Auricular Acupressure and Limb Massage for Neuropathic Pain in Spinal Cord Injury

Not Applicable

Not yet recruiting

• Conditions: Spinal Cord Injury

• Registration Number: NCT06700278
• Lead Sponsor: National Taiwan University Hospital

Brief Summary

This randomized controlled trial included 90 patients with spinal cord injury, divided into an experimental group and a control group (45 each). The experimental group received auricular acupressure alongside rehabilitation therapy, while the control group received body acupoint massage alongside rehabilitation therapy. The intervention targeted specific auricular and body acupoints, performed three times daily, five days a week, for three weeks.

Detailed Description

This study is a randomized controlled trial conducted in the rehabilitation ward of National Taiwan University Hospital, using a convenience sampling method. A total of 90 spinal cord injury patients who meet the inclusion criteria will be recruited and randomly assigned to either the experimental group (n=45) or the control group (n=45).

The experimental group will receive auricular acupressure in addition to rehabilitation therapy. The selected auricular acupoints include Shenmen (TF4), Subcortex (AT1), Liver (CO12), and Sympathetic (AH6a).

The control group will receive body acupoint massage in addition to rehabilitation therapy. The selected body acupoints include Quchi (LI11), Hegu (LI4), Sanyinjiao (SP6), and Zusanli (ST36).

Both groups will receive acupoint massage three times daily, with each acupoint being massaged for three minutes. The applied pressure will be adjusted to induce sensations of soreness, numbness, fullness, or mild pain. The intervention will be conducted five days per week for a total of three weeks.

Study Timeline

• Status Verified: 2024-11
• Study First Submitted: 2024-11-15
• Study First Submitted QC: 2024-11-19
• Study First Posted: 2024-11-21
• Last Update Submitted: 2025-02-24
• Last Update Posted: 2025-02-26
• Study Start: 2025-04-01
• Primary Completion: 2026-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

1. Over 18 years old.
2. Spinal cord injury due to traumatic or non-traumatic reasons.
3. Within one year after spinal cord injury.
4. Spinal cord injuries are classified into ASIA grades B to D.
5. DN4 scale ≥ 4 points and PainDETECT scale ≥ 19 points.
6. Able to communicate in Mandarin and Taiwanese or able to read and write Chinese.

Exclusion Criteria

1. The auricle and surrounding skin are injured, infected or susceptible.
2. Nerve block surgery has been performed previously.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Douleur Neuropathique 4 questions(DN4)	Before the intervention and on the 5th, 12th, and 19th days of the intervention.
PainDetect Pain Questionnaire	Before the intervention and on the 5th, 12th, and 19th days of the intervention.

Secondary Outcome Measures

Name	Time	Method
Barthel Index	Before the intervention and on the 5th, 12th, and 19th days of the intervention.
WHOQOL-BREF	Before the intervention and on the 5th, 12th, and 19th days of the intervention.