Cognitive Behavioural Therapy to Reduce Persistent Post-Surgical Pain After Fracture (SPOC_CBT)
Primary Purpose
Pain, Postoperative, Fractures, Closed, Fractures, Open
Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cognitive behavioural therapy
Sponsored by
About this trial
This is an interventional prevention trial for Pain, Postoperative focused on measuring fracture, persistent pain, cognitive behavioural therapy, post surgical pain, health-related quality of life
Eligibility Criteria
The inclusion criteria are:
- Adult men or women aged 18 years and older.
- Acute open or closed fracture(s) of the appendicular skeleton. Patients with multiple fractures may be included.
- Fracture treated operatively with internal fixation.
- Screened for eligibility within 6 weeks of their fracture.
- Cognitive ability and language skills required to participate in the CBT intervention (in the judgement of site research personnel).
- Able to start the CBT within 8 weeks of their fracture surgery.
- Provision of informed consent.
- Screen positive for unhelpful illness beliefs (SPOC scores ≥74), as assessed at 6 weeks' post-surgical fixation.
The exclusion criteria are:
- Fragility fracture.
- Stress fracture.
- Concomitant injury which, in the opinion of the attending surgeon, is likely to impair function for as long as or longer than the patient's extremity fracture.
- Active psychosis.
- Active suicidality.
- Active substance use disorder that, in the judgement of the treating surgeon, would interfere in the patient's ability to partake in the CBT and/or the study.
- Already participating in, or planning to start other psychological treatments (including CBT) within the duration of the study (12 months).
- Anticipated problems with the patient attending CBT sessions and/or returning for follow-up.
- Incarceration.
- Other reason to exclude the patient, as specified.
Sites / Locations
- St. Joseph Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
intervention - CBT
control
Arm Description
Participants in this arm will receive 6 weekly one-on-one, 1-hour sessions of Cognitive Behavioural Therapy session (intervention) in addition to receiving standard of care treatment for their fracture(s).
Participants in the control arm of the study will receive standard of care treatment for their fracture(s) but will not receive any Cognitive Behavioral Therapy.
Outcomes
Primary Outcome Measures
The prevalence of Persistent Post-Surgical Pain at 12 months' post-fracture
The primary outcomes are 1) PPSP according to the World Health Organization's (WHO) proposed definition, and 2) the prevalence of moderate to severe pain interference over 12 months post-fracture as assessed by an individual item from the Patient-Reported Outcomes Measurement Information System (PROMIS).
The WHO's definition requires 4 criteria for the diagnosis of PPSP: 1) Pain that began after surgery or a tissue trauma is experienced; 2) The pain is in an area of preceding surgery or tissue trauma, 3) The pain persisted for at least two months after the initiating event, and 4) The pain is not better explained by an infection, a malignancy, a pre-existing pain condition or any other alternative cause.
Secondary Outcome Measures
Short Form 12 (SF-12)
General health related quality of life will be assessed by the SF-12. The SF-12 is an established, reliable and validated health status measure.It is a self-administered, 12-item questionnaire that measures health-related quality of life in 8 domains related to physical, social, mental, and emotional functioning, bodily pain, and general health. Both physical and mental summary scores can be obtained. Each domain is scored separately from 0 (lowest level) to 100 (highest level).
Return to Function questionnaire
Return to function will be measured by when participants' return to work, household activities, and leisure activities, as well as when they achieve 80% of their pre-injury function. The return to function outcome will be assessed using the Return to Function questionnaire.
PROMIS-Physical Function 28
HRQL will also be assessed by the PROMIS-PF28, as recent research suggests it may be more sensitive to change than the SF-12. The PROMIS-PF is a standard for patient-reported outcomes research and practice and recommended for initial outcome assessment. Studies continue to support its construct validity and feasibility. The PROMIS-PF includes seven HRQoL domains: Physical Functioning, Anxiety, Depression, Fatigue, Sleep Disturbance, Social Functioning, and Pain. The PROMIS-Physical Function 28 will be used to assess seven health quality of life domains.
