| Literature DB >> 35055646 |
Francisco M Kovacs1,2, Natalia Burgos-Alonso2,3, Ana María Martín-Nogueras2,4, Jesús Seco-Calvo2,5,6.
Abstract
A systematic review was conducted to assess the efficacy and effectiveness of education programs to prevent and treat low back pain (LBP) in the Hispanic cultural setting. Electronic and manual searches identified 1148 unique references. Nine randomized clinical trials (RCTs) were included in this review. Methodological quality assessment and data extraction followed the recommendations from the Cochrane Back Pain Review Group. Education programs which were assessed focused on active management (3 studies), postural hygiene (7), exercise (4) and pain neurophysiology (1). Comparators were no intervention, usual care, exercise, other types of education, and different combinations of these procedures. Five RCTs had a low risk of bias. Results show that: (a) education programs in the school setting can transmit potentially useful knowledge for LBP prevention and (b) education programs for patients with LBP improve the outcomes of usual care, especially in terms of disability. Education on pain neurophysiology improves the results of education on exercise, and education on active management is more effective than "sham" education and education on postural hygiene. Future studies should assess the comparative or summatory effects of education on exercise, education on pain neurophysiology and education on active management, as well as explore their efficiency.Entities:
Keywords: Hispanic cultural setting; education programs; non-specific low back pain; systematic review
Mesh:
Year: 2022 PMID: 35055646 PMCID: PMC8776076 DOI: 10.3390/ijerph19020825
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Figure 1PRISMA Flow Diagram of This Study.
Main Characteristics of the Studies Included in the Systematic Review.
| Study | Study | Setting | Follow-Up | N° of Subjects Included in the Analysis | Age (Years) 1 | Intervention/s in the Experimental Group/s (EG) | Intervention/s in the Control Group (CG) | Statistical Analysis | Comments |
|---|---|---|---|---|---|---|---|---|---|
| Cluster randomized | Nursing homes | 6 months | N = 661 | M(R) | Usual care + 20 min talk, provided to groups of ≤20 participants, followed by hand out of a booklet (content consistent with the talk) | Usual care | Mixed linear random-effects models | The same physician provided the education programs to all groups. He was told that the same effect was expected in both EGs, he had no opinion on their comparative effectiveness (both before and after the study) and was blind to subjects’ recruitment and assessment. An independent observer was present at the talks, and reported no differences across groups | |
| Cluster randomized | Primary care | 6 months | N = 348 | M(IQR) | Usual care + EG1 and EG2: one 15 min talk on active management for low back pain, provided to groups of ≤20 participants, and handing out of a booklet with a consistent content | Usual care + one 15 min talk on the importance of weight control and healthy nutrition habits for the management of low back pain, provided to groups of ≤20 participants, and handing out of a booklet with a consistent content | Generalized estimating | Subjects in the CG were told that weight control was very important for LBP | |
| Cluster randomized | School | 98 days | N = 497 | M(R) 1 | Handing out of a booklet on active management in class, adapted for 8-year-old children | No intervention | Intraclass | ||
| Cluster randomized | School | 3 months | N = 137 | M(SD) | 6, one-hour sessions on postural hygiene + 4 talks on anatomy and physiology of the spine, pathophysiology of low back pain, risk factors, ergonomics, and postural hygiene + 2 “practical sessions”; postural analysis, carrying objects, balance, analysis of the content and form of carry for schoolbags, breathing and relaxation | No intervention | Repeated-measures analysis | ||
| Randomized controlled | Primary care | 9 months | N = 100 | M(SD) | Usual care + face-to-face explanation of the program to each participant + As many contacts with researchers as participants wished (they could contact the research team by phone 5 days/week), with at least one face-to-face patient visit once a year + a website-based, educational program, including videos in which explanations were provided using audio and subtitles. Three videos were planned to be seen daily, from Monday to Friday, for 9 months:
A 2 min video on postural hygiene at a computer workstation (ergonomically appropriate placement of the computer screen and the mouse pad, seat height, height of the armrest, etc.) A 7 min video on exercise (strengthening, flexibility, mobility and stretching, of abdominal, lumbar, hip and thigh muscles). Participants were asked not to perform any other physical exercise routine during the 9 month intervention period Viewing the same 2 min video on postural hygiene, once again + One reminder sent by e-mail (with instructions on how to access the Website), every day from Monday through Friday at 10 am, for 9 months | Usual care | Student’s | ||
| Cluster randomized | School | 3 months | N = 357 | M(R) | One educational session on ergonomic criteria for selecting, loading and carrying a backpack (including the criterion to restrict carried items in the backpack to the minimum required). The content and distribution of items in the backpack on that very day, were analyzed | No intervention | Student’s | ||
| Cluster randomized | School | 8 months | N = 84 | M(SD) 1 | Education on physical exercise, in two 13 min sessions of exercise per week, during 32 weeks | No intervention | Chi-square and | ||
| Cluster randomized | School | 3 months | N = 137 | M(SD) 1 | 6, one-hour sessions on postural hygiene | No intervention | One-way analysis of variance | ||
| RCT | Physical therapy practices | 3 months | N = 56 | M(SD) | Usual care + exercise (motor control exercises, stretching, and aerobic exercise):
Session 1: exercises were demonstrated and performed by participants under supervision of a physiotherapist Session 2 (one month later). Same as session 1, confirming proper execution of exercises Patients instructed to complete the exercise program on their own, daily for 3 months. Compliance assessed + education on neurophysiology of pain ( Session 1: verbal explanation + visual presentation + leaflet reinforcing contents. Session 2, one month later: content of session 1 was reinforced, and questions answered | Usual care + exercise (motor control exercises, stretching, and aerobic exercise):
Session 1: exercises were demonstrated and performed by participants under supervision of a physiotherapist. Session 2 (one month later). Same as session 1, confirming proper execution of exercises Patients instructed to complete the exercise program on their own, daily for 3 months. Compliance assessed | Pearson chi-square test and |
RCT, randomized clinical trial; I, intervention; EG, experimental group; CG, control group; M(R): mean (range). M(IQR): mean (IQR: interquartile range). M(SD): Mean (Standard Deviation). 1 As per the Spanish law, children are grouped in class based on year of birth (e.g., all the children born between 1 January 2015 and 31 December 2015, are grouped in the same class). Therefore, the age of all the students in a school class is homogenous.
Results.
| Study | Outcome | Results (At the End of Follow-Up) | Comments |
|---|---|---|---|
| Disability (RMDQ) |
Results at the cluster level. Results from mixed linear random-effects models: additional improvement over the control group [effect size (95%IC)]: | This study included subjects with and without low back pain when entering the study. | |
| Disability (RMDQ) | Results of the generalized estimating equations (GEE), adjusted for potential confounders, reflecting the improvement in each experimental group additional to the one in the control group [effect size (95% CI)] | ||
| Appropriate knowledge (scoring | Results of the generalized estimating equations (GEE), adjusted for potential confounders, reflecting the probability of “appropriate knowledge” in the EG over the CG [effect size (95% CI)] | ||
| Healthy habits score | Results from a repeated-measures analysis of co-variance (ANCOVA) | Actual scores in each group, are not disclosed (only graphically represented, separately for each of the items scored) | |
| Disability RMDQ | Change from baseline to post-intervention assessment (“intention to treat” analysis). | Only results from the “intention to treat” analysis are shown. Results from the “per protocol” analysis were consistent | |
| Weight of the backpack (kg) (mean ± SD) | Student’s | Calculations based on the Number Needed to Treat (NNT) suggest that for every 100 children following the education program, 51 will reduce the weight of their backpacks to <15% of their bodyweight | |
| Number (%) of subjects reporting LBP in the previous week | Student’s | ||
| “Healthy backpack use | Repeated-measures analysis of co-variance (ANCOVA): | Actual scores in each group are not disclosed (only graphically represented, separately for each of the items scored) | |
