<?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>IRCT2016110829264N2</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2016-11-29</date_registration>
      <primary_sponsor>Vice Chancellor for Research and Technology, Tarbiat Modares University</primary_sponsor>
      <public_title>evaluation of the acute effect of abdominal muscle taping in patients with non specific chronic low back pain</public_title>
      <acronym></acronym>
      <scientific_title>evaluation of the acute effect of abdominal muscle taping on endurance tests in patients with non specific chronic low back pain</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2016-05-21</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>52</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/23569</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Single blinded, Placebo: Used, Assignment: Crossover, Purpose: Treatment, Other design features: this study is one part of master thesis with registration number of (PZ 2863 322) developed in 2011. this thesis is fully traceable with ethic registration number of 5299424 from Medical Ethics Committee of the tarbiat modares university.</study_design>
      <phase>2</phase>
      <hc_freetext>chrionic low back pain.</hc_freetext>
      <i_freetext>Intervention 1: intervention group: 1- Supine isometric chest raise (SICR) test&#13;
The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position.&#13;
&#13;
2-Supine double straight-leg raise (SDSLR) test&#13;
The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance.&#13;
3-Abdominal drawing in maneuver&#13;
This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg.&#13;
&#13;
4-Taping techniques&#13;
The NCLBP participants were asked to lie in a supine position and their hips and knees were flexed at 45°. Depending on the NCLBP participant’s morphology, the length of three pieces of I-shaped strip Kinesio tape  was determined by measuring the distance between two anterior superior iliac spines (ASISs) and measuring the distance between the middle one-third of the intermediate line of the iliac crest to the inferior border of the 10th rib. Afterward, the Kinesio tapes were applied to the internal oblique muscles in the direction of the fibers from the origin to insertion with approximately 50% of their maximal length tension. For the transversus abdominus muscle, the Kinesio tape was applied horizontally between the two ASISs with approximately 50% of maximal length tension . Then, all of the measurements were repeated again in the same manner as they had been performed before taping. Intervention 2: placebo group: 1- Supine isometric chest raise (SICR) test The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position. 2-Supine double straight-leg raise (SDSLR) test The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance. 3-Abdominal drawing in maneuver This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg. 4-Taping techniques The NCLBP participants were asked to lie in a supine position and their hips and knees were flexed at 45°. Depending on the NCLBP participant’s morphology, the length of one pieces of I-shaped strip Kinesio tape was determined by measuring the distance between inferior border of the 10th rib bilaterally. Afterward, the Kinesio tape were applied to the inferior margin of 10th ribs above the umbilicus under no tension. Then, all of the measurements were repeated again in the same manner as they had been performed before taping. Intervention 3: healthy group 1- Supine isometric chest raise (SICR) test The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position. 2-Supine double straight-leg raise (SDSLR) test The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance. 3-Abdominal drawing in maneuver This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg.</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></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Seyyed Rasoul Bagheri</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Madadkaran Alley, Shahnazari Street, Madar Squar.</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 21 2222 8051</telephone>
        <email>rasool.bagheri@ymail.com</email>
        <affiliation>Department of Physiotherapy, School of Rehabilitation Sciences, Iran University of Medical Sciences </affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Mohammad Reza Pourahmadi</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Madadkaran Alley, Shahnazari Street, Madar Squar.</address>
        <city>Tehran</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 21 7783 6545</telephone>
        <email>pourahmadipt@gmail.com</email>
        <affiliation>Department of Physiotherapy, School of Rehabilitation Sciences, Iran University of Medical Sciences </affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>inclusion criteria:&#13;
 1-Non specific Chronic Low Back Pain (LBP persisting for more than 3 months in the absence of an underlying pathology); &#13;
2- age between 18 and 45 years;&#13;
3- pain between 3 and 6 on visual analogue scale (VAS), &#13;
exclusion criteria:&#13;
1-  history of abdominal surgery; &#13;
2-  abdominal hernia; &#13;
3-  pregnancy.</inclusion_criteria>
      <agemin>18 years</agemin>
      <agemax>45 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>M54.5</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>Loin pain, Low back strain</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Rehabilitation</i_code>
