Active Coping Program for Chronic Musculoskeletal Pain: A Controlled Clinical Study

Effectiveness of an Active Coping Program on Pain, Disability, and Psychosocial Factors in Patients With Chronic Musculoskeletal Pain: A Controlled Clinical Study

Chronic musculoskeletal pain is a highly prevalent condition that is often associated with persistent pain, physical disability, and maladaptive psychosocial factors such as pain catastrophizing, fear of movement, and central sensitization. These factors can contribute to pain persistence and reduced quality of life, highlighting the need for multimodal, non-pharmacological interventions that address both physical and psychological dimensions of pain.

The purpose of this study is to evaluate the effectiveness of an active coping program for patients with chronic musculoskeletal pain compared with usual care. The intervention is designed to promote active pain management strategies through education, movement-based exercises, and behavioral approaches aimed at improving pain coping, reducing disability, and addressing psychosocial contributors to chronic pain.

This is a controlled interventional study in which adult patients with chronic musculoskeletal pain will be allocated to either an intervention group receiving the active coping program or a control group receiving usual care. Outcome measures will be assessed at baseline and after completion of the intervention. Primary and secondary outcomes include pain-related disability, pain catastrophizing, fear of movement, symptoms of central sensitization, and health-related quality of life, measured using validated questionnaires.

The findings of this study are expected to provide evidence on the clinical effectiveness of an active coping approach in the management of chronic musculoskeletal pain and to support its implementation in routine clinical practice within primary care settings.

Inclusion Criteria:

• Adults aged 18 years or older.
• Diagnosis of chronic musculoskeletal pain, defined as pain persisting for more than 3 months.
• Ability to understand study procedures and complete self-reported questionnaires.
• Ability to participate in an active coping program involving education and movement-based activities.
• Provision of written informed consent.

Exclusion Criteria:

• Presence of serious neurological, rheumatologic, or systemic disease that may interfere with participation in the intervention or outcome assessment.
• Severe cognitive impairment or psychiatric condition that limits understanding of the study procedures.
• Ongoing participation in another structured pain management or rehabilitation program.
• Any medical condition that, in the opinion of the investigators, would make participation unsafe or compromise study results.