The Association of Provider Communication With Trust Among Adults With Sickle Cell Disease
| dc.contributor.author | Haywood, Carlton Jr. | |
| dc.contributor.author | Lanzkron, Sophie | |
| dc.contributor.author | Ratanawongsa, Neda | |
| dc.contributor.author | Bediako, Shawn M. | |
| dc.contributor.author | Lattimer, Lakshmi | |
| dc.contributor.author | Powe, Neil R. | |
| dc.contributor.author | Beach, Mary Catherine | |
| dc.date.accessioned | 2020-06-15T17:16:02Z | |
| dc.date.available | 2020-06-15T17:16:02Z | |
| dc.date.issued | 2010-03-03 | |
| dc.description.abstract | Background Adults with sickle cell disease often report poor interpersonal healthcare experiences, including poor communication with providers. However, the effect of these experiences on patient trust is unknown. Objective To determine the association between patient ratings of the previous quality of provider communication and current trust in the medical profession among adults with sickle cell disease. Research design Cross-sectional survey. Participants A total of 95 adults with sickle cell disease. Measurements The four-item Provider Communication Subscale from the Consumer Assessment of Healthcare Plans and Systems Survey; The five-item Wake Forest Trust in the Medical Profession Scale. Main results Better ratings of previous provider communication were significantly associated with higher levels of trust toward the medical profession. A 10% increase in provider communication rating was associated with a 3.76% increase in trust scores (p < 0.001, 95% CI [1.76%, 5.76%]), adjusting for patient-level demographic, clinical, and attitudinal characteristics. Conclusions Poorer patient ratings of provider communication are associated with lower trust toward the medical profession among adults with sickle cell disease. Future research should examine the impact of low trust in the medical profession on clinical outcomes in this population of patients. | en |
| dc.description.sponsorship | Dr. Haywood’s effort was supported by a National Research Service Award Minority Predoctoral Fellowship from National Heart, Lung, and Blood Institute Grant #: 5F31HL082037-03. This study was conducted with grant support from the Johns Hopkins Blaustein Pain Research Fund. The funding agencies did not have a role in the design, conduct, or reporting of the study. | en |
| dc.description.uri | https://link.springer.com/article/10.1007/s11606-009-1247-7 | en |
| dc.format.extent | 6 pages | en |
| dc.genre | journal articles postprints | en |
| dc.identifier | doi:10.13016/m2drud-l2ou | |
| dc.identifier.citation | Haywood, C., Lanzkron, S., Ratanawongsa, N. et al. The Association of Provider Communication with Trust among Adults with Sickle Cell Disease. J GEN INTERN MED 25, 543–548 (2010). https://doi.org/10.1007/s11606-009-1247-7 | en |
| dc.identifier.uri | https://doi.org/10.1007/s11606-009-1247-7 | |
| dc.identifier.uri | http://hdl.handle.net/11603/18894 | |
| dc.language.iso | en | en |
| dc.publisher | Springer Nature | en |
| dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
| dc.relation.ispartof | UMBC Psychology Department Collection | |
| dc.relation.ispartof | UMBC Faculty Collection | |
| dc.rights | This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author. | |
| dc.title | The Association of Provider Communication With Trust Among Adults With Sickle Cell Disease | en |
| dc.type | Text | en |