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NCT03261505 Clinical Trial

Mechanistic Studies on Video-guided Acupuncture Imagery Treatment of Knee Pain

Osteoarthritis, Knee Clinical Trial

Official title:
Mechanistic Studies on Video-guided Acupuncture Imagery Treatment of Knee Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03261505
Other study ID # 2017P000820
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 4, 2019
Est. completion date August 31, 2023

Study information
Verified date November 2023
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate brain response and connectivity changes evoked by video-guided acupuncture imagery treatment (VGAIT) and verum and sham acupuncture in knee osteoarthritis patients to elucidate the underlying brain mechanisms of mind-body interaction, imagery, and acupuncture.

Recruitment information / eligibility
Status Completed
Enrollment 125
Est. completion date August 31, 2023
Est. primary completion date August 29, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - Right-handed - Knee osteoarthritis patients - Ages 40 to 70 years old Exclusion Criteria: - Any contraindications to MRI scanning (claustrophobia, metal implants) - Current or past history of major medical, neurological, or psychiatric illness other than knee osteoarthritis (including high blood pressure, heart disorders, impaired elimination, stomach problems, major kidney or liver problems, bleeding problems, severe dehydration, history of diabetes, history of asthma or other respiratory condition) - Pregnancy - Non fluent English speaker

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Acupuncture
Patients will watch a video of themselves receiving acupuncture or a control video or receive real or sham acupuncture treatment.

Locations
Country Name City State
United States Athinoula A. Martinos Center for Biomedical Imaging Charlestown Massachusetts

Sponsors (1)
Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary fMRI signal increases 4 days; Sessions 2-5
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