Palliative Care
Conditions
Brief summary
The purpose of this study is to test the usability of PCforMe, a web-based preparation and engagement tool about palliative care, during a pre-visit pilot trial in outpatient palliative care at the Duke Cancer Institute Palliative Care Clinic.
Detailed description
The Investigator will 1:1 randomize patients to an Active Control arm or Intervention arm. Both arms will receive a tablet computer (iPad or Galaxy Tab based on preference) connected to the internet with disposable headphones to use for up to 30 minutes. Subjects in the Active Control arm will receive a list of three nationally-recognized websites to receive information on palliative care - www.palliativedoctors.org; getpalliativecare.org; and Wikipedia Palliative Care https://en.wikipedia.org/wiki/Palliative\_care). Intervention Arm subjects will receive access to PCforMe. PCforMe is an online, web-based, interactive tool to prepare patients for a clinical palliative care encounter. PCforMe is accessible through www.pcforme.org. It does not collect any patient information, including identifiers (e.g. name, email address, disease, location) or health information (e.g. disease, symptom severity or location). The system uses a combination of animated videos and user-answered questions to generate a Palliative Care Passport, which is a summary of information entered into the system. Research staff will print out the Passport for patients and hand it to them prior to the appointment. Queries for users include standard-of-care questions asked by palliative care clinicians, including areas that patients want to more learn about. No diagnoses, medication advice, or clinical assessments are made or given.
Interventions
BEHAVIORALAccess to PCforMe for review
Intervention Arm subjects will receive access to PCforMe.
BEHAVIORALAccess to three nationally-recognized Palliative Care websites for review
Subjects in the Active Control arm will receive a list of three nationally-recognized websites to receive information on palliative care
Sponsors
Duke University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Intervention model description
The Investigator will 1:1 randomize patients to an Active Control arm or Intervention arm. Both arms will receive a tablet computer (iPad or Galaxy Tab based on preference) connected to the internet with disposable headphones to use for up to 30 minutes. Subjects in the Active Control arm will receive a list of three nationally-recognized websites to receive information on palliative care - www.palliativedoctors.org; getpalliativecare.org; and Wikipedia Palliative Care https://en.wikipedia.org/wiki/Palliative\_care). Intervention Arm subjects will receive access to PCforMe.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Potential participants will be identified by reviewing clinic appointment listings in EPIC (e.g., diagnosis, date of diagnosis, date of clinic appointment, physician), and deemed eligible by the RA by meeting the following criteria: * Age \>18 * capacity to give consent * has a scheduled outpatient visit (initial consult) with a palliative care provider * ability to speak and understand English
Exclusion criteria
* Not meeting the inclusion requirements
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| System usability as measured by the system usability scale | 1 hour | To determine usability, the System Usability Scale will be administered to each participate. As described by usability.gov: The participant's scores for each question are converted to a new number, added together and then multiplied by 2.5 to convert the original scores of 0-40 to 0-100. Though the scores are 0-100, these are not percentages and should be considered only in terms of their percentile ranking. Based on research, a SUS score above a 68 would be considered above average and anything below 68 is below average, however the best way to interpret the participant's results involves normalizing the scores to produce a percentile ranking. The original scale is a 10-item, 5-point Likert scale. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Palliative Care knowledge | Baseline, up to 1 hour | Regarding the change in knowledge outcome, Two-side P value of \<0.05 will infer significance. The Palliative Care Knowledge instrument is a 4-item, multiple choice assessment of palliative care knowledge. Only one answer is correct. A change in knowledge of Palliative Care will be determined based on the answer provided in the follow-up assessment |
| Change in Perceived Efficacy for the Patient-Physician Interaction (PEPPI) | Baseline, up to 1 hour | Change in PEPPI will be determined using 5-point Likert response - 1 being Not at all Confident and 5 being Very Confident |
| Change in single-item Prepared item | Baseline, up to 1 hour | I feel prepared for my palliative care appointment (5-point Likert response - Strongly Disagree, Disagree, Neither Agree or Disagree, Agree, Strongly Agree) |
Countries
United States
Outcome results
None listed