<?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>IRCT20250704066369N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2025-07-29</date_registration>
      <primary_sponsor>Tehran University of Medical Sciences</primary_sponsor>
      <public_title>comparison of the immediate effect of dry needling and active release technique in amateur athlete's posterior thigh muscle shortness</public_title>
      <acronym></acronym>
      <scientific_title>Comparison of the immediate effect of dry needling and active release technique in amateur athletes with hamstring muscle shortness</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2025-08-10</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>34</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/84635</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Random assignment is performed using the Block Randomization method so that the number of participants in the two groups is balanced.
1. Determine the block size: Given that we have two groups in this study, the block size must be divisible by 2, which is the most common block size when we have two study groups, 4. From each block of 4, 2 people will be placed in Group A or the dry needling group and 2 people in Group B or the active release technique group.
2. All possible combinations for a block:
AABB, ABAB, ABBA, BBAA, BABA, BAAB
Since we want the total sample size of the study to be 34 people, 9 blocks will be randomly selected from all the permutations.
3. Allocation of individuals to blocks:
Each individual who enters the study is entered into the study based on the order of individuals in the selected block. For example, if the random block is AABB, the first two individuals enter group A and the second two individuals enter group B, and ultimately we will have two groups of 17 individuals, Blinding description: Eligible individuals, after being informed about the general treatment method and the purpose of the study, voluntarily fill out and sign the consent form. If they meet the inclusion criteria, they are randomly assigned to one of the treatment groups. Then, the initial characteristics and demographic information of the participants (including age, weight, height, gender, and body mass index) and pre-treatment evaluations are recorded by a trained assessor who is unaware of the study type. After this evaluation, a treatment session will be conducted by a trained therapist. Participants will also be re-evaluated immediately and 24 hours after the treatment by a trained assessor who is unaware of the type of treatment.</study_design>
      <phase>N/A</phase>
      <hc_freetext>Hamstring muscle shortness.</hc_freetext>
      <i_freetext>Intervention 1: Dry needling intervention group: This method is performed using disposable stainless steel needles (mm 0.3*60 DongBang). In this method, subjects are placed on the treatment table in a prone position, with their feet on the bed, and the hamstrings are needled at 3 points, each for 1 minute, using a rapid entry and exit technique in a conical shape. To standardize the approach and optimize the application of dry needling, points are needled approximately close to the movement points of the hamstring muscles. The first two points are at 30 and 60%, respectively, of a straight line drawn from the attachment of the ischial tuberosity to the long and short heads of the biceps femoris muscle and then to the head of the fibula. The third point is at 60% of a straight line extending from the ischial tuberosity (the attachment point of the semimembranosus and semitendinosus muscles) to the medial condyle of the femur. Intervention 2: Active release intervention group: Active release, compared to other manual therapies, is a unique technique in which the patient actively moves, while the therapist uses his or her hands to first palpate, then assess and release the soft tissue. In this method, the therapist encourages the patient to move actively by applying manual pressure to the affected areas, and the muscle is stretched from a short length to a long length. This combination of pressure and active movement helps to increase muscle flexibility. Steps: The patient lies prone on the bed, with the patient's feet hanging over the end of the bed. The therapist then finds the area of the muscle that is most tight by skin contact and palpation and applies gentle pressure to it. The patient bends and straightens their knee to stretch the muscle from its short length to its long length. This cycle is repeated five times.</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 relevant data that has been agreed to be published can be shared.

When:
6 months after results

To whom:
It will be accessible to everyone involved in the industry.

Conditions:
For researchers who are conducting research in this field and need information to improve their studies.

Where to obtain:
1.Email
2.Contact Number
3.Postal Address

How to obtain:
The individual submits their request, and after the necessary checks are made regarding how the data will be used, the individual's job scope, and the necessary documents are provided to the individual.کل

Comments:
</results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Nourodin nakhostin ansari</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 336, Shemiran Corner, Safi Alishah Street, Enghelab Street, Tehran, Faculty of Rehabilitation, Tehran University of Medical Sciences</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1148965111</zip>
        <telephone>+98 21 7753 3939</telephone>
        <email>nnansari@gmail.com</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fateme zahra sadat mirian khoshkroudi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>No. 336, Shemiran Corner, Safi Alishah Street, Enghelab Street, Tehran, Faculty of Rehabilitation, Tehran University of Medical Sciences</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip>1148965111</zip>
        <telephone>+98 21 7753 3939</telephone>
        <email>fatememirian70@gmail.com</email>
        <affiliation>Tehran University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>People between the ages of 18 and 40
People with hamstring shortness of 25 degrees or more
Regular exercise three times a week, for less than 6 hours, for at least 10 months</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>40 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria>Having a history of orthopedic or neurological problems
Low back pain during the study
Having a history of surgery in the back, hip, or knee joints
Having a recent history of hamstring strain
Being in a group of contraindications to the use of dry needling or active release
Having upper or lower motor neuron injury
Having a lower limb length discrepancy of more than 10 mm
Experience of any injury to the lower extremities within the last three months
Women during menstruation
Needle's phobia</exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>S76</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Injury of muscle, fascia and tendon at hip and thigh level</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Rehabilitation</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>Dry needling intervention group: This method is performed using disposable stainless steel needles (mm 0.3*60 DongBang). In this method, subjects are placed on the treatment table in a prone position, with their feet on the bed, and the hamstrings are needled at 3 points, each for 1 minute, using a rapid entry and exit technique in a conical shape. To standardize the approach and optimize the application of dry needling, points are needled approximately close to the movement points of the hamstring muscles. The first two points are at 30 and 60%, respectively, of a straight line drawn from the attachment of the ischial tuberosity to the long and short heads of the biceps femoris muscle and then to the head of the fibula. The third point is at 60% of a straight line extending from the ischial tuberosity (the attachment point of the semimembranosus and semitendinosus muscles) to the medial condyle of the femur.</i_keyword>
      <i_keyword>Active release intervention group: Active release, compared to other manual therapies, is a unique technique in which the patient actively moves, while the therapist uses his or her hands to first palpate, then assess and release the soft tissue. In this method, the therapist encourages the patient to move actively by applying manual pressure to the affected areas, and the muscle is stretched from a short length to a long length. This combination of pressure and active movement helps to increase muscle flexibility. Steps: The patient lies prone on the bed, with the patient's feet hanging over the end of the bed. The therapist then finds the area of the muscle that is most tight by skin contact and palpation and applies gentle pressure to it. The patient bends and straightens their knee to stretch the muscle from its short length to its long length. This cycle is repeated five times.</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Hamstring muscle flexibility. Timepoint: Before, immediately and 24 hour after intervention. Method of measurement: Goniometer and active knee extension test.</prim_outcome>
      <prim_outcome>Passive compliance. Timepoint: Before, immediately and 24 hour after intervention. Method of measurement: Calculation by formula.</prim_outcome>
      <prim_outcome>Passive peak torque. Timepoint: Before, immediately and 24 hour after intervention. Method of measurement: Manual dynamometer.</prim_outcome>
      <prim_outcome>Stretch tolerance. Timepoint: Before, immediately and 24 hour after intervention. Method of measurement: Goniometer.</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>Tehran University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2025-07-01</approval_date>
        <contact_name>Ethics committee of Tehran University of Medical Sciences</contact_name>
        <contact_address>Room 605, 6th Floor, Tehran University of Medical Sciences Headquarters Building,  Keshavarz Blvd and Qods Street junction, Tehran Tehran Tehran Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
