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NCT03485820 · ClinicalTrials.gov registry record · NA

A Novel Transition Program to Reduce Disability After Stroke

A NA study, sponsored by Washington University School of Medicine.

Completed
Registry status
NA
Development phase
185
Enrollment target

NCT03485820: Completed NA study, sponsored by Washington University School of Medicine.

NCT03485820 is a NA study that has completed, run by Washington University School of Medicine. The registered enrollment target is 185 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03485820, a NA study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
NA
Development phase
185 participants
Enrollment target

Study Summary

This study evaluates a program designed to help individuals transition home from inpatient rehabilitation following an ischemic or hemorrhagic stroke. Half of the participants will receive a stroke education program while the other half will receive an environmental modifications program.

Primary Outcome

The RNLI is a disability-related quality-of life-instrument used to measure participants' satisfaction with their home and community participation and has been validated on a population of community-dwelling individuals with chronic conditions. It uses an 11-item, 10 point scale, with higher scores indicating greater reintegration to normal living. The sum score is divided by 110 and then multiplied by 100 to obtain an adjusted score. Adjusted scores range from 0 to 100, with higher scores indic

Interventions

  • BEHAVIORAL COMPASS
  • BEHAVIORAL Stroke education

Trial Details

FieldValue
Enrollment Target 185 participants
Start Date 2018-01-09
Est. Completion 2024-02-28
Phase NA

What the finished NCT03485820 record still lists

NCT03485820 is an interventional study that assigns participants to a tested intervention. The registered 185 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 2 interventions - of which COMPASS is the first listed.

NCT03485820 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03485820 about?

NCT03485820 is a clinical study titled "A Novel Transition Program to Reduce Disability After Stroke". This study evaluates a program designed to help individuals transition home from inpatient rehabilitation following an ischemic or hemorrhagic stroke. Half of the participants will receive a stroke education program while the other half will receive an environmental modifications program.

What is the current status of trial NCT03485820?

This trial is currently completed. It is a NA study. The enrollment target is 185 participants. The study started on 2018-01-09. Estimated completion is 2024-02-28.

What interventions are being tested in trial NCT03485820?

The interventions under investigation include: COMPASS (BEHAVIORAL), Stroke education (BEHAVIORAL).

Who is sponsoring clinical trial NCT03485820?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03485820's enrollment target sits among peer trials

185 580th of 2000 higher than 1,420 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 NCT03485820, the US trial registry maintained by the National Library of Medicine. NCT03485820 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.