Chronic PainNCT06044649
Moderators and Mediators (M & M Trial) of Psychosocial Treatments of Chronic Pain
A study testing Cognitive Behavioral Therapy, Acceptance and Commitment Therapy and Emotional Awareness and Expression Therapy in people with Chronic Pain and Neck Pain, run by Rush University Medical Center at 2 sites in United States.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Pain, Neck Pain, Back Pain
- What is being tested?
- Cognitive Behavioral Therapy, Acceptance and Commitment Therapy and Emotional Awareness and Expression Therapy
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 408 participants
- Where
- 2 sitesUnited States
- Study dates
- 15 Nov 2023to 28 Feb 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Back/neck is primary pain location (e.g., back/neck pain greater than leg pain)
- Pain for at least 3 months and experienced 4 or more days/week for the past 6 months
- Pain intensity last week is >= 3 (0 to 10 rating scale)
- Pain interference last week is >= 3 (0 to 10 rating scale)
- At least age 18
- Lives in United States
Show all 11Show fewer
- Fluent in English
- Has personal computer/tablet and internet access
- Able to attend weekly sessions
- Willing to be randomized
- Seeking to improve their pain-related status via a psychological therapy
Who cannot join
- Past 2 years (treated for or having experienced):
- Complex regional pain syndrome
- Epilepsy/seizure disorder
- Autoimmune disease
- Liver disease
- Cancer
Show all 18Show fewer
- Heart disease
- Substance dependence or use disorder
- Schizophrenia or other psychotic disorder
- Bipolar disorder
- Obsessive-compulsive disorder
- Borderline personality disorder
- Suicide attempt or suicide intention or impulse
- Also:
- Major medical procedure scheduled within next 9 months
- Applied for/ litigating for pain-related disability/worker's compensation (past year).
- Major life event/stressor in past 6 months
- Cognitive impairment (screener score <=4)
Trial locations and contacts
2 sites in 1 country.
United States2 sites
Rush University Medical Center
Chicago, Illinois, 60612
Wayne State University
Detroit, Michigan, 48202
About this study
Official title: Comparative Mechanisms (Moderators, Mediators) of Psychosocial Treatments of Chronic Pain
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.
Read the detailed description
Chronic musculoskeletal pain (CP) is a major public health concern. A number of psychosocial treatments have emerged in recent decades to help address this problem. These interventions have been shown to be efficacious when compared to largely inert control conditions; however, recent meta-analyses indicate that most of these treatments are characterized by modest effects on primary outcomes. This is a critical shortcoming of these otherwise promising approaches. Rather than attempting to boost efficacy only by developing new and hopefully more powerful interventions, we can also look within our already proven treatments for ways to enhance the magnitude of treatment effects. One strategy 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. The findings from such research could be used to inform adaptations to existing treatment that enhance their benefits. A second strategy for increasing the beneficial effects of existing treatments 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, we 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 we will randomize 460 participants 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. We will conduct weekly assessments of both potential mediators and outcomes, as well as post-treatment and 6-month follow-up assessments. In addition to comparing the three treatments to each other (and TAU) for overall efficacy, we focus on two specific aims: Aim 1 is to identify mediators that are specific to treatments and those that are shared across treatments. Aim 2 is to identify baseline moderators of specific treatments and general predictors across treatments. This project can increase the effects of our psychosocial chronic pain treatments by identifying the most powerful treatment mechanisms - specific and shared -- and revealing for whom the mediator-outcome pathways are strongest. Via increased understanding of mediator and moderators, more effective pain treatment approaches can be developed, tested, and implemented.
- Conditions
- Chronic Pain, Neck Pain, Back Pain
- Being tested
- Cognitive Behavioral Therapy, Acceptance and Commitment Therapy, Emotional Awareness and Expression Therapy, Treatment as Usual
- Medical subject headings
- Chronic Pain, Neck Pain, Back Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cognitive Behavioral TherapyBehavioural
Also called CBT for chronic pain
CBT endorses a pain management model and teaches people skills to cope with chronic pain.
Acceptance and Commitment TherapyBehavioural
Also called ACT for chronic pain
ACT is based on an acceptance model that seeks to decrease pain avoidance behaviors and enhance engagement in valued, adaptive activities that contribute to fewer pain-related restrictions in functioning.
