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NCT01587183 · ClinicalTrials.gov registry record · NA

Running Against Prehypertension Trial (RAPT): A Pilot Trial

A NA study, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
22
Enrollment target

NCT01587183: Completed NA study, sponsored by University of California, San Francisco.

NCT01587183 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01587183, a NA study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
22 participants
Enrollment target

Study Summary

This study will test strategies to help people with prehypertension adopt a running program to reduce their blood pressure in the long term. This study will be a 12 week intervention of about 40 participants randomized to running educational material, group based running instruction, or group based running instruction focused on form and all given the option to use the supplemental mHealth intervention. The purpose of this study is to collect feasibility, acceptability and preliminary efficacy data in preparation for a larger planned NIH-R01 study.

Primary Outcome

We will determine feasibility associated with recruitment n by recruiting and retaining at least 75% of our intended sample.

Interventions

  • BEHAVIORAL Educational material control
  • BEHAVIORAL Group running style B
  • BEHAVIORAL Group running style A

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2012-03
Est. Completion 2013-06
Phase NA

What the finished NCT01587183 record still lists

NCT01587183 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 3 interventions - of which Educational material control is the first listed.

NCT01587183 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01587183 about?

NCT01587183 is a clinical study titled "Running Against Prehypertension Trial (RAPT): A Pilot Trial". This study will test strategies to help people with prehypertension adopt a running program to reduce their blood pressure in the long term. This study will be a 12 week intervention of about 40 participants randomized to running educational material, group based running instruction, or group based ...

What is the current status of trial NCT01587183?

This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2012-03. Estimated completion is 2013-06.

What interventions are being tested in trial NCT01587183?

The interventions under investigation include: Educational material control (BEHAVIORAL), Group running style B (BEHAVIORAL), Group running style A (BEHAVIORAL).

Who is sponsoring clinical trial NCT01587183?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01587183's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 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 NCT01587183, the US trial registry maintained by the National Library of Medicine. NCT01587183 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.