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. 2014 Nov 18;22:41. doi: 10.1186/s12998-014-0041-8

Table 4.

Intention to treat analysis

mCPR status treatment group time of measurement Outcome measures
VAS a ODI b SF-36 Pain c
(St. Dev.) (St. Dev.) (St. Dev.)
Negative on mCPR
SMT (n = 32)
  Baseline 58.44 (15.46) 35.13 (8.55) 5.56 (1.20)
  5-weeks 37.51 (28.89) 29.01 (14.66) 6.98 (1.66)
  12-weeks 43.29 (24.62) 32.14 (15.77) 6.41 (1.92)
  24-weeks 47.61 (25.66) 30.17 (15.69) 6.60 (2.06)
AET (n = 28)
  Baseline 65.36 (16.78) 37.04 (12.57) 5.35 (1.21)
  5-weeks 36.50 (33.77) 30.15 (17.71) 6.56 (2.33)
  12-weeks 42.00 (33.57) 32.91 (20.82) 6.54 (2.72)
  24-weeks 52.54 (27.24) 32.71 (18.64) 6.44 (2.47)
Positive on mCPR
SMT (n = 60)
  Baseline 61.25 (13.74) 33.62 (9.60) 5.78 (1.22)
  5-weeks 34.86 (31.18) 26.71 (15.06) 7.10 (2.22)
  12-weeks 40.43 (27.53) 29.64 (18.30) 6.57 (2.55)
  24-weeks 38.47 (26.99) 23.16 (15.74) 7.51 (2.71)
AET (n = 61)
  Baseline 55.38 (16.64) 31.44 (10.05) 6.00 (1.52)
  5-weeks 26.60 (33.48) 23.73 (17.14) 7.49 (2.57)
  12-weeks 36.30 (29.64) 25.94 (19.90) 7.05 (2.98)
  24-weeks 42.11 (31.77) 23.52 (18.98) 7.75 (3.08)

athe higher the number the higher the reported pain on a 100 point scale.

bthe higher the number the more disability reported due to pain on a 100 point scale.

cthe higher the number the less self-reported pain on the computed SF-36 pain subscale.