The Immediate Effects of Spinal Manipulative Therapy on Kinetic and Kinematic Symmetry.

Sponsor
University of Lisbon (Other)
Overall Status
Completed
CT.gov ID
NCT03361592
Collaborator
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. (Other)
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Study Details

Study Description

Brief Summary

Athletes have been exposed to an ever increasing training load and subsequent biomechanical overload due to a constant demand for performance enhancement. As a result, it is observed an increased rate of musculoskeletal problems, including spinal biomechanical dysfunctions that are often asymptomatic. These dysfunctions are believed to negatively influence a wide range of mechanical and physiological parameters such as muscle strength, range of motion, and symmetry, what could potentially influence sports performance.

Spinal Manipulative Therapy (SMT) is a safe and effective therapy for musculoskeletal disorders that has been increasingly utilized in sports. SMT purpose is to correct spinal joints biomechanical dysfunctions using a high-velocity, low-amplitude movement, applied at the paraphysiological space, beyond the passive joint range of motion.

Kinetic and kinematic symmetry can be measured in commonly utilized physical functional tests often used as indicators of athlete's performance. Symmetry Index calculation is used to verify bilateral asymmetries in static and dynamic tests.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Spinal Manipulative Therapy
  • Procedure: SHAM
N/A

Detailed Description

Therefore, the objective of this randomized controlled trial study is to measure the immediate effects of lumbar SMT on kinetic and kinematic symmetry of asymptomatic athletes, through of the use of three commonly used functional tests: Static posture, Free Squat, and Countermovement Jump (CMJ) are often used as indicators of athlete's performance. These quantitative data is important to assess training effectiveness and prevention/ rehabilitation programs outcomes. To our knowledge this is the first study on literature that measured the immediate effects of SMT on kinetic and kinematic symmetry.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized controlled single-blinded study.randomized controlled single-blinded study.
Masking:
Single (Outcomes Assessor)
Masking Description:
Participants were initially instructed about the study procedures with therapeutic interventions. After collected data, the participants were asked about the therapeutic intervention, if they are capable to identify which intervention were performed, SMT or SHAM, as parte of study protocol.
Primary Purpose:
Treatment
Official Title:
Immediate Effects of Spinal Manipulative Therapy (SMT) on Kinetic and Kinematic Symmetry on Functional Performance Tests: a Test-retest, Single-blinded, Randomized Controlled Trial.
Actual Study Start Date :
Sep 4, 2017
Actual Primary Completion Date :
Sep 22, 2017
Actual Study Completion Date :
Dec 5, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Spinal Manipulative Therapy

The participants assigned to the intervention group received the procedure Lumbar (SMT) was performed after baseline measurements, using Diversified techniques, aiming to correct vertebral dysfunctional segments after clinical assessment. Participants were asked to lay down prone on, to perform spinal motion palpation analysis was performed in order to evaluate the presence of dysfunction in vertebral segments of lumbar spine.

Procedure: Spinal Manipulative Therapy
Lumbar (SMT) was performed using Diversified techniques, aiming to correct vertebral dysfunctional lumbar segments. Participants were asked to lay down prone on, to perform spinal motion palpation analysis was in order to evaluate the presence of dysfunction in vertebral segments of lumbar spine.
Other Names:
  • Movement Disorders/therapy
  • Spinal Manipulation
  • Sham Comparator: Sham pre-load positioning SMT

    The participants assigned to the control group received the procedure "Sham" (pre-load positioning MVT). The Sham (SMT) was performed with participant body positioning in the lateral position, as the SMT intervention. The doctor followed the participant through the same position of (SMT) intervention, using the maintenance of set-up position, but no manipulative thrust was delivered. The therapist applied minimal pressure and slid their hands across the skin to mimic the manipulative trust. The position was maintained for approximately 1 minute in total, 30 seconds on each side, and none of force or researcher body weight were putted in this procedure, only minimal pressure common to stabilize the set up position of (SMT).

    Procedure: SHAM
    The "SHAM" (pre-load positioning SMT) was performed with participant body positioning in the lateral position, as the SMT intervention. The doctor followed the participant through the same position of (SMT) intervention, using the maintenance of set-up position, but no manipulative thrust was delivered. The therapist applied minimal pressure and slid their hands across the skin to mimic the manipulative trust. The position was maintained 30 seconds on each side, and none of force or researcher body weight were putted in this procedure, only minimal pressure common to stabilize the set up position of (SMT).
    Other Names:
  • Control Group
  • Outcome Measures

    Primary Outcome Measures

    1. Kinetic Symmetry (Lower Limbs Ground Reaction Forces) [5 min after lumbar SMT intervention]

      Lower Limbs Ground Reaction Forces measured by the force platforms

    Secondary Outcome Measures

    1. Kinematic Symmetry (Linear Global Joint Centers Vectors Displacement) [5 min after lumbar SMT intervention]

      Linear Global Joint Centers Vectors Displacement measured by the 3D motion capture system

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 35 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Inclusion criteria

    The inclusion criteria for sample followed the assumptions below:
    • All young student participants had to be of both sexes, age between 18-35 years old.

    • All participants had to be pain free or asymptomatic, with regards to low back pain, in order to create homogeneity within the study sample.

    • All participants had to have at least a minimal score, (low level) of physical activity, evaluated by (IPAQ) questionnaire (International Physical Activity Questionnaire). This was done on the argument that the minimal score, already shows that the participants were minimally physically active. This also contributed in an indirect way to assure a certain degree of sample homogeneity, scoring the minimal level of physical activity to include in the study;

    • All participants were required to show the subluxations or vertebral dysfunctions in their lumbar spine, detected by motion palpation. Through the purposive sampling, was allowed participants to officially take part in the study.

    Exclusion Criteria:
    The exclusion criteria for sample followed the assumptions below:
    • Participants who received medical, surgical or in addition manual interventions prior or during the study, were immediately excluded.

    • Participants who presented with any contraindications to manipulation on spine, which included but was not limited to osteomyelitis, tuberculosis, infectious arthritis, disc extrusion, hemangioma, vertebral malignancy and advanced spondylolisthesis

    • Participants who have participating of sports competitions or change in training routine during the collecting data, was immediately withdraw from the study.;

    • Participants with no vertebral dysfunction in the palpated lumbar joints were excluded of the study;

    • Participants who did not sign the informed consent form, or not agree of the conditions, or did not have conditions to compromise with the schedule, were immediately withdraw from the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bruno Araújo Procópio de Alvarenga Lisbon Portugal 1700-228

    Sponsors and Collaborators

    • University of Lisbon
    • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

    Investigators

    • Principal Investigator: Bruno Alvarenga, Phd, ULisboa

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Bruno Araújo Procópio de Alvarenga, PT, DC, Phd Student, Physiotherapist and Chiropractor, University of Lisbon
    ClinicalTrials.gov Identifier:
    NCT03361592
    Other Study ID Numbers:
    • Ulisboa
    First Posted:
    Dec 5, 2017
    Last Update Posted:
    May 3, 2018
    Last Verified:
    Apr 1, 2018
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Bruno Araújo Procópio de Alvarenga, PT, DC, Phd Student, Physiotherapist and Chiropractor, University of Lisbon
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 3, 2018