Emotional Awareness and Expression Therapy for People With Persistent Pain Following Orthopedic Trauma

Not Applicable

Not yet recruiting

• Conditions: Orthopaedic Trauma; Chronic Pain; Musculoskeletal Injury
• Interventions: Behavioral: Emotional Awareness and Expression Therapy

• Registration Number: NCT05989230
• Lead Sponsor: Johns Hopkins University

Brief Summary

The purpose of this single-arm trial is to determine the feasibility of emotional awareness and expression therapy (EAET) for individuals with persistent pain following orthopedic trauma. As part of this study, participants will be asked to attend weekly EAET treatment sessions and complete assessments (including pre-treatment, post-treatment, and follow-up) consisting of questionnaires and sensory testing procedures.

Detailed Description

Orthopedic trauma, resulting in severe injuries such as multiple fractures or amputation, occurs in approximately 3 million people annually in the United States; about half of these people experience persistent pain and psychological distress (depression, anxiety, posttraumatic stress disorder \[PTSD\] symptoms) 6 to 12 months post injury. Pain and distress exacerbate one another, are likely to persist, and relate to disability: half of patients report substantial disability 7 years post trauma. Medical interventions such as surgery promote survival; however, there is an urgent need to develop targeted psychological interventions to treat these disabling symptoms.

Few psychological interventions are available to treat pain and distress following orthopedic trauma. Emotional Awareness and Expression Therapy (EAET) is an 8-week psychological intervention recently developed for chronic pain conditions characterized by central sensitization. EAET is unique in treating pain and mood by targeting emotion regulation processes related to traumatic life events. Such events are ubiquitous following orthopedic trauma and recent findings show that EAET results in improvements in pain and mood; thus, it may be uniquely effective to address the needs of orthopedic trauma survivors. However, there are documented barriers to implementing psychological interventions in this population, so the feasibility of EAET is unknown. The purpose of this study is to test the feasibility of delivery and assessment of EAET for orthopedic trauma survivors with persistent pain in a single-arm trial. As part of this study, participants will be asked to do the following things:

* Attend EAET treatment with a mental health provider. Session will last around 60 minutes each.

* Complete baseline, post-treatment, and follow-up assessments. These assessments will ask patients to complete questionnaires related to physical and emotional health, as well as receive sensory testing in order to examine pain processing. The questionnaires will take 20-25 minutes. The sensory testing procedures will take about 20 minutes.

Study Timeline

• Status Verified: 2023-08
• Study First Submitted: 2023-08-03
• Study First Submitted QC: 2023-08-03
• Last Update Submitted: 2023-08-03
• Study First Posted: 2023-08-14
• Last Update Posted: 2023-08-14
• Study Start: 2024-08
• Primary Completion: 2025-12
• Study Completion: 2026-12

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• One or more acute orthopedic injuries

• The patient sustained an orthopedic injury including, but not limited to:

  • Pelvic or acetabulum fracture
  • Open/displaced comminuted fracture of long bones
  • Upper extremity injuries with a major nerve involvement
  • Injuries with significant injuries to major blood vessels
  • Traumatic amputation of big toe, thumb, or proximal to the wrist or ankle.

• Initial admission to the trauma or orthopedic center/service of the participating hospital OR all necessary screening and patient characteristic data available in medical record (determination based on information available at time of enrollment)

• 18 years old or older

• Received operative fixation for at least one acute orthopaedic injury at a participating hospital. Patients should be recruited at the time of primary injury, not revision or complication surgery

• Average Brief Pain Inventory Score > 3/10

• Presence of pain most days (> 3 days/week) for past three months

Exclusion Criteria

• peri-prosthetic fractures of the femur (regardless of etiology)

• non-ambulatory due to an associated spinal cord injury

• non-ambulatory pre-injury

• currently pregnant

• moderate or severe traumatic brain injury (TBI), as evidenced by intracranial hemorrhage present on admission CT

• major amputation(s) of the upper or lower extremities

• non-English speaking

• Likely to have severe problems with maintaining follow-up for any of the following reasons:

  • The patient has been diagnosed with a severe psychiatric conditions
  • The patient has current alcohol and/or drug addiction based on medical record or patient self-report.
  • The patient is intellectually challenged without adequate family support
  • The patient lives outside the hospital's catchment area
  • The patient follow-up is planned at another medical center
  • The patient is a prisoner
  • The patient is homeless
  • Other

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Emotional Awareness and Expression Therapy	Emotional Awareness and Expression Therapy	Emotional Awareness and Expression Therapy (EAET) is a non-pharmacological intervention designed to address persistent pain.

Primary Outcome Measures

Name	Time	Method
Therapist Fidelity (Questionnaire developed by study team)	8 Weeks	Percentage of treatment fidelity across all treatment sessions (study therapist self-report using questionnaire developed by study team).
Percentage of patients who indicate patient satisfaction and acceptability	8 Weeks	Percentage of patients who indicate treatment acceptability on the Treatment Evaluation Inventory-Short Form. This is a 9-item measure and participants respond using a 1-5 point likert scale for a possible total range of 9-45. Higher scores indicate greater satisfaction and acceptability.
Feasibility of Study Assessment	12 months	Measured by percent of follow-up assessments completed by participants.
Feasibility of Enrollment	24 months	Feasibility of enrollment will be measured by percentage of eligible patients who enroll in the study.
Feasibility of Retention	24 months	Feasibility of retention will be measured by percentage of participants who are retained over the duration of the study.
Feasibility of Recruitment	24 months	Feasibility of Recruitment will be measured by the enrollment of a full sample within two years of the start of the enrollment period.
Percentage of patient session attendance	8 weeks	Percentage of patients who complete 6 of 8 total EAET sessions.

Trial Locations

Locations (1)

Johns Hopkins School of Medicine; 🇺🇸 Baltimore, Maryland, United States