<?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>IRCT20201129049524N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2021-05-26</date_registration>
      <primary_sponsor>Razi University of Kermanshah</primary_sponsor>
      <public_title>The effect of aerobic exercise at home and turmeric supplementation in type 2 diabetes during Covid -19 quarantine</public_title>
      <acronym></acronym>
      <scientific_title>The effect of eight weeks of home aerobic exercise and turmeric supplementation on anthropometric indices, glycemic status, lipid profile and quality of life in middle-aged women with type 2 diabetes during Covid -19 quarantine</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2021-06-15</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>40</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/56329</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Used, Assignment: Parallel, Purpose: Prevention.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Type 2 diabetes.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Intervention group: Aerobic exercise group (10 people), 8 weeks of aerobic exercise with 3 sessions per week online, the first week with an intensity of 60% of maximum heart rate for 20 minutes and in the eighth week to 75% of maximum heart rate for 40 minutes Will take minutes; Thus, during the first 4 weeks with 60% of maximum heart rate for 30 minutes and 3 days per week and during the second 4 weeks with 75% of maximum heart rate for 45 minutes and 3 days per week. Intervention 2: Intervention group: Turmeric supplement group (n = 10), in the present study, a dose of 2100 mg of turmeric will be selected. Intervention 3: Intervention group: Aerobic exercise and turmeric supplementation, aerobic exercise group (10 people) and placebo, 8 weeks of aerobic exercise with 3 sessions per week online, the first week with an intensity of 60% maximum heart rate for 20 minutes and in the eighth week to 75% Maximum heart rate will reach 40 minutes; During the first 4 weeks with 60% of maximum heart rate for 30 minutes and 3 days a week and during the second 4 weeks with 75% of maximum heart rate for 45 minutes and 3 days a week and turmeric supplementation (10 people) In the present study, a dose of 2100 mg of turmeric will be selected. Intervention 4: Control group:No aerobic exercise and no turmeric supplement.</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 will be registered in SPSS and can be provided

When:
Access starts 9 months after the publication of all articles

To whom:
It will be available only to researchers working in academic and scientific institutions

Conditions:
All data can be used for citation.

Where to obtain:
m.ahmady@stu.razi.ac.ir
R.hoseini@razi.ac.ir

How to obtain:
If the description of the data needs is convincing, it will be delivered within 3 days

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Rastegar Hosseini</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Faculty of Physical Education and Sport Sciences, Kranshah City, Taq Bostan St., University Blvd., No.</address>
        <city>kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6714967346</zip>
        <telephone>+98 83 3423 3267</telephone>
        <email>Rastegar.hoseini@gmail.com</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Rastegar Hosseini</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 9, Razi University, Faculty of Physical Education and Sports Sciences, Daneshgah Blvd., University Boulevard, Kermanshah, Kermanshah</address>
        <city>kermanshah</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6714967346</zip>
        <telephone>+98 83 3423 3267</telephone>
        <email>R.hoseni@razi.ac.ir</email>
        <affiliation>Razi University of Kermanshah</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Non-insulin type 2 diabetes
HbA1C above 6
TG above 150 mg / dL
LDL above 100 mg / dL
Do not take antioxidants, multivitamin supplements and polyphenols in the last three months
Overweight body mass index (25 to 29.99 kg / m2)</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>65 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Change in the amount and type of medication used
Physical activity and diet during the study period
Fasting blood sugar greater than 200 mg / dL
LDL greater than 160 mg / dL
Acute heart disease, kidney, liver and thyroid failure
Severe gastrointestinal diseases and gastric ulcer
Gallstones
Pregnancy or breastfeeding</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code></hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Type 2 diabetes</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
      <i_code>Lifestyle</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Intervention group: Aerobic exercise group (10 people), 8 weeks of aerobic exercise with 3 sessions per week online, the first week with an intensity of 60% of maximum heart rate for 20 minutes and in the eighth week to 75% of maximum heart rate for 40 minutes Will take minutes; Thus, during the first 4 weeks with 60% of maximum heart rate for 30 minutes and 3 days per week and during the second 4 weeks with 75% of maximum heart rate for 45 minutes and 3 days per week</i_keyword>
      <i_keyword>Intervention group: Turmeric supplement group (n = 10), in the present study, a dose of 2100 mg of turmeric will be selected.</i_keyword>
      <i_keyword>Intervention group: Aerobic exercise and turmeric supplementation, aerobic exercise group (10 people) and placebo, 8 weeks of aerobic exercise with 3 sessions per week online, the first week with an intensity of 60% maximum heart rate for 20 minutes and in the eighth week to 75% Maximum heart rate will reach 40 minutes; During the first 4 weeks with 60% of maximum heart rate for 30 minutes and 3 days a week and during the second 4 weeks with 75% of maximum heart rate for 45 minutes and 3 days a week and turmeric supplementation (10 people) In the present study, a dose of 2100 mg of turmeric will be selected</i_keyword>
      <i_keyword>Control group:No aerobic exercise and no turmeric supplement</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Lipid profile. Timepoint: Before the intervention and after the end of the study. Method of measurement: Using a blood test.</prim_outcome>
      <prim_outcome>Glycemic indexes. Timepoint: Before the intervention and after the end of the study. Method of measurement: Using a blood test.</prim_outcome>
      <prim_outcome>Anthropometric indicators. Timepoint: Before the intervention and after the end of the study. Method of measurement: With little measuring tools.</prim_outcome>
      <prim_outcome>Quality of Life. Timepoint: Before the intervention and after the end of the study. Method of measurement: 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>Razi University of Kermanshah</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2021-05-12</approval_date>
        <contact_name>Ethics Committee of Razi University of Kermanshah</contact_name>
        <contact_address>Faculty of Physical Education and Sports Sciences, Kermanshah, No. 9, Razi University Blvd. kermanshah Kermanshah Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
