Author (year) Study quality | Outcome measures | Results pain | Results disability | Original review authors conclusions |
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Byström et al. (2013) [48] AMSTAR-2 Moderate | Pain: NRS, VAS Disability: ODI, RMDQ Follow-up: Short-term: > 6 wks ≤ 4 mo Intermediate: > 4 and ≤ 8 mo Long-term: > 8 and ≤ 15 mo | MCE > GE Short-term (7 trials) WMD = -7.89 (95%CI -10.95;-4.65) Intermediate (7 trials) WMD = -6.06 (95%CI -10.94; -1.18) MCE = MT All time periods (3 trials) MCE > MI Short-term (2 trials) WMD = -12.48 (95%CI -19.04; -5.93) Intermediate (2 trials) WMD = -10.18 (95%CI 16.64; -3.72) Long-term (2 trials) WMD = -13.32 (95%CI 19.75; -6.90) MCE > MM-PT Intermediate (4 trials) WMD = -14.20 (95%CI -21.23; -7.16) | MCE > GE Short-term (7 trials) WMD = -4.65 (95%CI -6.20; -3.11) Intermediate (7 trials) WMD = -4.86 (95%CI -8.59; -1.13) Long-term (7 trials) WMD = -4.72 (95%CI -8.81;—0.63) MCE > MT Short-term (3 trials) WMD = -6.12 (95%CI -11.94; -0.30) Intermediate (3 trials) WMD = -5.27 (95%CI -9.52; -1.01) Long-term (3 trials) WMD = -5.76 (95%CI -9.21; -2.32) MCE > MI Short-term (3 trials) WMD = -9.00 (95%CI 15.28; -2.73) Intermediate (3 trials) WMD = -5.62 (95%CI -10.46; -0.77) Long-term (3 trials) WMD = -6.64 (95%CI -11.72; -1.57) MCE > MM-PT Intermediate (4 trials) WMD = -12.98 (95%CI -19.49; -6.47) | MCE seem to be superior to several other treatments. More studies are needed to investigate subgroups. |
Elbayomy et al. (2018) [51] AMSTAR-2 Low | Pain: VAS Disability: RMDQ Follow up: Shortterm: ≤ 3 mo from randomization Intermediate term: between 3 and 12 mo Long-term: ≥ 12 mo from randomization | CE > GE Short-term (15 trials) MD = -1.18 (95%CI 1.68; -0.67) Intermediate (8 trials) MD = -0.92 (95%CI -1.5; -0.35) Long-term (5 trials) MD = -0.11 (95%CI -0.52; 0.31) CE = MT Short-term (2 trials) MD = 0.39 (95%CI -0.98; 0.20) Intermediate (3 trials) MD = -0.55 (95%CI -1.39; 0.29) Long-term (2 trials) MD = -0.26 (95%CI -0.87; 0.35) CE > MI Short-term (2 trials) MD = -1.26 (95%CI -1.85; -0.67) Intermediate (4 trials) MD = -1.25 (95%CI -2.01; -0.49) Long-term (3 trials) MD = -1.3 (95%CI -1.85; -0.74) CE > MM-PT Short-term (6 trials) MD = -0.35 (95%CI -0.99; 0.29) | CE > GE Short-term (14 trials) SMD = -0.98 (95%CI -1.46; -0.50) Intermediate (8 trials) SMD = -0.59 (95%CI -1.03; -0.15) Long-term (4 trials) SMD = -0.04(95%CI -0.21; 0.12) CE = MT Short-term (2 trials) SMD = -0.12 (95%CI -0.40; 0.16) Intermediate (3 trials) SMD = -0.09 (95%CI -0.31; 0.12) Long-term (3 trials) SMD = -0.07 (95%CI -0.27; 0.13) CE > MI Short-term (3 trials) SMD = -0.66 (95%CI -1.08; -0.24) Intermediate (4 trials) SMD = -0.37 (95%CI -0.75; 0.02) Long-term (3 trials) SMD = -0.29 (95%CI -0.73; 0.14) CE > MM-PT Short-term (3 trials) SMD = -0.5 (95%CI -0.87; -0.13) | CE reduced pain and disability at short and intermediate term more than GE, level of evidence from low to moderate. Low evidence support that CE reduce disability more than MT. No clinically important difference between CE and MT. Low to moderate evidence suggest CE has significant effect on pain more than MI at all follow-up periods and on disability at short-term. |