Full Information
NCT ID
NCT03196258
First Posted
June 13, 2017
Last Updated
February 20, 2020
Sponsor
McMaster University
Collaborators
Hamilton Academic Health Sciences Organization, Hamilton Health Sciences Corporation, Unity Health Toronto
1. Study Identification
Unique Protocol Identification Number
NCT03196258
Brief Title
Cognitive Behavioural Therapy to Reduce Persistent Post-Surgical Pain After Fracture
Acronym
SPOC_CBT
Official Title
Cognitive Behavioural Therapy to Improve Outcomes of High Risk Patients Following Internal Fixation of Extremity Fractures: A Randomized Controlled Trial (SPOC-CBT)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Terminated
Why Stopped
Feasibility issues with the study treatment (in-person CBT) resulted in the study ending earlier than anticipated.
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
June 1, 2019 (Actual)
Study Completion Date
December 1, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Hamilton Academic Health Sciences Organization, Hamilton Health Sciences Corporation, Unity Health Toronto
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
Psychological factors such as stress, distress, anxiety, depression, and poor coping strategies may be associated with ongoing pain following injuries such as fractures. In order to study this relationship, researchers at McMaster University have developed the Somatic Pre-Occupation and Coping (SPOC) questionnaire, which identifies illness beliefs that may help to predict which patients are at risk for ongoing pain, reduced quality of life, and delays in returning to work and leisure activities after a fracture requiring surgical treatment. Previous research using the SPOC questionnaire suggests the possibility that fracture patients with illness beliefs that put them at risk for developing ongoing pain could be identified early in the treatment process. These patients may benefit from cognitive behavioural therapy (CBT) which is designed to modify such thoughts with the goal of reducing ongoing pain and improving quality of life. The goal of this study is to determine if CBT is effective in reducing ongoing pain and improving quality of life in fracture patients who show illness beliefs that may place them at risk for developing ongoing pain.
Detailed Description
In North America, chronic non-cancer pain affects approximately 30% of the population, with similar rates in Europe and Australia. Surgery and trauma are frequently cited as triggering events responsible for the development of chronic pain. A survey of 5,130 patients attending 10 outpatient clinics located throughout North Britain found that 41% attributed their chronic pain to a traumatic event or surgery. The presence of persistent pain can have a major impact on patients' quality of life, including their ability to return to work and their daily activities.
The relationship between psychological factors, behaviors, and cognitive processes and the sensation of pain is well documented. Stress, distress, anxiety, depression, catastrophizing, fear-avoidance behaviors, and poor coping strategies appear to have a significant positive relationship with both acute and chronic pain. Evidence suggests that these psychological factors can cause alterations along the spinal and supraspinal pain pathways which influence the perception of pain. Previous studies suggest that patients' beliefs and expectations may be associated with clinical outcomes, including self-reported pain.
Clinical outcomes following operatively managed fractures of the extremities are variable and many patients continue to experience persistent pain and disability one-year after surgery and beyond. In a recent trial involving patients with open extremity fractures, 65% of patients reported moderate to very severe pain and 35% reported moderate to extreme pain interference at one-year. A systematic review of 20 observational studies of traumatic tibial fracture repairs found the mean incidence of persistent post-surgical pain (PPSP) was 47.4% (range: 10% to 86%) at an average of 23.9 months after surgery. Although several risk factors for PPSP have been identified, many, such as younger age and female gender, are non-modifiable and thus not amendable to direct intervention.
The effect of patients' beliefs and expectations on their recovery following traumatic injuries is an under-investigated area. In response to this gap, Busse et al. developed and evaluated the Somatic Pre-Occupation and Coping (SPOC) questionnaire to identify unhelpful illness beliefs that are predictive of poorer functional outcomes post-fracture. This self-administered questionnaire identified unhelpful illness beliefs among approximately one third of patients with operatively managed extremity fractures. Furthermore, high somatic pre-occupation and poor coping at 6-weeks post-fracture (as measured by the SPOC questionnaire) were found to be strongly associated with PPSP, functional limitations, unemployment, and reduced quality of life 1 year after fracture fixation. This suggests the possibility that fracture patients who exhibit unhelpful illness beliefs can be identified and targeted for concurrent therapy designed to modify such cognitions and improve prognosis. At present, however, there are no approaches that have been shown effective for improving recovery among high-risk patients.
