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Assessing the Efficacy of Imagined Acupuncture for Postoperative Acute Pain Management in Spinal Surgery

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to evaluate whether imagined acupuncture can reduce postoperative acute pain in adult patients undergoing spinal surgery. The main questions it aims to answer are: Does video-guided imagined acupuncture improve postoperative pain control? Does the intervention reduce opioid consumption and improve functional recovery in the immediate postoperative period? Researchers will compare the imagined acupuncture group to the control education video group to see if imagery-based intervention leads to better pain outcomes and reduced analgesic use. Participants will: Watch a 30-minute video once daily for 7 consecutive days after surgery Complete pain and function assessments during the hospital stay and postoperative follow-up

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Undergoing 1- to 2-level primary spine surgery

• Aged 18 years or older

• Willing and able to receive postoperative imagined acupuncture (VGAIT)

• Able to provide written informed consent

Locations
United States
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Jingping Wang Associate Professor
JWANG23@mgh.harvard.edu
6176432729
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2026-09-19
Participants
Target number of participants: 120
Treatments
Experimental: Group 1: Imagined Acupuncture Intervention
Participants assigned to Group 1 will receive standard postoperative care and a daily VGAIT session once per day for seven consecutive days following surgery. Each session will last approximately 30 minutes and will be guided by a standardized video designed to induce acupuncture imagery and mental engagement. VGAIT will be administered at the same time each day (e.g., 9:00 AM ± 30 minutes). VAS and ODI assessments will be administered following the completion of the video session. The initial video session will be administered once the patient has fully regained consciousness in the post-anesthesia care unit (PACU) following surgery.
Sham_comparator: Group 2: Education video
Participants in the control group will receive standard postoperative care and Education video without any simulated acupuncture intervention. VAS and ODI assessments will be conducted at the same intervals as in Group 1 for consistency and comparison.
Related Therapeutic Areas
Sponsors
Leads: Jingping Wang, MD, Ph.D.

This content was sourced from clinicaltrials.gov