| Disability (RMDQ), differences between scores at baseline and at 3 month follow-up | Between-group difference in the variation of the score (Pearson chi-square or Student’s | All differences were in favor of EG (a clinically positive change may imply a positive or negative score across variables, due to differences in the measuring instruments) |
EG, experimental group; CG, control group; CI, confidence interval. RMDQ: Roland–Morris Disability Questionnaire, ODI: Oswestry Low Back Pain Disability Index, VAS, visual analog scale, SF12: Spanish version of Short Form 12 (PCS; Physical Component Summary, MCS: Mental Component Summary), FAB-Phys: Fear Avoidance Beliefs on physical activity, CSQ: Coping Strategies Questionnaire, TSK: Spanish version of Tampa Scale for Kinesiophobia, PGIC: Patient Global Impression of Change, EQ-5D-3L (TTO): EuroQol-5Dimensions-3 Levels utility index (Time Trade-Off method). *: Shirado–Ito tests [53]. Scores ranges: RMDQ; 0 (no disability) to 24 (maximum disability). ODI: 0 (no disability) to 100 (maximum disability), VAS and NPRS: 0 (no pain) to 10 (worst imaginable pain). SF-12 PCS: 71.67 (best possible physical quality of life) to 2.86 (worst possible). SF-12 MCS: 71.24 (best possible mental quality of life) to 11.61 (worst possible). FAB-Phys: 0 (=no fear avoidance beliefs) to 30 (highest possible fear avoidance beliefs), CSQ: 0 = no catastrophizing, 36 = worst possible catastrophizing, EQ-5D-3L (TTO): 1 = best possible health-related quality of life (HRQL), 3 = worst possible HRQL. Shirado–Ito test; 120 s: best possible muscle endurance, 0 s: worst possible one. NPRS or NPRS11: Numeric Pain Rating Scale. TSK-11: 11 = no kinesiophobia, 44 = worst possible degree of kinesiophobia. PGIC: 7 (maximum possible self-perception of improvement) to 0 (minimum).
Sources of Risk of Bias [24].
| Bias Domain | Source of Bias | Studies | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Kovacs et al. (2007) [ | Albadalejo et al. | Kovacs et al. (2011) [ | Vidal et al. (2011) [ | Del Pozo-Cruz et al. (2012) [ | Gallardo Vidal | Rodriguez Garcia | Vidal et al. (2013) [ | Bodes-Pardo | ||
| Selection | (1) Was the method of randomization adequate? |
|
|
|
|
|
|
|
|
|
| Selection | (2) Was treatment allocation concealed? |
|
|
|
|
|
|
|
|
|
| Performance | (3) Was the patient blinded to the intervention? 1 |
|
|
|
|
|
|
|
|
|
| Performance | (4) Was the care provider blinded to the intervention? 2 |
|
|
|
|
|
|
|
|
|
| Detection | (5) Was the outcome assessor blinded to the intervention? |
|
|
|
|
|
|
|
|
|
| Attrition | (6) Was the drop-out rate described and acceptable? |
|
|
|
|
|
|
|
|
|
| Attrition | (7) Were all randomized participants analyzed in the group which they were allocated? |
|
|
|
|
|
|
|
|
|
| Reporting | (8) Are reports of the study free of suggestion of selective outcome reporting? |
|
|
|
|
|
|
|
|
|
| Selection | (9) Were the groups similar at baseline regarding the most important prognostic indicators, or were potential differences adjusted for at the analysis phase? |
|
|
|
|
|
|
|
|
|
| Performance | (10) Were cointerventions avoided |
|
|
|
|
|
|
|
|
|
| Performance | (11) Was the compliance acceptable in all groups? |
|
|
|
|
|
|
|
|
|
| Detection | (12) Was the timing of the outcome assessment similar in all groups? |
|
|
|
|
|
|
|
|
|
| Other | (13) Are other sources of potential bias unlikely? |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
1: Because of the nature of the intervention, patients could not be blinded to whether they were receiving an intervention. However, in Kovacs 2007 and Albadalejo 2010, patients in the different groups received the same intervention; only the content of the education program was different, patients did not know that other groups were receiving different contents, and patients’ expectations were managed to be similar across groups. 2: Because of the nature of the intervention, the care provider could not be blinded. However, in Kovacs 2007 the care provider who gave the talks had no preferences on the content of the different education programs which were implemented in the control and the two experimental groups, either at the beginning and at the end of the trial, had been informed that the same outcome was to be expected across groups, and an independent physician audited that no differences in credibility or enthusiasm could be detected during the talks. Key, possible answers: Yes No Unsure .