Assignment 3: Final Project - Comprehensive Literature Review
Assignment 3: Final Project - Comprehensive Literature Review
Assignment 3: Final Project - Comprehensive Literature Review
Jay Jalali
Yorkville University
Abstract
The comprehensive literature review explores research from 6 quantitive sources and 6
qualitative studies conducted over the last ten years on the use of Cognitive Behavioural Therapy
(CBT) and Physical Exercise (PE) interventions in Pain Self Management Programs (PSM) for
the treatment of various types of chronic pain. The purpose of the review was an overall
The use of Cognitive Behavioural Therapy (CBT) and Exercise for Pain Self Management
(PSM) Programs
Chronic pain is the leading cause of disability and a public health issue prevalent in
almost 20% of adults globally (Rice, 2016). It is defined as pain experienced for three months or
longer and is classified into primary pain, in which pain is a primary presenting feature, and
secondary pain, which includes pain persisting after surgery, trauma or associated with an
individually targeting the physical component of pain are often short term or non effective (Turk
et al., 2009). However, self pain management programs involving Cognitive Behavioural
Therapy (CBT) and Physical Exercise (PE) have been shown to be efficacious approaches to
Background
CBT for PSM follows a rationale that patients must understand cognitive and behavioural
influences of pain in order to combat and self manage pain related emotions and behavior (Bruns
and behaviours; CBT encourages patients with chronic pain to conceptualize pain as
manageable, gain an active role in controlling it and develop adaptive behavioural and cognitive
responses to functioning with pain (Bruns et al., 2006). Limited research additionally supports
this rationale, by combining CBT and interventions involving physical exercise (PE), to optimise
pain management and improve overall quality of life (Dysvik et al., 2004). While CBT targets
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Presently, not many studies have specifically examined the impact of combining specific
types of CBT and PE interventions on chronic pain and further research is required to evaluate
the intervention’s efficacy over long term periods (Natvig et al., 2010). This is because research
on PSM programs using both CBT and PE are sparse and comparisons are limited due to
differences in types of pain, service periods, program content, program intensity, result
evaluation approaches, and follow-up periods used (Joos et al., 2004). For the purpose of this
literature review individual and group PSM programs using qualitive and quantitate methods
involving adaptations of CBT and PE for various forms of pain, have been reviewed from the
Problem Statement
With existing literature on adaptations of CBT and PE use in PSM programs varying in
relation to types of pain treated, target population, length of program and follow up period; the
purpose of this literature review is an overall evaluation of program efficacy, components that
Literature Review
Scope of Research
6 qualitative (Charest et al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al.,
2014; Barker et al., 2012; Furnes et al., 2014) and 6 quantitative studies (Pincus et al., 2015;
Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016; Arakoski et al., 2015; Oey et al., 2016)
were conducted within hospitals, physical rehabilitation centres, secondary care clinics and
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research institutes in the United Kingdom, Italy, Canada, Australia, Finland, USA, Sweden and
the Netherlands.
Besides any individual inclusion and exclusion screening criteria, participants were
included based on type of pain experienced, have reported chronic pain for over 3 months
duration and referral from their medical practioner. The quantitive and qualitative studies
included participants that were aged 18 and over and 16 and over respectively. This inclusion of
studies based on a range of developed countries, treatment locations and vast participant age
groups allowed a broader scope of intervention review based on varying adaptations of treatment
options for pain type, length of intervention time, and the duration of post intervention follow up,
In relation to types of pain, quantitive studies evaluated PSM programs for neck pain
(Rocca et al., 2017), low-back pain(Pincus et al., 2015; Foti et al., 2016), geriatric pain (Wood et
al., 2013), osteoarthritis (Arakoski et al., 2015) and general chronic pain (not limited to pain
type) (Oey et al., 2016); while qualitative studies evaluated fibromyalgia (Charest et al., 2015),
orofacial pain (Peters et al., 2016), low back pain (Barker et al., 2012) and general chronic pain
(Nordin et al., 2013; Dekker et al., 2014; Furnes et al., 2014). All studies were only selected if
the PSM program had a psychological based CBT treatment framework covering over 50 percent
of the program content, included some form of PE education and was delivered and supervised
Research Methods
control trial groups (Pincus et al., 2015; Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016;
Arakoski et al., 2015) and 1used a quasi experimental design (Oey et al., 2016). The 5 qualitive
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studies used phenomenological (thematic) (Charest et al., 2015; Peters et al., 2016; Nordin et al.,
2013; Dekker et al., 2014; Furnes et al., 2014) and 1 grounded theory (Barker et al., 2012) study
The experimental method randomised control trial (RCT) studies revealed a range of
results in relation to outcomes of PSM programs on completion over a range of follow up periods
(Pincus et al., 2015; Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016; Arakoski et al.,
2015). The advantages of reviewing these experimental studies with the RCT group as an
independent variable is that it allowed observations of any changes in participants where the
intervention was withheld (Goodwin & Goodwin, 2017). Since statistical significance test results
were readily interpretable in these studies, it increased the reliability of results by reducing the
likelihood of type one and type two errors (Goodwin & Goodwin, 2017). Additionally,
distribution of prognostic factors, making different groups comparable to known and unknown
The disadvantages of this method were that the long-term logistics and participation of
both participants and practioner of the intervention were significantly distorted due to lack of
consistent participation, dropping out of participants and changing the practioner between studies
(Pincus et al., 2015; Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016; Arakoski et al.,
2015). Additionally, the ethical considerations were that some studies never considered a
thorough medical history of each participant in relation to previous pain treatment. There were
participants included that have had tried multiple prior pain treatments and were thus desperate
for a positive outcome. This made generalisation of results difficult because the samples seem to
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have people who enrol or get referred to studies seeking positive results (Pincus et al., 2015;
Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016; Arakoski et al., 2015).
