| Literature DB >> 24346291 |
Gisela C Miyamoto1, Leonardo O P Costa1, Cristina M N Cabral1.
Abstract
OBJECTIVE: To systematically review the available evidence on the efficacy of the Pilates method in patients with chronic nonspecific low back pain.Entities:
Mesh:
Year: 2013 PMID: 24346291 PMCID: PMC4207151 DOI: 10.1590/S1413-35552012005000127
Source DB: PubMed Journal: Braz J Phys Ther ISSN: 1413-3555 Impact factor: 3.377
Figure 1Selection process for studies included in the analysis.
Study characteristics.
| Authors | Participants | Intervention |
|---|---|---|
| Gladwell et al.[ | Mean age: CG: 45.9 years; PG: 36.9 years; n=34 | CG: Normal activities and pain relief PG: Pilates method-based floor exercises with strengthening of abdominal, gluteus and back muscles and progression with movement of the limbs, 6 sessions with 1 hour of duration for 6 weeks |
| Gender: CG: 4 male and 10 female; PG: 3 male and 17 female | ||
| Duration of symptoms (mean±SD): CG: 139±148; PG: 115±101 months | ||
| Rydeard et al.[ | Mean age: CG: 34 years; PG: 37 years; n=39 | CG: Normal care, such as medical appointments when necessary PG: Static Pilates method-based-exercises in floor with the following progression: addition of hip extension and exercises in the Reformer, 12 sessions with 1 hour of duration and a home-based program (duration of 15 minutes) for 4 weeks |
| Gender: CG: 8 male and 13 female; PG: 6 male and 12 female | ||
| Duration of symptoms (median (interquartile range)): CG: 108 (12-240) months; PG: 66 (6-324) months | ||
| Rajpal et al.[ | Mean age: CG: 21.6 years; PG: 22.1 years; n=32 | 30 consecutive sessions CG: McKenzie for sitting and standing posture correction, 3 repetitions performed 15-20 times per day PG: Pilates method-based exercises on the floor, with breathing exercises and deep abdominal muscle contraction in supine, quadruped and sitting positions, 10 repetitions of 10 seconds |
| Gender: female | ||
| Duration of symptoms: >3 months in both groups | ||
| Curnow et al.[ | No specification of the participants characteristics; n=39 | 18 sessions for 6 weeks The 3 groups performed 4 Pilates-based exercises on the floor; 2 exercises involved abdominal contraction, one involved lateral elevation of lower limbs in supine and one involved back muscles contraction, 40 repetitions of each exercise. PG A: no additional exercises PG B: exercises and relaxation, during 3-5 minutes PG C: exercises, relaxation (for 3-5 minutes) and posture training involving hip flexion and eccentric psoas contraction (20 repetitions) |
| Da Fonseca et al.[ | Mean age: CG: 34.4 years; PG: 31.6 years; n=17 | CG: No intervention PG: Pilates method-based floor exercises (with the activation of deep abdominal muscles), with the following progression: lower limb movements with static back position and dynamic back position, 15 sessions of 1 hour duration, 2 sessions per week |
| Gender: 5 male and 12 female | ||
| Duration of symptoms: >6 months in both groups | ||
| Quinn et al.[ | Mean age: CG: 44.1 years; PG: 41.8 years; n=29 | CG: No intervention PG: Pilates method-based exercises based on the Body Control Pilates program 31 , 6 to 8 1-hour sessions and 15 minutes at home, 5 times per week for 8 weeks |
| Gender: female | ||
| Duration of symptoms (mean±SD): CG: 49.2 (49.2) months; PG: 57.6 (38.4) months | ||
| Wajswelner et al.[ | Mean age: CG: 48.9 years; PG: 49.3 years; n=87 | 12 sessions, 1-hour duration, for 6 weeks, with exercises prescribed at home CG: General exercises used in the treatment (e.g., stationary bike, stretching, resistance training) and 4 exercises performed at home PG: 6 to 12 Pilates method-based exercises in the Reformer and Cadillac and 1 to 4 Pilates method-based exercises performed at home on the floor or with support of a chair or wall, involving back exercises in all planes of movement |
| Gender: CG: 20 male and 23 female; PG: 19 male and 25 female | ||
| Duration of symptoms (mean±SD): CG:14.2±12.7; GP: 13.6±14.2 years | ||
| Miyamoto et al.[ | Mean age: CG: 38,3 years; PG: 40,7 years; n=86 | 12 sessions for 6 weeks, 2 times per week GC: Educational booklet and 12 telephone calls during a 6-week period GP: Pilates method-based floor exercises involving deep abdominal muscle contraction with stretching or strengthening of the back and lower limb muscles; 12 sessions, 1-hour duration, for 6 weeks |
| Gender: CG: 9 male and 34 female; PG: 7 male and 36 female | ||
| Duration of symptoms (mean±SD): CG: 56.7±53.5; PG: 73.3±79.6 months |
*CG: control group
PG: Pilates group
Studies included in the comparison between Pilates and minimal intervention considering pain at short term
Studies included in the comparison between Pilates and other types of exercises considering pain at short term
Studies included in the comparison between Pilates and minimal intervention considering disability at short term
Details of the extraction of data from studies, in mean and standard deviation.
