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PCplanner for Idiopathic Pulmonary Fibrosis

N/A
Waitlist Available
Led By Christopher Cox, MD
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 16 weeks
Awards & highlights

Study Summary

This trial will test whether the PCplanner mobile app can help patients with idiopathic pulmonary fibrosis (a lung disease) and their clinicians to address needs and have advance care planning discussions.

Eligible Conditions
  • Idiopathic Pulmonary Fibrosis
  • Interstitial Lung Disease

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 16 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 16 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptability of intervention
Completion of intervention
Documentation of advance care planning in electronic health record
+1 more
Secondary outcome measures
Change in EuroQol - 5 Dimension (EQ-5D) score
Change in General Anxiety Disorder-7 (GAD-7) score
Change in Needs; Existential concerns; Symptoms; and Therapeutic interaction (NEST) scale
+4 more
Other outcome measures
Number of hospitalizations during study
Referral to hospice during study
Referral to palliative care specialist during study

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: PCplanner mobile app platformExperimental Treatment1 Intervention
Participants who are randomized to the intervention arm will complete surveys at 3 timepoints and will be given resources on advance care planning via PCplanner, the mobile app platform. They will receive a telephone call by the study team about a week after enrollment to answer any questions about the resources provided. If needs and questions are not resolved quickly after the clinic visit, then another layer of patient support with a telephone call by a palliative care specialist will be provided to the participant to help develop potential management plans.
Group II: Usual CareActive Control1 Intervention
Participants who are randomized to the usual care arm will complete surveys at 3 timepoints and receive usual care by pulmonary clinician.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PCplanner
2021
N/A
~200

Find a Location

Who is running the clinical trial?

Duke UniversityLead Sponsor
2,358 Previous Clinical Trials
3,420,026 Total Patients Enrolled
6 Trials studying Idiopathic Pulmonary Fibrosis
2,420 Patients Enrolled for Idiopathic Pulmonary Fibrosis
Christopher Cox, MDPrincipal InvestigatorDuke Health
2 Previous Clinical Trials
254 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What are the ambitions of this experiment?

"This medical study seeks to measure the completion of intervention over a period of up to 16 weeks. Secondary objectives focus on changes in Patient Health Questionnaire-9 (PHQ-9), EuroQol - 5 Dimension (EQ-5D) and Patient Health Questionnaire 10(PHQ-10). A diminished PHQ-9 score suggests no or mild depression, whereas an increased reading implies more severe distress; EQ 5D results generally range from 0 (poor quality of life) to 1 (exemplary wellbeing); lastly, higher PHQ–10 scores indicate symptoms are becoming increasingly bothersome."

Answered by AI

Are there still opportunities to take part in this research endeavor?

"Information from clinicaltrials.gov reveals that this trial is actively enrolling candidates; it was first posted on March 16th 2022 and has been recently updated with the same date."

Answered by AI

How many participants are being enrolled in this research investigation?

"Affirmative. Clinicaltrials.gov has the records of this medical research project, which was initially made public on March 16th 2022 and recently revised on the same date. 30 participants must be sourced from one single location for the trial to continue as planned."

Answered by AI
Recent research and studies
~14 spots leftby Apr 2025