With the quasi experimental study with 36 different groups over 10 years, the pre-post
results showed significant increases in improved general health between completers and non
completers of programs (Oey et al., 2016). The advantage of this method is that the larger sample
base increased external validity of results and laid the foundation for future randomised studies
(Goodwin & Goodwin, 2017). The disadvantage to this method was the existence of non
completion bias from incomplete pre and post-test outcome measure questionnaires not being
checked by instructors for competedness (Oey et al., 2016). Additionally, the generalization of
findings was somewhat reduced reduced because of more female than male participants in
The phenomenological studies included face to face group interviews and semi structured
interviews, with open ended questions for theme development of program elements (Charest et
al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al., 2014; Furnes et al., 2014). The
advantage of this method is that it did not seek to prove anything about the efficacy of PSM
(Richards & Morse, 2013). Since these studies were thematic in purpose it improved the
confidence of results because it was based on participant’s own words and narratives than any
researcher bias with interpretations (Richards & Morse, 2013). The disadvantage with this
method is that all the studies used samples that contained no more than 34 participants. The low
sampling number although rich in internal validity to individual studies, were not highly
externally valid because of the non wider generalisation of findings (Richards & Morse, 2013).
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Additionally, an ethical consideration with these research studies was the lack of member
checking or allowing participants to clarify intentions with answers, correct errors or provide
additional information; before publishing final interpretations and conclusions (Charest et al.,
2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al., 2014; Furnes et al., 2014).
The grounded theory study used semi structured interviews to comparative analysis of
pre, during and post program outcomes to identify narratives between a group of achieved
successful PSM results and a group that perceived no benefit (Barker et al., 2012).
The advantage of this method was increased credibility and richness of results because of the
different points in time (Richards & Morse, 2013). Although grounded theory offers theoretical
insight and not reproducibility, all the participants from the study were from one pain
management program and this reduced the transferability of the theory obtained to other pain
All quantitive study patients for lower back, neck pain, geriatric and general pain
revealed results that the group-based intervention were higher in acceptance of pain, lower
distress, disability and fear avoidance; more than the standard intervention of physiotherapy and
general exercises alone used in the control groups (Pincus et al., 2015; Rocca et al., 2017; Wood
et al., 2013; Foti et al., 2016;Oey et al., 2016).While the osteoarthritis study revealed there was
no hypothesis proven of the intervention effectiveness over the ordinary GP care group, with
negative impact seen in self efficacy of pain in control groups and smaller decline in emotional
well being for those in the intervention programme (Arakoski et al., 2015).
