A randomised controlled pilot study of Neuro Emotional technique for low back pai

Phase 2

Completed

• Conditions: ow back pain; Low back pain; Alternative and Complementary Medicine - Other alternative and complementary medicine

• Registration Number: ACTRN12607000650493
• Lead Sponsor: Mr. Peter Bablis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-12-20
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

participants suffering from low back pain less than three months

Exclusion Criteria

acute low back pain (<3 months duration); < 18 years of age; currently undergoing other manual therapy or psychological intervention; presence of red flag” conditions; pregnancy; abdominal pain; vascular disease; motor vehicle accident or falls in last 3 months; neurological signs and symptoms; organic kidney, urinary tract or reproductive disease; straight leg raise of < 30°; previous spinal surgery; and bowel, bladder or sexual dysfunction.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual Analog Scale (VAS) of how much pain you are experiencing right now. <br>VAS of the typical or average pain you experience.<br>VAS of pain at its best. <br>VAS of pain at its worst.[1 month]

Secondary Outcome Measures

Name	Time	Method
Distress and Risk Assessment Method (DRAM)[1 month];Oswestry Low Back Pain Questionnaire[1 month]