Effectiveness of adding a large dose of shoulder strengthening to current nonoperative care for subacromial impingement
The verdict
Does adding a large dose of extra shoulder strengthening exercises to standard non-surgical care improve outcomes for people with subacromial impingement?
Adding a high-volume home-based shoulder strengthening program on top of usual non-surgical care did not improve shoulder disability, strength, or pain compared with usual care alone. About half of all patients still had unacceptable symptoms after four months regardless of which group they were in.
ChallengesRead paper
Primary study200 ParticipantsStrong evidence
Key points
- 200 patients with long-standing subacromial impingement were randomised to usual care alone or usual care plus a progressive home elastic-band program designed to at least double the strengthening dose
- SPADI scores improved similarly in both groups by roughly 22 points, well below the 10-point threshold needed to declare the added program superior
- No between-group difference was found for any secondary outcome including shoulder strength, range of motion, pain, or quality of life
- Only 54% of the intervention group and 48% of the control group reached an acceptable symptom state at four months
- Patients in the intervention group spontaneously reduced time on usual-care exercise, suggesting many cannot or will not increase their overall exercise burden
How it was conducted
- Design
- Pragmatic double-blind randomised controlled superiority trial (SExSI Trial)
- Participants
- 200 adults aged 18-65 with subacromial impingement lasting more than 3 months referred to an orthopaedic outpatient clinic in Denmark
- Groups
- Control: usual non-surgical care. Intervention: usual care plus home-based progressive elastic-band shoulder strengthening program
- Add-on intervention
- Three rotator-cuff exercises with elastic band performed to contraction failure, 3 phases over 16 weeks, prescribed time under tension of approximately 12 hours
- Primary outcome
- Shoulder Pain and Disability Index (SPADI, 0-100) at 4-month follow-up; minimal clinically important difference set at 10 points
- Follow-up
- 5 weeks, 10 weeks, and 4 months
What they found
- Primary outcome SPADI, baseline to 4 months: intervention group improved by -22.1 points (95% CI, -26.6 to -17.6); control group improved by -22.7 points (95% CI, -26.4 to -19.0); between-group mean difference 0.6 points (95% CI, -5.5 to 6.6), P = .8518
- SPADI pain subscale between-group difference: 2.3 points (95% CI, -4.6 to 9.1)
- SPADI function subscale between-group difference: -0.7 points (95% CI, -6.7 to 5.3)
- Abduction strength between-group difference at 4 months: -0.01 Nm/kg (95% CI, -0.04 to 0.02), P = .6280
- External rotation strength between-group difference at 4 months: 0.01 Nm/kg (95% CI, -0.01 to 0.02), P = .2062
- Abduction range of motion between-group difference at 4 months: 3.7 degrees (95% CI, -4.6 to 12.1), P = .3819
- Patient Acceptable Symptom State (PASS) at 4 months: 54% intervention vs 48% control, P = .4127
- Global impression of change (recovered or much improved) at 4 months: 24% intervention vs 27% control, P = .5751
- Actual mean total time under tension completed in the intervention group: 2.9 hours (10,468 seconds) vs prescribed 12 hours
- Intervention group spent on average 35 min/week on usual-care exercise vs 51 min/week in the control group
- Post-hoc analysis adjusting for usual-care exercise time showed no between-group difference: MD 0.2 points (95% CI, -6.0 to 6.3)
- Symptom exacerbations lasting at least 1 week: 49 in intervention group, 47 in control group; no serious adverse events
Limitations
- Actual adherence to the add-on program (mean 2.9 hours) was substantially below the prescribed 12 hours, though the achieved dose was still argued to be clinically meaningful based on prior evidence
- Patients in the intervention group reduced time on usual-care exercise despite instructions not to, potentially diluting the between-group contrast
- Missing primary outcome data at 4 months was 19% overall and higher in the intervention group, although this was likely to bias results in favour of the intervention rather than against it
- The four-month follow-up may be too short to detect longer-term benefits of higher-dose strengthening, though it corresponds to the standard clinical decision point for reassessment
Why it matters
- For patients
- If you have shoulder impingement and are already doing physiotherapy-guided exercises, doing a large amount of additional home strengthening is unlikely to reduce your pain or disability further, and about half of people still have bothersome symptoms after four months of non-surgical care regardless.
- For clinicians
- This high-quality RCT shows that simply prescribing more volume of home-based rotator-cuff strengthening on top of usual care does not improve outcomes for subacromial impingement; future efforts should explore patient education, self-management support, and identifying which patients may benefit from second-line interventions including surgery.
- For readers
- The trial confirms that for a common and stubborn shoulder condition, more exercise is not automatically better, and highlights a significant treatment gap since roughly half of patients remain symptomatic after four months of best available non-surgical care.
Source
doi:10.1177/03635465211016008
Read the original paperClinically assessing this area? See the shoulder special tests.
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