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Effectiveness of an Electronic Decision Support System (DeSSBack) in Improving the Management of Low Back Pain

Not Applicable
Conditions
Lower Back Pain
Interventions
Other: DeSSBack
Registration Number
NCT04959669
Lead Sponsor
University of Malaya
Brief Summary

Low back pain is a common health problem where over than half a billion people worldwide suffers from it. In Malaysia, back pain is among the top ten reasons why people see a doctor. Although there are many guidelines available, healthcare professionals still find managing low back pain as challenging.

The Decision Support System for Low Back Pain (DeSSBack) has been developed by adopting and re-packaging STaRT system, incorporate with the local clinical practice guidelines and feedback from local experts. It aims to aid healthcare professionals in managing low back pain through a stratified approach.

The objective of the study is to evaluate the effectiveness of DeSSBack in improving the management of patients with low back pain in a primary care clinic. We hypothesise that the implementation of DeSSBack will improve the outcomes of low back pain patients including quality of life, emotional state and level of pain.

This study protocol presents the rationale and design of a cluster randomized controlled trial.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
210
Inclusion Criteria
  • Patient seeking care for low back pain at the primary care clinic in UMMC
  • Male and female
  • Age 18 years and above
  • Can understand Malay and English
Exclusion Criteria
  • Potentially serious pathology (eg: cauda equina compression, inflammatory arthritis, malignancy and etc)
  • Serious co morbidity
  • Psychiatric illness or personality disorder
  • Spinal surgery in the last 6 months
  • Pregnant
  • Already receiving treatment other than primary care for this episode of back pain
  • Inability to attend regular physiotherapy appointments.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupDeSSBackDeSSBack (Decision Support System for Low Back Pain)
Primary Outcome Measures
NameTimeMethod
Changes in health status measure for low back pain between baseline and 6-monthBaseline, 6-months

We are measuring the changes in health status with Rolland Morris Disability Questionnaire (RMDQ). The score ranges from a minimum of 0 to a maximum of 24. Greater levels of disability are reflected by higher scores.

Changes in health status measure for low back pain between baseline and 2-monthBaseline, 2-months

We are measuring the changes in health status with Rolland Morris Disability Questionnaire (RMDQ). The score ranges from a minimum of 0 to a maximum of 24. Greater levels of disability are reflected by higher scores.

Secondary Outcome Measures
NameTimeMethod
Changes in the Hospital Anxiety and Depression Scale (HADS) between baseline and 6-monthBaseline, 6-months

The HADS is a self-assessment questionnaire to assess states of anxiety and depression in the setting of hospital outpatient clinic. The minimum value is 0 and the maximum value is 21 for both anxiety and depression. The higher the score, the worse the outcome is.

Changes in the back pain severity score between baseline and 2-monthBaseline, 2-months

The back pain severity score is a self-assessment score to rate severity of the back pain. Patients would rate their back pain from 0 being no pain at all, to 10 being unbearable pain.

Changes in the back pain severity score between baseline and 6-monthBaseline, 6-months

The back pain severity score is a self-assessment score to rate severity of the back pain. Patients would rate their back pain from 0 being no pain at all, to 10 being unbearable pain.

Changes in the Hospital Anxiety and Depression Scale (HADS) between baseline and 2-monthBaseline, 2-months

The HADS is a self-assessment questionnaire to assess states of anxiety and depression in the setting of hospital outpatient clinic. The minimum value is 0 and the maximum value is 21 for both anxiety and depression. The higher the score, the worse the outcome is.

Trial Locations

Locations (1)

University of Malaya Medical Centre

🇲🇾

Kuala Lumpur, Malaysia

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