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NCT02597673 · ClinicalTrials.gov registry record · NA

Trial of Self-managed Approaches for Patellofemoral Pain Syndrome in Active Duty

A NA study, sponsored by University of Tennessee.

Completed
Registry status
NA
Development phase
132
Enrollment target

NCT02597673 is a NA study that has completed, run by University of Tennessee. The registered enrollment target is 132 participants.

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The verdict

NCT02597673, a NA study, has completed, sponsored by University of Tennessee.

COMPLETED
Registry status
NA
Development phase
132 participants
Enrollment target

Study Summary

The overall objective of this project is to compare the three home-managed treatment regimens for PFPS: neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), and NMES combined with TENS to a standard home exercise program (HEP). Each of the three treatment arms will be supplemented by HEP and compared to a group receiving standard HEP alone. The central hypothesis is that the combination of NMES with TENS will show significantly greater improvements in muscle strength, mobility, pain, daily activity and quality of life (QOL) than HEP alone. The investigators are examining: 1) whether the three treatment regimens are significantly more efficacious than standard HEP alone in improving lower extremity muscle strength, physical activity, mobility, pain, and quality of life; 2) lower extremity muscle strength, physical activity, mobility, pain, and quality of life differ significantly across the 4 time periods; 3) is there an interaction between treatment and time in relation to lower extremity muscle strength, physical activity, mobility, pain, and quality of life.

Interventions

  • DEVICE TENS
  • DEVICE NMES
  • OTHER Home Exercise Program (HEP)

Trial Details

FieldValue
Enrollment Target 132 participants
Start Date 2015-07
Est. Completion 2018-05-31
Phase NA

Sponsor

University of Tennessee

96 total trials

What the Registry Record Tells You About NCT02597673

The ClinicalTrials.gov registry entry for NCT02597673 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 132 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Tennessee, which has 96 total studies on file at ClinicalTrials.gov.

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

NCT02597673 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02597673 about?

NCT02597673 is a clinical study titled "Trial of Self-managed Approaches for Patellofemoral Pain Syndrome in Active Duty". The overall objective of this project is to compare the three home-managed treatment regimens for PFPS: neuromuscular electrical stimulation (NMES), transcutaneous electrical nerve stimulation (TENS), and NMES combined with TENS to a standard home exercise program (HEP). Each of the three treatment ...

What is the current status of trial NCT02597673?

This trial is currently completed. It is a NA study. The enrollment target is 132 participants. The study started on 2015-07. Estimated completion is 2018-05-31.

What interventions are being tested in trial NCT02597673?

The interventions under investigation include: TENS (DEVICE), NMES (DEVICE), Home Exercise Program (HEP) (OTHER).

Who is sponsoring clinical trial NCT02597673?

This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.