CompletedNot Applicable

Brief Intervention for Chronic Pain and History of Stressful Experiences

United States50 participantsStarted 2025-04-14

Plain-language summary

The goal of this study is to understand whether a brief, three session program can be helpful in reducing symptoms related to both chronic pain and stressful experiences/trauma.

Who can participate

Age range21 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Presence of a chronic pain condition (pain for at least 3 months or more) * History of psychosocial trauma or stressful experience (Adverse Childhood Events questionnaire \[ACEs\] score of ≥ 3 OR Trauma History Questionnaire Score \[THQ\] of ≥ 2) * English fluency * Access to a smartphone, laptop, or computer * Able to participate in the intervention via a virtual platform Exclusion Criteria: * Unable to participate in 3 weekly sessions * Unable to complete study procedures due to the presence of delirium, dementia, psychosis, or other cognitive impairment

What they're measuring

Feasibility of Recruitment

Timeframe: At screening

Treatment Completion

Timeframe: From enrollment to end of treatment at 4 weeks

Feasibility of Data Collection

Timeframe: At end of treatment at (~4 weeks post-enrollment), and at 1-month follow-up (~8 weeks post-enrollment)

Treatment Credibility

Timeframe: At end of treatment at (~4 weeks post-enrollment), and at 1-month follow-up (~8 weeks post-enrollment)

Treatment Helpfulness

Timeframe: At end of treatment at (~4 weeks post-enrollment), and at 1-month follow-up (~8 weeks post-enrollment)

Trial details

NCT IDNCT06983327

SponsorBrigham and Women's Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-11-28

View on ClinicalTrials.gov More Chronic Pain trials