Empowered patient: A program to improve people with Parkinson’s communication with health care professionals

IF 1.9 Q3 CLINICAL NEUROLOGY Clinical Parkinsonism Related Disorders Pub Date : 2022-01-01 DOI:10.1016/j.prdoa.2022.100156
Muhammed Shahriar Zaman , Setareh Ghahari , Mary Ann McColl
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引用次数: 0

Abstract

Background

Communication breakdown between patients and health care professionals poses an accessibility gap preventing adequate health care. The Empowered Patient Program was developed to support people with Parkinson’s in improving their health communication skills/strategies and thus facilitate the accessibility gap in their care.

Objective

Our pilot study aimed to test the feasibility and preliminary effect of the Empowered Patient Program within a small cohort of individuals with Parkinson’s disease.

Methods

We completed a pre-test-post-test pilot study. Eight participants completed the Empowered Patient Program for this pilot study. Data collection was completed by administering a questionnaire prior to the program, immediately after program completion, and three months post-completion. We additionally conducted two telephone interviews with the participants to qualitatively gather feedback on the program.

Results

The program elucidated statistically significant improvement across domains/areas of knowledge (p = 0.01) and self-perceived communication skills (p = 0.04) among the participants. Through feedback from the patient interviews, it was confirmed that these significant improvements were owed largely to the high level of organization, intuitive user interface, and suitable content of the program for this cohort.

Conclusions

The Empowered Patient Program pilot resulted in a desired outcome indicating its satisfactory development. The next steps are to test the Empowered Patient program in a larger sample.

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授权病人:一个改善帕金森患者与卫生保健专业人员沟通的项目
患者与医护人员之间的沟通中断造成了可及性差距,阻碍了充分的医疗保健。制定赋权患者方案是为了支持帕金森患者改善其健康沟通技巧/策略,从而缩小其护理的可及性差距。我们的试点研究旨在在帕金森病患者的小队列中测试授权患者计划的可行性和初步效果。方法:我们完成了一项前测后测的中试研究。8名参与者完成了这项试点研究的授权患者计划。数据收集通过在项目前、项目完成后和项目完成后三个月进行问卷调查来完成。我们还与参与者进行了两次电话访谈,以定性地收集对该计划的反馈。结果该方案在知识领域(p = 0.01)和自我感知的沟通技巧(p = 0.04)上有统计学意义的改善。通过患者访谈的反馈,我们确认这些显著的改善在很大程度上归功于高水平的组织、直观的用户界面和适合该队列的程序内容。结论授权患者项目试点取得了令人满意的效果。接下来的步骤是在更大的样本中测试授权患者程序。
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来源期刊
Clinical Parkinsonism  Related Disorders
Clinical Parkinsonism Related Disorders Medicine-Neurology (clinical)
CiteScore
2.70
自引率
0.00%
发文量
50
审稿时长
98 days
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