Randomised controlled trials (RCTs), controlled clinical trials (CCTs) or studies of other design that assessed rehabilitation (immobilisation, early controlled mobilisation or early active mobilisation) were eligible for inclusion. Studies needed to describe at least two groups with a minimum of 10 digits per group. Eligible outcome measures were at least one of: body functions; manual dexterity or co-ordination; health-related quality of life; pain; and return to work.
Included studies assessed direct postoperative immobilisation (plaster splint), early active mobilisation (with static splint or palmar blocking splint) and early controlled mobilisation (dynamic splints, thermoplastic splints) compared to each other. Where reported, mean age ranged from 28 to 35 years. Duration of follow-up ranged from four weeks to six months.
Studies were selected by one reviewer and discussed with a second.