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Single Session Pain Education

Primary Purpose

Chronic Pain

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Single session pain education class
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain

Eligibility Criteria

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

Inclusion Criteria:

  • chronic pain patients, pain longer than 3 months
  • ability to adhere to and complete study protocols

Exclusion Criteria:

  • not fluent in English
  • recent injury at the discretion of the researcher
  • previous completion of pain education class at the discretion of the researcher
  • current cancer diagnosis or other medical condition at the discretion of the researcher

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Pain Education

    wait list control

    Arm Description

    Participant will attend a single session pain education course

    Participants will be wait listed then receive intervention

    Outcomes

    Primary Outcome Measures

    Mean change in Tampa scale for kinesiophobia at three months
    TSK is a measure of kinesiophobia in people who have chronic pain

    Secondary Outcome Measures

    Full Information

    First Posted
    April 26, 2021
    Last Updated
    April 26, 2021
    Sponsor
    Stanford University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04865822
    Brief Title
    Single Session Pain Education
    Official Title
    Single Session Pain Education for Chronic Pain
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 1, 2021 (Anticipated)
    Primary Completion Date
    September 1, 2023 (Anticipated)
    Study Completion Date
    September 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Stanford University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    To pilot single session pain education classes aimed at improving outcomes and behaviors in patients with chronic pain.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Pain

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Pain Education
    Arm Type
    Experimental
    Arm Description
    Participant will attend a single session pain education course
    Arm Title
    wait list control
    Arm Type
    No Intervention
    Arm Description
    Participants will be wait listed then receive intervention
    Intervention Type
    Behavioral
    Intervention Name(s)
    Single session pain education class
    Intervention Description
    Pain education classes will be provided in person group or virtual settings
    Primary Outcome Measure Information:
    Title
    Mean change in Tampa scale for kinesiophobia at three months
    Description
    TSK is a measure of kinesiophobia in people who have chronic pain
    Time Frame
    month 3

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: chronic pain patients, pain longer than 3 months ability to adhere to and complete study protocols Exclusion Criteria: not fluent in English recent injury at the discretion of the researcher previous completion of pain education class at the discretion of the researcher current cancer diagnosis or other medical condition at the discretion of the researcher

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Single Session Pain Education

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