Purpose

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.

Conditions

Eligibility

Eligible Ages
Over 21 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Brief Intervention
  • Behavioral: Trauma Focused Emotional Awareness and Expression Therapy (EAET)
    The intervention is three-session program which includes pain neuroscience education, education on the relationship between trauma and chronic pain, and skills training to reduce pain- and stress-related symptoms.

Recruiting Locations

Brigham and Women's Hospital
Chestnut Hill, Massachusetts 02467
Contact:
Jolin B Yamin, PhD
857-352-3292
jyamin@bwh.harvard.edu

More Details

Status
Recruiting
Sponsor
Brigham and Women's Hospital

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.