<?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>IRCT20220129053855N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2022-10-12</date_registration>
      <primary_sponsor>Iran University of Medical Sciences</primary_sponsor>
      <public_title>The effect of Range Of Motion training on Activity Daily Living of patients with hip fractures that admitted to orthopedic ward</public_title>
      <acronym></acronym>
      <scientific_title>The effect of Range Of Motion training on Activity Daily Living of patients with hip fractures that admitted to orthopedic ward</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2022-09-23</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>40</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/62030</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: N/A, Blinding: Not blinded, Placebo: Not used, Assignment: Single, Purpose: Education/Guidance.</study_design>
      <phase>N/A</phase>
      <hc_freetext>hip fracture.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: The present study is a semi-experimental study with a pre-test-post-test design and a control group. First, after the proposal is approved by the research council and the code of ethics is obtained from the vice president of research, the researcher sends a letter of introduction to the research environment from the university, and then goes to the research environment and while introducing himself to them, obtains permission to carry out the activity. Also, in order to conduct the research, in order to access the research samples, visit the orthopedic department of Shahid Beheshti Hospital in Babol and select your samples from among the patients hospitalized in the orthopedic departments with hip fracture using a continuous sampling method and in a simple random manner and based on the inclusion criteria. and then they will be divided into two test and control groups in a simple random manner.. Before any intervention and measurement, the written consent form of the company in the study will be completed by the subjects in order to prevent contamination of the researcher's information first from the patients. The hospital that suffers from hip fracture selects 40 patients for the test group and after the completion of the above number, the next 40 patients for the control group. Before doing any interventionand measurement, the written consent form of the company in the study will be completed by the subjects and it will be collected along with the patient's demographic profile form.Then, the daily life activities questionnaire will be completed by all patients of both groups (test and control) at the beginning of the work. For the test group, training sessions are started after the patient's surgery with the permission of the patient's treating physician, and during the hospitalization period and every day for 10-15 minutes until the discharge, training sessions are conducted by the researcher and for the convenience of the test group members, the sessions are held in a separate room. It will also be possible to continue the exercises at home using a training booklet that contains sports pictures and in the form of training how to move in detail and how to perform daily activities. The question of being able to contact the researcher at the time of dischargeMore about this source textSource text required for additional translation informationSend feedbackSide panels. Intervention 2: Control group: After 24 hours after the surgery, the control group will receive only the routine exercises and trainings of the department by the personnel after 24 hours after the surgery. In order to prevent contamination, the researcher first selects the test group based on the entry criteria and until the desired number is reached. He will perform this activity until the discharge and then select the control group and examine it for a week until the discharge.Considering that a month later, both the control and test groups will go to the clinic, the educational pamphlet will be given to the control group at the end, but the test group will receive the pamphlet from the beginning.</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:
The present study is a quasi-experimental with pre-test-post-test design and with a control group. First, after the proposal is approved by the Research Council and the code of ethics is obtained from the Vice Chancellor, the researcher sends a request for a letter of introduction to the research environment from the university and then refers to the research environment and introduces himself to them and obtains permission to carry out activities.

When:
Training sessions begin after the patient's surgery with the permission of the patient's physician, and during the hospital stay and every day for 10-15 minutes until discharge by the researcher and for the convenience of the test group, sessions will be held in a separate room. The house will be done using an educational booklet that contains sports pictures and in the form of training on how to move in detail and how to perform daily activities, and the samples will be given a phone number so that they can contact the researcher in case of any problems or questions. In addition, the control group will not experience any training protocol during the test and will receive daily activities and routines, but at the end of the work, the control group will be given a training booklet. Then one month after dischargeThe patient of the experimental group will refer to the clinic to check the daily life activities questionnaire again.