| Authors | Participants | Before treatment | After treatment | 6 months after randomization | Results |
|---|---|---|---|---|---|
| Gladwell et al.[ | CG: 14 | CG: Pain RMVAS: 2.4 (0.9); | CG: Pain RMVAS: 2.4 (0.8); | --- | Statistically significant improvement in pain (p <0.05) but not disability |
| PG: 20 | Disability OSWDQ: 24.1 (13.4) | Disability OSWDQ: 18.1 (13.0) | |||
| PG: Pain RMVAS: 2.7 (0.9); | CG: Pain RMVAS: 2.2 (0.9); | ||||
| Disability OSWDQ: 19.7 (9.8) | Disability OSWDQ: 18.1 (11.2) | ||||
| Rydeard et al.[ | CG: 18 | CG: Pain: NRS-101: 30.4 (1.8); | CG: Pain NRS-101: 33.9 (1.5); | --- | Statistically significant improvement in pain (p=0.002) and disability (p=0.023) |
| PG: 21 | Disability RM: 4.2 (3.4) | Disability RM: 3.2 (0.4) | |||
| PG: Pain NRS-101: 23,0 (1,8); | PG: Pain NRS-101: 18.3 (1.5); | ||||
| Disability RM: 3,1 (2.8) | Disability RM: 2.0 (0.3) | ||||
| Rajpal et al.[ | CG: 15 | CG: Pain VAS: 4.4 (1.5) | CG: Pain VAS: 2.1 (0.8) | --- | Statistically significant improvement in pain (p<0.05) |
| PG: 17 | PG: Pain VAS: 5.6 (0.7) | PG: Pain VAS: 2.1 (0.7) | --- | Only statistically significant difference between Group A and B, with greater improvement in Group B (p=0.02) | |
| Curnow et al.[ | PG A: 13 | Without values | Without values | ||
| PG B: 14 | |||||
| PG C: 12 | |||||
| Da Fonseca et al.[ | CG: 9 | CG: Pain VAS: 6.1 (1.8) | CG: Pain VAS: 4.9 (2.5) | --- | Statistically significant improvement in pain (p<0.05) |
| PG: 8 | PG: Pain VAS: 5.9 (2.0) | PG: Pain VAS: 3.0 (3.4) | |||
| Quinn et al.[ | CG: 14 | CG: Pain VAS -101: 39.9 (19.9); | CG: Pain VAS -101: 44.6 (14.7); | --- | Statistically significant improvement in pain (p<0.05) but not disability |
| PG: 15 | Disability RM: 7.7 (5.0) | Disability RM: 7.5 (1.7) | |||
| PG: Pain VAS -101: 40.4 (14.6); | PG: Pain VAS -101: 30.9. (15.2); | ||||
| Disability RM: 6.9 (4.6) | Disability RM: 5.4 (1.0) | ||||
| Wajswelner et al.[ | CG: 43 | CG: Pain NRS: 4.6 (1.8); Disability | CG: Pain NRS: 3.2 (2.1); Disability | CG: Pain NRS: 2.2 (1.7); Disability | No statistically significant difference for any comparison at short and medium term |
| PG: 44 | Quebec: 23.9 (14.0) | Quebec: 17.1 (13.4) | Quebec: 13.0 (11.4) | ||
| PG: Pain NRS: 4.9 (1.6); Disability | PG: Pain NRS: 2.8 (1.6); Disability | PG: Pain NRS: 2.5 (1.8); Disability | |||
| Quebec: 28.1 (11.4) | Quebec: 15.3 (9.1) | Quebec: 14.1 (10.4) | |||
| Miyamoto et al.[ | CG: 43 | GC: Pain NRS: 6.5 (1.7); Disability | GC: Pain NRS: 5.2 (2.3); Disability | GC: Pain NRS: 5.3 (2.3); Disability | Statistically significant improvement in pain and disability (p<0.05) at short term but not at medium term |
| PG: 43 | RM: 10.5 (5.4) | RM: 7.1 (5.7) | RM: 6.7 (5.6) | ||
| GP: Pain NRS: 6.6 (1.5); Disability | GP: Pain NRS: 3.1 (2.3); Disability | GP: Pain NRS: 4.5 (2.2); Disability | |||
| RM: 9.7 (4.5) | RM: 3.6 (3.4) | RM: 4.5 (4.5) |
*CG: control group
PG: Pilates group
VAS: visual analogue scale (0-10) for pain evaluation
OSWDQ: Oswestry Low Back Pain Disability Questionnaire (0-100) for disability evaluation
