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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02887430
Other study ID # UHREC/2016/2/011
Secondary ID
Status Not yet recruiting
Phase Phase 0
First received August 19, 2016
Last updated September 6, 2016
Start date September 2016
Est. completion date February 2017

Study information

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

Clinical Trial 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.


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.


Recruitment information / eligibility

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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Screening


Related Conditions & MeSH terms


Intervention

Other:
foot reflexology therapy
standard care and foot reflexology

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universiti Sultan Zainal Abidin

Outcome

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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