Cacchio 2009b
Methods | RCT | |
Participants | Country: Italy Sample size: 24 Participants (8 in each group) Inclusion criteria: first ischaemic or haemorrhagic stroke (> 6 months); diagnosis of CRPS‐type 1 (pain VAS > 4 cm) Exclusion criteria: intra‐articular shoulder injection in the previous 6 months or systemic corticosteroid in the previous 4 months; another obvious explanation for pain; prior surgery to shoulder or neck region; serious uncontrolled medical conditions; global aphasia or cognitive impairments interfering with understanding instructions, motor testing and treatment; visual impairments interfering with aims of the study; evidence of recent alcohol or drug abuse; or severe depression |
|
Interventions | 3 arms:
1, 2 and 3: 5 days a week; 30 minutes of therapy for 4 weeks |
|
Outcomes | Outcomes were recorded at baseline and after the intervention period
|
|
Notes | Published and unpublished data; we only analysed the first intervention period (4 weeks); we summarised groups 2 and 3 to one control group | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Block randomisation; sequence generation method not stated |
Allocation concealment (selection bias) | Low risk | A therapist not involved in the treatments; opened sealed envelopes and assigned appointments according to treatment group (authors' statement) |
ITT analysis | Low risk | Results were analysed on an ITT basis |
Blinding of outcome assessment (detection bias) primary outcome | Low risk | Assessors were blinded to group allocation |