You are viewing an expired study

This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please browse nearby listings below.

Click here to view additional nearby studies or search for clinical trials.

Tuscaloosa, Alabama 35401

  • Chronic Pain Due to Injury

Purpose:

Chronic pain is a significant public health problem that affects over 116 million Americans, costs $600 billion annually, and is unequally borne by people in low-income brackets, especially ethnic minorities. Many individuals also have health literacy deficits (difficulty understanding their illness and difficulty navigating the health care system for treatment) putting them at a greater disadvantage. Treatment usually relies on expensive medical interventions that often have negative side-effects. Psychosocial treatments, like Pain Education and Cognitive-Behavioral Therapy (CBT), show promise, but are usually unavailable. Clinicians are poorly equipped to provide psychosocial treatments to patients with low health literacy. CBT has not been adapted and supported for use in individuals with low health literacy, and even educational materials are often poorly adapted for their needs. To address this problem, the PI completed a small trial showing benefits from health literacy-adapted pain education and CBT groups for chronic pain in a population with low income and low health literacy. Patients in both treatments reported lower pain by the end of treatment, and the effects were maintained at one year. Patients in the CBT group also reported less depression. The current study uses a larger sample, and directly compares these psychosocial treatments to medical treatment-as-usual to seek better evidence for or against their widespread use in community settings. Our research questions: 1. In people with chronic pain and low income and/or low literacy, does participating in a health-literacy-adapted psychosocial treatment improve their pain and interference in daily activities due to pain by the end of treatment when compared with a group receiving typical medical care, and are these effects maintained 6 months later? 2. Does participation in the CBT pain management group improve symptoms of depression better than a pain education group by the end of treatment, and are these effects maintained 6 months later? In partnership with a federally qualified health center, we will enroll 294 patients with chronic pain. Main outcomes will be patient-reported pain intensity, pain interference, depression, and perceived change. From an earlier trial, we expect that our participants will be ~75% female and ~70% African American, and will have low literacy and low income (~60% in the low 15% nationally on word reading, and 90% at or below the poverty threshold).


Study summary:

Study Description Chronic pain is a major public health problem that is compounded by a number of health-related disparities. Low health literacy presents a notable access barrier to effective treatment as it produces cumulative education and communication deficits. Standard care employs biomedical approaches that are expensive, often invasive, and limited in accessibility and long-term effectiveness. Psychosocial treatments are efficacious, yet few psychosocial interventions have adequately addressed the significant health literacy barriers that exclude a substantial portion of disadvantaged individuals from the benefits of treatment. Research Questions: 1. In individuals with chronic pain and low socioeconomic standing who are receiving care at a federally qualified health center in the Southern US, does participating in a health-literacy-adapted psychosocial treatment group improve their self-reported pain intensity and interference in physical functioning by the end of treatment when compared with a group receiving standard medical care, and are these effects maintained 6 months later? 2. In these same individuals, does participation in the CBT pain management group improve depressive symptoms better than a pain education group by the end of treatment, and are these effects maintained 6 months later? The proposed study will build on researcher experience developing and evaluating psychosocial treatments for chronic pain in individuals with low socioeconomic standing (SES) and on strong partnerships with community health centers to evaluate two innovative, health-literacy-adapted psychosocial interventions for chronic pain. Both interventions integrate patient feedback, expert opinion, and qualitative patient data. DESIGN We propose a three-group, community-based randomized, controlled, comparative effectiveness trial. Participants will be patients receiving care from a federally qualified primary care clinic. Patients are expected to be mostly ethnic minority females living below the poverty line with significant unmet need for chronic pain treatment. Patients will be randomly assigned by group to a standard medical treatment control, a pain education group, or a cognitive-behavioral therapy group. Primary outcomes are patient-reported pain intensity, pain interference in physical functioning, and psychological symptoms, all highly relevant to patient-provider decision-making. Aims: 1. Evaluate the feasibility, acceptability, and comparative effectiveness of health literacy-adapted psychosocial group treatments to a standard-treatment control. 2. Evaluate the comparative effectiveness of treatment groups on depressive symptoms, and evaluate all outcomes for heterogeneity of treatment effects. STUDY IMPACT - Systems: Produces a new, low-cost treatment option for community health clinics. - Providers: Offers options for treatments over and above surgery and medication. - Patients: Provides information to patients on the benefits of psychosocial treatment on outcomes that matter.


Criteria:

Inclusion Criteria: 1. Must be at least 19 yrs-old in order to consent to treatment. 2. Must have received at least one diagnosis consistent with chronic pain by a physician at one of the participating primary care clinics. 3. Must have experienced pain most days of the month for 3 months, and although pain may have more than one pain source, all pain must be non-malignant (e.g., not cancer- or HIV-related). 4. Must be able to speak and understand English. 5. Must have a telephone or other avenue of communication for contact regarding the study. Exclusion Criteria: 1. Must not demonstrate significant cognitive impairment (based on results of a cognitive screener). 2. Must not have current, uncontrolled serious psychological disturbance (e.g., schizophrenia, bipolar disorder) or active substance abuse (based on responses to a structured diagnostic interview). 3. Must have minimal literacy skills (i.e., read at the 1st grade level). 4. Must have been stabilized for at least 4 weeks on current pain and psychotropic medication regimen to reduce potential confounds to treatment results. 5. Must not have a surgery scheduled for the intervention period (~3 months). 6. Must neither be currently receiving a psychosocial treatment for pain (though they may be receiving psychotherapy for non-pain difficulties) nor be a participant in our previous treatment studies.


Study is Available At:


Original ID:

10-021-ME


NCT ID:

NCT01967342


Secondary ID:

Easygrants 941


Study Acronym:

LAMP


Brief Title:

Literacy-Adapted Psychosocial Treatments for Chronic Pain --- "Learning About Mastering/My Pain"


Official Title:

Reducing Disparities With Literacy-Adapted Psychosocial Treatments for Chronic Pain: A Comparative Trial


Overall Status:

Active, not recruiting


Study Phase:

N/A


Genders:

Both


Minimum Age:

19 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

University of Alabama, Tuscaloosa


Oversight Authority:

  • United States: Institutional Review Board
  • United States: Data and Safety Monitoring Board


Reasons Why Stopped:


Study Type:

Interventional


Study Design:

Allocation: Randomized, Endpoint Classification: E


Number of Arms:

3


Number of Groups:

0


Total Enrollment:

299


Enrollment Type:

Actual


Overall Contact Information

Official Name:Beverly E. Thorn, Ph.D.
Principal Investigator
University of Alabama at Birmingham

Study Dates

Start Date:May 2013
Completion Date:August 2016
Completion Type:Anticipated
Primary Completion Date:February 2016
Primary Completion Type:Anticipated
Verification Date:January 2016
Last Changed Date:January 11, 2016
First Received Date:October 16, 2013

Study Outcomes

Outcome Type:Secondary Outcome
Measure:Patient Global Impression of Change (PGIC)
Time Frame:Retrospective self-report at posttreatment (~Week 12)
Safety Issues:False
Description:We will measure perceived change on 7 key domains of interest: (a) Pain Intensity; (b) Pain Interference; (c) Pain Acceptance; (d) Pain Coping; and (e) Negative Thoughts about Pain. For each condition, we will publish the percentages of participants endor
Outcome Type:Secondary Outcome
Measure:Patient Health Questionnaire - 9 (PHQ-9)
Time Frame:Change from baseline to the end of treatment (10-14 weeks)
Safety Issues:False
Description:We will use the PHQ-9 at several key points in treatment to identify patient change in depressive symptoms. The IMMPACT publications only provided recommendations for the Beck Depression Inventory, which was deemed less satisfactory than the PHQ-9 for the
Outcome Type:Secondary Outcome
Measure:Brief Pain Inventory-Interference (BPI-Interference)
Time Frame:Change from baseline to the end of treatment (10-14 weeks)
Safety Issues:False
Description:We intend to compare mean pre-post changes in BPI-Interference between treatment groups and the usual care group to test for treatment effectiveness on pain interference in daily life. Using IMMPACT recommendations for clinically important change, a minim
Outcome Type:Primary Outcome
Measure:Brief Pain Inventory-Intensity (BPI-Intensity)
Time Frame:Change from baseline to the end of treatment (10-14 weeks)
Safety Issues:False
Description:We intend to compare mean pre-post changes in BPI-Intensity between treatment groups and the usual care group to test for treatment effectiveness at reducing pain intensity. Using the Initiative on Methods, Measurements, and Pain Assessment in Clinical Tr

