Evidence from available studies is insufficient to establish the definitive efficacy of PA in preventing or reducing CPSP. Future trials should clearly define intervention parameters and employ active control groups to strengthen methodological rigor. Incorporation of more comprehensive pain assessments will allow investigation of mechanisms of efficacy, as well as differential impact among patients.PROSPERO ID CRD42025626850.
Munõz-Vergara et al. (Fri,) studied this question.