Emotional Awareness and Expression TherapyBehavioural
Also called EAET for chronic pain
EAET advocates a pain treatment model in which pain can be substantially reduced by helping people learn that their pain is brain-based and can be substantially reduced or eliminated by decreasing fear of pain and of various emotional/interpersonal problems.
Treatment as UsualOther
Also called TAU
Participants assigned to TAU will not receive any additional psychosocial treatment beyond the other treatments they were receiving before enrolling in this study.
| Study group | Role | What they receive |
|---|---|---|
| Cognitive Behavioral Therapy | Experimental | 8-session, individual, Cognitive Behavioral Therapy delivered remotely by skilled CBT therapists Receives: Behavioral: Cognitive Behavioral Therapy |
| Acceptance and Commitment Therapy | Experimental | 8-session, individual, Acceptance and Commitment Therapy delivered remotely by skilled ACT therapists Receives: Behavioral: Acceptance and Commitment Therapy |
| Emotional Awareness and Expression Therapy | Experimental | 8-session, individual, Emotional Awareness and Expression Therapy delivered remotely by skilled EAET Receives: Behavioral: Emotional Awareness and Expression Therapy |
| Treatment As Usual | Other | In this control condition, participants will engage in their usual care for neck/back pain with no additional experimental intervention Receives: Other: Treatment as Usual |
What is being measured
The primary outcome is the main question the study is designed to answer.
Brief Pain Inventory (BPI) - Pain Severity
4-item measure of pain severity over past week (range 0 to 10; higher scores = worse pain severity)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference - Short Form 8a
8-item measure of pain interference over past week (range1 to 5; higher scores = more pain interference)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Secondary outcomes (21)
Patient Global Impression of Change
1-item measure of overall health change since the start of the study (range 1 to 7; higher scores = more health improvement)
Measured: Weekly during treatment to post-treatment and 6-month follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Physical Function - Short Form 10a
4-item measure of current physical function (range 1 to 5; higher scores = poorer physical function)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Anxiety - Short Form
4-item measure of anxiety symptoms in the past week (range 1 to 5; higher scores = more anxiety symptoms)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Depression - Short Form
4-item measure of depression symptoms in the past week (range 1 to 5; higher scores = more depression symptoms)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient Health Questionnaire - Depression
8-item measure of depression symptoms in the past week (range 0 to 3; higher scores = more depression symptoms)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Fatigue - Short Form
4-item measure of fatigue in the past week (range 1 to 5; higher scores = more fatigue)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Sleep Disturbance - Short Form
4-item measure of sleep disturbance in the past week (range 1 to 5; higher scores = more sleep disturbance)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Anger - Short Form 5a
5-item measure of anger in the past week (range 1 to 5; higher scores = more anger)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Positive and Negative Affect Schedule (PANAS) - Positive Affect - Short Form
5-item measure of positive affect in the past week (range 1 to 5; higher scores = more positive affectivity)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Posttraumatic Stress Disorder Checklist (PCL) - Short Form
5-item measure of trauma symptoms in the past week (range 1 to 4; higher scores = worse PTSD symptoms)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Pain Stages of Change Questionnaire (PSOCQ): Preparation and action
13-item measure on current readiness to adopt self-management for pain, Preparation and Action items only (range 1 to 5; higher scores = more ready to change)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Opioid Use
1-item measure on opioid use in past 7 days (range 1 to 7; higher scores = more days)
Measured: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Employment
3-item measure on current employment (options for current status and qualitative responses)
Measured: Baseline to post-treatment and 6-month follow-up
Post-Treatment Satisfaction Questionnaire
8-item measure on patient post-treatment satisfaction (range 1 to 10; higher scores = more satisfied - also included qualitative responses)
Measured: Post-Treatment to 6-Month Follow-Up
Levels of Emotional Awareness Scale (LEAS) - Forms A and B
10-item measure of current emotional awareness (includes qualitative responses); responses coded for levels of emotional awareness; higher = greater awareness; Form A baseline and Form B at post-treatment
Measured: Baseline
Other Pain Treatments and Health Care Use
2-item measure of health care currently, the past 6 months, and the past 4 weeks (2 items with yes/no responses and remaining range 0 to 4; higher scores = more treatment)
Measured: Baseline to post-treatment and 6-month follow-up
Inventory of Interpersonal Problems (IIP)
32-item measure of current interpersonal problems (range 0 to 4; higher scores = more interpersonal problems)
Measured: Baseline to post-treatment and 6-month follow-up
American College of Rheumatology (ACR) Fibromyalgia Diagnostic Criteria - 2011
8-item measure on fibromyalgia symptoms in the past week (items with yes/no responses, a checklist, and remaining range 0 to 3; higher scores = worse fibromyalgia symptoms)
Measured: Baseline to post-treatment and 6-month follow-up
Psychological Flexibility Scale (PSYFlex)
6-item measure of psychological flexibility in the past week (range 0 to 5; higher scores = higher psychological flexibility)
Measured: Baseline to post-treatment and 6-month follow-up
The Tobacco, Alcohol, Prescription medications, and other Substance (TAPS) Tool - Part II
9-item measure on substance use in the past week (yes/no responses); higher scores = more use
Measured: Baseline to post-treatment and 6-month follow-up
Posttraumatic Stress Disorder Checklist (PCL)
20-item measure of PTSD symptoms in the past month (range 0 to 4; higher scores = worse PTSD symptoms)
Measured: Baseline to post-treatment and 6-month follow-up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Sep 2023
- Study start15 Nov 2023
- Primary completion30 Aug 2026 (estimated)
- Study completion28 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic PainStudies of the same condition, open and under way.