Ferreira et al. (2006) [49] AMSTAR-2 Low | Pain: VAS Disability: RMDQ Follow up: Short-term: ≤ 3 mo Intermediate term: ≥ 3 and ≤ 12 mo Long-term: ≥ 12 mo | MCE > UC Short-term (2 trials) ES = -21 (95%CI -32; -9) Intermediate (2 trials) ES = -24 (95%CI -38; -1) MCE = MT Short-term / Long-term (2 trials) NR in text MCE + Educ > MM Short-term (2 trials) ES = -11 (95%CI -13; -9) Intermediate (2 trials) ES = -11 (95%CI -18; -5) Long-term (1 trial) ES = -9 (95%CI -15; -3) MCE + UC = UC Short-term (3 trials): NR | MCE = MT Short-term (2 trials) ES = -5 (95%CI -12; 1) Intermediate term (2 trials) ES = -9 (95%CI -16; -2) MCE = MT Short/ long-term (2 trials) NR in text MCE + Educ > MM Short-term (2 trials) ES = -20 (95%CI -27; -13) Intermediate (2 trials) ES = -4 (95%CI -7; -1) MCE + Educ = MM Long-term (1 trial) ES = -3 (95%CI -6; 0) MCE + UC = UC Short-term (3 trials): NR | The authors suggest that specific stabilization exercise is an effective treatment option for many forms of spinal pain. It is not clear if the improvements in pain and disability are associated with changes in the pattern of muscle activation. |
Gomes-Neto et al. (2017) [52] AMSTAR-2 Moderate | Pain: VAS Disability: RMDQ Follow up: Post-intervention | MCE > GE Baseline to study end (8 trials) WMD = -1.03 (95%CI -1.79; 0.27) MCE = MT Baseline to study end (3 trials) WMD = -0.38 (95%CI -0.98; 0.22) | MCE > GE Baseline to study end (4 trials) WMD = -5.41 (95%CI -8.34; -2.49) MCE = MT Baseline to study end (3 trials) WMD = -0.17 (95%CI -0.38; 0.03) | Based on relatively low-quality data that led to a high risk of bias. Additional research is required to ascertain the positive effects of MCE over time. |
Henao & Bedoya (2016) [40] AMSTAR-2 low | Pain: VAS Disability: ODI, RMDQ Follow-up: Short-term: post-intervention (6–8 wks) Intermediate term: 3 mo Long-term: > 6 mo | MCE = GE No difference between MCE and GE in short or long-term (1 trial) | MCE = GE No difference between MCE and GE in short or long-term (1 trial) | Although there are no differences between MCE and GE concerning pain and disability in people in chronic LBP there is uncertainty as to whether there is consensus in defined exercise protocols of MCE and GE. It is necessary to develop an exercise protocol that demonstrates evidence that favors optimal lumbo-pelvic stability. |
Luomajoki et al. (2018) [53] AMSTAR-2 Moderate | Pain: VAS, NRS Disability: ODI, RMDQ Follow-up: Short-term: post-intervention Long-term: ≥ 12 mo | MvCE > control Short-term (9 trials) SMD = -0.39 (95%CI -0.69; -0.04) Long-term (5 trials) SMD = -0.27 (95%CI -0.62; -0.09) | MvCE > control Short-term (11 trials) SMD = -0.38 (95%CI -0.68; -0.09) Long-term (6 trials) SMD = 0.37 (95%CI -0.61; 0.04) | MvCE may be more effective in disability in the short and long-term compared to other interventions. Pain was reduced through MvCE treatment in short but not in long-term. |