To whom:
Researchers working in academic and scientific institutes

Conditions:
No copy

Where to obtain:
Contact number 09118559018
Email Rad561492@gmail.comبا

How to obtain:
It can be accessed using the contact number and email

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Rahele Faraji Fard</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Shahid Salehi Gotab Road, village below the border</address>
        <city>Babol</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4734181670</zip>
        <telephone>+98 11 3262 9616</telephone>
        <email>Rad561492@gmail.com</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Rahele Faraji Fard</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>SHahid Salehi Gatab Road,VillageBelowTheBorder</address>
        <city>Babol</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>4734181670</zip>
        <telephone>+98 11 3262 9616</telephone>
        <email>Rad561492@gmail.com</email>
        <affiliation>Iran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Age between 18 and 65 years
No heart, lung, kidney, muscle, skeletal disease
history of major surgery
,No restrictions on range of motion (ROM)
,No restrictions on daily activities due to other physical injuries
No restrictions on daily activities due to psychological damage.
Patients with physical pain or lack of energy to perform activities</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>65 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Taking nonsteroidal anti-inflammatory drugs during the stud
Exacerbation of symptoms and pain
unwillingness of the patient to continue treatment
,Do not attend training classes for more than two consecutive
sessionsOccurrence of any unpredictable stressful event during the intervention</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M84.4</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Pathological fracture, not elsewhere  classified</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: The present study is a semi-experimental study with a pre-test-post-test design and a control group. First, after the proposal is approved by the research council and the code of ethics is obtained from the vice president of research, the researcher sends a letter of introduction to the research environment from the university, and then goes to the research environment and while introducing himself to them, obtains permission to carry out the activity. Also, in order to conduct the research, in order to access the research samples, visit the orthopedic department of Shahid Beheshti Hospital in Babol and select your samples from among the patients hospitalized in the orthopedic departments with hip fracture using a continuous sampling method and in a simple random manner and based on the inclusion criteria. and then they will be divided into two test and control groups in a simple random manner.. Before any intervention and measurement, the written consent form of the company in the study will be completed by the subjects in order to prevent contamination of the researcher's information first from the patients. The hospital that suffers from hip fracture selects 40 patients for the test group and after the completion of the above number, the next 40 patients for the control group. Before doing any interventionand measurement, the written consent form of the company in the study will be completed by the subjects and it will be collected along with the patient's demographic profile form.Then, the daily life activities questionnaire will be completed by all patients of both groups (test and control) at the beginning of the work. For the test group, training sessions are started after the patient's surgery with the permission of the patient's treating physician, and during the hospitalization period and every day for 10-15 minutes until the discharge, training sessions are conducted by the researcher and for the convenience of the test group members, the sessions are held in a separate room. It will also be possible to continue the exercises at home using a training booklet that contains sports pictures and in the form of training how to move in detail and how to perform daily activities. The question of being able to contact the researcher at the time of dischargeMore about this source textSource text required for additional translation informationSend feedbackSide panels</i_keyword>
      <i_keyword>Control group: After 24 hours after the surgery, the control group will receive only the routine exercises and trainings of the department by the personnel after 24 hours after the surgery. In order to prevent contamination, the researcher first selects the test group based on the entry criteria and until the desired number is reached. He will perform this activity until the discharge and then select the control group and examine it for a week until the discharge.Considering that a month later, both the control and test groups will go to the clinic, the educational pamphlet will be given to the control group at the end, but the test group will receive the pamphlet from the beginning.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Barthel Index (daily life activities)The original version of the instrument was in English and was designed in 1965 in the United States by Dorothea Barthel and Mahoney Florence. This tool has 10 questions and 0-5-10-15 style scoring and measures the state of self-sufficiency in daily life activities. Timepoint: Training sessions begin after the patient's surgery with the permission of the patient's physician, and are taught by the researcher during the hospital stay and every day for 10-15 minutes until discharge. Method of measurement: Lawton Index (instrumental activities of daily living)This index was designed by Lawton and Brody in 1969 to measure the skills related to independence in life. This tool has eight items, which include the items of using the phone, shopping, preparing food, tidying the house (housekeeping), washing clothes, moving with vehicles, the ability to accept responsibility, taking one's own medicine, and financial ability. . Each item includes a score of one (more ability) and a score of zero (less ability), and in women, the total score of the questionnaire is eight, which means independent performance in instrumental activities of daily life, but in men, the item is preparing food, washing Clothes and housekeeping are removed and the total score is calculated out of five (Lawton and Brody, 1969). In its Persian version, due to the lack of difference between men and women in the above questions, the total scores for women and men were considered eight (Soltanmohamadi et al., 2014).</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Activity daily living are the skills and tasks that a person deals with during the day and do their daily affairs, they are one of the most basic components of life. Timepoint: In order to check ADL daily life activities, the standard questionnaire of ADL daily life activities will be used. In this way, before starting the exercises in both groups, the questionnaire is completed first, and after the training of the range of motion exercises in the test group and the routine training of the department, it is also completed at the time of discharge one week later and one month later in the clinic. Method of measurement: In this questionnaire, 7 items are examined, each item has three points (0, 1, and 2), and the score 1 to 6 is classified as dependent, 7 to 10 as necessary, and 11 to 14 as independent. The general index of ADL ranges from zero to 14.</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>Iran University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2022-01-02</approval_date>
        <contact_name>Ethics Committee of Iran University of Medical Sciences</contact_name>
        <contact_address>Shahid Salehi-Gotab road, village below the border Babol Mazandaran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
