Assessing the Patient Experience in Cancer Care

Mayo Clinic

Status: Completed

Conditions: Gastrointestinal Neoplasm; Sarcoma; Melanoma; Breast Neoplasm; Gynecological Neoplasm; Genitourinary Neoplasm; Endocrine Gland Neoplasm; Brain Neoplasm; Lung Neoplasm; Head and Neck Neoplasm

Study type: Observational

Funder types: Other; NIH

Identifiers

NCT01621295

R01AT006515 (U.S. NIH Grant/Contract)

11-006682

Details and patient eligibility

About

Communication is an important component of comprehensive cancer care impacting patient satisfaction, adherence, and quality of life. The wide array of issues addressed in cancer clinical interactions makes communicating about a broad range of topics (including quality of life, communication, symptom control, complementary/alternative therapies, costs, treatment burden, prognosis, anxiety, side-effects, sexual function, palliative care options, etc.) especially interesting and potentially challenging. Some of these topics may not be routinely addressed in the clinical interaction or may require consultative support from other members of the comprehensive cancer care team. One frequently overlooked critical element in research on communication between cancer clinicians, their patients, and their primary care clinicians is describing real-time consultations between patients and their clinicians. These interactions provide rich material for assessing key psycho-social dynamics and identifying issues that patients find important in their care. In order to devise systems of care that optimize the patient experience, it is critical that clinicians and researchers understand, appreciate, and systematically characterize the richness and complexity of the decision-making process in routine cancer consultations between cancer patients and their treating clinicians. This study seeks to assess the patient experience in cancer care by observing patients and their physicians in their clinical interactions and following them for several months to see how their care went. By describing in-depth the conversations and experiences of patients in these clinical interactions, this study will lay the foundation for practice-based interventions to optimize patients' interactions with their cancer care teams.

Enrollment: 408 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Age greater than or equal to 18 years
• Histological confirmation of: brain, breast, endocrine, gastrointestinal, genitourinary, gynecological, head/neck, lung, melanoma, or sarcoma malignancies.
• Speak English or Spanish
• Not enrolled in hospice
• In any of the following phases of the cancer control continuum: initial diagnosis, initial treatment, early survivorship, or recurrence.
• Provide written informed consent

Exclusion Criteria: