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Clinical Trials/IRCT2016080620888N6
IRCT2016080620888N6CompletedPhase 2

Comparing the Effects of Standard Rehabilitation Protocol and Standard Rehabilitation Protocol in Combination with Exercise Therapy, on Functional Disability and Pain in Subjects Affected by Non Specific Low Back Pain

Isfahan University of Medical Sciences, Vice Chancellory of Research and Technology0 sites40 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
40

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20 years to 55 years (—)
Sex
All

Inclusion Criteria

  • Inclusion Criteria: meeting at least 5 items of following items: remaining pain even after 7 days of treatment; pain duration less than 6 weeks; no symptoms distal to the knee; one or more hypo-mobile segments in the lumbar spines; Oswestry disability score = 25%; pain intensity = 30% (Visual Analogue Scale).
  • Exclusion criteria: spine fracture/surgery in the previous 6 months; pregnancy; neoplasia; infection of the spine; visceral pain; systemic disorders; radicular pain due to radiculopathy in last 6 months; sensory impairments; abnormal deep tendon reflexes or muscular weakness due to nerve compression; neurological claudication; psychiatric disorders; osteoporosis; corticosteroid therapy; receiving spinal manipulation previously for the same LBP episode; back pain; segmental spinal instability; administering narcotics; those who may not cooperate; those with contraindications for spinal manipulation; those who meet red flag conditions like fever; trauma; unusual weight loss.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Isfahan University of Medical Sciences, Vice Chancellory of Research and Technology

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