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Empowering Through Understanding: Simplifying Patients' Rights for Better Outcomes

Empowering Through Understanding: Simplifying Patients\' Rights for Better Outcomes

Empowering Through Understanding: Simplifying Patients' Rights for Better Outcomes

As practitioners in the field of speech-language pathology, we are acutely aware of the power of language and communication. The National Survey of Patients’ Bill of Rights Statutes sheds light on a critical issue: the complexity of language used in Patients' Bill of Rights (PBOR) documents. This complexity often prevents patients from understanding their rights, ultimately impacting their care and empowerment.

The Challenge of Readability

The study reveals that PBOR documents are often written at a reading level far above the average U.S. adult's reading capacity, which is at an 8th-grade level. The average readability of these documents is at a 14th-grade level, with some reaching as high as a 17th-grade level. This disparity creates a barrier for patients, who may not fully comprehend their rights, leading to a passive role in their healthcare journey.

Implications for Practitioners

For practitioners, this presents an opportunity to advocate for change. By understanding the impact of readability on patient comprehension, we can push for the use of plain language in PBOR documents. This change can foster a more inclusive healthcare environment where patients feel informed and empowered to participate actively in their care.

Strategies for Improvement

Encouraging Further Research

While the study provides valuable insights, it also highlights the need for further research into the effects of document readability on patient outcomes. Practitioners can contribute by conducting studies within their own institutions to assess the impact of simplified language on patient understanding and satisfaction.

By prioritizing clear communication, we can help ensure that patients are not only aware of their rights but are also empowered to exercise them. This shift towards patient-centered communication aligns with our mission at TinyEYE to create positive outcomes for children and their families through effective online therapy services.

To read the original research paper, please follow this link: National Survey of Patients’ Bill of Rights Statutes.


Citation: Paasche-Orlow, M. K., Jacob, D. M., Hochhauser, M., & Parker, R. M. (2009). National survey of patients’ bill of rights statutes. Journal of General Internal Medicine, 24(4), 489-494. https://doi.org/10.1007/s11606-009-0914-z
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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in online therapy apply today!

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