Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01559948 · ClinicalTrials.gov registry record · NA

Effectiveness of the Compression Belt for Patients With Sacroiliac Joint Pain

A NA study, sponsored by Texas Woman's University.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT01559948 is a NA study that has completed, run by Texas Woman's University. The registered enrollment target is 30 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01559948, a NA study, has completed, sponsored by Texas Woman's University.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

The purpose of this randomized clinical trial is to examine the usefulness of the addition of a pelvic compression belt to a lumbopelvic stabilization program for patients with sacroiliac joint pain by comparing lumbopelvic stabilization exercises with a pelvic compression belt to lumbopelvic stabilization exercises alone. Outcome measures including the Modified Oswestry Low Back Pain Disability Index (OSW), the percentage change of TrA and IO muscle thickness (i.e. muscle contraction from rest to contract) utilizing ultrasound imaging, the Numeric Pain Rating Scale (NPRS) for pain, and a subjective rating of overall perceived improvement using the Global Rating of Change (GROC) scale will be collected. Hypothesis: The OSW scores and NPRS scores will be lower for those who receive the compression belt in addition to the lumbopelvic stabilization program as compared to those who receive the lumbopelvic stabilization alone. The percent change of muscle thickness for the deep abdominals as well as the GROC scores will be higher for those who receive the compression belt in addition to the lumbopelvic stabilization program as compared to those who receive the lumbopelvic stabilization alone.

Interventions

  • BEHAVIORAL Lumbopelvic stabilization exercise
  • DEVICE Sacroiliac joint belt

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2012-01
Est. Completion 2014-02
Phase NA

Sponsor

Texas Woman's University

51 total trials

What the Registry Record Tells You About NCT01559948

The ClinicalTrials.gov registry entry for NCT01559948 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Texas Woman's University, which has 51 total studies on file at ClinicalTrials.gov.

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

NCT01559948 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01559948 about?

NCT01559948 is a clinical study titled "Effectiveness of the Compression Belt for Patients With Sacroiliac Joint Pain". The purpose of this randomized clinical trial is to examine the usefulness of the addition of a pelvic compression belt to a lumbopelvic stabilization program for patients with sacroiliac joint pain by comparing lumbopelvic stabilization exercises with a pelvic compression belt to lumbopelvic stabil...

What is the current status of trial NCT01559948?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2012-01. Estimated completion is 2014-02.

What interventions are being tested in trial NCT01559948?

The interventions under investigation include: Lumbopelvic stabilization exercise (BEHAVIORAL), Sacroiliac joint belt (DEVICE).

Who is sponsoring clinical trial NCT01559948?

This trial is sponsored by Texas Woman's University, which has 51 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.