The Efficacy of A Smartphone Application in Treating Non-Specific Low Back Pain

Low Back Pain Clinical Trial

Official title:

The Efficacy and Compliance of Using A Smartphone Application in Treating Non-Specific Low Back Pain Among Office Employees: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03994458
• Other study ID #: 20180429
• Status: Completed
• Phase: N/A
• Start date: August 1, 2019
• Est. completion date: February 1, 2020

Study information

• Verified date: February 2020
• Source: Jordan University of Science and Technology
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Evaluating the efficacy of a newly developed self-monitored mobile application in reducing office workers low back pain.

Description:

II. Introduction and Hypothesis of the Study:

Around 12% to 33% of the adult workforce are affected by low back pain (LBP) each year. Furthermore 70% to 95% of the adults are predicted to have back pain at least once in their lifetime (Van Tulder et al., 2006, Karthikeyan et al., 2013). There are numerus applications for self-management of LBP. These applications provided patients with cost-effective alternative management for their LBP. However, most of these available applications are of a low quality, because they were developed without an evidence-based vision (Machado et al., 2016).

Hypothesis:

1. All participants who will use the full access of the LBP application for six weeks will demonstrate significant decrease in low back pain intensity as measured by Visual Analogue Scale (VAS).

2. All participants who will use the full access of the LBP application for six weeks will demonstrate significant decrease in disability as measured by Oswestry Disability Index (ODI).

3. All participants who will use the full access of the LBP application for six weeks will demonstrate significant perceptual satisfaction and gained benefit as measured by self-rated survey questions.

III. Aims of the study: This study aims to evaluate the efficacy and compliance in using a standardized evidence-based LBP application among office employees who suffer from non-specific LBP, in randomized controlled trial.

IV. Materials and Methods: A smartphone application will be programed to deliver home-based exercises and advices targeting LBPP. 30 participants who has LBP, had been at least 5 years office worker have a 5 hours of working, will be recruited for a randomized controlled trial, participants who have any spine or spinal cord disease will be excluded. Participants will be compared according who will get full access to the application for non-specific LBP management with those who will get a limited version of the application. Both groups will use their versions of the application for 6 weeks, a follow-up will be done after 6 weeks. Visual Analog Scale (VAS), will be used to assess intensity of the LBP, and Oswestry Disability Index (ODI) will be used to assess the disability that had been caused by LBP. Descriptive statistics will be represented in means and standard deviations. Change scores between groups (experimental vs control) will be compared using ANCOVA model.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 41
• Est. completion date: February 1, 2020
• Est. primary completion date: January 1, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 30 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Being office worker for at least 5 years with at least 5 hours of working daily behind the desk.

2. Middle age adults, age between 30 and 55 years old.

3. Complains of LBP at least for 3 months measured by self-report

4. Scored at least 3 point on a 0-10 Visual Analog Scale.

5. Owning an android smartphone.

Exclusion Criteria:

1. Pregnancy.

2. Diagnosed with disc herniation with radiculopathy pain.

3. Structural deformities as in Scoliosis, or Kyphosis, or Lordosis.

4. Spinal tumor.

5. Ankylosing spondylitis, spondylolisthesis.

6. Had a spine surgery or significant trauma in the past 6 months.

7. Low mental ability of not being able to use smartphone.

Related Conditions & MeSH terms

• Back Pain
• Low Back Pain

Intervention

Behavioral:
• Smartphone Full version application
Android smartphone experimental application include: rehabilitative self-administered evidence-based exercises (Strengthening and stretching), ergonomics, and education related to low back pain. The application includes videos, photos, text, and reminders.
• Samartphone limited version application
Android smartphone placebo application include: ineffective content that does not help in treating low back pain. The application includes only five posts in the general instruction and advises section about proper nutrition and few irrelevant reminders.

Locations

Country	Name	City	State
Jordan	Jordan University of Science and Technology	Irbid

Sponsors (1)

Lead Sponsor	Collaborator
Jordan University of Science and Technology

Country where clinical trial is conducted

Jordan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Visual Analog Scale (VAS) scores	A measure used to evaluate pain related to low back pain. Score range is 0-10, where higher scores indicate more pain.	Change from basleine to 6 weeks will be assessed.
Primary	Change in Oswestry Disability Questionnaire (ODQ) scores	A measure used to evaluate disability related to low back pain. Score range is 0-100, where higher scores indicate more disability.	Change from basleine to 6 weeks will be assessed.
Secondary	Change in 12-item Short Form Health Survey (SF-12) scores	A measure of health related quality of life includes Physical Component Summary (PCS) and Mental Component Summary (MCS) scores. Score range is 0-100, where higher scores indicate better health related quality of life.	Change from basleine to 6 weeks will be assessed.
Secondary	Change in Depression, Anxiety, and Stress Scale (DASS21) scores	A measure used to assess mental health symptoms over the last week. Score range is 0-21, where higher scores indicate worse mental health.	Change from basleine to 6 weeks will be assessed.
Secondary	Change in Pittsburgh Sleep Quality Index (PSQI) scores	The PSQI assess sleep quality over previous month.Score range is 0-21, where higher scores indicate worse sleep quality.	Change from basleine to 6 weeks will be assessed.
Secondary	Change in International Physical Activity Questionnaire -short form (IPAQ-SF) scores	A measure collects the occurrence and time of physical activity with continuous high, moderate and low intensity for at least ten minutes during the previous 7 days. A higher score in this measure indicates higher physical activity level.	Change from basleine to 6 weeks will be assessed.