ClinicalTrials.gov
ClinicalTrials.gov Menu

High(Deadlift) Versus Low Intensity Motor Control Exercises on Low Back Pain

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01061632
Recruitment Status : Completed
First Posted : February 3, 2010
Last Update Posted : March 8, 2013
Sponsor:
Collaborators:
Umeå University
Norrlandskliniken
County Council of Norrbotten, Sweden
Information provided by (Responsible Party):
Luleå Tekniska Universitet

Brief Summary:
The aim of the study is to evaluate and compare the effects of high-intensity (deadlift) versus low-intensity motor control exercises on selfrated pain, function and symptoms on patients with peripherally mediated pain

Condition or disease Intervention/treatment Phase
Low Back Pain Procedure: High intensity motor control exercise (deadlift) Procedure: Low intensity motor control exercise Phase 2

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 70 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effects of High(Deadlift) Versus Low Intensity Motor Control Exercises on Patients With Peripherally Mediated Low Back Pain
Study Start Date : January 2010
Actual Primary Completion Date : March 2010
Actual Study Completion Date : January 2011

Resource links provided by the National Library of Medicine

U.S. FDA Resources


Intervention Details:
    Procedure: High intensity motor control exercise (deadlift)
    12 treatment sessions over a 8 week period is planned for the high intensity motor control exercise.
    Procedure: Low intensity motor control exercise
    12 sessions of low intensity motor control exercises over 8 weeks


Primary Outcome Measures :
  1. Selfrated function, symptoms and pain-rating [ Time Frame: 8 weeks, 6 month, 12 month ]

Secondary Outcome Measures :
  1. Functional capacity [ Time Frame: 8 weeks, 6 months ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   25 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • low back pain over 3 month
  • the pain must originate locally from the lowe back and be nociceptive

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01061632


Sponsors and Collaborators
Luleå Tekniska Universitet
Umeå University
Norrlandskliniken
County Council of Norrbotten, Sweden
Investigators
Study Director: Kerstin Öhrling, As professor Lulea University of Technology

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Luleå Tekniska Universitet
ClinicalTrials.gov Identifier: NCT01061632     History of Changes
Other Study ID Numbers: LTU_marklyft
First Posted: February 3, 2010    Key Record Dates
Last Update Posted: March 8, 2013
Last Verified: March 2013

Keywords provided by Luleå Tekniska Universitet:
deadlift
motor control
exercises
pain
function
functional capacity

Additional relevant MeSH terms:
Back Pain
Low Back Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms