Study Summary

One hundred thirteen patients with persistent non-cancer pain were randomized to receive iSelf-help (n=56) or an in-person pain management program (n=57). The primary outcome was the Modified Roland-Morris Disability Questionnaire (RMDQ). Secondary outcomes included DASS-21 (anxiety, depression, stress), Brief Pain Inventory (intensity, interference), EQ-5D-5L VAS, Pain Self-Efficacy (PSEQ), Pain Catastrophizing (PCS), acceptance, satisfaction, attendance, adverse events, and costs. Outcomes were assessed post-intervention, and at 3 and 6 months. Overall, the results revealed iSelf-help was non-inferior to in-person care for RMDQ at 6 months and for several secondary domains; pain intensity did not meet non-inferiority. iSelf-help showed similar satisfaction, greater accessibility, and lower delivery cost per participant, suggesting an effective, more accessible alternative to expand service capacity.