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Completed

NCT Number: NCT05084209

Preparing Patient-Caregiver Dyads with Parkinson's Disease for Future Decision Making

Persons with Parkinson's disease and family care partners are often unprepared to make difficult, future medical decisions. Earlier conversations about future medical decisions between persons with Parkinson's disease and family care partners are needed before communication and cognitive difficulties become severe. In this study, the investigators will pilot test a novel dyadic intervention to help persons with Parkinson's disease and family care partners make future medical decisions. The investigators hypothesize the intervention will be feasible and acceptable among persons with Parkinson's disease and family care partners.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Purdue University

West Lafayette, Indiana, 47907-2069, United States

About this study

Investigators are looking for pairs of participants consisting of a person with a diagnosis of Parkinson's Disease, and a family care partner who is most likely to help make medical decisions in the future.

For this study, pairs will complete a survey to understand how engaged participants are in discussing future medical decisions, demographics, and the severity of Parkinson's disease. This survey will take about 15 minutes. Then, participants will work through a medical decision making support intervention together. Completing the intervention in-person, on the phone, or via video conferencing is acceptable. The resources will provide information on future medical decisions participants may need to make. The intervention is completely online and will take about 60 minutes to complete. Participants will have 2 weeks to complete the intervention.

The investigators will call participants a week after enrollment to ask about technical difficulties completing the intervention, provide assistance with intervention material navigation as needed, and answer questions about the intervention. Participants will receive another online survey 2 weeks after enrollment to understand engagement in discussing future medical decisions, and acceptability of the intervention. The 2 week survey will take about 15 minutes to complete.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Person with Parkinson's Disease Inclusion Criteria:

  • Self-report a clinical diagnosis of Parkinson Disease
  • Does not have a diagnosis of dementia
  • Speak and read English
  • Have access to a reliable phone or internet connection
  • Have access to an online connection through a smartphone, tablet, or computer device
  • Be comfortable navigating websites or have someone available to assist
  • Agree to be audio recorded during intervention

Care Partner Inclusion Criteria:

  • Self-identify as the family member who will likely make medical decisions for the person with Parkinson Disease in the future OR who is the legally appointed health care representative
  • Self-report not having a diagnosis of dementia
  • Speak and read English
  • Have access to a reliable phone or internet connection
  • Have access to an online connection through a smartphone, tablet, or computer device
  • Be comfortable navigating websites or have someone available to assist
  • Agree to be audio recorded during intervention

Exclusion criteria

  • Cannot see well enough to see words on a newspaper even with corrective lenses
  • Used the intervention resources before
  • If cognition is questionable and cannot pass consent understanding questions

Treatment and study plan

Parkinson's medical decision making support

Behavioral

Participants will be asked to view and work through medical decision making support resources. The resources will include information on medical decisions that may occur in Parkinson's disease, and general medical decisions that anyone may need to make (i.e. choosing a medical decision maker). The resources will also include suggestions on how to discuss these decisions.

Primary outcomes

  1. Change from baseline Advance Care Planning Engagement Survey at 2 weeks

    Time frame: Baseline, 2 weeks post intervention

    Assesses knowledge, contemplation, self-efficacy, and readiness on a 5-point Likert scale.

  2. Intervention feasibility/acceptability

    Time frame: 2 weeks post intervention

    Ratings of ease of use, helpfulness, and likeliness of recommending the intervention to others on Likert-scales.

Sponsors and collaborators

Lead sponsor

Purdue University

Other

Registry information

Official study title

Preparing Patient-Caregiver Dyads with Parkinson's Disease for End-of-Life Decision Making

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Oct 19, 2021
Registry last updated
Feb 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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