Skip to main content
. 2018 Oct 31;2018(10):CD011887. doi: 10.1002/14651858.CD011887.pub2

Zhu 2015.

Methods Randomized clinical trial
Participants Stroke patients hospitalized in Jiaxing Rehabilitation Medical Center were recruited
70 participants: 35 experimental group; 35 control group
Inclusion criteria: patients who met the diagnosis for stroke formulated in the 4th National Academic Conference on Cerebrovascular Disease in 1995, and were confirmed as having a stroke upon CT or MRI; first‐episode patients who began rehabilitation therapy within 6 months, for whom the sitting balance was ≥ Level 1, and the FMA score was ≥ 15 for upper extremity motor function; patients with a stable condition; patients with a normal Kinesthetic and Visual Imagery Questionnaire score; patients who were 42 to 75 years of age; patients who provided informed consent and were willing to participate in the study
Exclusion criteria: patients with cognitive impairment MMSE score of < 24 in patients with a junior high school education or < 17 if illiterate; patients with severe upper limb spasticity; patients with severe bone joint malformation or myopathy; patients with severe diseases of the heart, lung, liver, or kidney
Mean (SD) age: experimental group: 57.75 (15.57) years, control group: 56.89 (14.93) years
Stroke details: not reported by authors
Stroke phase: acute
Interventions Experimental group additionally watched a video showing a specific action of the upper limb and then performed the same exercise after watching 30 videos
Control group received conventional drug treatment and traditional physical and occupational therapy
Control group received conventional therapy 2 to 5 hours per day, 6 times per week for 8 weeks. Experimental group had additional 30 minutes per day, 6 times per week, for 8 weeks
Outcomes Outcomes recorded at baseline and post‐intervention
Muscle tone of elbow flexor and forearm pronator: MAS
Upper limb function: FMA of the upper limb
Activities of daily living: BI
Notes
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Random number table
Allocation concealment (selection bias) High risk Authors did not report if there was allocation concealment, but randomization type classifies the allocation concealment as high risk
Blinding of participants and personnel (performance bias) 
 All outcomes Low risk No blinding, but the outcome is not likely to be influenced by lack of blinding
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk Evaluators were unaware of the participant grouping status and did not participate in the treatment
Incomplete outcome data (attrition bias) 
 All outcomes Low risk 9 participants were excluded from analysis: 4 from experimental group and 5 from control group. Participants were excluded for absence on 3 consecutive days of intervention and aggravated condition of the participant. Nevertheless the reasons were reported and they have no direct relationship with the outcomes studied, and there is not a substantial imbalance in final number of participants in each group considered for analysis
Selective reporting (reporting bias) Low risk The study protocol is not available but it is clear that the published reports include all expected outcomes, including those that were pre‐specified
Other bias Low risk  

ADLs: activities of daily living
 ARAT: Action Research Arm Test
 BBT: Box and Block Test
 BDI: Beck Depression Inventory
 BI: Barthel Index
 CG: control group
 CMCT: center‐motion conduction time
 CPT: conventional physical therapy
 CT: computed tomography
 EG: experimental group
 FAT: Frenchay Arm Test
 FAST: Florida Apraxia Screening Test
 FIM: Functional Independence Measure
 FMA: Fugl‐Meyer Assessment
 fMRI: functional magnetic resonance
 MAL: Motor Activity Log
 MAS: Modified Ashworth Scale
 MBI: Modified Barthel Index
 MEP: motor evoked potential amplitudes
 MI: Motricity Index
 MMSE: mini‐mental state examination
 MRI: magnetic resonance imaging
 NHPT: Nine Hole Peg test
 OTI: observation‐to‐imitate
 PP: physical practice
 SD: standard deviation
 SIS: Stroke Impact Scale
 TMS: transcranial magnetic stimulation
 VAS: visual analogue scale
 WMFT: Wolf Motor Function Test