Clinical Research Directory

Inclusion Criteria: * Participants aged 18 to 65 years. * Participants must have a confirmed diagnosis of Reflex Sympathetic Dystrophy (CRPS) Type I, affecting the wrist, according to the Budapest Criteria. * Participants must experience chronic wrist pain for at least 3 months but not more than 24 months. * Participants must be able to offer written informed consent and participate in the study willingly. * Participants must demonstrate sufficient cognitive function to understand the training protocols (assessed via screening tools such as the Mini-Mental State Examination). Exclusion Criteria: * Participants who have undergone any surgical intervention for the wrist (other than the injury that led to RSD), or those with traumatic injuries that cause structural damage will be excluded. * Participants with significant neurological disorders affecting the upper limb. * Individuals with active psychiatric conditions, such as severe depression, anxiety, or psychosis which may impair participation in the study. * Participants with poorly controlled medical conditions such as diabetes, cardiovascular disease, or autoimmune disorders that could interfere with treatment outcomes or the ability to participate in the study.