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

NCT04917107 · ClinicalTrials.gov registry record · NA

CREATION: A Clinical Trial of Qigong for Neuropathic Pain Relief in Adults With Spinal Cord Injury

A NA study, sponsored by University of Minnesota.

Terminated
Registry status
NA
Development phase
23
Enrollment target

NCT04917107 is a NA study that was terminated before completion, run by University of Minnesota. The registered enrollment target is 23 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04917107, a NA study, was terminated before completion, sponsored by University of Minnesota.

TERMINATED
Registry status
NA
Development phase
23 participants
Enrollment target

Study Summary

Between 39-67% of the 294,000 Americans who have a SCI suffer from long-term debilitating neuropathic pain, interfering with rehabilitation, general activity, mobility, mood, sleep, and quality of life. Pain can hinder any potential for functional improvement that could be obtained during rehabilitation. Yet, neuropathic pain is refractory to many treatments. Current interventions, such as medications and physical therapy, result in less than 50% reduction in pain for only about one third of the people trying them, calling for new treatment options. Qigong, a mind and body approach that incorporates gentle body movements, paired with a focus on breathing and body awareness to promote health and wellness, could reduce SCI-related neuropathic pain. If the hypothesis is supported, the resulting work could be transformative in demonstrating a potentially effective therapy for civilians, military Service members, and Veterans with SCI and neuropathic pain. The following provides the scientific basis for this hypothesis and establishes the rationale for this approach. This study also includes an optional, remote, quasi-experimental substudy, in which all participants will receive Qigong for 12 weeks, followed by 6 weeks followup.

Interventions

  • BEHAVIORAL Qigong

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2021-07-01
Est. Completion 2023-02-01
Phase NA

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT04917107

The ClinicalTrials.gov registry entry for NCT04917107 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Qigong is the first listed.

NCT04917107 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04917107 about?

NCT04917107 is a clinical study titled "CREATION: A Clinical Trial of Qigong for Neuropathic Pain Relief in Adults With Spinal Cord Injury". Between 39-67% of the 294,000 Americans who have a SCI suffer from long-term debilitating neuropathic pain, interfering with rehabilitation, general activity, mobility, mood, sleep, and quality of life. Pain can hinder any potential for functional improvement that could be obtained during rehabilita...

What is the current status of trial NCT04917107?

This trial is currently terminated. It is a NA study. The enrollment target is 23 participants. The study started on 2021-07-01. Estimated completion is 2023-02-01.

What interventions are being tested in trial NCT04917107?

The interventions under investigation include: Qigong (BEHAVIORAL).

Who is sponsoring clinical trial NCT04917107?

This trial is sponsored by University of Minnesota, which has 966 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.