NCT04814992

Brief Summary

A significant number of patients develop chronic post-surgical pain (CPSP) following knee replacement surgery. Proposed is the testing of a novel computer-assisted behavioral intervention integrating motivational interviewing in the 4 weeks prior to surgery to address the risk factors for CPSP, with the expectation that severity of post-op pain and the incidence of CPSP will be reduced.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

4 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2020

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

March 17, 2021

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 24, 2021

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2023

Completed
10 months until next milestone

Results Posted

Study results publicly available

October 17, 2024

Completed
Last Updated

October 17, 2024

Status Verified

July 1, 2024

Enrollment Period

3.2 years

First QC Date

March 17, 2021

Results QC Date

January 23, 2024

Last Update Submit

July 29, 2024

Conditions

Keywords

CPSPChronic Post-Surgical PainCognitive Behavioral TherapyTotal Knee ArthroplastyMotivational InterviewingOpioid Taper

Outcome Measures

Primary Outcomes (1)

  • Preoperative Chronic Pain Severity

    The severity of preoperative chronic pain will be evaluated with the Brief Pain Inventory (BPI), along two dimensions: intensity and interference. Pain intensity is rated on a 0 (no pain) to 10 (worst pain imaginable) scale as the worst in the past 24 hours, least in the past 24 hours, average pain and current pain. Pain interference is measured in 7 areas: general activity, mood, walking ability, work, sleep, enjoyment of life and relationships on a 0 (no interference) to 10 (interferes completely) scale. The composite mean of these scores are used as a pain interference score. BPI scores will be collected at baseline and compared to those collected just prior to surgery and at 3- and 6-month follow-up. Higher composite mean scores represent more pain interference (worse outcome).

    prior to surgery, approximately 6 weeks following baseline.

Secondary Outcomes (10)

  • Preoperative Opioid Use

    prior to surgery, approximately 6 weeks following baseline

  • Post-operative Opioid Use

    6-months

  • Pre-Op Depression

    pre-operation, approximately 6 weeks following baseline

  • Post-Op Depression

    6-months

  • Pre-Op Anxiety

    pre-operation, approximately 6 weeks following baseline

  • +5 more secondary outcomes

Study Arms (2)

Computer-Assisted Preoperative CBT Intervention

ACTIVE COMPARATOR

Patients will receive the computer-assisted preoperative CBT intervention (n=75). A particularly promising internet-based CBT pain program for the population of interest, PAINTrainer, demonstrated improved pain, function, coping and global health in patients with chronic knee arthritic pain in comparison to an internet education control, with benefits persisting for up to 52 weeks. In addition to the PAINTrainer, there will be an integration of a motivational interviewing (MI) intervention delivered by a trained "coach" across the sessions about (1) the benefits of opioid tapering for post-operative pain control, (2) approaches for safely tapering, (3) identifying and managing withdrawal symptoms patients may experience.

Behavioral: Computer-Assisted Preoperative CBT Intervention (PAINTrainer)

Treatment-as-usual (control)

NO INTERVENTION

Patients scheduled to undergo total joint arthroplasty at the study site are automatically enrolled in a mandatory 4-hour education class delivered by a nurse educator or physical therapist. Utilizing an in-person Powerpoint presentation format, patients are informed about pre-habilitation exercises to do prior to surgery; what to expect the day of surgery; the multimodal analgesia protocol used in the perioperative period; options for anesthesia and analgesia; and the expectation of physical therapy after surgery.

Interventions

Subjects will be asked to complete eight (8) 30- to 45-minute educational sessions during the 4 weeks prior to your surgery. In addition to the computer based training sessions, there is a motivational interviewing component that requires subjects to meet with a member of the study team weekly for a total of four (4) 30- to 45-minute meetings to help manage opioid medication use. It is expected that subject participation in this arm of the study will be a total of 12 hours over the course of the entire study.

Computer-Assisted Preoperative CBT Intervention

Eligibility Criteria

Age22 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Males and females, age \> 21 years
  • Chronic non-malignant pain of at least 3 months duration
  • Morphine equivalent daily dose (MEDD) \> 40 milligrams for at least 3 months
  • Able to enroll at least 4 weeks prior to planned surgery
  • Able to speak, read and comprehend in English at the 6th grade or higher proficiency

You may not qualify if:

  • Pain of malignant origin
  • Current or past history of opioid use disorder (including those on medication-assisted therapy)
  • Revision of TKA
  • Comorbid CNS disease such as dementia, HIV, psychosis, poorly controlled bipolar disorder or any condition interfering with informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Penn Medicine University City

Philadelphia, Pennsylvania, 19104, United States

Location

Penn Presbyterian Medical Center

Philadelphia, Pennsylvania, 19104, United States

Location

Pennsylvania Hospital

Philadelphia, Pennsylvania, 19129, United States

Location

Penn Medicine Radnor

Radnor, Pennsylvania, 19087, United States

Location

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Related Links

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Results Point of Contact

Title
Dr. Peggy Compton
Organization
University of Pennsylvania

Study Officials

  • Martin D Cheatle, PhD

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR
  • Peggy Compton, RN, PhD, FAAN

    University of Pennsylvania

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: A randomized clinical trial is proposed to evaluate the efficacy of the novel computer-assisted preoperative CBT with integrating motivational interviewing intervention to affect acute and chronic post-operative pain outcomes. Specifically, 90 adult patients over the age of 21 meeting study inclusion criteria and preparing to undergo TKA at the Department of Orthopedic Surgery at Penn Presbyterian Medical Center, Penn Medicine University City, Penn Medicine Radnor, and Pennsylvania Hospital will be randomized to either receive the computer-assisted preoperative CBT intervention (n=45) or treatment-as-usual (control, n=45).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor, van Ameringen Endowed Chair

Study Record Dates

First Submitted

March 17, 2021

First Posted

March 24, 2021

Study Start

October 1, 2020

Primary Completion

December 31, 2023

Study Completion

December 31, 2023

Last Updated

October 17, 2024

Results First Posted

October 17, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

All records will be kept strictly confidential. No one except the researchers will know the subjects are in a research study. Data forms for the collection of health and study data will be coded with each subject's unique identification number. No data form will identify the participants by name. Hardcopies of data forms will be kept in locked files with keys held only by the study investigators. All electronic data will be stored with the password and firewall protected REDCap data collection and management system of the U Penn School of Nursing. No presentation or publication of the results of this study will refer to the individual participants or present information that would identify any participant. All persons working on the proposed work will have completed HIPAA training and the Collaborative Institutional Training Initiative (CITI) Basic Courses in the Protection of Human Research Subjects and Biomedical Focus Responsible Conduct of Research (RCR) modules.

Locations