<?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>IRCT20260417069089N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-06-01</date_registration>
      <primary_sponsor>university of kurdistan</primary_sponsor>
      <public_title>Comparing the effectiveness of eight weeks of dynamic neuromuscular stability training on improving balance and lower limb strength in elderly men</public_title>
      <acronym></acronym>
      <scientific_title>Comparing the effectiveness of eight weeks of dynamic neuromuscular stability training on improving balance and lower limb strength in elderly men</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-06-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>22</target_size>
      <recruitment_status>Pending</recruitment_status>
      <url>https://irct.ir/trial/90520</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Randomization description: This study will use a simple randomization method. Participants will be randomly assigned to two groups: an exercise intervention group and a control group. Randomization will be performed at the individual level, with each of the 22 study participants placed in one of the two groups. A computer sequence will be used to randomly assign participants to each group. This method provides high precision and reproducibility and minimizes selection bias. The sequence of participant allocation was generated using a block randomization method with variable block sizes (e.g., 4 and 8) and a 1:1 allocation ratio to ensure a balanced distribution of participants across the two groups. This randomization sequence was generated by a dedicated computer program or a validated statistical software. Specifically, SPSS version 26 was used to generate the allocation sequence.</study_design>
      <phase>N/A</phase>
      <hc_freetext>AGEING.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Intervention group: The training steps will include a dynamic neuromuscular stabilization exercise protocol. The training period will be 8 weeks, three sessions per week, and each session will be 50 minutes. Each session will include 5 minutes of warm-up exercises, 40 minutes of dynamic neuromuscular stabilization exercises, and 5 minutes of cool-down exercises. The training movements will include diaphragmatic breathing, supine 90-90, prone, rolling, side sitting, oblique sitting, three-legged standing, kneeling, squatting, and standing. Intervention 2: Control group: NON-ACTIVITY.</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:
En All data is potentially shareable after de-identifying individuals.

When:
One years AFTER publication

To whom:
All people who study ageing in scientific institutions, as well as ageing people themselves

Conditions:
The information extracted from the present work can be used by sports coaches who are designing training programs, older adults, and gerontology specialists to improve their performance.

Where to obtain:
After publishing the data in reputable journals, the reader, after studying and being interested in the topic in question, is first referred to the author responsible for the work whose email address and phone number are mentioned in the article. In the second stage, the other authors of the article are contacted using your email. In the third stage, they can go to the place where the research was conducted, i.e. the university, and obtain information from the university's research department.

How to obtain:
Since the publication of the article takes one year, readers who are interested in this field can immediately message or email the responsible author after one year and when the article is published. The responsible author will provide the person with relevant data and appropriate information as soon as possible and on the same day.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>saber saedmocheshi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>university</address>
        <city>sanandaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6639115831</zip>
        <telephone>0098 87 334600</telephone>
        <email>saedmocheshi@uok.ac.ir</email>
        <affiliation>university of kurdistan</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>saber saedmocheshi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>university</address>
        <city>sanandaj</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6639115831</zip>
        <telephone>0098 87 334600</telephone>
        <email>saedmocheshi@uok.ac.ir</email>
        <affiliation>university of kurdistan</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>No history of acute injury
Not having vision problems
Not having a hearing problem
Ear and ear canal disorders
No history of stroke</inclusion_criteria>
      <agemin>60 years</agemin>
      <agemax>79 years</agemax>
      <gender>Male</gender>
      <exclusion_criteria></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>Other</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Intervention group: The training steps will include a dynamic neuromuscular stabilization exercise protocol. The training period will be 8 weeks, three sessions per week, and each session will be 50 minutes. Each session will include 5 minutes of warm-up exercises, 40 minutes of dynamic neuromuscular stabilization exercises, and 5 minutes of cool-down exercises. The training movements will include diaphragmatic breathing, supine 90-90, prone, rolling, side sitting, oblique sitting, three-legged standing, kneeling, squatting, and standing.</i_keyword>
      <i_keyword>Control group: NON-ACTIVITY</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>STRENGHT MUSCLE. Timepoint: Before the start of the intervention and 60 days after the start of the intervention. Method of measurement: Before the start of the intervention and 60 days after the start of the intervention.</prim_outcome>
      <prim_outcome>BALANCE. Timepoint: Before the start of the intervention and 60 days after the start of the intervention. Method of measurement: Using functional tests.</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>university of kurdistan</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-11-03</approval_date>
        <contact_name>university of kurdistan</contact_name>
        <contact_address>university sanandaj Kurdistan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
