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. 2014 Mar 14;2014(3):CD003007. doi: 10.1002/14651858.CD003007.pub3

Choi 2005.

Methods Randomised
Participants 75 patients, mean age 46.09 years, male and female, with primarily leg pain not responding to conservative treatment, who had undergone discectomy
Interventions Intervention (I: n = 35): advice, lumbar extension exercise handout, home exercise for six weeks, then intensive training for 12 weeks. MedX system, which restricts hip and pelvic motion Control (C: n = 40): advice, lumbar extension exercise handout, six weeks of home‐based exercise, continued for another 12 weeks
Outcomes Pain intensity (VAS): largely decreased in both exercise and control groups after 12 weeks of extension exercise. (I) 2.51 and (C) 4.3 (P < 0.05) post‐treatment, (I) 1.5 and (C) 1.3 at one year (no significant difference). Functional status (ODI): Postoperative ODI scores were improved compared with preoperative ODI scores (I) 24.6 and (C) 30.6 post‐treatment (no significant difference). Return to work: More than 92% returned to work within six months after surgery. (I) 87% and (C) 24% returned within four months
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Participants were randomly assigned/participants and methods paragraph one
Allocation concealment (selection bias) Unclear risk Participants were randomly assigned/participants and methods paragraph one
Blinding (performance bias and detection bias) 
 All outcomes ‐ patients? High risk Home based versus clinic based
Blinding (performance bias and detection bias) 
 All outcomes ‐ care providers? High risk Home based versus clinic based
Blinding (performance bias and detection bias) 
 All outcomes ‐ outcome assessors? High risk Participants were not blinded, patient reported outcomes
Incomplete outcome data (attrition bias) 
 All outcomes ‐ drop‐outs? High risk Five of 40 IG dropout (patient and methods paragraph two and Table 1), less than 20% but not similar in groups
Incomplete outcome data (attrition bias) 
 All outcomes ‐ ITT analysis? High risk Five dropouts
Selective reporting (reporting bias) Low risk Pain VAS, function ODI
Similarity of baseline characteristics? Unclear risk Only age reported, 51.05 versus 42.02, = significantly different
Co‐interventions avoided or similar? Unclear risk Not described
Compliance acceptable? Unclear risk Not described
Timing outcome assessments similar? Low risk Patients and methods paragraph four: baseline six weeks, paragraph six: follow‐up at 12 weeks, one year