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The Parkinson’s Disease Questionnaire-39 (PDQ-39) is a standardized tool used to assess the quality of life in individuals diagnosed with Parkinson's disease. This comprehensive instrument includes 39 items, each designed to evaluate particular aspects of living with Parkinson’s. These items are sorted into eight distinct categories, encompassing dimensions such as mobility, emotional well-being, and activities of daily living. By providing a detailed overview of a patient's health status, the PDQ-39 serves clinicians and researchers in identifying areas that may require targeted interventions or therapeutic focus.
Using the PDQ-39 involves patients self-reporting their experiences across various facets of their condition. The questionnaire is structured to be user-friendly, prompting individuals to reflect on their health experiences in the preceding month. Responses are scored on a five-point scale, ranging from "never" to "always". This format ensures that results are both comprehensive and reflective of the patient’s overall wellbeing. Clinicians can analyze these scores to interpret which specific domains of the patient's life are most impacted by the disease.
Scores from the PDQ-39 are calculated by summing the responses within each of the eight domains and converting them into percentages. This transformation helps in standardizing results across different patient populations. A higher percentage score indicates poorer quality of life or greater impact of Parkinson's symptoms. Healthcare providers often use these scores to tailor individualized management plans and measure treatment efficacy over time.
The PDQ-39 is divided into eight key domains:
Each domain provides insights into specific areas of impact, guiding clinicians in fine-tuning treatment approaches.
The PDQ-39 is predominantly used by neurologists, researchers, and healthcare providers who specialize in managing Parkinson’s disease. Additionally, it can be employed by caregivers and family members who are involved in caregiving roles to better understand the specific challenges faced by the patient and facilitate more informed discussions with medical professionals.


The PDQ-39 is a legally recognized tool within healthcare systems and research contexts. It must be administered and interpreted by qualified professionals within the bounds of medical confidentiality and ethical guidelines. While the questionnaire itself does not dictate legal decisions, data derived can influence healthcare policies and coverage considerations for patients with Parkinson’s disease.
The PDQ-39 is available in both digital and paper formats, allowing flexibility in how it is administered:
Healthcare facilities may choose one format over the other based on logistical considerations and patient preferences.
Each of these terms is integral to both the administration and interpretation of the PDQ-39, providing structure and clarity for users.
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