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NCT06126887 · ClinicalTrials.gov registry record · NA
Evaluation of Efficacy and Comfort: A Trial on the Incrediwear Back Brace in Patients With Chronic Lower Back Pain
A NA study of Low Back Pain and Back Pain, sponsored by Johns Hopkins University.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT06126887 is a NA study of Low Back Pain and Back Pain that has completed, run by Johns Hopkins University. The registered enrollment target is 100 participants, below the 503-participant average among 122 other Low Back Pain trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06126887, a NA study of Low Back Pain and Back Pain, has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The investigators hypothesize that the utilization of Incrediwear's Back Brace, compared to a sham brace and a standard-issue brace, will lead to better brace adherence, increased patient satisfaction, reduced pain medication usage, and improved functional disability among non-surgical chronic LBP patients.
Conditions Studied
Interventions
- DEVICE Incrediwear Daytime Back Brace
- DEVICE Incrediwear Sham Daytime Back Brace
- DEVICE Control Daytime Back Brace
- DEVICE Incrediwear 24 Hour Back Brace
Study Locations (1)
Maryland
- Johns Hopkins Health Care & Surgery Center - Howard County Medical Center - Columbia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-01-09 |
| Est. Completion | 2024-11-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06126887
The ClinicalTrials.gov registry entry for NCT06126887 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 503-participant average among 122 other Low Back Pain trials with a reported enrollment target (80% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Low Back Pain appearing as the primary indexed condition, and to 4 interventions - of which Incrediwear Daytime Back Brace is the first listed.
NCT06126887 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT06126887 about?
NCT06126887 is a clinical study titled "Evaluation of Efficacy and Comfort: A Trial on the Incrediwear Back Brace in Patients With Chronic Lower Back Pain". The investigators hypothesize that the utilization of Incrediwear's Back Brace, compared to a sham brace and a standard-issue brace, will lead to better brace adherence, increased patient satisfaction, reduced pain medication usage, and improved functional disability among non-surgical chronic LBP p...
What is the current status of trial NCT06126887?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2024-01-09. Estimated completion is 2024-11-30.
What conditions does trial NCT06126887 study?
This clinical trial studies the following conditions: Low Back Pain, Back Pain.
What interventions are being tested in trial NCT06126887?
The interventions under investigation include: Incrediwear Daytime Back Brace (DEVICE), Incrediwear Sham Daytime Back Brace (DEVICE), Control Daytime Back Brace (DEVICE), Incrediwear 24 Hour Back Brace (DEVICE).
Who is sponsoring clinical trial NCT06126887?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06126887 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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