      <i_code>Treatment - Drugs</i_code>
      <i_code>Treatment - Drugs</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>intervention group: 1- Supine isometric chest raise (SICR) test&#13;
The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position.&#13;
&#13;
2-Supine double straight-leg raise (SDSLR) test&#13;
The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance.&#13;
3-Abdominal drawing in maneuver&#13;
This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg.&#13;
&#13;
4-Taping techniques&#13;
The NCLBP participants were asked to lie in a supine position and their hips and knees were flexed at 45°. Depending on the NCLBP participant’s morphology, the length of three pieces of I-shaped strip Kinesio tape  was determined by measuring the distance between two anterior superior iliac spines (ASISs) and measuring the distance between the middle one-third of the intermediate line of the iliac crest to the inferior border of the 10th rib. Afterward, the Kinesio tapes were applied to the internal oblique muscles in the direction of the fibers from the origin to insertion with approximately 50% of their maximal length tension. For the transversus abdominus muscle, the Kinesio tape was applied horizontally between the two ASISs with approximately 50% of maximal length tension . Then, all of the measurements were repeated again in the same manner as they had been performed before taping.</i_keyword>
      <i_keyword>placebo group: 1- Supine isometric chest raise (SICR) test The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position. 2-Supine double straight-leg raise (SDSLR) test The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance. 3-Abdominal drawing in maneuver This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg. 4-Taping techniques The NCLBP participants were asked to lie in a supine position and their hips and knees were flexed at 45°. Depending on the NCLBP participant’s morphology, the length of one pieces of I-shaped strip Kinesio tape was determined by measuring the distance between inferior border of the 10th rib bilaterally. Afterward, the Kinesio tape were applied to the inferior margin of 10th ribs above the umbilicus under no tension. Then, all of the measurements were repeated again in the same manner as they had been performed before taping.</i_keyword>
      <i_keyword>healthy group 1- Supine isometric chest raise (SICR) test The participant's position was supine on the treatment table with the hands crossed on his/her chest. The hips and knees were flexed at 45° and the feet were placed flat on the table. The participant was requested to lift neck and upper trunk from the table until the inferior angles of scapulae had risen clear of the table and hold this position as long as possible. The maximal hold time was then recorded in seconds, and the test was terminated when the participant was unable to maintain the test position. 2-Supine double straight-leg raise (SDSLR) test The participant was asked to lie in a supine position with the hips and knees extended. The hands were also placed in a relaxed position near his/her body. The participant was then instructed to raise both legs from the table to approximately 20° and hold them as long as possible without any tilting in the pelvis. During the test, pelvic tilt was monitored by an experienced physical therapist. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain knee clearance. 3-Abdominal drawing in maneuver This was done with the participant lying supine on the treatment table with the hands were placed in a relaxed position near the body. The hips and knees were flexed at 45° and the feet were placed flat on the table. In addition, a pressure biofeedback monitor (sphygmomanometer) was placed below the lumbar lordosis between the L1 and S1 vertebrae. The cuff of the sphygmomanometer was inflated to 20 mmHg using an air pump to fill the space between the lumbar spine and treatment table. The participant was then requested to contract his/her deep abdominal musculature by drawing the navel up in a cephalad direction and in toward the spine. The participant was instructed to push his/her back against the cuff and maintain the pressure at 40 (±10) mmHg as long as possible. The maximal hold time was recorded in seconds, and the test was terminated when the participant was unable to maintain the pressure at 40 (±10) mmHg</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Supine isometric chest raise test. Timepoint: before and after taping. Method of measurement: The maximal hold time in seconds.</prim_outcome>
      <prim_outcome>Supine double straight-leg raise test. Timepoint: before and after taping. Method of measurement: The maximal hold time in seconds.</prim_outcome>
      <prim_outcome>Abdominal drawing in maneuver. Timepoint: before and after taping. Method of measurement: The maximal hold time in seconds.</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>Vice Chancellor for Research and Technology, Tarbiat Modares University</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2011-02-26</approval_date>
        <contact_name>Ethics Committee of the Tarbiat Modares university</contact_name>
        <contact_address>Jalal Al Ahmad street ,Tehran. Tehran  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