Macedo et al. (2009) [54] AMSTAR-2 Moderate | Pain: VAS Disability: ODI Follow up: Short term: ≤ 3 mo Intermediate term: > 3 and < 12 mo Long term: ≥ 12 mo | MCE = GE All time intervals Short term (4 trials) Intermediate (3 trials) Long term (3 trials) MCE > MT Intermediate (4 trials) WMD = -5.7 (95%CI -10.7; -0.8) MCE > MI Short-term (7 trials) WMD = -14.3 (95%CI -20.4; -8.1) Intermediate (7 trials) WMD = -13.6 (95%CI -22.4; -4.1) Long-term (7 trials) WMD = -14.4 (95%CI -23.1; -5.7) | MCE > GE Short-term (5 trials) WMD = -5.1 (95%CI -8.7; -1.4) MCE > MT Intermediate (4 trials) WMD = -4.0 (95%CI -7.6; -0.4) MCE > MI Long-term (7 trials) WMD = -10.8 95%CI (-18.7; -2.8) | MCE is more effective than MI and add benefit to another form of intervention in reducing pain and disability in LBP. The optimal implementation of MCE is unclear. Future trials need to study dosage parameters, feedback and subgroups. |
Niederer & Mueller (2020) [55] AMSTAR-2 Moderate | Pain: NRS, VAS Disability: ODI, RM Follow-up: Short-term: ≥ 1 < 3 mo Intermediate term: > 3 ≤ 12 mo Long term > 12 mo | MCE > Inactive, passive or other exercise Overall (13 trials) SMD = -0.46 (95%CI -0.78; -0.14) MCE > GE Short-term (3 trials) SMD = -0.53 (95%CI -1.20; -0.14) Intermediate (6 trials) SMD = -0.23 (95%CI -0.46; 0.01) Long-term (3 trials) SMD =- 0.29 (95%CI -0.56; -0.01) MCE = Inactive, passive Short-term (3 trials) SMD = -0.03 (95%CI -1.88; 0.03) Intermediate and long-term No difference | MCE > Inactive, passive or other exercise Overall (12 trials) SMD = -0.44 (95%CI -0.88; -0.09) MCE = GE Short-term (4 trials) SMD = 0.45 (95%CI -1.51; 0.60) Intermediate (5 trials) SMD = -0.16 (95%CI -0.37; -0.04) Long-term (3 trials) SMD = -0.25 (95%CI -0.59; 0.10) MCE = Inactive, passive Short-term (4 trials) SMD = -0.82 (95%CI -1.59; 0.04) Intermediate and Long-term No difference | MCE lead, with low to moderate quality evidence, to a sustainable improvement in pain intensity and disability in chronic non-specific LBP compared to an inactive or passive control group or compared to other exercises. |
Saragiotto et al. (2016) [16] AMSTAR-2 High | Pain: VAS Disability: RMDQ Follow-up: Short-term: 4–10 wks Intermediate term: 3–6 mo Long-term: 12–36 mo | MCE > GE Short-term (13 trials) MD = -7.53 (95%CI -10.54; -4.52) MCE = GE Intermediate and Long-term No difference MCE = MT No difference at any time point MCE > MI Short-term MD = -10.01 (95%CI -15.67; -4.35) intermediate MD = -12.61 (95%CI -20.53; -4.69) Long-term MD = -12.97 (95%CI -18.51; -7.42) MCE > GE + EPA Short-term MD = -30.18 (95%CI -35.32; -25.05) Intermediate MD = -19.39 (-36.83; -1.96) | MCE > GE Short-term (11 trials) MD = -4.82 (95%CI -6.95; -2.68) MCE = GE Intermediate and Long-term No difference MCE = MT No difference at any time point MCE > MI Short-term MD = -8.63(95%CI -14.78; -2.47) Intermediate MD = -5.47, (95%CI -9.17; -1.77) Long-term MD = -5.96 (95%CI -9.81; -2.11) MCE > GE and EPA Short-term MD = -20.83 (95%CI -28.07; -13.59) Intermediate MD = -11.5 (95%CI -20.69; -2.31) | MCE probably provides better improvements in pain, function and global impression of recovery than MI at all follow-up periods. MCE may provide slightly better improvements than exercise and EPA for pain, disability, global impression of recovery and the physical component of QoL in the short/intermediate term. There is probably little or no difference between MCE and MT for all outcomes and follow-up periods. |
