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NCT04245852 · ClinicalTrials.gov registry record · NA

Does a Video-based Education Tool Related to Strengthening Result in Different Functional Outcomes Compared to Traditional Physical Therapy Education for Patients?

A NA study, sponsored by University of Illinois at Chicago.

Terminated
Registry status
NA
Development phase
5
Enrollment target

NCT04245852: Clinical Trial NA study, sponsored by University of Illinois at Chicago.

NCT04245852 is a NA study that was terminated before completion, run by University of Illinois at Chicago. The registered enrollment target is 5 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04245852, a NA study, was terminated before completion, sponsored by University of Illinois at Chicago.

TERMINATED
Registry status
NA
Development phase
5 participants
Enrollment target

Study Summary

• Patients receiving physical therapy (PT) at the University of Illinois at Chicago Faculty Practice (UICFP) meeting inclusion and exclusion criteria will be randomly assigned to one of two groups: control group (CG) receiving standard care and an experimental group (EG) receiving standard care in addition to being provided a strength education video (SEV). The SEV is a short video designed to provide instructions clarifying how to do strength-based exercises by monitoring a fatigue response with a set of any exercise. The EG will watch the video with headphones in the waiting room of the UICFP on an iPad. The EG will also be provided a handout with a link and QR code to the video on YouTube.com. Functional changes with PT will be tracked for both groups using a Patient Specific Functional Scale (PSFS) questionnaire at initial evaluation, follow up at session 3 or 4, and at any date of anticipated discharge. Basic demographic data (age, sex), dates of data collection, and any discharge dates will be tracked as well. If questions arise regarding the content of the SEV then the treating physical therapist will be permitted to answer and apply the content at their discretion. All therapists will have pre-approved the content of the video to ensure there are no contradictions to their usual methods of care. Data will be gathered for up to 3 months.

Primary Outcome

The Patient Specific Functional Scale (PSFS) is a clinical outcome tool that was designed and validated for the purpose of tracking changes in function for patients with a wide variety of clinical conditions. This is measuring up to three patient identified important activities which are each scored on a 0 to 10 scale. On this scale 0 indicates "unable to perform activity" and 10 indicates "able to perform activity"

Interventions

  • OTHER Strength education video
  • OTHER standard PT care

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2020-02-11
Est. Completion 2020-11-16
Phase NA
University of Illinois at Chicago

430 total trials

Why NCT04245852 stopped before completion

NCT04245852 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

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

NCT04245852 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04245852 about?

NCT04245852 is a clinical study titled "Does a Video-based Education Tool Related to Strengthening Result in Different Functional Outcomes Compared to Traditional Physical Therapy Education for Patients?". • Patients receiving physical therapy (PT) at the University of Illinois at Chicago Faculty Practice (UICFP) meeting inclusion and exclusion criteria will be randomly assigned to one of two groups: control group (CG) receiving standard care and an experimental group (EG) receiving standard care in a...

What is the current status of trial NCT04245852?

This trial is currently terminated. It is a NA study. The enrollment target is 5 participants. The study started on 2020-02-11. Estimated completion is 2020-11-16.

What interventions are being tested in trial NCT04245852?

The interventions under investigation include: Strength education video (OTHER), standard PT care (OTHER).

Who is sponsoring clinical trial NCT04245852?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04245852's enrollment target sits among peer trials

5 1988th of 2000 higher than 5 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 NCT04245852, the US trial registry maintained by the National Library of Medicine. NCT04245852 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.