The effects of spinal manipulation added to exercise on pain and quality of life
In short
For thoracic (mid-back) spinal pain, does adding spinal manipulation to exercise relieve pain and improve quality of life more than exercise alone?
Adding spinal manipulation to exercise gave better pain relief and quality of life than exercise alone at the end of the 8-session treatment course, but that extra benefit had disappeared by the 12-week follow-up. Exercise alone held its gains while the manipulation advantage faded.
Mixed pictureRead paper
Primary study100 ParticipantsModerate evidence
Key points
- This single-centre randomized controlled trial compared manipulation plus exercise against exercise alone in 100 adults with thoracic spinal pain.
- Both groups improved significantly in pain and in all SF-36 quality-of-life domains over the study.
- After the 8th session the manipulation-plus-exercise group had significantly better pain and quality-of-life scores than exercise alone.
- At the 12-week follow-up there was no significant difference between the groups, because the manipulation group's gains faded while the exercise group's held.
- Authors suggest the manipulation benefit is short-term, possibly reflecting regression to the mean.
How it was conducted
- Design
- Open-label parallel-group randomized controlled trial (single centre, Lahore, Pakistan), computer-generated randomization with SNOSE allocation concealment, assessors and participants blinded
- Participants
- 100 adults with nonspecific thoracic (T1 to T12) spinal pain and mobility deficit, ages 16 to 60 (127 assessed, 27 excluded)
- Groups
- Experimental (n=50): high-velocity low-amplitude thoracic manipulation plus thoracic strengthening exercises. Control (n=50): thoracic exercises alone
- Dose and timing
- Twice weekly for 4 weeks, 8 sessions total; assessed at baseline, after 1st session, after 8th session, and at 12-week follow-up
- Primary outcomes
- Pain on a 10 cm visual analogue scale (VAS); quality of life on the SF-36
- Analysis
- Intention-to-treat with last observation carried forward; repeated-measures ANOVA (within group) and independent t-test (between group)
What they found
- Within both groups, VAS and all 8 SF-36 domains improved significantly (p<0.001).
- After the 8th session the manipulation group had significantly better pain, with a between-group mean difference of 1.14 (95% CI 0.62 to 1.65), and significantly better scores on all SF-36 domains (p<0.05).
- VAS fell from 6.50 (1.55) at baseline to 2.26 (1.08) after the 8th session in the experimental group, versus 6.58 (1.41) to 3.40 (1.48) in the control group.
- SF-36 physical functioning after the 8th session was 64.70 (16.94) experimental versus 55.46 (22.35) control.
- At the 12-week follow-up there was no significant between-group difference for pain or any quality-of-life domain (p>0.05); experimental-group VAS rose to 2.46 (1.23) while control-group VAS continued to 2.74 (1.06).
- Within the experimental group, quality of life dropped significantly from the 8th session to the 12-week follow-up (p<0.05 for all domains).
Limitations
- Data came from a single centre, limiting how widely the results apply.
- Follow-up was only 12 weeks, so longer-term effects are unknown.
- The manipulation force was not measured, so the treatment dose cannot be standardized or reproduced precisely.
- Pain chronicity (acute versus chronic) was not recorded, and acute and chronic pain may respond differently.
Why it matters
- For patients
- If you have mid-back pain, adding manipulation to your exercise program may speed up early pain relief, but exercise alone appears to hold its benefit better over a few months.
- For clinicians
- Thoracic manipulation can be a useful short-term add-on to exercise for thoracic spinal pain, but it offered no advantage over exercise alone by 12 weeks, so exercise should remain the foundation of care.
- For readers
- This is the first RCT testing manipulation added to exercise for thoracic spinal pain, and it shows a real but short-lived extra benefit that does not persist once treatment stops.
Source
doi:10.1155/2023/7537335
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