The study was a randomizedcontrol trial and the subjects were divided in two groupsA and B. The subjects were briefed about the study andduly signed informed consent forms were obtained.Inclusion criteria- Subjects between the age of 35-60, in stage 3 of Brunnstrom recovery stages of thearm (BRS-A) and hand (BRS-H),2intact cognition andperception and clients with non- traumatic stroke wererecruite