CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 7 enrolled
Drug / intervention
patientMpower platform +1 moreother
Likely dose
Not stated in record
Key inclusion· 4
  • Confirmed diagnosis of idiopathic pulmonary fibrosis (IPF)
  • Daily unrestricted access to smartphone or tablet device at home
  • Demonstrated understanding of protocol and correct use of Spirobank Smart spirometer and patientMpower platform
  • Able and willing to perform spirometry every day at home
Key exclusion· 3
  • Significant confusion or any concomitant medical condition limiting ability to record symptoms or use home spirometer regularly
  • New prescription of antifibrotic therapy (pirfenidone, nintedanib) within 4 weeks before baseline visit
  • Recent IPF exacerbation or clinically significant change in medical condition within 4 weeks before baseline visit

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03104322
NCT03104322N/ACompleted

A Randomised, Crossover Study of Self-monitoring of Symptoms and Spirometry Via the patientMpower Platform in Patients With Idiopathic Pulmonary Fibrosis

patientMpower Ltd.·interventional·Posted Apr 7, 2017·Updated Apr 2, 2019

In Brief

A clinical study evaluating patientMpower platform and usual care for Idiopathic Pulmonary Fibrosis. Completed, enrolled 7 participants across 1 site.

Detailed Summary

Pilot-scale, open-label, fixed-order, two-period crossover study in idiopathic pulmonary fibrosis (IPF) over 16 weeks. Patients will use an electronic health journal (patientMpower platform) to record treatment compliance, forced vital capacity (FVC; daily), impact of IPF on daily life (weekly) and other symptoms. Objectives are to characterise acceptability of patientMpower platform from patient \& healthcare professional perspective, impact of active engagement and self-monitoring using patientMpower platform on Patient Reported Outcome Measures (PROMs) in IPF, impact of patientMpower platform on medication compliance and correlation between patient-reported PROMs \& FVC and clinical outcomes.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIreland

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedApr 7, 2017
Enrollment StartJun 15, 2017
Primary CompletionMar 9, 2018
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 9.2 years ago

Interventions

patientMpower platformother

electronic health journal for patient to record compliance, spirometry, impact on daily life and symptoms

usual careother

usual care