RECRUITING

Moderators and Mediators (M & M Trial) of Psychosocial Treatments of Chronic Pain

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Chronic musculoskeletal pain (CP) is a major public health concern. Psychosocial treatments have been shown to be efficacious when compared to largely inert control conditions, but they are characterized by modest effects on primary outcomes. One strategy to boost efficacy is to increase our understanding of treatment mediators. Studies of mediators that directly compare different treatments with each other are needed to determine which mediators are treatment-specific, which are shared across treatments, and which contribute the most to clinical outcomes. Another strategy is to identify the patient characteristics that moderate treatment responses. Research is needed that is guided by theoretical models and that tests moderators across multiple treatments. Identifying subgroups of patients more likely to respond to one or another treatment can advance precision medicine by informing a priori patient-treatment matches that can optimize treatment effects. To accomplish these goals, the authors will conduct a randomized clinical trial to compare the mediators and moderators of the clinical effects of Cognitive-Behavioral Therapy (CBT), Acceptance and Commitment Therapy (ACT), and Emotional Awareness and Expression Therapy (EAET) on adults with chronic spinal (axial) pain. Following baseline assessment of outcome variables as well as potential mediators and moderators, 460 participants will be randomized to CBT, ACT, EAET, or treatment-as-usual control (TAU). The three treatments will be conducted as individual therapy provided weekly for 8 weeks via telehealth. The researchers will conduct weekly assessments of both potential mediators and outcomes, as well as post-treatment and 6-month follow-up assessments. The goal of the study is to identify the most powerful treatment mechanisms - specific and shared -- and reveal for whom the mediator-outcome pathways are strongest.This project can increase the effects of our psychosocial chronic pain treatments by identifying the most effective treatment mechanisms and by informing patient-treatment matches that can optimize treatment effects.

Official Title

Comparative Mechanisms (Moderators, Mediators) of Psychosocial Treatments of Chronic Pain

Quick Facts

Study Start:2023-11-15
Study Completion:2027-03-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06044649

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Back/neck is primary pain location (e.g., back/neck pain greater than leg pain)
  2. * Pain for at least 3 months and experienced 4 or more days/week for the past 6 months
  3. * Pain intensity last week is \>= 3 (0 to 10 rating scale)
  4. * Pain interference last week is \>= 3 (0 to 10 rating scale)
  5. * At least age 18
  6. * Lives in United States (and in a state that has psychology license agreement: PSYPACT)
  7. * Fluent in English
  8. * Has personal computer/tablet and internet access
  9. * Able to attend weekly sessions
  10. * Willing to be randomized
  11. * Seeking to improve their pain-related status via a psychological therapy
  1. * Complex regional pain syndrome
  2. * Epilepsy/seizure disorder
  3. * Autoimmune disease
  4. * Liver disease
  5. * Cancer
  6. * Heart disease
  7. * Substance dependence or use disorder
  8. * Schizophrenia or other psychotic disorder
  9. * Bipolar disorder
  10. * Obsessive-compulsive disorder
  11. * Borderline personality disorder
  12. * Suicide attempt or suicide intention or impulse
  13. * Major medical procedure scheduled within next 9 months
  14. * Applied for/ litigating for pain-related disability/worker's compensation (past year).
  15. * Major life event/stressor in past 6 months
  16. * Cognitive impairment (screener score \<=4)

Contacts and Locations

Study Contact

John W Burns, PhD
CONTACT
312-942-0379
john_burns@rush.edu
Mark A Lumley, PhD
CONTACT
313-577-2247
mlumley@wayne.edu

Principal Investigator

John W Burns, PhD
PRINCIPAL_INVESTIGATOR
Rush University Medical Center

Study Locations (Sites)

Rush University Medical Center
Chicago, Illinois, 60612
United States
Wayne State University
Detroit, Michigan, 48202
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

  • John W Burns, PhD, PRINCIPAL_INVESTIGATOR, Rush University Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-11-15
Study Completion Date2027-03-30

Study Record Updates

Study Start Date2023-11-15
Study Completion Date2027-03-30

Terms related to this study

Additional Relevant MeSH Terms

  • Chronic Pain
  • Neck Pain
  • Back Pain