The findings from the FLOW trial highlight the importance of patient beliefs in recovery from orthopaedic trauma. A number of systematic reviews have shown patients' perceptions regarding their illness experience can be modified, and that such efforts can improve outcomes. Moss-Morris and colleagues explored the effect of CBT among patients attending a multidisciplinary chronic pain clinic and found that changes in cognitive processes accounted for 26% of the variation in improved health-related quality of life scores. Collectively, these findings suggest that targeting and modifying unhelpful beliefs through CBT may provide an effective strategy to improve outcomes among high-risk trauma patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative, Fractures, Closed, Fractures, Open
Keywords
fracture, persistent pain, cognitive behavioural therapy, post surgical pain, health-related quality of life
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants with operatively managed extremity fractures who screen positive for unhelpful illness beliefs (SPOC scores ≥78) 6-weeks post-fracture fixation will be randomized to receive either 6 weekly one-on-one, 1-hour sessions of cognitive behavioral therapy (CBT) or standard of care (control). Outcomes will be assessed at 3 months, 6 months, 9 months, and 12 months' post-fracture
Masking
None (Open Label)
Masking Description
Eligible participants will be randomized to 1 of 2 groups: 1) CBT intervention or 2) standard of care. Due to the nature of the intervention, it will not be feasible to blind participants, treating surgeons, or CBT therapists to treatment allocation. The data analyst and Steering Committee will be blinded to treatment allocation
Allocation
Randomized
Enrollment
8 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intervention - CBT
Arm Type
Experimental
Arm Description
Participants in this arm will receive 6 weekly one-on-one, 1-hour sessions of Cognitive Behavioural Therapy session (intervention) in addition to receiving standard of care treatment for their fracture(s).
Arm Title
control
Arm Type
No Intervention
Arm Description
Participants in the control arm of the study will receive standard of care treatment for their fracture(s) but will not receive any Cognitive Behavioral Therapy.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioural therapy
Other Intervention Name(s)
CBT
Intervention Description
Participants who are randomized to the CBT intervention are required to start CBT within 8 weeks of their fracture surgery. The CBT intervention will consist of 6 weekly one-on-one, 1-hour sessions that will focus on addressing maladaptive beliefs related to pain and recovery as well as teaching skills to enhance coping and management of pain symptoms. The specific focus of CBT sessions will be informed by each individual patient's responses on the SPOC questionnaire. All other aspects of post-operative care will be at the discretion of participant's surgeon
Primary Outcome Measure Information:
Title
The prevalence of Persistent Post-Surgical Pain at 12 months' post-fracture
Description
The primary outcomes are 1) PPSP according to the World Health Organization's (WHO) proposed definition, and 2) the prevalence of moderate to severe pain interference over 12 months post-fracture as assessed by an individual item from the Patient-Reported Outcomes Measurement Information System (PROMIS).
The WHO's definition requires 4 criteria for the diagnosis of PPSP: 1) Pain that began after surgery or a tissue trauma is experienced; 2) The pain is in an area of preceding surgery or tissue trauma, 3) The pain persisted for at least two months after the initiating event, and 4) The pain is not better explained by an infection, a malignancy, a pre-existing pain condition or any other alternative cause.
Time Frame
12 months post-fracture
Secondary Outcome Measure Information:
Title
Short Form 12 (SF-12)
Description
General health related quality of life will be assessed by the SF-12. The SF-12 is an established, reliable and validated health status measure.It is a self-administered, 12-item questionnaire that measures health-related quality of life in 8 domains related to physical, social, mental, and emotional functioning, bodily pain, and general health. Both physical and mental summary scores can be obtained. Each domain is scored separately from 0 (lowest level) to 100 (highest level).
Time Frame
1 year
Title
Return to Function questionnaire
Description
Return to function will be measured by when participants' return to work, household activities, and leisure activities, as well as when they achieve 80% of their pre-injury function. The return to function outcome will be assessed using the Return to Function questionnaire.
Time Frame
1 year
Title
PROMIS-Physical Function 28
Description
HRQL will also be assessed by the PROMIS-PF28, as recent research suggests it may be more sensitive to change than the SF-12. The PROMIS-PF is a standard for patient-reported outcomes research and practice and recommended for initial outcome assessment. Studies continue to support its construct validity and feasibility. The PROMIS-PF includes seven HRQoL domains: Physical Functioning, Anxiety, Depression, Fatigue, Sleep Disturbance, Social Functioning, and Pain. The PROMIS-Physical Function 28 will be used to assess seven health quality of life domains.
