<?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>IRCT20241020063435N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2024-10-26</date_registration>
      <primary_sponsor>Razi University of Kermanshah</primary_sponsor>
      <public_title>Effects of a Session of Aerobic exercise with moderate-Intensity and intermittent exercise with high intensity on craving and appetite control in overweight and obese women</public_title>
      <acronym></acronym>
      <scientific_title>Effects of One Session Moderate-Intensity Aerobic Training and High-Intensity Interval Training on Food Craving- Food Choices- and Some Psychological Factors Related to Appetite Control in Overweight and Obese Women</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2024-10-26</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>15</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/79743</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Crossover, Purpose: Supportive, Randomization description: In this study, the order of subject exposure to 3 different conditions (moderate intensity aerobic exercise, high intensity intermittent exercise and control condition) will be randomized by Latin square method. For this purpose, first, using the website www.random.org, each subject will be randomly assigned a number between 1 and 15 as an identification code. Then, the English letters A.B.C will be assigned to the three intervention conditions and a Latin square with three rows and three columns will be created. Finally, participants number 1 to 5 are placed in the sequence of the first row, participants number 6 to 10 are placed in the sequence of the second row, and participants number 11 to 15 are placed in the sequence of the third row.</study_design>
      <phase>3</phase>
      <hc_freetext>overweight and obesity.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: In this research, all the subjects will be exposed to two intervention conditions with an interval of at least 7 days, including 1- aerobic exercise with moderate intensity, 2- intermittent exercise with high intensity. Intervention 2: Control group: In this study, all the subjects will watch a documentary film for 30 minutes that does not have any spiritual, psychological, emotional or motivational effects.</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:
All data can be shared after de-identifying subjects.

When:
6-9 months after printing the results

To whom:
Supervisor and executive researcher

Conditions:
Meta-analysis research

Where to obtain:
Take action by sending an e-mail to Amirabbas Monazzami, supervisor, at monazzami.amirabbas@gmail.com and Chnour Ghaderi, researcher, at chnourghaderi77@gmail.com.

How to obtain:
In case of an official request, the relevant reasons are announced and full details are mentioned, the data will be sent via email after 72 hours.

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Amir Abbas Monazzami</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Taq Bostan, University Street, Razi University, Faculty of Sports Sciences</address>
        <city>Kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6714414971</zip>
        <telephone>+98 83 3427 7605</telephone>
        <email>monazzami.amirabbas@gmail.com</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Amir Abbas Monazzami</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Taq Bostan, University Street, Razi University, Faculty of Sports Sciences</address>
        <city>Kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6714414971</zip>
        <telephone>+98 83 3427 7605</telephone>
        <email>monazzami.amirabbas@gmail.com</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age range from 18 to 40 years
A resident of Kermanshah
Body mass index (BMI) between 25 and 35 kg/m2
Having food cravings (getting a total score of 108 or higher from the 15-item food craving questionnaire and the 12-item visual analog food craving questionnaire)
Obtaining a certificate of non-prohibition of participation in sports training program from the doctor</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>40 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Smoking, alcohol and drugs
Abnormalities or musculoskeletal disorders
Participation in weight loss programs in the last 6 months
Participating in a regular exercise program in the past 6 months</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>E66</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Overweight and obesity</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Treatment - Devices</i_code>
      <i_code>Placebo</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: In this research, all the subjects will be exposed to two intervention conditions with an interval of at least 7 days, including 1- aerobic exercise with moderate intensity, 2- intermittent exercise with high intensity.</i_keyword>
      <i_keyword>Control group: In this study, all the subjects will watch a documentary film for 30 minutes that does not have any spiritual, psychological, emotional or motivational effects.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Food cravings. Timepoint: 24 and 48 hours after completing the interventions. Method of measurement: 15-item food craving questionnaire and 12-item visual analogue food craving questionnaire.</prim_outcome>
      <prim_outcome>Food preference. Timepoint: Before and after the interventions. Method of measurement: Online food preference questionnaire software.</prim_outcome>
      <prim_outcome>Appetite. Timepoint: 1, 2, 4, 24 and 48 hours after the intervention. Method of measurement: Visual analogue subjective scale of appetite.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Impulsiveness. Timepoint: Before and after the interventions. Method of measurement: Go/no go cognitive test software.</sec_outcome>
      <sec_outcome>Risky decision making. Timepoint: Before and after the interventions. Method of measurement: Iowa gambling cognitive test software.</sec_outcome>
      <sec_outcome>Cognitive flexibility. Timepoint: Before and after the interventions. Method of measurement: 20-question cognitive flexibility questionnaire.</sec_outcome>
      <sec_outcome>Sense of pleasure. Timepoint: Before and after the interventions. Method of measurement: 11-item emotion scale.</sec_outcome>
      <sec_outcome>Arousal level. Timepoint: Before and after the interventions. Method of measurement: 6-point scale of perceived arousal.</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>Razi University of Kermanshah</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2024-07-03</approval_date>
        <contact_name>Research Ethics Committee of Razi University</contact_name>
        <contact_address>Taq Bostan, University Street, Razi University, Faculty of Sports Sciences Kermanshah Kermanshah Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
