Source
cureus
Abstract
Adults living with sickle cell disease (SCD) experience high rates of chronic pain, depression, and anxiety, which significantly impair quality of life. Despite this burden, access to mental health services remains limited, and mental health providers often report limited training or apprehension in treating patients with chronic pain. To address these gaps, we implemented a psychotherapeutic skills group co-created and led by clinical psychology postdoctoral residents and tailored for adults with SCD. The program aimed to reduce depression, anxiety, and chronic pain interference in the enrolled patients.
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