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Advance
Back School
1.Information
about the anatomy and function of the spine,
spinal biomechanics,
pathology physiology back disorders,
epidemiology.
Now a days, this part of back school (giving
information) is limited as compared to the back
school in 1969
3. Active Exercises
Active protection of the spine by active exercises,
Example
A. Flank breathing versus diaphragmatic breathing:
The pressure-changes in the abdomen resulting from
diaphragmatic breathing causes some instability in the
low back. Flank breathing maintains the tension in the
abdominal muscles. (So there is no instability in the lower
back).
We teach patients
S y s t e m a t i c R e v i e w
2011
RCT
3
2013
2011
2008
Search methods
MEDLINE
EMBASE databases and
the Cochrane Central Register of Controlled
Trials
Trials reported in English, Dutch, French or
German.
The literature search :
articles updated to November 2004.
OBJECTIVES
The objective of this systematic review was to
determine if back schools are more effective
than other treatments or no treatment for
patients with non-specific LBP.
METHODS
Criteria for considering studies for this review
Types of studies
Only randomized controlled trials (RCTs) were
included.
Nonrandomized trials were excluded.
Types of participants
Randomized controlled trials that included
subjects with
nonspecific LBP,
aged 18 to 70 years, were included.
Types of interventions
Randomized controlled trials in which one of the
treatments consisted of a back school type of
intervention were included.
1. return to work,
2. pain (VAS),
3. a global measure of improvement (overall
improvement, proportion of patients recovered,
subjective improvement of symptoms), and
4. functional status (expressed on a back-specific
index, such as the Roland Disability
Questionnaire or the Oswestry Scale) were
included .
meta-analysis, but
CONCLUSIONS
There is moderate evidence that back schools
conducted in occupational settings seem to be
more effective for patients with recurrent and
chronic LBP (as opposed to patients from the
general population or primary/secondary care)
than other treatments.
The most promising interventions consisted of a
modification of the Swedish back school and
were quite intensive (a three to five-week stay
in a specialized centre).
Objective
The purpose of this study was to compare the
effectiveness of Back School and McKenzie
methods in patients with chronic nonspecific
low back pain.
Design
The study was a prospectively registered,
2-arm randomized controlled trial with a
blinded assessor.
Setting
Outpatient physical therapy clinic of the
Universidade Cidade de Sao Paulo, Brazil.
From July 2010 and July 2012.
Inclusion Criteria
nonspecific low back pain of at least 3
months duration
between 18 and 80 years of age.
Exclusion Criteria
Patients with any contraindication to physical
exercise (American College of Sports Medicine)
serious spinal pathology
(eg, tumors,fractures, inflammatory diseases)
previous spinal surgery
nerve root compromise
cardiorespiratory illnesses or
pregnancy were excluded.
Randomization
A total of 148 subjects were enrolled out
of which :
74 were randomized into the Back School
group and
remaining 74 were assigned into the
McKenzie group
Interventions
Participants from both groups received 4, onehour sessions over 4 weeks, once a week.
All participants received the exercises under the
supervision of the physical therapist.
At the end of each treatment session,
participants were asked to perform the same
exercises at home once a day (3 sets of 10
repetitions that could be performed on the same
day or in different times of day depending on the
patients availability).
McKenzie group
Result
The author observed a reduction in pain intensity
and disability after treatment (1 month) in both
groups.
Participants allocated to the McKenzie group had
greater improvements in disability (treatment
effect;2.37 points, 95% CI;0.76 to 3.99) after
treatment (at 1-month follow-up).
There was no statistically significant between
group difference for pain (treatment effect:0.66
points, 95% CI:0.29 to 1.62).
Most of the
observed at
maintained
randomization
outcomes.
improvements in outcomes
short-term follow-up were
at 3 and 6 months after
for both primary and secondary
Conclusion
Patients allocated to the McKenzie group
experienced greater improvements in disability,
but not in pain intensity, after treatment
compared with patients allocated to the Back
School group, but the magnitude of this effect
was small and possibly of doubtful clinical
importance.
Objective:
To evaluate the effectiveness of the addition of
back school to exercise and physical treatment
modalities in relieving pain and improving the
functional status of patients with chronic low
back pain.
