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NCT01752010 · ClinicalTrials.gov registry record · NA

Comparing Acupuncture, BioModulator, and Transcutaneous Electrical Nerve Stimulation for Symptomatic Treatment of Chronic Pain.

A NA study of Depression and Chronic Pain, sponsored by Samueli Institute for Information Biology.

Completed
Registry status
NA
Development phase
98
Enrollment target
1
Study location

NCT01752010 is a NA study of Depression and Chronic Pain that has completed, run by Samueli Institute for Information Biology. The registered enrollment target is 98 participants, below the 786-participant average among 679 other Depression trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01752010, a NA study of Depression and Chronic Pain, has completed, sponsored by Samueli Institute for Information Biology.

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

Study Summary

The primary objective of this preliminary study is to compare the Tennant BioModulator with Transcutaneous Electrical Nerve Stimulation (TENS) and Traditional Chinese Acupuncture for the management of chronic pain among injured service members. The secondary objective is to investigate any associative effects or benefits on sleep, Post-Traumatic Stress Disorder (PTSD) symptoms, or depression.

Conditions Studied

Depression Chronic Pain Sleep PTSD Symptoms

Interventions

  • OTHER Traditional Chinese Acupuncture
  • DEVICE Tennant™ Biomodulator Treatment
  • DEVICE Transcutaneous electrical nerve stimulation (TENS) Treatment

Study Locations (1)

Texas

  • Brooke Army Medical Center - Fort Sam Houston

Trial Details

FieldValue
Enrollment Target 98 participants
Start Date 2010-05
Est. Completion 2014-04
Phase NA

Sponsor

Samueli Institute for Information Biology

8 total trials

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What the Registry Record Tells You About NCT01752010

The ClinicalTrials.gov registry entry for NCT01752010 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 98 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 786-participant average among 679 other Depression trials with a reported enrollment target (88% lower). The listed sponsor is Samueli Institute for Information Biology, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Depression appearing as the primary indexed condition, and to 3 interventions - of which Traditional Chinese Acupuncture is the first listed.

NCT01752010 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT01752010 about?

NCT01752010 is a clinical study titled "Comparing Acupuncture, BioModulator, and Transcutaneous Electrical Nerve Stimulation for Symptomatic Treatment of Chronic Pain.". The primary objective of this preliminary study is to compare the Tennant BioModulator with Transcutaneous Electrical Nerve Stimulation (TENS) and Traditional Chinese Acupuncture for the management of chronic pain among injured service members. The secondary objective is to investigate any associati...

What is the current status of trial NCT01752010?

This trial is currently completed. It is a NA study. The enrollment target is 98 participants. The study started on 2010-05. Estimated completion is 2014-04.

What conditions does trial NCT01752010 study?

This clinical trial studies the following conditions: Depression, Chronic Pain, Sleep, PTSD Symptoms.

What interventions are being tested in trial NCT01752010?

The interventions under investigation include: Traditional Chinese Acupuncture (OTHER), Tennant™ Biomodulator Treatment (DEVICE), Transcutaneous electrical nerve stimulation (TENS) Treatment (DEVICE).

Who is sponsoring clinical trial NCT01752010?

This trial is sponsored by Samueli Institute for Information Biology, which has 8 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01752010 being conducted?

This trial has 1 study location across Texas. 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

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.