NCT00555802

Brief Summary

The purpose of this study was to evaluate the efficacy of motor control exercises. For this, before and after motor control and general exercises, we determined transverses abdominis and multifidus thickness, activity limitation and pain. We hypothesized that the motor control exercises would increase transverses abdominis and multifidus muscles thickness. Activity limitation and pain would decrease following two protocols that it was more in motor control group than general one.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
49

participants targeted

Target at P25-P50 for not_applicable low-back-pain

Timeline
Completed

Started Apr 2006

Typical duration for not_applicable low-back-pain

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2006

Completed
1.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2007

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

November 8, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 9, 2007

Completed
Last Updated

January 29, 2008

Status Verified

November 1, 2007

First QC Date

November 8, 2007

Last Update Submit

January 25, 2008

Conditions

Keywords

Low Back PainMotor Control ExerciseGeneral exerciseUltrasonography, MultifidusTransversus abdominisRandomized Controlled trial.

Outcome Measures

Primary Outcomes (1)

  • Before and after intervention, we assessed the multifidus and abdominal muscles thickness (mm) using a 7.5 MHz B-mode transducer ultrasound, pain through visual analog scale and activity limitation through Back Performance Scale.

    Baseline, 16 weeks

Secondary Outcomes (1)

  • Weight, Age, height,BMI,Current duration of pain,Time since first onset

    baseline

Interventions

exercise

Also known as: training

Eligibility Criteria

Age20 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • nonspecific low back pain with or without leg pain of at least 3 months duration
  • currently seeking care for low back pain
  • aged greater than 18 and less than 80 years
  • suitable for motor control exercise based on clinical assessment
  • The patients must also have sufficient knowledge of the Persian language to understand instructions

You may not qualify if:

  • suspected or confirmed serious spinal pathology (fracture, metastatic, inflammatory or infective diseases of the spine, cauda equine syndrome, widespread neurological disorder)
  • suspected or confirmed pregnancy
  • nerve root compromise (2 of strength, reflex or sensation affected for same nerve root)
  • spinal surgery
  • any of the contraindications to exercise listed on page 42 of the ACSM guidelines

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dept. of physiotherapy, Zahedan university of medical scinces

Zahedan, Sistan & Bladchestan, Iran

Location

Related Publications (1)

  • Maher CG, Latimer J, Hodges PW, Refshauge KM, Moseley GL, Herbert RD, Costa LO, McAuley J. The effect of motor control exercise versus placebo in patients with chronic low back pain [ACTRN012605000262606]. BMC Musculoskelet Disord. 2005 Nov 4;6:54. doi: 10.1186/1471-2474-6-54.

    PMID: 16271149BACKGROUND

Related Links

MeSH Terms

Conditions

Low Back Pain

Interventions

Exercise

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Asghar Akbari

    Deputy of research, Zahedan university of medical scinces

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

November 8, 2007

First Posted

November 9, 2007

Study Start

April 1, 2006

Study Completion

November 1, 2007

Last Updated

January 29, 2008

Record last verified: 2007-11

Locations