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NCT03634527 · ClinicalTrials.gov registry record · NA

Auricular Point Acupressure: Examining the Scientific Underpinnings of Pain Relief

A NA study, sponsored by Johns Hopkins University.

Terminated
Registry status
NA
Development phase
15
Enrollment target

NCT03634527: Clinical Trial NA study, sponsored by Johns Hopkins University.

NCT03634527 is a NA study that was terminated before completion, run by Johns Hopkins University. The registered enrollment target is 15 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03634527, a NA study, was terminated before completion, sponsored by Johns Hopkins University.

TERMINATED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

Chemotherapy-induced peripheral neuropathy (CIPN)-numbness, burning and stunning pain distributed in hands and feet-is a major challenge among cancer patients. Even after completion of chemotherapy, CIPN persists among \~30-40% of cancer patients, which can negatively impact quality of life. The only drug (duloxetine) better than placebo in a randomized control trial improved pain intensity by 0.72 points on a scale of 0-10, which cannot manage CIPN effectively. A better pain management strategy clearly needs to be developed. The investigators propose to test auricular point acupressure (APA), a non-invasive, easily administered, patient-controlled, and non-pharmacological strategy, to provide rapid, safe, and effective pain relief so that cancer patients can self-manage their CIPN. APA involves an acupuncture-like stimulation of the ear without needles. With APA, small seeds are taped to specific ear points. The patient is taught to apply pressure to the seeds, with the thumb and index finger, three times a day (morning, noon, and evening) for three minutes each session to achieve pain relief. The investigators have developed a detailed APA protocol to teach health-care providers without experience in acupuncture and traditional Chinese Medicine that investigators can learn about APA in brief educational seminars as a treatment including the systematic identification of ear points (called auricular diagnosis). The investigators teach methods that enable patients to continue using APA to self-manage their pain. However APA is not available in current U.S. health care setting yet. Quantitative sensory testing (QST) and fMRI in acupuncture have provided new objective methods for measuring pain. QST provides an evaluation of peripheral and central mechanisms of pain by quantifying stimulus-evoked negative and positive sensory phenomena to evaluate a participant's perception of threshold values regarding pain generated through touch (A beta fibers), warmth (C fibers),

Interventions

  • BEHAVIORAL Auricular Point Acupressure
  • BEHAVIORAL Control Auricular Point Acupressure-

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2018-02-15
Est. Completion 2019-01-30
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT03634527

The ClinicalTrials.gov registry entry for NCT03634527 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Auricular Point Acupressure is the first listed.

NCT03634527 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03634527 about?

NCT03634527 is a clinical study titled "Auricular Point Acupressure: Examining the Scientific Underpinnings of Pain Relief". Chemotherapy-induced peripheral neuropathy (CIPN)-numbness, burning and stunning pain distributed in hands and feet-is a major challenge among cancer patients. Even after completion of chemotherapy, CIPN persists among \~30-40% of cancer patients, which can negatively impact quality of life. The onl...

What is the current status of trial NCT03634527?

This trial is currently terminated. It is a NA study. The enrollment target is 15 participants. The study started on 2018-02-15. Estimated completion is 2019-01-30.

What interventions are being tested in trial NCT03634527?

The interventions under investigation include: Auricular Point Acupressure (BEHAVIORAL), Control Auricular Point Acupressure- (BEHAVIORAL).

Who is sponsoring clinical trial NCT03634527?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

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

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, the data changelog, or report a data error.