Increasing Days at Work Using Function-Centered Rehabilitation in Nonacute Nonspecific Low Back Pain: A Randomized Controlled Trial
Adult
Male
Chi-Square Distribution
Rehabilitation
Pain
Middle Aged
Statistics, Nonparametric
3. Good health
03 medical and health sciences
Treatment Outcome
0302 clinical medicine
Randomized controlled trial
Sick leave
Linear Models
Humans
Low back pain
Female
Single-Blind Method
Sick Leave
Low Back Pain
Physical Therapy Modalities
Pain Measurement
DOI:
10.1016/j.apmr.2004.10.044
Publication Date:
2005-05-06T22:48:44Z
AUTHORS (8)
ABSTRACT
To evaluate the effect of function-centered compared with pain-centered inpatient rehabilitation in patients whose absence from work is due to chronic nonspecific low back pain (LBP).Single-blinded randomized controlled trial with follow-up assessments immediately after treatment and at 3 months.Center for work rehabilitation in Switzerland.Patients with more than 6 weeks of work absence due to chronic nonspecific LBP (N=174; 137 men, 37 women; mean age +/- standard deviation, 42+/-8 y; mean sick leave before study, 6.5 mo).Function-centered treatment (FCT) (4h/d, 6d/wk, for 3 wk) consisted of work simulation, strength, endurance, and cardiovascular training. Pain-centered treatment (PCT) (2.5h/d, 6d/wk, for 3 wk) used a mini back school, individually selected passive and active mobilization, stretching, and low-intensity strength training.The number of days at work in 3 months after treatment, self-efficacy, lifting capacity, pain, mobility, strength, and global perceived effect. Effect sizes (ESs) (Cohen d ) were defined as small (ES range, 0.2-0.5), moderate (ES range, 0.5-0.8), and large (ES, >0.8).Groups were comparable at baseline. Moderate ESs for the FCT group versus PCT group were found for days at work (25.9 d vs 15.8d, ES=.36, P =.029), self-efficacy (5.9 points vs -7.4 points, ES=.55, P =.003), and lifting capacity (2.3 kg vs 0.2 kg, ES=.54, P =.004).Function-centered rehabilitation increases the number of work days, self-efficacy, and lifting capacity in patients with nonacute nonspecific LBP.
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