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Clinical Trials/NCT02714803
NCT02714803
Completed
Phase 2

Assistant Professor

Ataturk Training and Research Hospital1 site in 1 country61 target enrollmentMarch 2015
ConditionsLow Back Pain

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Ataturk Training and Research Hospital
Enrollment
61
Locations
1
Primary Endpoint
Change in low back pain intensity as measured by Visual Analog Scale
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The aim of this study is to compare of different massage techniques plus conservative aplications in low back pain treatment.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
October 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Ataturk Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Seyda TOPRAK CELENAY

Assistant Professor

Ataturk Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Having non specific low back pain without any relevant ongoing pathologies such as disc prolapse, spondylolisthesis, fractures, tumor, osteoporosis, infection
  • Willing to participate

Exclusion Criteria

  • Spinal surgery in the past 6 months or having to undergo surgery or invasive examinations during the study;
  • neurological disease;
  • psychiatric disease;
  • serious chronic disease that could interfere with the outcomes (e.g., cardiovascular disease, epilepsy, rheumatoid arthritis),
  • pregnant during the study

Outcomes

Primary Outcomes

Change in low back pain intensity as measured by Visual Analog Scale

Time Frame: Change from baseline low back pain intensity at 2 weeks

Secondary Outcomes

  • Change in psychologic statue as assessed by Hospital Anxiety and Depression Scale(Change from baseline psychologic statue at 2 weeks)
  • Change in quality of life as assessed by Short Form-36(Change from baseline quality of life at 2 weeks)
  • Change in functional statue as assessed by Oswestry Disability Index(Change from baseline functional statue at 2 weeks)

Study Sites (1)

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