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Exploratory outcome 1: Fracture healing complications
Description
fracture healing complications as assessed by the treating surgeon (including wound healing problems, infection (superficial and deep), hardware failure, hardware breakage, and non-union),
Time Frame
1 year
Title
Exploratory outcome 2: time to fracture healing
Description
time to clinical fracture healing, as assessed by the treating surgeon. To determine if CBT versus usual care reduces the incidence of fracture healing complications within 12-months post-fracture
Time Frame
1 year
Title
Exploratory outcome 3: opioid use
Description
Patient-reported use of opioid class medications. ) to determine if CBT versus usual care reduces the proportion of participants taking opioid class medications at 6 months and 12 months.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
The inclusion criteria are:
Adult men or women aged 18 years and older.
Acute open or closed fracture(s) of the appendicular skeleton. Patients with multiple fractures may be included.
Fracture treated operatively with internal fixation.
Screened for eligibility within 6 weeks of their fracture.
Cognitive ability and language skills required to participate in the CBT intervention (in the judgement of site research personnel).
Able to start the CBT within 8 weeks of their fracture surgery.
Provision of informed consent.
Screen positive for unhelpful illness beliefs (SPOC scores ≥74), as assessed at 6 weeks' post-surgical fixation.
The exclusion criteria are:
Fragility fracture.
Stress fracture.
Concomitant injury which, in the opinion of the attending surgeon, is likely to impair function for as long as or longer than the patient's extremity fracture.
Active psychosis.
Active suicidality.
Active substance use disorder that, in the judgement of the treating surgeon, would interfere in the patient's ability to partake in the CBT and/or the study.
Already participating in, or planning to start other psychological treatments (including CBT) within the duration of the study (12 months).
Anticipated problems with the patient attending CBT sessions and/or returning for follow-up.
Incarceration.
Other reason to exclude the patient, as specified.
Facility Information:
Facility Name
St. Joseph Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N4A6
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Description
28. Hamner J, Dewitt B. The Development of a Preference-based Scoring System for PROMIS (PROPr): A Technical Report v 1.1. [Internet] 2017;available from: http://janelhanmer.pitt.edu/documents/technicalreportv1.1.pdf (accessed August 29, 2017).
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https://www.google.ca/search?q=Wang+L%2C+Chang+Y%2C+Kennedy+SA%2C+Hong+PJ%2C+Chow+N%2C+Coubon+R+et+al.+Perioperative+Psychotherapy+for+Persistent+Post-Surgical+Pain+and+Physical+Impairment%3A+A+Meta-Analysis+of+Randomized+Trials.+Br+J+Anaesth.+2017%3B%5Bin+review%5D&oq=Wang+L%2C+Chang+Y%2C+Kennedy+SA%2C+Hong+PJ%2C+Chow+N%2C+Coubon+R+et+al.+Perioperative+Psychotherapy+for+Persistent+Post-Surgical+Pain+and+Physical+Impairment%3A+A+Meta-Analysis+of+Randomized+Trials.+Br+J+Anaesth.+2017%3B%5Bin+review%5D&aqs=chrome..69i57.453j0j9&sourceid=chrome&ie=UTF-8
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Wang L, Chang Y, Kennedy SA, Hong PJ, Chow N, Coubon R et al. Perioperative Psychotherapy for Persistent Post-Surgical Pain and Physical Impairment: A Meta-Analysis of Randomized Trials. Br J Anaesth. 2017;[in review]
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Hamner J, Dewitt B. The Development of a Preference-based Scoring System for PROMIS (PROPr): A Technical Report v 1.1 [internet] 2017; available from: http//janelhanmer.pitt.edu/documents/technicalreportv1.1.pdf (accessed August 29, 2017)
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https://academic.oup.com/ije/article/46/2/746/2741997
Description
Li G, Taljaard M, Van den Heuvel ER, Levine MA, Cook DJ, Wells GA, et al. An introduction to multiplicity issues in clinical trials: the what, why, when and how. Int J Epidemiol. 2017;46(2):746-55
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Cognitive Behavioural Therapy to Reduce Persistent Post-Surgical Pain After Fracture
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