Global Posture Reeducation (GPR) Compared To Isostretching in Chronic Low Back Pain Patients

Sponsor
Centro Universitario de Maringa (Other)
Overall Status
Unknown status
CT.gov ID
NCT01468298
Collaborator
(none)
40
1
2
16
2.5

Study Details

Study Description

Brief Summary

The aim of this study was to investigate the changes in posture, flexibility, muscle strength, functional capacity, heart rate(HR), peripheral oxygen saturation, systolic blood pressure, diastolic blood pressure and intensity of pain in chronic low back pain underwent to Isostretching and GPR.

Condition or Disease Intervention/Treatment Phase
  • Other: Isostretching
  • Other: Global Posture Reeducation
Early Phase 1

Detailed Description

It was selected 40 patients, from 40 to 59 years old, with chronic low back pain from CESUMAR Physiotherapy Clinic-Schoo. These were evaluated before and after treatment regarding posture by SAPO computer program; flexibility for lumbar Schober testing, sit and reach; muscle strength by dynamometry for trunk extensors and the maximum repetition test in a minute to abdominal and trunk extensors; functional capacity by Rolland-Morris Questionnaire; pain by visual analog scale; heart rate(HR) by polar frequencymetric; peripheral oxygen saturation by Finger Pulse Oximeter; and systolic and diastolic blood pressure with a Sphygmomanometer. The sample was divided in two groups (1-GPR with 11 patients, 2-Isostretching with 10 patients). All patients were accompanied by an individual treatment program composed by 12 sessions of 45 minutes, twice a week. It was considered statistically significant p values <0.05 obtained from the Student's t test.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparing the Global Posture Reeducation With Isostretching in Chronic Low Back Pain Patients
Study Start Date :
Aug 1, 2010
Actual Primary Completion Date :
Oct 1, 2011
Anticipated Study Completion Date :
Dec 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Isostretching

Other: Isostretching
All of patients were accompanied by an individual treatment program composed by 12 sessions of 45 minutes, twice a week. The Isostretching method includes therapeutic different postures, lying, sitting or standing, and the positions were selected according to the postural changes of each patient, identified in the assessment. The Isostretching protocol involves nine positions held for a period of nine breaths, and every three cycles, the patient should rest for a period. The physical therapist used verbal commands to emphasize pursed lip breathing, self growth, curvatures correction and isometric of abdominal, paravertebral, quadriceps and gluteal muscles with the aim of optimizing the stretching and discouraging compensatory movements.
Other Names:
  • postural reeducation
  • Active Comparator: Global Posture Reeducation

    Other: Global Posture Reeducation
    All patients were accompanied by an individual treatment program composed by 12 sessions of 45 minutes, twice a week, involving a series of active gentle movements and postures aimed at realigning joints, stretching shortened muscles and enhancing the contraction of antagonist muscles, thus avoiding postural asymmetry. The positions were selected according to the postural changes of each patient, identified in the assessment and these therapeutic postures imply an active involvement of the patient. The protocol includes three therapeutic postures, lying, sitting or standing, to be held for 15 minutes each. The physical therapist used verbal commands and manual contact to maintain the alignment and make the necessary postural corrections, with the aim of discouraging compensatory movements.
    Other Names:
  • postural reeducation
  • Outcome Measures

    Primary Outcome Measures

    1. functional capacity [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      Low back patients functional capacity were evaluated before and after 10 sesssions treatment regarding by Rolland-Morris Questionnaire.

    Secondary Outcome Measures

    1. Posture [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      Posture were evaluated before and after 10 sessions treatment regarding posture by computer SAPO (Softwere Avaluation Posture Online) program.

    2. flexibility [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      These were evaluated before and after 10 sessions treatment regarding posture, flexibility for lumbar Schober testing and sit and reach.

    3. muscle strength [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      These were evaluated before and after 10 sessions treatment regarding muscle strength by dynamometry for trunk extensors and the maximum repetition test in a minute to abdominal and trunk extensors.

    4. heart rate(HR) [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      It was measured heart rate (HR)by polar frequencymetric at start and for every 15 minutes in 10 sessions therapy.

    5. peripheral oxygen saturation [Before and after 10 sessions and for every 15 minutes in therapyPatients will be followed for the duration of 10 sessions, an expected average of 5 weeks..]

      It was measured peripheral oxygen saturation (SpO2) by Finger Pulse Oximeter at start and for every 15 minutes in therapy.

    6. systolic blood pressure [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks..]

      It was measured systolic blood pressure (SBP) with a Sphygmomanometer at start and for every 15 minutes in 10 sessions therapy. Blood pressure measurement was obtained by arterial occlusion by inflation of the cuff, correlating to the auscultation of the heartbeat with the values recorded in the column of mercury. The sounds perceived during the blood pressure measurement procedure are called Korotkoff sounds, and classified into five phases, with phase 1 (first sound) corresponding to the value of systolic blood pressure (SBP).

    7. diastolic blood pressure [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      It was measured diastolic blood pressure (DBP) with a Sphygmomanometer at start and for every 15 minutes in 10 sessions therapy.Blood Ppressure measurement was obtained by arterial occlusion by inflation of the cuff, correlating to the auscultation of the heartbeat with the values recorded in the column of mercury. The sounds perceived during the blood pressure measurement procedure are called Korotkoff sounds, and classified into five phases, with phase 5 (muffling or disappearance of sound) corresponding value of diastolic blood pressure (DBP).

    8. Intensity of Pain [Patients will be followed for the duration of 10 sessions, an expected average of 5 weeks.]

      The low back intensity of pain were evaluated before and after 10 sessions treatment regarding pain by visual analog scale.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • patients with non-specific LBP in its chronic phase (pain lasting more than 12 weeks), from 40 to 60 years old.
    Exclusion Criteria:
    • scheduling conflicts

    • lack of transportation

    • disease that compromises their health during the treatment

    • uncontrolled hypertension

    • fibromyalgia

    • history of spinal surgery in the last six months

    • patients with neurological diseases

    • individuals who demonstrate inability to understand or physical restraint for the exercises.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centro Universitário de Maringá Maringá Paraná Brazil 87050390

    Sponsors and Collaborators

    • Centro Universitario de Maringa

    Investigators

    • Principal Investigator: Ligia M Facci, doctor, Centro Universitario de Maringa

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ligia Maria Facci, Principal Investigator, Clinical Professor, Centro Universitario de Maringa
    ClinicalTrials.gov Identifier:
    NCT01468298
    Other Study ID Numbers:
    • 249/2010
    First Posted:
    Nov 9, 2011
    Last Update Posted:
    Nov 9, 2011
    Last Verified:
    Oct 1, 2011
    Keywords provided by Ligia Maria Facci, Principal Investigator, Clinical Professor, Centro Universitario de Maringa
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 9, 2011