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Cognitive Behavioral Therapy for Painful Diabetic Neuropathy

Primary Purpose

Diabetic Neuropathy

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cognitive behavioral therapy
standard medical care
Sponsored by
VA Connecticut Healthcare System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Neuropathy focused on measuring diabetes, neuropathy, chronic pain, Cognitive behavioral therapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • type 2 diabetes mellitus
  • daily lower extremity pain or discomfort (burning, tingling or other parasthesias) for at least 3 months
  • documented trial of at least one medication for neuropathic pain
  • pain of at least 4 on a 0-10 numeric rating scale

Exclusion Criteria:

  • acute medical condition, substance abuse, or psychiatric condition that would impair ability to participate
  • dementia (MMSE score of 23 or lower)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    standard care

    CBT

    Arm Description

    Medical care including medication for neuropathic pain

    Outcomes

    Primary Outcome Measures

    Pain intensity score (NRS)

    Secondary Outcome Measures

    pain-related disability (MPI) and emotional functioning

    Full Information

    First Posted
    January 24, 2009
    Last Updated
    July 27, 2011
    Sponsor
    VA Connecticut Healthcare System
    Collaborators
    Donaghue Medical Research Foundation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00830011
    Brief Title
    Cognitive Behavioral Therapy for Painful Diabetic Neuropathy
    Official Title
    Cognitive Behavioral Therapy for Painful Diabetic Neuropathy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2004 (undefined)
    Primary Completion Date
    June 2009 (Actual)
    Study Completion Date
    December 2009 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    VA Connecticut Healthcare System
    Collaborators
    Donaghue Medical Research Foundation

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary objective of this study is to evaluate the usefulness of cognitive behavioral therapy (CBT) for the management of painful diabetic neuropathy. Participants will be randomly assigned to one of two treatment conditions: CBT plus standard medical care or standard medical care alone. CBT will be offered in ten, ninety-minute group sessions and will be provided by a psychologist with experience in the management of both diabetes and chronic pain. CBT will involve teaching and encouraging practice of adaptive pain coping skills such as relaxation skills, activity pacing, and positive self-statements, among others. This study will allow us to determine which treatment is superior in terms of improvements in pain management, functioning and overall quality of life.
    Detailed Description
    Research Design: A randomized mixed factorial controlled design will be employed in which CBT plus standard pharmaceutical care (CBT/SC) is compared to a standard pharmaceutical care (SC) treatment condition. Participants will be randomized in equal numbers to the two conditions. Repeated assessments of key outcome domains will occur at pretreatment/baseline and at 12, 24 and 36 weeks following baseline. Methodology: Study participants will be evaluated pre-treatment (baseline), 12 weeks post-baseline (post-treatment) and at 24 and 36 weeks post-baseline (follow-up). Baseline assessment will include a neurological examination with a nerve conduction study to confirm the diagnosis of diabetic neuropathy. The primary outcome measure will be pain intensity. Secondary outcome measures will be pain quality, pain-related disability, physical and emotional functioning. Measures of treatment feasibility will also be examined. Participants receiving CBT will attend 10 weekly, group treatment sessions of 90 minutes. A target sample size of approximately 120 participants will be recruited.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetic Neuropathy
    Keywords
    diabetes, neuropathy, chronic pain, Cognitive behavioral therapy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    standard care
    Arm Type
    Active Comparator
    Arm Description
    Medical care including medication for neuropathic pain
    Arm Title
    CBT
    Arm Type
    Active Comparator
    Intervention Type
    Behavioral
    Intervention Name(s)
    cognitive behavioral therapy
    Intervention Description
    Ten sessions of manualized CBT delivered by a PhD level psychologist
    Intervention Type
    Other
    Intervention Name(s)
    standard medical care
    Intervention Description
    any care recommended by physician for treatment of diabetic neuropathy including medication.
    Primary Outcome Measure Information:
    Title
    Pain intensity score (NRS)
    Time Frame
    post treatment and follow-up (24 and 36 weeks)
    Secondary Outcome Measure Information:
    Title
    pain-related disability (MPI) and emotional functioning
    Time Frame
    post treatment and followup (24 and 36 weeks)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: type 2 diabetes mellitus daily lower extremity pain or discomfort (burning, tingling or other parasthesias) for at least 3 months documented trial of at least one medication for neuropathic pain pain of at least 4 on a 0-10 numeric rating scale Exclusion Criteria: acute medical condition, substance abuse, or psychiatric condition that would impair ability to participate dementia (MMSE score of 23 or lower)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Robert Kerns, PhD
    Organizational Affiliation
    VA Connecticut Healthcare System
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    33070667
    Citation
    Higgins DM, Heapy AA, Buta E, LaChappelle KM, Serowik KL, Czlapinski R, Kerns RD. A randomized controlled trial of cognitive behavioral therapy compared with diabetes education for diabetic peripheral neuropathic pain. J Health Psychol. 2022 Mar;27(3):649-662. doi: 10.1177/1359105320962262. Epub 2020 Oct 19.
    Results Reference
    derived
    Links:
    URL
    http://www.diabetes.org
    Description
    American Diabetes Association

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    Cognitive Behavioral Therapy for Painful Diabetic Neuropathy

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