Design:
A randomized controlled trial.
Setting
Physical Medicine and Rehabilitation Clinic of
Meram Medical Faculty of Selcuk University,
Turkey
Inclusion Criteria
Patients who had had non-specific low back
pain
low back pain for longer than 12 weeks
without neurological deficits
Exclusion Criteria
subjects who had
continuous pain with a score above 8 on VAS,
age 18 years,
who had already attended the back school
programme,
who had undergone previous surgery,
who had structural anomalies,
spinal cord compressions,
severe instabilities,
severe osteoporosis,
acute infections,
severe cardiovascular or metabolic diseases,
who were pregnant, and
those with a body mass index above 30kg/m2
Evaluation criteria
Patients were evaluated
at the beginning,
after the treatment and
at 3 months post-treatment
1. for pain severity by VAS and
1. for functional aspects by Oswestry Low
Back Pain Disability Questionnaire (ODQ)
Sample
A total of 160 patients, who were referred or
self-referred to our outpatient clinic with
CLBP took part in this study.
Interventions
1. Exercise programme.
lumbar flexion exercises,
lumbar extension and
lumbar stretching exercises, and
strengthening exercises for the thighs.
The exercise programme was run by the same
physiotherapist, who was blinded to which
group the patient was allocated to,
in patient groups of 5 in an exercise room.
2. Physical therapy
A physical therapy programme, including
TENS,
ultrasound and
hot pack
once daily,
5 days a week
for 2 weeks,
totaling 10 sessions
Randomization
Samples were randomized in to two groups
Group 1 and Group 2
RESULTS
A total of 146 patients completed the study
and attended the third-month control visits .
The mean age in the BSG
was 47.25 years (SD 11.22 years), whereas it
was 51.36 years (SD 9.65 years) in the CG.
There was no statistically significant
difference between the groups in terms of
age, gender, body mass index, occupation or
education (p > 0.05).
Within-groups
The decrease in VAS and ODQ values preand post-treatment was statistically
significant in both study groups
(VAS: 95% CI = 4.685.15; 5.125.58, ODQ:
95% CI = 39.8342.18; 43.5945.94, for BSGCG, respectively).
These result were statistically significant (p
< 0.01).
Between-groups
There was a significant reduction in VAS in the
BSG compared with the CG after the treatments
and at 3 months post-treatment
(0.665, 95% CI = 0.5640.767 and 0.205,
95% CI = 0.070 0.340).
These results were statistically significant
(p = 0.010 and p = 0.002, respectively).
DISCUSSION
The author
observed that a back school
programme has an effect on pain and disability
when given in addition to physical treatment
modalities and exercises.
This effect was observed post-treatment and
at 3 months follow-up.
Objectives
To evaluate the effectiveness of a back school
program in
pain,
functional status,
quality of life, and in anxiety and
depression
in patients with non-specific low back pain.
Exclusion criteria
This constituted
previous back surgery,
spinal tumor,
spinal fracture,
pregnancy,
fibromyalgia,
inflammatory or infectious spinal diseases
and
litigant patients
Procedures
1. Intervention group:
back school program,
which consisted of 5 one-hour group sessions
(four
consecutive once a week sessions and a fifth
reinforcement session after 30 days).
Sessions were instructed by a rheumatologist
and a physical therapist for groups of 10
participants.
Control group:
patients were seen at 3 medical visits within a
four-week period (Week 1; Week 2; Week 4)
and at a fourth visit 30 days after Week 4.
Each medical visit was conducted by a
rheumatologist (other than the back school
instructor).
Follow-up assessment
The first assessment (T0) took place
immediately after randomization and before
initiating the intervention at a maximum
interval of seven days.
Other assessment visits took place 30 (T30), 60
(T60) and 120 (T120) days after initiating the
intervention.
Results
There were no significant differences in the
baseline characteristics between the two
groups.
Fifty-five patients completed the study.
The intervention group showed a significant
improvement in the general health domain,
assessed by SF-36, and also in the reduction of
acetaminophen and NSAID intake.
Conclusion
The back school program was more effective
than any educational intervention in general
health status and in decreasing acetaminophen
and NSAID intake.
It was ineffective in the other quality of life
domains, in pain, functional status, anxiety and
depression.