Objective:We reviewed and appraised the existing evidence of in vivo manifestations of residual force enhancement in human skeletal muscles and assessed,through a meta-analysis,the effect of an immediate history of eccentric contraction on the subsequent torque capacity of voluntary and electrically evoked muscle contractions.Methods:Our search was conducted from database inception to May 2020.Descriptive information was extracted from,and quality was assessed for,45 studies.Meta-analyses and metaregressions were used to analyze residual torque enhancement and its dependence on the angular ampli-tude of the preceding eccentric contraction.Results:Procedures varied across studies with regards to muscle group tested,angular stretch amplitude,randomization of contractions,time window analyzed,and verbal command.Torque capacity in isometric (constant muscle tendon unit length and joint angle) contractions preceded by an eccentric contraction was typically greater compared to purely isometric contractions,and this effect was greater for electrically evoked muscle contractions than voluntary contractions.Residual torque enhancement differed across muscle groups for the voluntary contractions,with a significant enhancement in torque observed for the adductor pollicis,ankle dorsiflexors,ankle plantar flexors,and knee extensors,but not for the elbow and knee flexors.Meta-regressions revealed that the angular amplitude of the eccentric contraction (normalized to the respective joint\'s full range of motion) was not associated with the residual torque enhancement observed.Conclusion:There is evidence of residual torque enhancement for most,but not all,muscle groups,and residual torque enhancement is greater for electrically evoked than for voluntary contractions.Contrary to our hypothesis,and contrary to generally accepted findings on isolated muscle preparations,residual torque enhancement in voluntary and electrically evoked contractions does not seem to depend on the angular amplitude of the preceding eccentric contraction.