Background
Colorectal cancer (CRC) symptoms are often vague and vary in severity, intensity, type, and timing. Receipt of medical care is dependent on symptom recognition and assessment, which may impede timely diagnosis.
Objective
To describe and categorize how CRC patients coped with symptoms prior to seeking medical care, examine socio-demographic differences in these coping strategies, and determine the strategies associated with time to seek medical care and overall time to diagnosis.
Methods
244 Caucasian and African Americans in Virginia and Ohio diagnosed with CRC who experienced symptoms prior to diagnosis were administered a semi-structured interview and the Brief COPE questionnaire.
Results
83% used more than one coping strategy. Common symptom-specific coping strategies were to wait-and-see, self-treat, and rationalize symptoms. Males were more likely to ‘wait-and-see’ (p<.001); African Americans and Medicaid recipients were more likely to self-treat via lifestyle changes (p’s<.01). Younger individuals (< 50) had higher Brief COPE reframing, planning, and humor scores; those with lower education and income had higher denial scores (p’s<.01). Using more symptom-specific coping strategies and engaging in avoidance/denial was associated with longer time to seek medical care and overall time to diagnosis (p’s<.01).
Conclusions
Individuals experiencing CRC symptoms use multiple, diverse coping strategies which are influenced by socio-demographic characteristics. Denial is particularly relevant for delay in seeking care and timely diagnosis.
Implications for Practice
Public health campaigns could focus on secondary prevention of CRC by targeting at-risk groups like males, African Americans, or Medicaid recipients, who choose waiting or self-treatment in response to initial symptoms.