<?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>IRCT20230410057876N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-07-20</date_registration>
      <primary_sponsor>Mashhad University of Medical Sciences</primary_sponsor>
      <public_title>Abdominal Muscles Training in groin pain</public_title>
      <acronym></acronym>
      <scientific_title>Effectiveness of hip muscle training with and without focus on abdominal muscles on pain, range of motion, hip muscle strength, physical performance and patient-reported outcomes in athletes with longstanding adductor-related groin pain: A randomized controlled trial</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-06-10</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>30</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/83406</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: In this study, a block randomization method of size four will be used to allocate participants to two treatment groups. Each block will include two participants from the control group (A) and two participants from the intervention group (B). In order to reduce bias and maintain statistical balance between groups, different orders of block sequences will be considered. Allowed combinations include: AABB, ABAB, ABBA, BBAA, BABA, and BAAB.
Random sequences will be generated using the reputable website Sealedenvelope.com. The resulting sequences will be placed in opaque, sealed envelopes, and upon participant arrival, the sample allocator will randomly open one of the envelopes. The participant will be assigned to the appropriate group according to the order listed on the envelope.
In order to conceal allocation and prevent bias in the selection process, sealed envelopes will be used and will be prepared by individuals unaware of the study contents, Blinding description: In this study, a blinding approach will be implemented involving both the outcome assessor and the data analyst. An independent evaluator will be designated as the outcome assessor, who will have no involvement in the study design, intervention delivery, or group allocation process. The assessor will remain fully blinded to the group assignments and intervention details. Clinical outcomes will be evaluated at two time points: baseline (prior to the intervention) and immediately after completion of the intervention period (week 8).

Furthermore, data analysis will be conducted under blinded conditions. Prior to statistical processing, the dataset will be anonymized such that group identifiers are replaced with neutral codes (e.g., Group 1 and Group 2). The analyst will receive the de-identified data and will be unaware of the actual treatment allocation until the analysis is finalized.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Longstanding groin pain related to the adductor muscles.</hc_freetext>
      <i_freetext>Intervention 1: Intervention group: Athletes in the intervention group will perform exercises under the supervision of one of two sports physiotherapists in the sports club for 6 weeks (3 days per week, odd days). Both physiotherapists will be trained in advance to provide a standard therapeutic exercise. Since the reduction in the strength of adductor muscles is evident in people with chronic groin pain and therapeutic exercise focused on isometric and eccentric strength of adductor and abductor muscles has been recommended in previous studies to reduce pain and restore function in athletes with chronic groin pain, the exercises provided for the muscles in question will also include these types of contractions, since in athletes with chronic groin pain, these two muscles are more likely to change than others among the trunk muscles. Therefore, exercises with maximum contraction of these muscles are recommended. The therapeutic exercise program of the intervention group includes strengthening the thigh muscles along with strengthening the abdominal muscles. The approximate duration of each session will be 60 minutes. Warm-up, fixed hip adduction, bilateral hip adduction, lateral hip adduction, hip abduction/adduction glide, machine adduction, Copenhagen adduction. Core exercises: Plank with leg raise, crunch, bird-dog exercise. Intervention 2: Control group: Athletes in the control group will be supervised by one of two sports physiotherapists in a sports club for 6 weeks (3 days per week, even days). Both physiotherapists will be trained in advance to provide a standard therapeutic exercise. Research shows that weakness in adductor muscle contractions is a common problem in people with chronic groin pain. Also, previous studies have shown that therapeutic exercises focusing on strengthening isometric and eccentric contractions of adductor and abductor muscles can help reduce pain and improve performance in athletes. Therefore, the proposed exercises will include these types of contractions. The approximate duration of each session will be 45 minutes. Warm-up, fixed thigh adduction, bilateral thigh adduction, lateral thigh adduction, thigh abduction/adduction, adduction with a device, Copenhagen adduction.</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:
Only information related to the primary outcome (pain during function) can be shared after the study is completed.

