Clinical Trials Directory

Trials / Completed

CompletedNCT02448888

Prevention and Treatment of Chronic Low Back Pain Through an Adapted Exercise Program

Prevention and Treatment of Chronic Low Back Pain Through an Adapted Exercise Program and General Exercise Recommendations Tailored to the Job on an Assembly Line Training Versus General Exercise Recommendations: Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Universidad San Jorge · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Objective: The purpose of this study is to investigate the effects of a adapted exercise program and general exercise recommendations compared with only general exercise recommendations for the management of chronic back pain among the workers of BSH (Bosch Siemens Hausgeräte), a manufacturing company.

Detailed description

Design: Randomized controlled trial. Participants: Subjects (N\_40 volunteers) experimental group (n\_20) control group (n\_20). All of the participants needs to be diagnosed with chronic back pain by a physician. Participants are going to be randomly assigned to two groups: a control group (CG), and experimental group (EG). Intervention: The experimental group is going to follow a home-exercise program designed specifically to compensate the overloads and strength necessities of the workplace, the patient enter the description of the workplace in a mobile application (APP) and the APP shows specific exercises that the patient needs to practice. The exercise program includes muscle strengthening, flexibility, and endurance training, during 2 months, 3 times/week and generla recommendations. The control group is going to receive only general recommendation (ACSM recommendations) with the same kind of mobile application to control the amount of exercise that each patient performs during the week. Data on pain intensity (BPI short form, Brief Pain Inventory), disability (Oswestry Low Back Pain Disability Questionnaire), functional assessment of the lumbar spine (EMG Flexion-relaxation test), amount of weekly physical activity (IPAQ), and number of sick leaves are going to be measured immediately before and after intervention and 3 months after the end of the intervention period.

Conditions

Interventions

TypeNameDescription
OTHERAdapted exercise2 months, 3 times/week
OTHERGeneral exercise recommendations2 months, 3 times/week

Timeline

Start date
2015-01-01
Primary completion
2015-11-01
Completion
2016-05-01
First posted
2015-05-20
Last updated
2016-11-09

Locations

2 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT02448888. Inclusion in this directory is not an endorsement.