Study designs of evaluations included in the review
Experimental and quasi-experimental studies were eligible for inclusion. The included studies were crossover randomised controlled trials (RCTs), various types of observational studies and case reports.
Specific interventions included in the review
Studies that used casting as the main intervention were eligible for inclusion.
In the included studies, casts were applied to ankle plantar flexors, elbow flexors, wrist flexors, and both ankle and knee flexors. The participants wore casts from one day to a mean of 102 days, and in most cases the time spent in a cast was determined on an individual basis. Some participants had casts applied to more than one joint. In some studies the patients were weight bearing through the casts; in other studies the degree of weight bearing was not explicitly stated. The participants in the studies were also receiving rehabilitation including medical and pharmacological treatments.
Participants included in the review
Studies of adults with an acquired brain injury, whom the investigators described as having spasticity, were eligible for inclusion. Studies of children (aged less than 16 years) and people with cerebral palsy were excluded. Most of the included studies were of patients with a traumatic brain injury; other studies included patients with cerebrovascular accident, cerebral hypoxia, cerebral ischaemia, cerebral aneurysm and 'other'. All of the included studies were of patients in the acute or subacute stage of recovery.
Outcomes assessed in the review
The inclusion criteria were not specified in terms of outcomes. The outcomes assessed in the review were spasticity, passive range of motion (PROM) and 'function'. The included studies measured spasticity using clinical improvement, the joint angle at which a stretch reflex was elicited plus the ability to perform rapid alternating movements, and vibratory inhibition using electromyography. Two studies measured PROM using a standardised torque-controlled measure, but most studies did not report the reliability or validity of the methods used to measure PROM. Studies used different scales to measure function or ambulation. Most of the studies assessed the outcomes when the cast was finally removed, but 2 studies assessed PROM from 5 to 684 days and 1 month after casting, respectively.
How were decisions on the relevance of primary studies made?
The authors did not state how the papers were selected for the review, or how many reviewers performed the selection.