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NCT02996435 · ClinicalTrials.gov registry record · Phase 4

Smartphones to Improve Rivaroxaban ADHEREnce in Atrial Fibrillation

A Phase 4 study, sponsored by Janssen Scientific Affairs.

Completed
Registry status
Phase 4
Development phase
139
Enrollment target

NCT02996435: Completed Phase 4 study, sponsored by Janssen Scientific Affairs.

NCT02996435 is a Phase 4 study that has completed, run by Janssen Scientific Affairs. The registered enrollment target is 139 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02996435, a Phase 4 study, has completed, sponsored by Janssen Scientific Affairs.

COMPLETED
Registry status
Phase 4
Development phase
139 participants
Enrollment target

Study Summary

The primary purpose of this study is to evaluate the effectiveness of an intervention with a mobile adherence platform, compared to physician- or nurse-guided standard of care, to improve medication adherence to rivaroxaban in participants who have recently initiated treatment with rivaroxaban for stroke prevention in atrial fibrillation based on an assessment of the proportion of days covered (PDC) of rivaroxaban treatment.

Primary Outcome

Adherence to rivaroxaban medication will be estimated based on validated PDC algorithm. PDC (expressed as percentage) defined as non-hospitalized days during which oral anticoagulant (OAC) will be supplied and consumed over total observation time duration during which rivaroxaban should have been consumed.

Interventions

  • OTHER No Intervention
  • BEHAVIORAL Mobile Application Intervention

Trial Details

FieldValue
Enrollment Target 139 participants
Start Date 2016-12-21
Est. Completion 2018-03-22
Phase Phase 4
Janssen Scientific Affairs

37 total trials

What the finished NCT02996435 record still lists

NCT02996435 is an interventional study that assigns participants to a tested intervention. The registered 139 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 2 interventions - of which No Intervention is the first listed.

NCT02996435 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02996435 about?

NCT02996435 is a clinical study titled "Smartphones to Improve Rivaroxaban ADHEREnce in Atrial Fibrillation". The primary purpose of this study is to evaluate the effectiveness of an intervention with a mobile adherence platform, compared to physician- or nurse-guided standard of care, to improve medication adherence to rivaroxaban in participants who have recently initiated treatment with rivaroxaban for s...

What is the current status of trial NCT02996435?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 139 participants. The study started on 2016-12-21. Estimated completion is 2018-03-22.

What interventions are being tested in trial NCT02996435?

The interventions under investigation include: No Intervention (OTHER), Mobile Application Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT02996435?

This trial is sponsored by Janssen Scientific Affairs, which has 37 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02996435's enrollment target sits among peer trials

139 593rd of 2000 higher than 1,408 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02996435, the US trial registry maintained by the National Library of Medicine. NCT02996435 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.