<?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>IRCT20261005071302N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-10-13</date_registration>
      <primary_sponsor>Shiraz University of Medical Sciences</primary_sponsor>
      <public_title>impact of yoga on the general health and mindfulness</public_title>
      <acronym></acronym>
      <scientific_title>investigating the impact of yoga on the general health and mindfulness of female nursing student</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-12-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>144</target_size>
      <recruitment_status>Pending</recruitment_status>
      <url>https://irct.ir/trial/93866</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Other, Purpose: Health service research, Randomization description: This study is a randomized controlled clinical trial with a parallel design. The unit of randomization was individual, and participants were assigned to the two groups (yoga intervention and control) using blocked randomization with a block size of 12 and a 1:1 allocation ratio. The random sequence was generated by the statistical consultant using software (producing a list of 12-member blocks with a total length of 144). The randomization tool consisted of a block randomization allocation table, which was used by the researcher to enroll and assign participants to the groups. Allocation concealment was achieved through this same block randomization allocation table, whereby the statistical consultant determined the sequence and the researcher enrolled participants and assigned them to groups accordingly. Stratified randomization was not used in this study, and blinding was not performed (the study was conducted as open-label); the only measure taken was preventing information transfer between the two groups.</study_design>
      <phase>N/A</phase>
      <hc_freetext>yoga, general health, mindfulness.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: 8 sessions of offline yoga training (one session per week via video) for 8 consecutive weeks, along with daily physical exercises performed by participants at home or in student dormitories (standard yoga meditation). Before the start of the training sessions, an in-person orientation and educational session will be conducted by the researchers regarding yoga, its goals, how to perform it, and the intervention process. Then, in the intervention group, yoga sessions will be held virtually in 8 sessions over 8 consecutive weeks (one one-hour session per week) under the supervision of the researchers. To follow up on performing the exercises at home/dormitory and to address possible problems, daily telephone contact or communication through the Bale social network will be carried out, and a daily report form will be completed by the student and reviewed by the researcher. First, stretching and warm-up exercises, then the sun salutation exercise and other intermediate yoga asanas such as back bend, forward bend, standing and seated side bend, hero, child's pose, boat, triangle, etc., and then breathing exercises or pranayama (alternate nostril breathing and abdominal breathing) and meditation and relaxation will be performed. Intervention 2: Control group: no intervention will be performed.</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 statistical data may be made available upon reasonable request by email to the corresponding author and subject to obtaining permission from the relevant research center. Access will be limited to anonymized data and relevant supporting documents, where applicable. No personally identifiable information or documents containing confidential participant information will be shared. Requests will be reviewed to ensure compliance with institutional policies, ethical requirements, and data confidentiality regulations.

When:
After the article is published

To whom:
Researchers affiliated with academic, scientific, or other relevant institutions may request access to the study’s de-identified statistical data and relevant supporting documents by contacting the corresponding author via email. All requests will be reviewed on a case-by-case basis, and access will be granted subject to approval by the relevant research center and compliance with institutional policies, ethical requirements, and data confidentiality regulations. Researchers from industry or other organizations may also submit requests under the same conditions. Only anonymized data will be shared.

Conditions:
Data and documents may be accessed and used only after obtaining the required permission from the relevant research center and complying with all applicable legal, ethical, and institutional requirements. Data must be used solely for the approved research purposes while maintaining confidentiality.

Where to obtain:
After publication, applicants may request access to the de-identified study data and relevant documents by emailing the corresponding author. Access is subject to obtaining the required permission from the relevant research center and complying with applicable legal and ethical requirements.

How to obtain:
After publication, applicants should email the corresponding author with a formal request specifying the intended use of the data. Access will be provided after obtaining the required permission from the relevant research center and fulfilling applicable legal and ethical requirements. The process may take up to three months.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Neda Jamalimoghadam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Fatemeh (PBUH) School of Nursing and Midwifery, Namazi Hospital, Namazi Square, Shiraz, Iran.</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۷۱۹۳۶۱۳۱۱۹</zip>
        <telephone>+98 71 3647 4254</telephone>
        <email>nedajamali21@yahoo.com</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Neda Jamalimoghadam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Fatemeh (PBUH) School of Nursing and Midwifery, Namazi Hospital, Namazi Square, Shiraz, Iran.</address>
        <city>Shiraz</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>۷۱۹۳۶۱۳۱۱۹</zip>
        <telephone>+98 71 3647 4254</telephone>
        <email>nedajamali21@yahoo.com</email>
        <affiliation>Shiraz University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Being a female undergraduate nursing student.
Being enrolled in the fourth to eighth semester of the nursing program.
Having completed at least two semesters of clinical training/clinical practice.
Willingness to participate in the study and sign the written informed consent form.
Ability and willingness to attend the initial face-to-face orientation and training session and participate in the eight-week yoga intervention.
Having access to a smartphone and the Internet to receive educational videos, communicate with the researcher, and submit daily exercise reports.
Not having participated regularly in yoga, meditation, relaxation exercises, breathing exercises, or other mind–body practices during the study.
Having no physical or medical limitation that would interfere with performing yoga exercises, based on self-report and, if necessary, medical assessment.</inclusion_criteria>
      <agemin>20 years</agemin>
      <agemax>no limit</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Withdrawal from the study at any stage for any reason, without the need to provide an explanation.
Failure to attend two or more of the eight scheduled yoga sessions.
Failure to perform the prescribed daily exercises for three or more days in a week, resulting in inadequate adherence to the intervention.
Repeated failure to complete the daily exercise checklist or submit the required exercise reports.
Development of any acute illness, physical injury, or musculoskeletal condition that makes performing yoga exercises impossible or medically inappropriate.
Concurrent participation in another intervention study that may affect the outcomes of the present study.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Y93.42</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Activity, yoga</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: 8 sessions of offline yoga training (one session per week via video) for 8 consecutive weeks, along with daily physical exercises performed by participants at home or in student dormitories (standard yoga meditation). Before the start of the training sessions, an in-person orientation and educational session will be conducted by the researchers regarding yoga, its goals, how to perform it, and the intervention process. Then, in the intervention group, yoga sessions will be held virtually in 8 sessions over 8 consecutive weeks (one one-hour session per week) under the supervision of the researchers. To follow up on performing the exercises at home/dormitory and to address possible problems, daily telephone contact or communication through the Bale social network will be carried out, and a daily report form will be completed by the student and reviewed by the researcher. First, stretching and warm-up exercises, then the sun salutation exercise and other intermediate yoga asanas such as back bend, forward bend, standing and seated side bend, hero, child's pose, boat, triangle, etc., and then breathing exercises or pranayama (alternate nostril breathing and abdominal breathing) and meditation and relaxation will be performed.</i_keyword>
      <i_keyword>Control group: no intervention will be performed.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Mindfulness, general health. Timepoint: Measurement of general health and mindfulness before the intervention, immediately after, and one and three months after the intervention. Method of measurement: Goldberg General Health Questionnaire, Baer Mindfulness Questionnaire.</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>Shiraz University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-09-12</approval_date>
        <contact_name>Schools of Nursing and Midwifery, Management and Medical Information Science - Shiraz University of </contact_name>
        <contact_address>Fatemeh (S) School of Nursing and Midwifery, Namazi Hospital, Namazi Square, Shiraz Shiraz Fars Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
