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NCT03270124 · ClinicalTrials.gov registry record · NA

A pragmatiC sTrategy to Promote actIVity and Enhance Quality of Life AFTER Transcatheter Aortic Valve Replacement

A NA study, sponsored by Vanderbilt University Medical Center.

Completed
Registry status
NA
Development phase
85
Enrollment target

NCT03270124: Completed NA study, sponsored by Vanderbilt University Medical Center.

NCT03270124 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 85 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03270124, a NA study, has completed, sponsored by Vanderbilt University Medical Center.

COMPLETED
Registry status
NA
Development phase
85 participants
Enrollment target

Study Summary

This study is being performed in patients who have undergone transcatheter aortic valve replacement (TAVR) for aortic stenosis. The goal is to obtain pilot and feasibility data on a novel post-procedure rehabilitation strategy, including a daily activity goal using a fitness tracking device (Fitbit Alta HR) and in-home resistance training exercises targeting muscles related to activities of daily living. We will evaluate the effect of these interventions on physical performance and several quality of life domains.

Primary Outcome

Average daily steps over the intervention period

Interventions

  • BEHAVIORAL Daily Activity Goal
  • BEHAVIORAL Resistance Exercises
  • BEHAVIORAL Daily Activity Recording

Trial Details

FieldValue
Enrollment Target 85 participants
Start Date 2017-11-07
Est. Completion 2020-03-25
Phase NA

What the finished NCT03270124 record still lists

NCT03270124 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 85 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 3 interventions - of which Daily Activity Goal is the first listed.

NCT03270124 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03270124 about?

NCT03270124 is a clinical study titled "A pragmatiC sTrategy to Promote actIVity and Enhance Quality of Life AFTER Transcatheter Aortic Valve Replacement". This study is being performed in patients who have undergone transcatheter aortic valve replacement (TAVR) for aortic stenosis. The goal is to obtain pilot and feasibility data on a novel post-procedure rehabilitation strategy, including a daily activity goal using a fitness tracking device (Fitbit ...

What is the current status of trial NCT03270124?

This trial is currently completed. It is a NA study. The enrollment target is 85 participants. The study started on 2017-11-07. Estimated completion is 2020-03-25.

What interventions are being tested in trial NCT03270124?

The interventions under investigation include: Daily Activity Goal (BEHAVIORAL), Resistance Exercises (BEHAVIORAL), Daily Activity Recording (BEHAVIORAL).

Who is sponsoring clinical trial NCT03270124?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03270124's enrollment target sits among peer trials

85 980th of 2000 higher than 1,018 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT03270124, the US trial registry maintained by the National Library of Medicine. NCT03270124 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.