Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
ID07179016

A Pragmatic, Randomized Controlled Trial of a Auricular Point Acupressure - Self-Management (APA-SM) Program for Chronic Musculoskeletal Pain Among Rural Populations

Led by The University of Texas Health Science Center, Houston · Updated on 2025-10-01

693

Participants Needed

3

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating an Auricular Point Acupressure Self-Management (APA-SM) program for people with chronic musculoskeletal pain (CMP) living in rural areas. This study aims to compare the effectiveness of three approaches: APA-SM self-guided with remote training, APA-SM with in-person training, and an education control group. The goal is to improve pain intensity, pain interference, and daily activity over a 4-week intervention period, with follow-ups up to 6 months. The study also looks at clinical pain measures and analgesic use over time. Participants will be randomly assigned to one of three groups: self-guided APA-SM with remote training using a smartphone app, APA-SM with in-person training, or a control group receiving pain education without APA practice. The APA-SM program uses a noninvasive, needle-free technique based on acupuncture principles, supported by videos and guidance through the app or in-person sessions. The control group will receive pain self-management education through the app without APA content. During the study, participants will use the app to monitor their progress and self-administer APA where applicable. Assessments include surveys measuring pain, function, mood, sleep, substance use, and quality of life before and after the 4-week intervention and at 1, 3, and 6 months post-intervention. Researchers will also evaluate implementation outcomes and cost-effectiveness. The total study duration for participants includes the intervention and follow-up assessments, with recruitment planned over 3.5 to 4 years.

CONDITIONS

Brief Title

Evaluating the Auricular Point Acupressure-Self Management Program for Chronic Musculoskeletal Pain Among Rural Populations

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Receive any pain management for chronic musculoskeletal pain in neck, back, shoulder, hands, hips, knees, or feet
  • Have chronic musculoskeletal pain rated 4 or higher on a 0-10 scale that has lasted at least 3 months or caused pain on at least half the days in the past 6 months
  • Age between 18 and 85 years
  • Live in a rural area
Not Eligible

You will not qualify if you...

  • Severe ear skin disorders such as eczema or lupus that require medical intervention, or severe allergy to tape
  • Unable or unwilling to provide informed consent
  • Use of hearing aids that may block placement of seeds for acupressure
  • Not living in a rural area

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Treatment

Duration - 4 weeks

Participants engage in the Auricular Point Acupressure-Self Management program or receive pain education to manage chronic musculoskeletal pain.

1 baseline visit and 1 post-intervention visit

Follow-up

Duration - 6 months

Participants are followed up to assess pain and other outcomes at 1 month, 3 months, and 6 months after treatment.

3 follow-up visits

Trial Site Locations

Total: 3 locations

1

University of South Carolina

Columbia, South Carolina, United States, 29208

Actively Recruiting

2

University of North Texas Health Science Center at Fort Worth

Fort Worth, Texas, United States, 76107

Not Yet Recruiting

3

The University of Texas Health science Center at Houston

Houston, Texas, United States, 77030

Not Yet Recruiting

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Research Team

J

Jennifer Kawi, PhD, MSN, FNP-BC, CNE, FAAN

J

Jungkyung Min, PhD, MS, RN

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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