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NCT01061632 Clinical Trial

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

Low Back Pain Clinical Trial

Official title:
Effects of High(Deadlift) Versus Low Intensity Motor Control Exercises on Patients With Peripherally Mediated Low Back Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01061632
Other study ID # LTU_marklyft
Secondary ID
Status Completed
Phase Phase 2
First received January 20, 2010
Last updated March 7, 2013
Start date January 2010
Est. completion date January 2011

Study information
Verified date March 2013
Source Luleå Tekniska Universitet
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial 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

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date January 2011
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- low back pain over 3 month

- the pain must originate locally from the lowe back and be nociceptive

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

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

Locations
Country Name City State
n/a

Sponsors (4)
Lead Sponsor Collaborator
Luleå Tekniska Universitet County Council of Norrbotten, Sweden, Norrlandskliniken, Umeå University

Outcome
Type Measure Description Time frame Safety issue
Primary Selfrated function, symptoms and pain-rating 8 weeks, 6 month, 12 month Yes
Secondary Functional capacity 8 weeks, 6 months Yes
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