Clinical Trials Directory

Trials / Completed

CompletedNCT02189070

The PAtient Preference Analysis of Yearly Follow-up After PCI (PAPAYA)

What Patients Really Want - Patient Preferences Regarding Annual Follow-up After Medical Interventions: The PAPAYA Study

Status
Completed
Phase
Study type
Observational
Enrollment
2,566 (actual)
Sponsor
Thorax Centrum Twente · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the preference of patients regarding the approach for follow-up after percutaneous coronary intervention (PCI) procedures. We hypothesize that patients prefer questionnaires for annual follow-up assessment when compared to telephone or email.

Detailed description

Rationale: Assessment and reporting of long-term clinical follow-up after medical interventions is essential for transparency of medical care and its quality improvement. However follow-up adherence is a serious challenge in clinical trials. Taking the patient preference of the mode of follow-up into account is likely to enhance trial adherence, reduce withdrawals, and facilitate a longer follow-up duration. No data on patient preference of annual follow-up have been reported. Objective: To investigate the patient preference of approach to obtain follow-up information after percutaneous coronary intervention (PCI) Study design: Single-center, prospective, observational registry Study population: All patients enrolled in the percutaneous coronary intervention studies TWENTE trial (a broad study population reflecting real-world PCI patients) and DUTCH PEERS trial (an all-comers population), who were treated at Thoraxcentrum Twente in Enschede between June 2008 and May 2012 Intervention: All subjects will receive a questionnaire with questions regarding their preference with regards to the approach of acquiring follow-up information after PCI. Main study endpoints: * The primary endpoint is the patient preference on how to be approached for annual follow-up after PCI procedures. * Secondary endpoints include 1. least preferred approach of follow-up 2. the preferred number of follow-up moments per year 3. the from the patients' perspective maximum acceptable number of questions to be answered 4. the assessment of potential relationships between the most and least preferred approach of assessment and patient age, gender urgency of PCI treatment, and history of previous revascularizations

Conditions

Timeline

Start date
2013-07-01
Primary completion
2014-08-01
Completion
2014-09-01
First posted
2014-07-14
Last updated
2015-05-14

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02189070. Inclusion in this directory is not an endorsement.