Smith et al. (2014) [56] AMSTAR-2 High | Pain: VAS Disability: RMDQ Follow-up: Short-term: ≤ 3 mo Intermediate term: > 3 and < 12 mo Long term: ≥ 12 mo | MCE > Any treatment/control Short-term (22 trials) MD = -7.93 (95%CI -11.74; -4.12) Intermediate (22 trials) MD = -6.10 (95%CI -10.54; -1.65) Long-term (22 trials) MD = -6.39 (95%CI -10.14; -2.65) MCE > GE Short-term MD = -7.75 (95%CI -12.23; -3.27) Intermediate MD = -4.24 (95%CI -8.27; -0.21) MCE = GE Long-term MD = -3.06 (95%CI -6.74; 0.63) | MCE > Any treatment/control Short-term (24 trials) MD = -3.61 (95%CI -6.53 to -0.70) Long-term (24 trials) MD = -3.92 (95%CI -7.25 to -0.59) MCE = Any treatment/control Intermediate no difference MD = -2.31 (95%CI -5.85; 1.23) MCE > GE Short-term MD = -3.63 (95%CI -6.69; -0.58) Intermediate MD = -3.56 (95%CI -6.47; -0.66) MCE = GE Long-term No difference | MCE improve LBP symptoms, but are no better than any other form of active exercise in the long-term. |
Wang et al. (2012) [57] AMSTAR-2 Low | Pain: VAS, NRS Disability: RM, ODI Follow-up: Short term: < 3 mo Intermediate: 6 mo Long term: ≥ 12 mo | MCE > GE Short-term MD = -1.29 (95%CI -2.47; -0.11) MCE = GE No difference at intermediate or long-term | MCE > GE Short-term MD = -7.14 (95%CI -11.64; -2.65) MCE = GE No difference at intermediate or long-term | Compared to GE, MCE is more effective in decreasing pain and may improve physical function in patients with chronic LBP in the short-term but not in long-term. |
Zhang et al. (2021) [58] AMSTAR2 High | Pain NRS, VAS Disability RMDQ, ODI QLBPDSQ Follow up Posttreatment Intermediate 6 mo Long-term 12 and 24 mo | MCE > other exercises Posttreatment (11 trials) WMD = -0.65 (95%CI -1.05; -0.25) MCE = other exercises Intermediate 6 months (2 trials) WMD = -0.09 (95%CI -0.31; 0.14) Long-term 12 mo (3 trials) WMD = -0.13 (95%CI -0.32; 0.06) MCE = MT Posttreatment (4 trials) WMD = -0.06 (95%CI -0.26, 0.13) Intermediate 6 mo (2 trials) WMD = 0.25 (95%CI -0.48; 0.01) Long-term 12 mo (1 trial) WMD = 0.00 (95%CI -0.33; 0.33) Long term 24 mo (1 trial) WMD = -0.08 (95%CI -0.54; 0.38) MCE > MI Posttreatment (4 trials) WMD = -0.44 (95%CI -0.78, -0.09) MCE = MI Intermediate 6 mo (2 trials) WMD = -0.23 (95%CI -0.49; 0.04) Long-term 12 mo (1 trial) WMD = 0.04 (95%CI -0.31; 0.22) Long-term 24 mo (1 trial) WMD = -0.50 (95%CI -1.06; 0.07) | MCE > other exercises Posttreatment (11 trials) WMD = -0.56 (95%CI -0.98; -0.18) MCE = other exercises Intermediate 6 mo (2 trials) WMD = -0.16 (95%CI -0.39; 0.07) Long-term 12 mo (2 trials) WMD = -0.10 (95%CI -0,33; 0.13) MCE = MT Posttreatment (4 trials) WMD = 0.12 (95%CI -0.10, 0.35) Intermediate 6 mo (2 trials) WMD = -0.07 (95%CI -0.30; 0.16) Long-term 12 mo (2 trials) WMD = -0.16 (95%CI -0.39; 0.08) Long-term 24 mo (1 trial) WMD = -0.19 (95%CI -0.66; 0.27) MCE > MI Posttreatment (4 trials) WMD = -0.70 (95%CI -1.40, -0.01) MCE = MI Intermediate 6 mo (2 trials) WMD = -0.15 (95%CI -0.41; 0.12) Long-term 12 mo (2 trial) WMD = -0.12 (95%CI -0.38; 0.14) Long-term 24 mo (1 trial) WMD = -0.00 (95%CI -0.56; 0.56) | Low to very low quality of evidence supported that MCE resulted in a reduction of pain and disability posttreatment than other treatments for NSCLBP. |