriate stretching and exercise movements to relieve tension caused by static and improper postures will be developed—movements that can be performed within the dental work environment. Using artificial intelligence tools, the content will be prepared as illustrative pictorial messages with detailed explanations. To achieve this goal, 16 educational posters will be designed, each containing clear and motivational explanations including a full description of the movement, targeted body region, recommended daily frequency, and repetitions per session. These posters will be delivered to participants via online platforms. Participants will be instructed to include these exercises in their daily routines and perform them at least three times during each work shift. Furthermore, they will be asked to notify the researcher through a reaction whenever they perform the instructed movements.By the end of the eighth week, participants are expected to be familiar with and able to correctly perform all 16 stretching exercises related to upper limb and neck discomfort.At the conclusion of the two‑month intervention, the dental practitioners’ upper limb disability levels will be reassessed using the DASH to evaluate the effectiveness of the designed educational intervention..</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:
De identified individual participant data including baseline demographic variables and the shortened Disabilities of the Arm, Shoulder and Hand questionnaire scores at baseline and after completion of the 2 month training period; along with the data dictionary and the study protocol

When:
Access will start 6 months after publication of the main results and will remain available for 5 years

To whom:
Researchers from universities and scientific centers who has specific scientific aims

Conditions:
Use is permitted only for scientific purposes such as meta analysis, systematic reviews, and secondary analyses related to the study objectives; only de identified data will be shared; requestors must sign a data use agreement, agree not to attempt re identification, not to share data with third parties, and to cite the trial registration in any resulting publications

Where to obtain:
Requests should be sent to the principal investigator: Ali Moradi, email Ali.moradi206@gmail.com
, mobile 0098 9359385871

How to obtain:
Requestors submit a written application including the proposed project title, objectives, analysis plan, and institutional details; the research team reviews the request; if approved, a data use agreement is signed and the de identified dataset, data dictionary, and protocol are provided electronically

Comments:
The informed consent form will not be publicly shared due to confidentiality and research ethics considerations</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Ali Moradi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Dentistry, Hamadan University of Medical Sciences, Shahid Fahmideh Boulevard, Pajouhesh Crossroad, Hamadan, Iran</address>
        <city>Hamadan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6517838843</zip>
        <telephone>+98 935 938 5871</telephone>
        <email>Ali.moradi206@gmail.com</email>
        <affiliation>Hamedan University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Ali Moradi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Dentistry, Hamadan University of Medical Sciences, Shahid Fahmideh Boulevard, Pajouhesh Crossroad, Hamadan, Iran</address>
        <city>Hamadan</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6517838678</zip>
        <telephone>+98 935 938 5871</telephone>
        <email>Ali.moradi206@gmail.com</email>
        <affiliation>Hamedan University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>At least 1 year of work experience (one year after completing mandatory service)
Being a dentist
Age 27 to 65 years</inclusion_criteria>
      <agemin>27 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Unwillingness to participate in the study</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M79.1</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Myalgia</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: The level of upper limb disability among participants who meet the study’s inclusion criteria will be measured using the DASH (Disabilities of the Arm, Shoulder, and Hand) instrument. Subsequently, participants will undergo a "two‑month ergonomics educational intervention" comprised of the following components: Part I – Classroom‑based Instruction Based on scientific content and published research articles, two virtual training sessions will be held on the Skyroom platform during the fourth and sixth weeks of the intervention. 1) First session (approximately one hour): This session will address ergonomic risk factors such as improper posture, prolonged working hours, repetitive movements, vibration, and unsuitable hand tools in clinical environments. The aim is to ensure that dentists become familiar with the causes of musculoskeletal disorders and are able to recognize them effectively in their workplaces. 2) Second session (approximately one hour): This session will focus on strategies for mitigating the identified ergonomic risk factors. Participants will be introduced to appropriate workstation designs, healthy behavioral habits, ergonomic hand tools, and related topics. They will be expected to select and implement suitable solutions according to the risk factors identified in their own work settings.Part II – Social network‑based TrainingDrawing upon scientific sources and published articles, appropriate stretching and exercise movements to relieve tension caused by static and improper postures will be developed—movements that can be performed within the dental work environment. Using artificial intelligence tools, the content will be prepared as illustrative pictorial messages with detailed explanations. To achieve this goal, 16 educational posters will be designed, each containing clear and motivational explanations including a full description of the movement, targeted body region, recommended daily frequency, and repetitions per session. These posters will be delivered to participants via online platforms. Participants will be instructed to include these exercises in their daily routines and perform them at least three times during each work shift. Furthermore, they will be asked to notify the researcher through a reaction whenever they perform the instructed movements.By the end of the eighth week, participants are expected to be familiar with and able to correctly perform all 16 stretching exercises related to upper limb and neck discomfort.At the conclusion of the two‑month intervention, the dental practitioners’ upper limb disability levels will be reassessed using the DASH to evaluate the effectiveness of the designed educational intervention.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Total score of the shortened Disabilities of the Arm, Shoulder and Hand questionnaire (range 0 to 100; higher scores indicate greater functional disability). Timepoint: At baseline (before training) and 2 months after training. Method of measurement: the shortened Disabilities of the Arm, Shoulder and Hand questionnaire.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Subscale score for upper extremity symptoms and function in the shortened Disabilities of the Arm, Shoulder and Hand questionnaire. Timepoint: At baseline (before training) and after completion of the 2-month training period. Method of measurement: the shortened Disabilities of the Arm, Shoulder and Hand questionnaire and the subscale score was calculated.</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>Hamedan University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-09-20</approval_date>
        <contact_name>Ethics committee of Hamadan University of Medical Sciences</contact_name>
        <contact_address>Hamadan University of Medical Sciences, Shahid Fahmideh St, Hamadan Hamadan Hamadan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
