<?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>IRCT20171031037124N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2017-12-09</date_registration>
      <primary_sponsor>Vice chancellor for research Deputy of Education in University of Social Welfare and Rehabilitati</primary_sponsor>
      <public_title>The investigation of the impact of different types of education on  physical activity among older people</public_title>
      <acronym>education of  physical activity among older people</acronym>
      <scientific_title>The investigation of the impact of different types of education on knowledge, attitude and practice of physical activity among older people</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2017-06-22</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/27548</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention, Other design features: The randomized clinical trial will done on 120 older adults who were chosen by block random sampling. The Control group, the intervention group 1 (discussion group training), the intervention group 2(face to face training) and the intervention group 3 (e- learning) each will have 30 members. The control group will receive no interventions. For intervention groups 1, 2, and 3, the physical activity will be trained by the trainer in 4 sessions by discussion group, face to face training and e- learning methods respectively.  Knowledge, attitude and behavior (physical activity) questionnaire will be completed at the beginning, one month after and 3 months after the beginning of the study for each of the for groups, Randomization description: For Randomization, the block randomization method will be used. In this study, 16 blocks will be designed, each block will have 8 members, In which the letters A, B, C and D will be symbols for the control, face-to-face, discussion and electronic groups respectively. The first block will be considered as (AABBCCDD) and based on the first one, the other blocks will be designed using permutation.</study_design>
      <phase>N/A</phase>
      <hc_freetext>physical activity in older adults.</hc_freetext>
      <i_freetext>Intervention 1: Control group: This group will have 30 members whose members will not receive any intervention during the study. A knowledge, attitude, and behavior (physical activity) questionnaire will be completed at the start of the study one month after the start of. Intervention 2: Intervention Group 1 ( education of discussion group): This group will have 30 members. Physical activity training will be presented in a discussion group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionnaire. Intervention 3: Intervention Group 2 ( education of face to face group): This group will have 30 members. Physical activity training will be presented in a face to face group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionn. Intervention 4: Intervention Group 3 ( education of e-learning ): This group will have 30 members. Physical activity training will be presented in a e-learning group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionnaire will.</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>Undecided - It is not yet known if there will be a plan to make this available</results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>shahab papi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>kodakyar Ave., daneshjo Blvd.,Evin, tehran</address>
        <city>tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985713834</zip>
        <telephone>+98 21 2218 0083</telephone>
        <email>sh.papi@uswr.ac.ir</email>
        <affiliation>University of Social Welfare and Rehabilitation Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>robab sahaf</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>kodakyar Ave., daneshjo Blvd.,Evin, tehran</address>
        <city>tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1985713834</zip>
        <telephone>+98 21 2218 0154</telephone>
        <email>robabsahaf@gmail.com</email>
        <affiliation>University of Social Welfare and Rehabilitation Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age 60 years and over
the ability to complete and answer to the questions of the questionnaire
ability to communicate
the ability to read and write in Persian and to use cell phone and electric Apps such as telegram &amp; what’s up.
Signed consent form for participation into the program</inclusion_criteria>
      <agemin>60 years</agemin>
      <agemax>139 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>No diagnosed specific mental and physical disease(self report) which prohibits physical activity</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>Z72.3</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Lack of physical exercise</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>Control group: This group will have 30 members whose members will not receive any intervention during the study. A knowledge, attitude, and behavior (physical activity) questionnaire will be completed at the start of the study one month after the start of</i_keyword>
      <i_keyword>Intervention Group 1 ( education of discussion group): This group will have 30 members. Physical activity training will be presented in a discussion group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionnaire</i_keyword>
      <i_keyword>Intervention Group 2 ( education of face to face group): This group will have 30 members. Physical activity training will be presented in a face to face group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionn</i_keyword>
      <i_keyword>Intervention Group 3 ( education of e-learning ): This group will have 30 members. Physical activity training will be presented in a e-learning group  in 4 sessions by the trainer. A knowledge, attitude, and behavior (physical activity) questionnaire will</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Knowledge. Timepoint: in the first session (before starting the intervention), immediately after the end of the intervention, and 3 months after the intervention. Method of measurement: Knowledge assessment questionnaire, which is a researcher made and has 13 questions.</prim_outcome>
      <prim_outcome>Attitude. Timepoint: in the first session (before starting the intervention), immediately after the end of the intervention, and 3 months after the intervention. Method of measurement: kenyon's attitudes toward physical activities.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Behavior. Timepoint: in the first session (before starting the intervention), immediately after the end of the intervention, and 3 months after the intervention. Method of measurement: CHAMPS physical activity questionnaire.</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>Vice chancellor for research Deputy of Education in University of Social Welfare and Rehabilitati</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2017-09-23</approval_date>
        <contact_name>Ethics committee of University of Social Welfare and Rehabilitation Sciences</contact_name>
        <contact_address>kodakyar Ave., daneshjo Blvd.,Evin tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