- More trials run by Rush University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 4-arm parallel randomized clinical trial comparing three therapies with each other and with a treatment as usual control
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 408 participants (actual)
Sponsor and investigators
- Lead sponsor
- Rush University Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Wayne State University
- Responsible party
- Sponsor
- Investigators
- John W Burns, PhD, Principal investigator, Rush University Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06044649
- Sponsor's protocol ID
- 22010705
- Status last verified
- Jun 2026
- First submitted
- 11 Sep 2023
- Last updated
- 24 Jun 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Mechanisms (Moderators, Mediators) of Psychosocial Treatments of Chronic Pain
- ClinicalTrials.gov ID
- NCT06044649
- Acronym / sponsor ID
- 22010705
- Conditions
- Chronic Pain, Neck Pain, Back Pain
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 408 participants (actual)
- Lead sponsor
- Rush University Medical CenterUniversity, hospital or other
- Collaborators
- Wayne State University
- Study start
- 15 Nov 2023 (actual)
- Primary completion
- 30 Aug 2026 (estimated)
- Study completion
- 28 Feb 2027 (estimated)
- First posted
- 21 Sep 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Chronic musculoskeletal pain (CP) is a major public health concern. A number of psychosocial treatments have emerged in recent decades to help address this problem. These interventions have been shown to be efficacious when compared to largely inert control conditions; however, recent meta-analyses indicate that most of these treatments are characterized by modest effects on primary outcomes. This is a critical shortcoming of these otherwise promising approaches. Rather than attempting to boost efficacy only by developing new and hopefully more powerful interventions, we can also look within our already proven treatments for ways to enhance the magnitude of treatment effects. One strategy 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. The findings from such research could be used to inform adaptations to existing treatment that enhance their benefits. A second strategy for increasing the beneficial effects of existing treatments 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, we 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 we will randomize 460 participants 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. We will conduct weekly assessments of both potential mediators and outcomes, as well as post-treatment and 6-month follow-up assessments. In addition to comparing the three treatments to each other (and TAU) for overall efficacy, we focus on two specific aims: Aim 1 is to identify mediators that are specific to treatments and those that are shared across treatments. Aim 2 is to identify baseline moderators of specific treatments and general predictors across treatments. This project can increase the effects of our psychosocial chronic pain treatments by identifying the most powerful treatment mechanisms - specific and shared -- and revealing for whom the mediator-outcome pathways are strongest. Via increased understanding of mediator and moderators, more effective pain treatment approaches can be developed, tested, and implemented.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 4
- Model description
- 4-arm parallel randomized clinical trial comparing three therapies with each other and with a treatment as usual control
| Arm | Type | Receives |
|---|---|---|
| Cognitive Behavioral Therapy | Experimental | Behavioral: Cognitive Behavioral Therapy8-session, individual, Cognitive Behavioral Therapy delivered remotely by skilled CBT therapists |
| Acceptance and Commitment Therapy | Experimental | Behavioral: Acceptance and Commitment Therapy8-session, individual, Acceptance and Commitment Therapy delivered remotely by skilled ACT therapists |
| Emotional Awareness and Expression Therapy | Experimental | Behavioral: Emotional Awareness and Expression Therapy8-session, individual, Emotional Awareness and Expression Therapy delivered remotely by skilled EAET |
| Treatment As Usual | Other | Other: Treatment as UsualIn this control condition, participants will engage in their usual care for neck/back pain with no additional experimental intervention |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (11 listed)
- Back/neck is primary pain location (e.g., back/neck pain greater than leg pain)
- Pain for at least 3 months and experienced 4 or more days/week for the past 6 months
- Pain intensity last week is >= 3 (0 to 10 rating scale)