When:
One year after the publication of the article

To whom:
Researchers affiliated with academic and scientific institutions

Conditions:
Studies in the relevant field with an official letter of introduction from academic institutions

Where to obtain:
Email: Rafsanjanidh@mums.ac.ir
Hossein Rafsanjani Deh Ghazi

How to obtain:
After obtaining an introduction letter from academic institutions and attaching the request to the Deputy of Research and Technologyی

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Hossein Rafsanjani Deh Ghazi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Mashhad - Azadi Square - East Gate of Ferdowsi University of Mashhad - University Campus - Faculty of Allied Medical Sciences and Rehabilitation</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9177948964</zip>
        <telephone>+98 51 3884 6728</telephone>
        <email>Rafsanjanidh@mums.ac.ir</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Hossein Negahban</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Mashhad - Azadi Square - East Gate of Ferdowsi University of Mashhad - University Campus - Faculty of Allied Medical Sciences and Rehabilitation</address>
        <city>Mashhad</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>9177948964</zip>
        <telephone>+98 51 3884 6710</telephone>
        <email>Honegahban@yahoo.com</email>
        <affiliation>Mashhad University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Athletes aged 18 to 50
Groin pain lasting at least 2 months
Groin pain during or after sports activity
Pain location at the junction of the adductor tendon to the pubic bone
Motivation to return to sports participation at the pre-injury level
Pain location at the junction of the adductor tendon to the pubic bone
Pain at the junction of the adductor tendon to the pubic bone during resisted adduction
Tenderness of the adductor tendons and/or their attachment to the pubic bone</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>50 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Palpable hernia in the inguinal or femoral region, or pain over the conjoined tendon
Clinical symptoms of prostatitis or urinary tract infection
Lower back pain in the T10 to L5 vertebral region
Hip osteoarthritis
Clinical suspicion of nerve entrapment syndrome involving the ilioinguinal, genitofemoral, or lateral femoral cutaneous nerve
Inability to perform an active sports program
Use of anticoagulant medications
Instability of the medial collateral ligament of the affected knee(s)</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>S76.2</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Injury of adductor muscle, fascia and tendon of thigh</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: Athletes in the intervention group will perform exercises under the supervision of one of two sports physiotherapists in the sports club for 6 weeks (3 days per week, odd days). Both physiotherapists will be trained in advance to provide a standard therapeutic exercise. Since the reduction in the strength of adductor muscles is evident in people with chronic groin pain and therapeutic exercise focused on isometric and eccentric strength of adductor and abductor muscles has been recommended in previous studies to reduce pain and restore function in athletes with chronic groin pain, the exercises provided for the muscles in question will also include these types of contractions, since in athletes with chronic groin pain, these two muscles are more likely to change than others among the trunk muscles. Therefore, exercises with maximum contraction of these muscles are recommended. The therapeutic exercise program of the intervention group includes strengthening the thigh muscles along with strengthening the abdominal muscles. The approximate duration of each session will be 60 minutes. Warm-up, fixed hip adduction, bilateral hip adduction, lateral hip adduction, hip abduction/adduction glide, machine adduction, Copenhagen adduction. Core exercises: Plank with leg raise, crunch, bird-dog exercise</i_keyword>
      <i_keyword>Control group: Athletes in the control group will be supervised by one of two sports physiotherapists in a sports club for 6 weeks (3 days per week, even days). Both physiotherapists will be trained in advance to provide a standard therapeutic exercise. Research shows that weakness in adductor muscle contractions is a common problem in people with chronic groin pain. Also, previous studies have shown that therapeutic exercises focusing on strengthening isometric and eccentric contractions of adductor and abductor muscles can help reduce pain and improve performance in athletes. Therefore, the proposed exercises will include these types of contractions. The approximate duration of each session will be 45 minutes. Warm-up, fixed thigh adduction, bilateral thigh adduction, lateral thigh adduction, thigh abduction/adduction, adduction with a device, Copenhagen adduction</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Pain during functional activity. Timepoint: Before the start of the intervention - After six weeks of intervention. Method of measurement: Visual Analogue Scale (VAS).</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Pain during resisted contraction. Timepoint: Before the start of the intervention - After six weeks of intervention. Method of measurement: Visual analogue scale (VAS).</sec_outcome>
      <sec_outcome>Range of Motion. Timepoint: Before the start of the intervention - After six weeks of intervention. Method of measurement: Bent Knee Fall Out test.</sec_outcome>
      <sec_outcome>Strength. Timepoint: Before the start of the intervention - After six weeks of intervention. Method of measurement: Handheld dynamometer.</sec_outcome>
      <sec_outcome>Patient-centered outcomes. Timepoint: Before the start of the intervention - After six weeks of intervention. Method of measurement: The Copenhagen Hip and Groin Outcome Scale (HAGOS).</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>Mashhad university of medical sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-04-28</approval_date>
        <contact_name>Ethics Committee of Mashhad University of Medical Sciences</contact_name>
        <contact_address>Mashhad - Azadi Square - East Gate of Ferdowsi University of Mashhad - University Campus Mashhad Razavi Khorasan Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