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Among qualitive studies a hope and collective belief narrative was fundamental to groups
and was likely linked to rehabilitation and recovery. This was supported in content
interpretations that patients with no hope made no recovery and patients with a positive outlook
had restored hope with living with pain. This restoration of hope of patients hinged upon the
programs ability to deconstruct their fears, provide acceptable understanding of pain and
reconstruction of self ability (Charest et al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker
A common theme among all types of studies were that they built new cognitive
behavioural skills and self acceptance skills including belief modification and challenging
perception had decreased in participants by the end of treatment, suggesting the importance of
functional exercises and cognitive behavioural therapy in sustaining modified pain perception
All qualitive studies revealed common themes that encounters with the group facilitators
and fellow participants were fundamental to acceptance and productive outcomes; from
underlying causes for their pain condition and previously felt stigmatised and not believed by
others (clinicians, family members, friends and acquaintances), when sharing their pain
experiences. Thus, feeling understood and believed during the program was essential to feeling
comfortable discussing and validating their symptoms and engage without feeling judged in the
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intervention (Charest et al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al., 2014;
In the long term strong therapeutic alliance was built over repeated sessions from
continual nonjudgmental and open exchanges, feeling valued, guided problem solving and
family, friends, and work environment positively influenced “self-discovery” and made
individuals “feel empowered” to continue to use the strategies following the intervention outside
the program (Pincus et al., 2015; Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016;
Some qualitative findings revealed that the day to day self management of chronic pain
post program completion has practical challenges in relation to time dedication needed to
practice CBT techniques and practicing exercises learnt, in isolation versus while in group
settings (Charest et al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al., 2014; Barker
et al., 2012; Furnes et al., 2014). Furthermore, avoiding or practicing the challenging thoughts of
pain caused mental conflict, which at times reduced coping effects from increased focus on pain
related thoughts. In some participants the lack of commitment with practicing the strategies post
program led to feelings of guilt and increased self criticism in addition to pain acceptance being
It was understood that the meaning and intervention act of accepting pain seemed
counterproductive to those holding fixed biomedical beliefs towards their pain and this led to
continual inner conflict from focusing on pain reduction, leading to perceptions of the program
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as unhelpful (Charest et al., 2015; Peters et al., 2016; Nordin et al., 2013; Dekker et al., 2014;
Summary
The overall review of all studies revealed that the there were efficacious therapeutic
outcomes in participants experiencing different pain types, treated in various types of centres
during and after the use of adaptations of CBT and PE for PSM programs. This literature review
also demonstrated the various components that contribute to program experience and challenges
Implications
approaches, which are a critical component of CBT centered care and shared decision making,
the review implicates the need for improved communication among stakeholders (i.e., patients,
clinicians, family, and friends) to increase the overall efficacy of self-management strategies
(William et al., 2020; Devan et al., 2018). For patients, interventions can incorporate strategies to
with treatment goals, and clarifications on their personal pain management plans (William et al.,
populations should be introduced to allow for more shared understandings and validation during
and recognize biopsychosocial struggle needed for continual coping, this acknowledgement and
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empathetic approach could possibly grow trust in the intervention and strengthen therapeutic
alliances by low drop out rates (William et al., 2020; Devan et al., 2018).
The main themes and learnings offered by these research outcomes from different
countries, chronic pain types and treatment centres should now add to the existing knowledge
needed to: (a) empower decisions of managing pain and maintaining sustainable lifestyles within
a more informed biopsychosocial model, (b) tailor treatments to pain types and individual needs,
and (c) synergise multidisciplinary expertise of physical therapists and psychologists in order to
effectively co-deliver these programs consistently (William et al., 2020; Devan et al., 2018).
More practically, this means research outcomes can be applied to make programs more daily
living applicable and transferable across pain types; by screening patients and matching their
specific requirements to interventions and continually seeking to develop and test cross-
disciplinary with shared delivery outcomes for patient progress (William et al., 2020; Devan et
al., 2018).
An idea for improvement of future quantitive research would be the use of standard
measures to improve comparability across studies (Goodwin & Goodwin, 2017). Although some
studies used commonly accepted measures for pain, catastrophizing and fear outcomes, there
were a range of different measurement methods for subjective experiences, theme variations
A potential quantitative research bias problem worth noting here is many experimental
studies were designed in a way that primary outcomes were psychological abstraction
characterising presumed process (for example, acceptance of pain) rather than tangible outcomes
of living with pain (Pincus et al., 2015; Rocca et al., 2017; Wood et al., 2013; Foti et al., 2016;
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Arakoski et al., 2015; Oey et al., 2016). Oftentimes such inferential abstractions are
misunderstood by patients and variably measured by researchers, since chronic pain patients
identify with a varied range of outcomes compared to what is currently assessed (Biguet 2016).
With the quality of research reviewed and various trials of CBT and PE used in PSM
programs, there is less discovery value for any further randomised controlled trials (RCTs) and
phenomenological studies for standard CBT in the management of pain. Glasziou & Chalmers
(2018) suggest that resources to investigating the efficacy of CBT in people with chronic pain
should not be allocated to small trials, regardless of pain condition, since research waste is a risk.
Research resources should instead be targeted to larger multi-centre studies for different types of
psychological therapies for people with chronic pain, including extension of established CBT
Additionally, all trials can allow individual patient data to be made available to facilitate
individual patient analysis and pooling of data to identify outcome variances, since some studies
may suggest ways to maximise treatment benefits that were previously untested(William et al.,
2020). This will be beneficial because there is extensive preclinical interest and research in
behavioural treatment for PSM but any advancement to into clinical level studies have been
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