- Pain interference last week is >= 3 (0 to 10 rating scale)
- At least age 18
Key exclusion criteria (18 listed)
- Complex regional pain syndrome
- Epilepsy/seizure disorder
- Autoimmune disease
- Liver disease
- Cancer
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cognitive Behavioral TherapyAlso: CBT for chronic painCBT endorses a pain management model and teaches people skills to cope with chronic pain. | Behavioural | Cognitive Behavioral Therapy |
| Acceptance and Commitment TherapyAlso: ACT for chronic painACT is based on an acceptance model that seeks to decrease pain avoidance behaviors and enhance engagement in valued, adaptive activities that contribute to fewer pain-related restrictions in functioning. | Behavioural | Acceptance and Commitment Therapy |
| Emotional Awareness and Expression TherapyAlso: EAET for chronic painEAET advocates a pain treatment model in which pain can be substantially reduced by helping people learn that their pain is brain-based and can be substantially reduced or eliminated by decreasing fear of pain and of various emotional/interpersonal problems. | Behavioural | Emotional Awareness and Expression Therapy |
| Treatment as UsualAlso: TAUParticipants assigned to TAU will not receive any additional psychosocial treatment beyond the other treatments they were receiving before enrolling in this study. | Other | Treatment As Usual |
Primary outcome
Brief Pain Inventory (BPI) - Pain Severity
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
4-item measure of pain severity over past week (range 0 to 10; higher scores = worse pain severity)
Patient-Reported Outcome Measurement Information System (PROMIS) - Pain Interference - Short Form 8a
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
8-item measure of pain interference over past week (range1 to 5; higher scores = more pain interference)
21 secondary outcomes
Patient Global Impression of Change
Time frame: Weekly during treatment to post-treatment and 6-month follow-up
Patient-Reported Outcome Measurement Information System (PROMIS) - Physical Function - Short Form 10a
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Anxiety - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Depression - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient Health Questionnaire - Depression
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Fatigue - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Sleep Disturbance - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Patient-Reported Outcome Measurement Information System (PROMIS) - Emotional Distress - Anger - Short Form 5a
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Positive and Negative Affect Schedule (PANAS) - Positive Affect - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Posttraumatic Stress Disorder Checklist (PCL) - Short Form
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Pain Stages of Change Questionnaire (PSOCQ): Preparation and action
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Opioid Use
Time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment
Employment
Time frame: Baseline to post-treatment and 6-month follow-up
Post-Treatment Satisfaction Questionnaire
Time frame: Post-Treatment to 6-Month Follow-Up
Levels of Emotional Awareness Scale (LEAS) - Forms A and B
Time frame: Baseline
Other Pain Treatments and Health Care Use
Time frame: Baseline to post-treatment and 6-month follow-up
Inventory of Interpersonal Problems (IIP)
Time frame: Baseline to post-treatment and 6-month follow-up
American College of Rheumatology (ACR) Fibromyalgia Diagnostic Criteria - 2011
Time frame: Baseline to post-treatment and 6-month follow-up
Psychological Flexibility Scale (PSYFlex)
Time frame: Baseline to post-treatment and 6-month follow-up
The Tobacco, Alcohol, Prescription medications, and other Substance (TAPS) Tool - Part II
Time frame: Baseline to post-treatment and 6-month follow-up
Posttraumatic Stress Disorder Checklist (PCL)
Time frame: Baseline to post-treatment and 6-month follow-up
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John W Burns, PhD principal investigator
Rush University Medical Center
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Cognitive Behavioral Therapy, Acceptance and Commitment Therapy and Emotional Awareness and Expression Therapy in people with Chronic Pain and Neck Pain, run by Rush University Medical Center at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 11 inclusion and 18 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Brief Pain Inventory (BPI) - Pain Severity (time frame: Baseline to post-treatment and 6-month follow-up, and weekly during treatment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026.