Clinical Trial

Multidimensional Assessment of Chronic Pain in Severe Haemophilia A

Recruiting
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Record status
This record was last updated August 1, 2025 (before its estimated October 3, 2025 completion). Its status may not reflect the trial's current state.
Summary
Introduction: Haemophilia is a congenital coagulopathy characterised by haemarthrosis, mainly in the knees, ankles and elbows. Prophylactic treatment is the most effective therapeutic option for preventing or minimising these bleeds. Bispecific monoclonal antibodies have been shown to be effective in reducing bleeding in patients with haemophilia. Objectives: To investigate the associations between chronic residual pain and pain catastrophising, perceived self-efficacy regarding the disease and treatment, and body image and perception of visible disability. Methods. Multicentre cross-sectional cohort studies. 109 patients with severe haemophilia A from different regions of Spain will be included in the study. The primary variable will be chronic residual pain and its functional interference (Brief Pain Inventory-Short Form). Secondary variables will be pain catastrophising (Pain Catastrophising Scale), perceived self-efficacy regarding the disease and treatment (Pain Self-Efficacy Questionnaire), and body image and perception of visible disability (Body Image Scale). Potential confounding variables will include sociodemographic variables (age and educational level), clinical variables (time on monoclonal antibody treatment and number of previous bleeds in the last 12 months) and anthropometric variables (body mass index). Expected results: It is expected that residual chronic pain will persist in patients with severe haemophilia A treated with monoclonal antibodies and that it will be associated with greater catastrophising, lower self-efficacy and poorer body image, modulating the experience of pain beyond bleeding control.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-07-24.
Status change: Not Yet Recruiting → Recruiting 2025-07-31
Trial Details
NCT Number NCT07096349
Lead Sponsor Investigación en Hemofilia y Fisioterapia
Conditions Hemophilia A Without Inhibitor
Enrollment 109 participants
Start Date 2025-07-30
Primary Completion 2025-10-03 (estimated)
Study Completion 2025-10-26 (estimated)
Updated on ClinicalTrials.gov 2025-08-01