<?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>IRCT20251115068000N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-09-14</date_registration>
      <primary_sponsor>Yazd University</primary_sponsor>
      <public_title>Effect of Attentional Strategies on Dynamic Stability and Movement Smoothness in Older Adults With and Without Mild Cognitive Impairment</public_title>
      <acronym></acronym>
      <scientific_title>Effects of Different Attentional Focus Strategies on Dynamic Stability and Movement Smoothness During Perturbed Gait: An Optimal Control–Based Analysis in Older Adults With and Without Mild Cognitive Impairment</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-09-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>38</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/93234</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Not randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Blinding description: This study will be conducted with blinding at the level of participants and outcome assessors. Participants will not be informed of their own cognitive status or that of other participants, specifically whether they belong to the cognitively healthy older adults group or the mild cognitive impairment (MCI) group. Due to the nature of the study and the need to provide specific instructions for performing the different attentional conditions, blinding participants to the type of attentional condition is not possible. Outcome assessors and personnel responsible for data processing and analysis will also be blinded to the participants’ group status, and the data will be coded using unique identification codes for analysis. The principal investigator and the researcher responsible for conducting the experimental procedures will not be blinded to participants’ group status because access to this information is necessary for proper implementation of the study protocol. Therefore, blinding in this study will be applied to participants’ cognitive status and to outcome assessment and data analysis, whereas blinding of the principal investigator and the researcher conducting the experimental procedures is not feasible due to the nature of the study protocol.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Mild Cognitive Impairment.</hc_freetext>
      <i_freetext>Intervention 1: Control group: Older adults without mild cognitive impairment; perturbation walking under baseline, internal, near external, and far external attentional conditions. Intervention 2: Intervention group: Older adults with mild cognitive impairment; the same task under the four attentional conditions.</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>No - There is not a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for not sharing IPD is Data related to the study protocol and statistical analysis plan may be available from the corresponding author upon reasonable request after publication of the study results. Individual participant data, informed consent forms, and identifiable information will not be publicly shared to protect participant confidentiality.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Mostafa Haj Lotfalian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Safaeie, Yazd university</address>
        <city>Yazd</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۸۹۱۵۸۱۸۴۱۱</zip>
        <telephone>+98 35 3123 3385</telephone>
        <email>M.HAJLOTFALIAN@YAZD.AC.IR</email>
        <affiliation>Yazd University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mostafa Haj Lotfalian</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Safaeie, Yazd university</address>
        <city>Yazd</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۸۹۱۵۸۱۸۴۱۱</zip>
        <telephone>+98 35 3123 3385</telephone>
        <email>M.HAJLOTFALIAN@YAZD.AC.IR</email>
        <affiliation>Yazd University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age 60–80 years, ability to walk independently without an assistive device, absence of acute neurological, musculoskeletal, or other conditions that may affect walking or balance, and provision of written informed consent to participate in the study. For older adults with mild cognitive impairment, confirmation of mild cognitive impairment based on the cognitive assessment criteria specified in the study protocol is also required.</inclusion_criteria>
      <agemin>60 years</agemin>
      <agemax>80 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>History of severe neurological, musculoskeletal, or other disorders affecting walking or balance; severe visual or hearing impairment; inability to walk independently without an assistive device; history of a severe fall within the previous six months; or failure to meet the required cognitive criteria for assignment to the respective study group.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>F06.7</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Mild cognitive disorder</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Behavior</i_code>
      <i_code>Behavior</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Control group: Older adults without mild cognitive impairment; perturbation walking under baseline, internal, near external, and far external attentional conditions.</i_keyword>
      <i_keyword>Intervention group: Older adults with mild cognitive impairment; the same task under the four attentional conditions.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Dynamic stability based on the distance between the extrapolated center of mass and the base of support. Timepoint: During all four attentional conditions in a single testing session. Method of measurement: Calculated using the Margin of Stability from movement data and the position of the center of mass and base of support.</prim_outcome>
      <prim_outcome>Movement smoothness based on linear and angular jerk. Timepoint: During all four attentional conditions in a single testing session. Method of measurement: Calculated from linear and angular jerk derived from the recorded kinematic data during walking.</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>Yazd University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-08-15</approval_date>
        <contact_name>Research Ethics Committees of Tehran University - Faculty of Sport Sciences and Health</contact_name>
        <contact_address>North Kargar Street, 15th Street, University of Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
