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Implementing the Aphasia ASK Program: Enhancing Mood and Quality of Life for People with Aphasia

Implementing the Aphasia ASK Program: Enhancing Mood and Quality of Life for People with Aphasia

Introduction

The psychosocial impact of aphasia following a stroke is profound, affecting not only the individual but also their family members. The research article titled "Reducing the psychosocial impact of aphasia on mood and quality of life in people with aphasia and the impact of caregiving in family members through the Aphasia Action Success Knowledge (Aphasia ASK) program: study protocol for a randomized controlled trial" provides valuable insights into addressing these challenges. This blog explores how practitioners can leverage the findings from this study to improve their therapeutic interventions and outcomes for individuals with aphasia and their families.

The Importance of Early Intervention

Early intervention is crucial in managing the mood and quality of life for individuals with aphasia. The Aphasia ASK program, as outlined in the study, offers a structured approach to achieve this. By implementing this program, practitioners can provide targeted support that not only addresses the communication barriers associated with aphasia but also mitigates the risk of depression, which is prevalent in 62% to 70% of individuals with aphasia post-stroke.

Key Findings from the Aphasia ASK Program

The study conducted a multicenter, cluster-randomized controlled trial to evaluate the efficacy of the Aphasia ASK program. The primary outcomes focused on mood and quality of life at 12 months post-stroke, while secondary outcomes assessed the impact on family members, including caregiver burden and mental health.

Implementing the Aphasia ASK Program in Practice

For practitioners, integrating the Aphasia ASK program into their therapeutic repertoire can be transformative. Here are steps to consider:

Encouraging Further Research

While the Aphasia ASK program shows promise, continued research is essential to refine and expand its application. Practitioners are encouraged to contribute to ongoing studies and share their findings to enhance the collective understanding of effective aphasia interventions.

Conclusion

The Aphasia ASK program represents a significant advancement in addressing the psychosocial impacts of aphasia. By adopting this evidence-based approach, practitioners can improve outcomes for individuals with aphasia and their families, ultimately enhancing their quality of life. To read the original research paper, please follow this link: Reducing the psychosocial impact of aphasia on mood and quality of life in people with aphasia and the impact of caregiving in family members through the Aphasia Action Success Knowledge (Aphasia ASK) program: study protocol for a randomized controlled trial.


Citation: Worrall, L., Ryan, B., Hudson, K., Kneebone, I., Simmons-Mackie, N., Khan, A., Hoffmann, T., Power, E., & Togher, L. (2016). Reducing the psychosocial impact of aphasia on mood and quality of life in people with aphasia and the impact of caregiving in family members through the Aphasia Action Success Knowledge (Aphasia ASK) program: study protocol for a randomized controlled trial. Trials, 17(153). https://doi.org/10.1186/s13063-016-1257-9
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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