Clinical Trials Directory

Trials / Completed

CompletedNCT06044714

Effects of Acupuncture on Perceived Stress and Health in Military Service Members

Effects of Acupuncture on Perceived Stress and Health in Military Service Members and Veterans

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
86 (actual)
Sponsor
United States Naval Medical Center, San Diego · Federal
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The goal of this is to investigate the effect of a Manual Standardized Stress Acupuncture (MSSA) protocol as an adjunct treatment to a short-term mindfulness therapy for perceived stress and general health in service members (i.e., active duty military personnel and veterans). The specific aims of this study are Aim 1) To evaluate the effectiveness of a brief MSSA as an adjunct treatment with a short-term Mindfulness-Based Stress Reduction (MBSR) compared with MBSR alone for perceived stress and general health in service members. Aim 2) To describe any perceived benefits of MSSA as an adjunct treatment with MBSR compared with MBSR alone for perceived stress and general health. Participants will be asked to complete an informed consent if eligible for the study and randomized into two groups: 1) Participants in the experimental group will receive MSSA in addition to MBSR. 2) Participants in the control group will receive MBSR only. Researchers will compare experimental and control groups to see if the interventions mitigated perceived stress and improved the health of the participants.

Conditions

Interventions

TypeNameDescription
PROCEDUREManual Standardized Stress Acupuncture (MSSA)Participants in the experimental group will receive 4 weekly sessions of MSSA, which consists of 8 acupuncture points: bilateral auricular (ear) shen men, GV- 20, GV-24.5 (Yin Tang), bilateral LI-4, and bilateral LR-3. Needles are left in situ for 30 minutes per session.
BEHAVIORALMindfulness-Based Stress Reduction (MBSR)Participants will receive four sessions of MBSR group psychotherapy (no more than 10 participants per group session) via Microsoft Teams. The first session will be 90 minutes followed by three 60-minute weekly sessions.

Timeline

Start date
2024-09-01
Primary completion
2025-10-31
Completion
2025-10-31
First posted
2023-09-21
Last updated
2026-01-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06044714. Inclusion in this directory is not an endorsement.