Study Interventions

Intervention Type:Behavioral
Name:Pain Ed
Description:A 10-week psychosocial group treatment for chronic pain that focuses on providing information about the development, course, and treatment of chronic pain, as well as information about factors associated with reduced pain (e.g., sleep). In particular, it seeks to empower patients to take ownership of their chronic pain care through building deeper knowledge about their pain condition and their interactions with the health care system.
Arm Name:Pain Ed
Other Name:EDU
Intervention Type:Behavioral
Name:CBT for Pain
Description:A 10-week psychosocial group treatment for chronic pain that focuses on providing information and skills about the development, course, and treatment of chronic pain, as well as information about factors associated with reduced pain (e.g., sleep). In particular, it seeks to empower patients to self-manage their chronic pain through building deeper knowledge about and better skills for improving their pain condition and their interactions with the health care system.
Arm Name:CBT for Pain
Other Name:Cognitive-Behavioral Therapy for Pain
Intervention Type:Other
Name:Usual Care
Description:A comparison condition in which patients receive standard individualized medical care from the federally qualified health center partnering on this study. Care can include basic biological interventions, such as medication or surgery, as well as supplementary care such as chiropractic or physical therapy. However, cost has a pragmatic influence on the amount of services provided, sought, and received.
Arm Name:Pain Ed
Other Name:UC

Study Arms

Study Arm Type:Experimental
Arm Name:Pain Ed
Description:Pain Education: A psychosocial treatment group focusing on providing core pain education to low-income patients who may not have received this information due to existing barriers that often includes limited health literacy.
Study Arm Type:Experimental
Arm Name:CBT for Pain
Description:Cognitive-Behavioral Therapy for Pain: A psychosocial treatment group focusing on providing core pain education and cognitive-behavior skills to low-income patients who may not have received this information due to existing barriers that often includes limited health literacy.
Study Arm Type:Active Comparator
Arm Name:Usual Care
Description:Usual Care (Medical Treatment-as-Usual: A control/comparison condition in which patients receive on-going standard care at the federally qualified health center partnering in this research. Facets of care may include medication, surgery, chiropractic, and physical therapy, among others, which are available to all patients in all arms.

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:University of Alabama, Tuscaloosa
Agency Class:Other
Agency Type:Collaborator
Agency Name:Patient-Centered Outcomes Research Institute

Sample and Retention Information

There are no available Sample and Retention Information

Study References

Reference Type:Reference
Citation:Thorn BE, Day MA, Burns J, Kuhajda MC, Gaskins SW, Sweeney K, McConley R, Ward LC, Cabbil C. Randomized trial of group cognitive behavioral therapy compared with a pain education control for low-literacy rural people with chronic pain. Pain. 2011 Dec;152(12):2710-20. doi: 10.1016/j.pain.2011.07.007. Epub 2011 Sep 14.
PMID:21920668
Reference Type:Reference
Citation:Day MA, Thorn BE, Kapoor S. A qualitative analysis of a randomized controlled trial comparing a cognitive-behavioral treatment with education. J Pain. 2011 Sep;12(9):941-52. doi: 10.1016/j.jpain.2011.02.354. Epub 2011 Aug 11.
PMID:21839689
Reference Type:Reference
Citation:Kuhajda MC, Thorn BE, Gaskins SW, Day MA, Cabbil CM. Literacy and cultural adaptations for cognitive behavioral therapy in a rural pain population. Transl Behav Med. 2011 Jun;1(2):216-23. doi: 10.1007/s13142-011-0026-2.
PMID:24073046
Reference Type:Reference
Citation:Day MA, Thorn BE. The relationship of demographic and psychosocial variables to pain-related outcomes in a rural chronic pain population. Pain. 2010 Nov;151(2):467-74. doi: 10.1016/j.pain.2010.08.015.
PMID:20817401
Reference Type:Reference
Citation:Campbell LC. Addressing literacy as a barrier in delivery and evaluation of cognitive-behavioral therapy for pain management. Pain. 2011 Dec;152(12):2679-80. doi: 10.1016/j.pain.2011.09.004. Epub 2011 Sep 29.
PMID:21963312
Reference Type:Reference
Citation:Thorn BE, Burns JW. Common and specific treatment mechanisms in psychosocial pain interventions: the need for a new research agenda. Pain. 2011 Apr;152(4):705-6. doi: 10.1016/j.pain.2010.12.017. Epub 2011 Jan 11.
PMID:21227586

Data Source: ClinicalTrials.gov

Date Processed: April 03, 2020

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


This study is not currently recruiting Study Participants. The form below is not enabled.