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Behavioural Intervention
Standard Acupuncture / Moxibustion for Neuropathic Pain
N/A
Waitlist Available
Research Sponsored by New York University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline rating of pain intensity after 6 wks of twice-wkly treatment sessions (the end of the treatment phase) and at weeks 9, 11 and 15 (the follow-up phase - determine change and sustainability)
Awards & highlights
Study Summary
This trial assesses the efficacy of novel non-pharmacologic pain management approaches to reduce HIV-related DSP pain and improve quality of life.
Eligible Conditions
- Neuropathic Pain
- Pain
- Neuropathy
- HIV/AIDS
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline rating of general health after 6 wks of twice-wkly treatment sessions (the end of the treatment phase) and at weeks 9, 11 and 15 (the follow-up phase - determine change and sustainability)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline rating of general health after 6 wks of twice-wkly treatment sessions (the end of the treatment phase) and at weeks 9, 11 and 15 (the follow-up phase - determine change and sustainability)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Gracely Pain Scale (GPS)
Secondary outcome measures
Clinical Global Severity Improvement Scale (CGIs)
Medical Outcome Survey - HIV (MOS-HIV)
NIH PROMIS Pain Scale
+2 moreTrial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: Standard (fixed) protocol Acu/Moxa - ActiveExperimental Treatment1 Intervention
Standard (Fixed) Acupuncture / Moxibustion Active Protocol
Subjects receive active standard Acu/Moxa protocol aimed at reducing neuropathic pain/discomfort.
Group II: Individualized (tailored) protocol Acu/Moxa - ActiveExperimental Treatment1 Intervention
Individualized (Tailored) Active Acupuncture / Moxibustion Protocol
Subjects receive active individualized Acu/Moxa protocol based on traditional Chinese medicine assessment aimed reducing neuropathic pain/discomfort.
Group III: Sham Acu/Placebo Moxa (Control)Active Control1 Intervention
Sham Acu/Placebo Moxa (Control)
Note. All subjects randomized to the Control will be offered 12 active protocol acupuncture/ moxibustion treatments, at no cost, at the end of their study participation.
Group IV: WaitList (Control)Active Control1 Intervention
WaitList (Control) No treatment. Subjects receive all aspects of study participation with the exception of exposure to Acupuncture / Moxibustion.
Note. All subjects randomized to the Control will then be offered 12 active protocol acupuncture/ moxibustion treatments, at no cost, at the end of their study participation.
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Who is running the clinical trial?
New York UniversityLead Sponsor
226 Previous Clinical Trials
314,059 Total Patients Enrolled
1 Trials studying Neuropathic Pain
44 Patients Enrolled for Neuropathic Pain
National Institutes of Health (NIH)NIH
2,696 Previous Clinical Trials
6,952,392 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is it feasible for individuals to join this medical experiment at present?
"At present, clinicaltrials.gov confirms that the trial is actively recruiting. This venture was first announced on January 14th 2019 and its most recent update occurred October 26th 2021."
Answered by AI
What is the scope of this research's participants?
"Affirmative. The clinical trial directory on clinicaltrials.gov demonstrates that this medical study, initially published on January 14th 2019, is actively seeking patients. Thus far they have enlisted 196 participants from a single location."
Answered by AI
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