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Clinical Trials/NCT03046030
NCT03046030CompletedNot Applicable

Mechanistic Studies on Video-guided Acupuncture Imagery Treatment of Pain

Massachusetts General Hospital1 site in 1 country27 target enrollmentStarted: January 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
27
Locations
1
Primary Endpoint
fMRI signal increases

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Right handed healthy male and female adults aged 18-60
  • •No contraindications to fMRI scanning

Exclusion Criteria

  • •Current or past history of major medical, neurological, or psychiatric illness
  • •Any pain disorder
  • •Pregnancy
  • •Non-fluent speaker of English

Arms & Interventions

Healthy Volunteers

Experimental

In this experiment, we will apply a crossover design in healthy subjects. Each subject will receive four treatments in four separate sessions: 1) VGAIT, 2) VGAIT control condition, 3) real acupuncture, and 4) sham acupuncture. Each session will be separated by at least 7 days. Subjects will participate in five experimental sessions: a training and familiarity behavioral session and four fMRI sessions during which the subject will receive one of the four treatments.

Intervention: VGAIT (Other)

Healthy Volunteers

Experimental

In this experiment, we will apply a crossover design in healthy subjects. Each subject will receive four treatments in four separate sessions: 1) VGAIT, 2) VGAIT control condition, 3) real acupuncture, and 4) sham acupuncture. Each session will be separated by at least 7 days. Subjects will participate in five experimental sessions: a training and familiarity behavioral session and four fMRI sessions during which the subject will receive one of the four treatments.

Intervention: Real acupuncture (Other)

Healthy Volunteers

Experimental

In this experiment, we will apply a crossover design in healthy subjects. Each subject will receive four treatments in four separate sessions: 1) VGAIT, 2) VGAIT control condition, 3) real acupuncture, and 4) sham acupuncture. Each session will be separated by at least 7 days. Subjects will participate in five experimental sessions: a training and familiarity behavioral session and four fMRI sessions during which the subject will receive one of the four treatments.

Intervention: Sham acupuncture (Other)

Healthy Volunteers

Experimental

In this experiment, we will apply a crossover design in healthy subjects. Each subject will receive four treatments in four separate sessions: 1) VGAIT, 2) VGAIT control condition, 3) real acupuncture, and 4) sham acupuncture. Each session will be separated by at least 7 days. Subjects will participate in five experimental sessions: a training and familiarity behavioral session and four fMRI sessions during which the subject will receive one of the four treatments.

Intervention: VGAIT control (Other)

Outcomes

Primary Outcomes

fMRI signal increases

Time Frame: 4 days; Sessions 2-5

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jian Kong

Associate Professor

Massachusetts General Hospital

Study Sites (1)

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