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NCT03688282 · ClinicalTrials.gov registry record · NA

Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2

A NA study of Osteopenia, sponsored by Theranova, L.L.C..

Completed
Registry status
NA
Development phase
18
Enrollment target
1
Study location

NCT03688282 is a NA study of Osteopenia that has completed, run by Theranova, L.L.C.. The registered enrollment target is 18 participants, below the 110-participant average among 9 other Osteopenia trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03688282, a NA study of Osteopenia, has completed, sponsored by Theranova, L.L.C..

COMPLETED
Registry status
NA
Development phase
18 participants
Enrollment target
1
Study location

Study Summary

The wearable vibration device aims to consistently deliver vibrations directly to the hip and spine and allowing use during many everyday activities. We propose that demonstrating higher rates of compliance and consistent delivery of optimal force, with accelerometer feedback, will provide a superior alternative to whole body vibration and is plausibly more effective at preventing bone loss in postmenopausal women than vibration platforms in the home setting.

Conditions Studied

Interventions

  • DEVICE Wearable vibration belt
  • DEVICE Sham, wearing belt

Study Locations (1)

Nebraska

  • University of Nebraska Medical Center - Omaha

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2018-07-11
Est. Completion 2019-04-17
Phase NA

Sponsor

Theranova, L.L.C.

11 total trials

What the Registry Record Tells You About NCT03688282

The ClinicalTrials.gov registry entry for NCT03688282 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 110-participant average among 9 other Osteopenia trials with a reported enrollment target (84% lower). The listed sponsor is Theranova, L.L.C., which has 11 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Osteopenia appearing as the primary indexed condition, and to 2 interventions - of which Wearable vibration belt is the first listed.

NCT03688282 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT03688282 about?

NCT03688282 is a clinical study titled "Wearable Vibration Device to Prevent Bone Loss in Postmenopausal Women--Aim 2". The wearable vibration device aims to consistently deliver vibrations directly to the hip and spine and allowing use during many everyday activities. We propose that demonstrating higher rates of compliance and consistent delivery of optimal force, with accelerometer feedback, will provide a superio...

What is the current status of trial NCT03688282?

This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2018-07-11. Estimated completion is 2019-04-17.

What conditions does trial NCT03688282 study?

This clinical trial studies the following conditions: Osteopenia.

What interventions are being tested in trial NCT03688282?

The interventions under investigation include: Wearable vibration belt (DEVICE), Sham, wearing belt (DEVICE).

Who is sponsoring clinical trial NCT03688282?

This trial is sponsored by Theranova, L.L.C., which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03688282 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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