Skip to main content
Clinical Trials/NCT02887430
NCT02887430
Unknown
Early Phase 1

The Effect of Foot Reflexology Therapy on Pain Intensity and Health-related Quality of Life in People With Non-specific Low Back Pain

Universiti Sultan Zainal Abidin0 sites100 target enrollmentSeptember 2016
ConditionsLow Back Pain

Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Universiti Sultan Zainal Abidin
Enrollment
100
Primary Endpoint
mean time in days to the recovery of pain
Last Updated
9 years ago

Overview

Brief Summary

The aim of this study was to investigate whether the eight therapy session with foot reflexology can reduce pain intensity when applied as an addition to the standards care of low back pain according to the Malaysian low back pain management guidelines.

Detailed Description

Low back pain is a common health complaint in most societies. Many treatments for low back pain aim to reduce suffering quicken recovery and minimize recurrence or development of chronic disability. However, low back pain continues as a societal enigma. The aim of this study was to investigate whether the eight therapy session with foot reflexology can reduce pain intensity when applied as an addition to standards care of low back pain according to the Malaysian low back pain management guidelines. Analysis of health-related quality of life will also be carried out.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
February 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

nor dalila marican

Principle investigator

Universiti Sultan Zainal Abidin

Eligibility Criteria

Inclusion Criteria

  • Have been medically diagnosed with a non-specific low back pain.
  • Have not received treatment for low back pain within the previous 2 weeks.
  • Are at least 18 years old.
  • Have both feet and all toes intact and free from wounds.
  • Have not undergone any other complementary and alternative therapies during the study.

Exclusion Criteria

  • Have severe coexistent disease and serious pathology or systemic illness.
  • Have a specific diagnosed cause of back pain (infection, tumour, osteoporosis, fracture, an inflammatory condition or cauda equine syndrome).
  • Have plantar fasciitis.
  • Lack the ability to read and write Malaysia language.
  • Had plans to move out of the area.

Outcomes

Primary Outcomes

mean time in days to the recovery of pain

Time Frame: 5 months

the mean time in days to the recovery of pain is measured at the first day the patient scores 0 to 10 point on the visual analog scale (VAS)

Secondary Outcomes

  • demographic information(3 month)
  • side effects of treatment(5 month)
  • health-related quality of life(5 months)

Similar Trials