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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01061632
First Posted: February 3, 2010
Last Update Posted: March 8, 2013
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.
Collaborators:
Umeå University
Norrlandskliniken
County Council of Norrbotten, Sweden
Information provided by (Responsible Party):
Luleå Tekniska Universitet
January 20, 2010
February 3, 2010
March 8, 2013
January 2010
March 2010   (Final data collection date for primary outcome measure)
Selfrated function, symptoms and pain-rating [ Time Frame: 8 weeks, 6 month, 12 month ]
Same as current
Complete list of historical versions of study NCT01061632 on ClinicalTrials.gov Archive Site
Functional capacity [ Time Frame: 8 weeks, 6 months ]
Same as current
Not Provided
Not Provided
 
High(Deadlift) Versus Low Intensity Motor Control Exercises on Low Back Pain
Effects of High(Deadlift) Versus Low Intensity Motor Control Exercises on Patients With Peripherally Mediated Low Back Pain
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
Not Provided
Interventional
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Low Back Pain
  • 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
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
70
January 2011
March 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria:

Sexes Eligible for Study: All
25 Years to 60 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
 
NCT01061632
LTU_marklyft
No
Not Provided
Not Provided
Luleå Tekniska Universitet
Luleå Tekniska Universitet
  • Umeå University
  • Norrlandskliniken
  • County Council of Norrbotten, Sweden
Study Director: Kerstin Öhrling, As professor Lulea University of Technology
Luleå Tekniska Universitet
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP