<?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>IRCT20260729070428N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2026-09-04</date_registration>
      <primary_sponsor>Islamic Azad University</primary_sponsor>
      <public_title>Effectiveness of combined exercises (resistance and endurance)</public_title>
      <acronym></acronym>
      <scientific_title>The effectiveness of combined exercises (resistance and endurance) on body image shame and body management in overweight women.</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2026-09-20</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/92966</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance, Randomization description: In this study, a simple randomization method is used to assign participants to two experimental groups (combined resistance and endurance exercises) and control. The randomization unit in this study is overweight women eligible for the study in Izeh County. First, a complete list of volunteers who have been selected based on the study entry and exit criteria is prepared. Then, each participant is assigned a unique numerical identification code. These codes are entered into the Random Number Generator software and a random number is generated for each individual. After generating these numbers, the participants are sorted in ascending order based on the value of the random number. Then, the individuals are assigned to two groups; sequentially, the first 15 people on the list are assigned to the experimental group (combined exercise intervention) and the next 15 people are assigned to the control group. With this method, the order of entry into the study and the researcher's knowledge of the participants will not play any role in determining the group. To conceal allocation, the person responsible for entering data and performing the randomization process in the software will be independent of the trainers implementing the exercise protocol and the evaluators of the research variables (body image shame and body management) and will not have the opportunity to know the process of implementing the sessions or changes in the allocation of individuals. Also, the identification codes of the participants will be kept confidential and separate from their other personal information. Therefore, it will not be possible to predict the assigned group for each participant before the randomization process, Blinding description: In order to control bias and improve internal validity of the study, this study was designed with a double-blind protocol; in this way, the outcome assessor and data analyst will be kept unaware of the allocation of overweight women to the experimental (combined exercise) and control groups. In this process, the outcome assessor will collect data related to body image shame and body management at all stages of the pre-test and post-test, without knowing the assigned group of the participants, in order to prevent bias in the measurement; also, all raw data will be provided to the statistical analyst with anonymous codes (such as groups 1 and 2), and the true nature of the groups will not be revealed until the end of the data analysis process. All allocation steps will be performed by an independent person from the research team, and decoding of allocation codes will be done only after the final completion of the statistical analyses.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Psychological problems caused by obesity.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Combined training sessions (resistance and endurance) will be implemented based on the standard protocol designed by Sobhanipour et al. (2016; 2019). This intervention will be conducted in the form of 90-minute group sessions for the experimental group. Combined training is an approach designed to improve functional capabilities and body composition, reduce body image shame, and strengthen body management strategies. It helps overweight women rebuild their body evaluation patterns by promoting the perception of physical competence, reducing negative body sensitivities, and increasing self-efficacy resulting from physiological adaptations. The structure of the sessions of this intervention has main implementation axes; each session begins with a 10-minute general warm-up and preparation of the musculoskeletal system and ends with a 10-minute cool-down and return to the initial state, and the main body of the exercise includes two parts: endurance and resistance training; The endurance part includes continuous running on a treadmill with an initial intensity of 40% of maximum oxygen consumption for 35 minutes, the intensity and duration of which are increased according to the progress of the subjects every week to an intensity of 75% and a duration of 60 minutes, and the resistance part includes leg press, chest press, front thigh, butterfly, back thigh, shoulder, lateral pull (lat from behind) and bicep curl movements, which are performed in 3 sets of 12 repetitions in an interval manner (with a rest of 2 to 3 minutes between sets and 1 minute between movements) and with an initial training load of 30% of one repetition maximum, and 5% of the overload is added every two weeks to reach 60% of maximum strength. The main emphasis of these exercises is homogenization and control of training pressure based on the Borg Pressure Perception Index (Borg Scale) and gradual progression of workload in order to reduce negative evaluations of the body and improve control and management of physical dimensions. Intervention 2: Control group: They do not receive any intervention or treatment.</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>No - There is not a plan to make this available</results_IPD_plan>
      <results_IPD_description>Justification or reason for not sharing IPD is rticipant data is completely confidential and I do not intend to publish it.</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Arezou Zamzam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Muslim Alley,. Sattarkhan Street.</address>
        <city>Iezh</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6391647754</zip>
        <telephone>+98 916 739 5083</telephone>
        <email>arezouzamzam80@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Arezou Zamzam</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Muslim Alley,. Sattarkhan Street.</address>
        <city>Iezh</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>6391647754</zip>
        <telephone>+98 916 739 5083</telephone>
        <email>arezouzamzam80@gmail.com</email>
        <affiliation>Islamic Azad University</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Be between 18 and 35 years old.
Be overweight.
Provide informed consent for participation in the study.</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>35 years</agemax>
      <gender>Female</gender>
      <exclusion_criteria>Having a physical illness that interferes with the treatment process.
Use of psychiatric medications.
History of substance or drug abuse.</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>E66.9</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Obesity, unspecified</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>N/A</i_code>
      <i_code>N/A</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Intervention group: Combined training sessions (resistance and endurance) will be implemented based on the standard protocol designed by Sobhanipour et al. (2016; 2019). This intervention will be conducted in the form of 90-minute group sessions for the experimental group. Combined training is an approach designed to improve functional capabilities and body composition, reduce body image shame, and strengthen body management strategies. It helps overweight women rebuild their body evaluation patterns by promoting the perception of physical competence, reducing negative body sensitivities, and increasing self-efficacy resulting from physiological adaptations. The structure of the sessions of this intervention has main implementation axes; each session begins with a 10-minute general warm-up and preparation of the musculoskeletal system and ends with a 10-minute cool-down and return to the initial state, and the main body of the exercise includes two parts: endurance and resistance training; The endurance part includes continuous running on a treadmill with an initial intensity of 40% of maximum oxygen consumption for 35 minutes, the intensity and duration of which are increased according to the progress of the subjects every week to an intensity of 75% and a duration of 60 minutes, and the resistance part includes leg press, chest press, front thigh, butterfly, back thigh, shoulder, lateral pull (lat from behind) and bicep curl movements, which are performed in 3 sets of 12 repetitions in an interval manner (with a rest of 2 to 3 minutes between sets and 1 minute between movements) and with an initial training load of 30% of one repetition maximum, and 5% of the overload is added every two weeks to reach 60% of maximum strength. The main emphasis of these exercises is homogenization and control of training pressure based on the Borg Pressure Perception Index (Borg Scale) and gradual progression of workload in order to reduce negative evaluations of the body and improve control and management of physical dimensions.</i_keyword>
      <i_keyword>Control group: They do not receive any intervention or treatment.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Shame on the picture. Timepoint: before performing the intervention and two weeks after completion of the intervention. Method of measurement: Kesh and Pruzinski Body Image Questionnaire (1983).</prim_outcome>
      <prim_outcome>Body management. Timepoint: before performing the intervention and two weeks after completion of the intervention. Method of measurement: Manakhani and Rakibi Body Management Questionnaire (2019).</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>Islamic Azad University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2026-06-30</approval_date>
        <contact_name>Behbahan Islamic Azad University Ethics Committee</contact_name>
        <contact_address>Shahid Bayani St., Amir Kabir Blvd. بهبهان Khouzestan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