RMVAS: Roland Morris pain rating visual analogue scale (0-10) for pain evaluation
NRS: 101-point numerical rating scale (0-100) for pain evaluation
RM: Roland Morris Disability Questionnaire (0-24) for disability evaluation
VAS-101: visual analogue scale (0-100) for pain evaluation
NRS: numerical rating scale (0-10) for pain evaluation
Evaluation of methodological quality.
| Criteria | Gladwell et al.[ | Rydeard et al.[ | Rajpal et al.[ | Curnow et al.[ | Da Fonseca et al.[ | Quinn et al.[ | Wajswelner et al.[ | Miyamoto et al.[ |
|---|---|---|---|---|---|---|---|---|
| 1. Eligibility criteria were specified | yes | yes | yes | no | yes | yes | yes | yes |
| 2. Subjects were randomly allocated to groups (in a crossover study, subjects were randomly allocated an order in which treatments were received) | yes | yes | yes | yes | yes | yes | yes | yes |
| 3. Allocation was concealed | no | yes | no | no | no | yes | yes | yes |
| 4. The groups were similar at baseline regarding the most important prognostic indicators | yes | yes | no | no | yes | yes | yes | yes |
| 5. There was blinding of all subjects | no | no | no | no | no | no | no | no |
| 6. There was blinding of all therapists who administered the therapy | no | no | no | no | no | no | no | no |
| 7. There was blinding of all assessors who measured at least one key outcome | yes | yes | no | no | no | yes | no | yes |
| 8. Measures of at least one key outcome were obtained from more than 85% of the subjects initially allocated to groups | no | yes | yes | no | yes | no | yes | yes |
| 9. All subjects for whom outcome measures were available received the treatment or control condition as allocated or, when this was not the case, data for at least one key outcome was analysed by "intention to treat" | no | yes | no | no | no | yes | yes | yes |
| 10. The results of between-group statistical comparisons are reported for at least one key outcome | yes | yes | yes | yes | no | yes | yes | yes |
| 1. The study provides both point measures and measures of variability for at least one key outcome | yes | yes | yes | no | yes | yes | yes | yes |
| Score 0/10 | 5 | 8 | 4 | 2 | 4 | 7 | 7 | 8 |
*yes=1 point; no=0; Criterion 1 was not used to calculate the PEDro score.
Figure 2Forest plot of the results of the meta-analysis. A) Comparison of the Pilates method with minimal intervention for pain. The values shown are the average effects (difference between means) and the 95% confidence interval. The average effect was calculated using a fixed-effects model for short-term pain relief. B) Comparison of the Pilates method with other types of exercises for pain. The values shown are the average effects (difference between means) and the 95% confidence interval. The average effect was calculated using a fixed-effects model for short-term pain relief. C) Comparison of the Pilates method with minimal intervention for disability. The values shown are the average effects (difference between means) and the 95% confidence interval. The average effect was calculated using a random-effects model for short-term changes in disability.