Developing a Tailored Psychosocial Education Intervention for Chronic Pain Management for Asian Americans
CompletedNot applicableNCT06725329
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Chronic pain is a major population health issue affecting more than 100 million Americans and variations in chronic pain experiences have been widely documented, including differences in pain burden and likelihood of undertreatment. Evidence regarding chronic pain experiences of Asian Americans is limited, as are resources and evidence-based programs for this group. Our exploratory, developmental study will provide evidence of feasibility and acceptability of a tailored psychosocial education intervention to reduce pain catastrophizing and improve pain outcomes for Asian Americans.
Study details
- Official title
- Developing a Tailored Psychosocial Education Intervention for Chronic Pain Management for Asian Americans in the Community
- Conditions
- Interventions
- Behavioral: A tailored psychosocial education intervention
- Sponsor
- George Washington University
- Collaborators
- National Institutes of Health (NIH); National Institute of Nursing Research (NINR)
- Start date
- 2025-03-08
- Primary completion
- 2026-02-17
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 2
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Female and male 2. ≥ 18 years old 3. Self-reported foreign born Korean Americans 4. Self-reported pain most days of the month for at least 3 months 5. Pain must be non-malignant, but may have more than one pain source Exclusion Criteria: 1. Having malignant pain (e.g., cancer or HIV-related) 2. Demonstrating significant cognitive impairment (based on results of a cognitive screener-Short Portable Mental Status Questionnaire) 3. Having current, uncontrolled serious psychological disturbance (e.g., schizophrenia, bipolar disorder) or active substance abuse based on self-report 4. Having low literacy skills in Korean or English (unable to understand the written consent and to sign) 5. Undergoing other psychosocial treatment for pain * If excluding a population or group that may benefit from the research, please provide justification: We will exclude children. The original intervention (LAMP) trial has established for efficacy in reducing chronic pain outcomes in adult population. Children are not our target population as we focus on developing a culturally tailored chronic pain management program based on LAMP.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06725329