Imagined Acupuncture for Postoperative Pain After Spinal Surgery
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Jingping Wang, MD, Ph.D.
- Study ID
- NCT07197710
- Status
- Recruiting
Conditions
- Pain Management
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- video-guided acupuncture imagery treatment (VGAIT) — OTHERUnlike traditional acupuncture, VGAIT can be self-administered and does not require physical needle insertion, making it a practical alternative for patients seeking non-invasive pain management.
- Education video — OTHEREducation video about postoperative precautions
Study Details
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
Key Dates
- Start date
- Oct 1, 2025
- Status verified
- Sep 2025
- Primary completion
- Sep 19, 2026
- Completion
- Sep 19, 2026
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Group 1: Imagined Acupuncture InterventionParticipants 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 videoParticipants 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.
Primary Outcome Measure
Pain Scores (VAS) [ Time Frame: During the first postoperative week (Days 0-6) ]
Central Contacts
- Jingping Wang Associate Professor6176432729
Locations (1)
| Facility | City | State | ZIP |
|---|---|---|---|
| Massachusetts General Hospital | Boston | Massachusetts | 02114 |
Find similar trials in Boston, MA
Related Studies
- Psilocybin in Cancer Pain StudyPHASE2 · Recruiting · Yvan Beaussant, MD, MSci · Boston, Massachusetts
- Effectiveness of Bupivacaine, Ketorolac, Ketamine, vs Bupivacaine Alone in Reducing Postoperative Pocket PainPHASE1 · Not Yet Recruiting · Kansas City Heart Rhythm Research Foundation · Loma Linda, California
- Efficacy of Liposomal Bupivacaine Post SeptorhinoplastyPHASE3 · Enrolling By Invitation · Jessyka Lighthall · Hershey, Pennsylvania
- Local Anesthesia for Facial FracturesPHASE2 · Recruiting · Washington University School of Medicine · St Louis, Missouri