Low Back Pain Clinical Trial
Official title:
The Effect of Foot Reflexology Therapy on Pain Intensity and Health-related Quality of Life in People With Non-specific Low Back Pain
Verified date | September 2016 |
Source | Universiti Sultan Zainal Abidin |
Contact | n/a |
Is FDA regulated | No |
Health authority | Malaysia: Institutional Review Board |
Study type | Interventional |
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.
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | February 2017 |
Est. primary completion date | October 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
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. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Screening
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Universiti Sultan Zainal Abidin |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | mean time in days to the recovery of pain | 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) | 5 months | No |
Secondary | demographic information | demographic information including age, ethnicity, marital status, educational level, weight, height, household monthly income, smoking status, alcohol consumption, co-morbid disease and categories of low back pain. | 3 month | No |
Secondary | side effects of treatment | reporting of possible side effects of the treatment, both reflexology and medication | 5 month | No |
Secondary | health-related quality of life | measuring mean of health-related quality of life using Euro-quality of life 5D questionnaire before and after intervention | 5 months | No |
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