Development and validation of a cystic fibrosis patient and family member experience of care survey

Karen Homa, Kathryn A. Sabadosa, Eugene C. Nelson, William H. Rogers, Bruce C. Marshall

Research output: Contribution to journalArticle

Abstract

Objective: The purpose of this study was to develop a cystic fibrosis (CF)-specific patient and family experience of care survey that CF care centers could use to inform quality improvement efforts. Methods: A literature search and query of CF care centers was conducted to identify existing surveys. Individuals with CF, their families, and health care professionals were also asked what to include. Following this process, a draft survey was developed and then reviewed by focus groups. Finally, a version was piloted at 25 CF care centers to validate and further refine the instrument. Results: No CF-specific surveys were found in the literature. Focus group participants stated that they understood the survey questions and that they covered important aspects of care, particularly infection control. The pilot test of the instrument with 485 participants supported its validity by demonstrating significant differences across centers and that most of the 3 care dimensions had acceptable internal consistency (Cronbach α: adults, 0.71-0.85; children, 0.68-0.79). Conclusion: A CF-specific patient and family experience of care survey was developed with input from individuals with CF, their families, and health care professionals. The instrument was validated and has been deployed to CF care centers.

Original languageEnglish (US)
Pages (from-to)100-116
Number of pages17
JournalQuality management in health care
Volume22
Issue number2
DOIs
StatePublished - Apr 1 2013
Externally publishedYes

Keywords

  • Cystic fibrosis
  • Health care surveys
  • Patient experience of care
  • Quality of care

ASJC Scopus subject areas

  • Leadership and Management
  • Health(social science)
  • Health Policy
  • Care Planning

Fingerprint Dive into the research topics of 'Development and validation of a cystic fibrosis patient and family member experience of care survey'. Together they form a unique fingerprint.

  • Cite this