Pilot Testing A Theory-Driven Self-Management Intervention for Chronic Musculoskeletal Pain
Completed · Not applicable
Conditions studied: Chronic Musculoskeletal Pain
In brief
The proposed randomized control trial will evaluate auricular point acupressure (APA) treatment administered by the participant themselves with the use of a phone app on chronic musculoskeletal pain (CMP) outcomes. This study will randomly assign participants into three groups: (1) Self-guided mAPA (S-mAPA), (2) In-Person Training + mAPA (IP-mAPA), and (3) Usual Care Control (UC). EMA will be used to assess momentary pain outcomes and APA adherence. Data will be collected at pre- (T1), post-completion of intervention (T2), follow-ups at post 1M- (primary endpoint) (T3), 2M (T4), and 3M (secondary endpoint, long-term sustained effect) (T5) for a total of four assessments.
Key facts
- Study ID
- NCT05020470
- Run by
- Johns Hopkins University
- People needed
- 37
- Starts
- 2021-09-22
- Expected to finish
- 2022-08-11
- Last updated by the study team
- 2023-06-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adults 18 years of age or older.
- Receiving outpatient pain treatment for CMP condition (e.g., pain in the back, hip, knee, upper extremity, lower extremity, neck, pelvic, headache/migraine).
- Chronic pain ≥ 4 on a scale of 0-10 point numerical pain, persisting for at least 3 months or has resulted in pain on at least half the days in the past 6 months.
You may not qualify if…
- Disease that might confound therapeutic effects or explanation of outcomes, i.e., infection, malignant tumors, or autoimmune diseases.
- Severe ear skin issues.
- Use of some types of hearing aids (size may obstruct the placement of seeds)
- Concurrent major psychiatric disorder (i.e., participant self-report).
- Pregnant women will be excluded from the study based on the self-reported data.
Where it is running
- Johns Hopkins School of Nursing — Baltimore, Maryland, United States
- University of Nevada, Las Vegas — Las Vegas, Nevada, United States
Full record on ClinicalTrials.gov
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