2 Review of Literature
2.5 THE COGNITIVE-BEHAVIOURAL FRAMEWORK IN PAIN PSYCHOLOGY .1 Theory
The CB perspective presented by Turk et al. (1983) is the most widely accepted model in the field of pain psychology. The CB approach to chronic pain is based on several propositions (Keefe et al. 1992, Turk and Rudy 1992), the central one being that an individual'ʹs emotions and behavioural activity in response to an event are influenced by the cognitive appraisal and interpretation of that event. The CB perspective on pain grew out of developments in pain theory dating back to Melzack and Wall'ʹs gate control theory (1965). The gate control theory has two main principles. Firstly, the gating mechanism in the dorsal horn of the spinal cord can control the transmission of nociceptive signals from a peripheral site to the brain. Secondly, the spinal gating of noxious signals is controlled not only by input from the periphery, but also by input from higher brain centres responsible for thoughts, feelings, and behaviours. The gate control theory provides an explanation for why some psychological factors (e.g. active coping, optimism) can reduce pain while others (e.g.
anxiety, depression) can increase pain.
In rehabilitation, CB approaches aim to improve the way that individuals manage and cope with their pain. Rather than trying to find a biological explanation for the pain problem, CB treatments focus on returning control to the sufferer. Patients with chronic pain are viewed as active processors of information. They have negative expectations about their own ability and responsibility to exert any control over their pain. Moreover, they often view themselves as helpless. Such negative, maladaptive appraisals of their situation and their personal efficacy may reinforce the experience of demoralization, inactivity, and overreaction to nociceptive stimulation. Such cognitive appraisals and expectations are postulated as having an effect on behaviour, leading to reduced effort and activity as well as increased psychological distress (Turk and Rudy 1992).
CB treatments for pain commonly cover three main elements (Dixon et al. 2007).
Firstly, they try to provide an educational rationale, such as the gate control theory (Melzack and Wall 1965), that helps the patients to better understand the interrelated nature of their thoughts, feelings, behaviour and pain perceptions. The second element is comprised of therapist-‐‑guided training in cognitive and behavioural coping strategies such as progressive relaxation training, brief relaxation methods, goal setting, activity pacing, imagery, and strategies for modifying overly negative thoughts related to pain. The final element involves home practice of coping skills and learning how to apply these skills to pain-‐‑related situations in daily life. With these methods, patients may feel that they regain control of their lives, and are able to do more and feel better.
2.5.2 Applications for knee osteoarthritis patients
The drawing of conclusions on psychological interventions for knee OA is difficult due to the variability among previous studies, which have been heterogeneous in terms of the intervention (group or individual programmes, of different lengths), underlying theory and methods. In the recent Cochrane review (Kroon et al. 2014) on OA self-‐‑management programmes many interventions included behavioural and cognitive components as a part of the programme but other conservative treatment modalities, such as exercise, were also incorporated. Thus, the impact and significance of the CB part of the intervention is difficult to determine.
Studies applying plain CB interventions for knee OA patients are presented in Table 4.
All in all, seven out of eight studies have used an intervention called pain coping skills training (PCST), and at least partly the same researchers have been involved in them. One of the earliest studies was a three-‐‑arm RCT testing a 10-‐‑week group-‐‑based PCST programme in comparison to arthritis educational (AE) classes and standard care (SC) (Keefe et al. 1990a, Keefe et al. 1990b). In this study, knee OA was diagnosed on the basis of medical evaluation and radiographic examination. However, more detailed information was not given on the radiographic findings or diagnostic criteria used. The results regarding pain reduction were short-‐‑lived. There were significant differences between the PCST and AE groups in physical and psychological function in favour of the PCST group.
Interestingly however, these differences were not present between PCST and SC groups.
Next, Keefe et al. (1996, 1999) studied the efficacy of a group-‐‑based spouse-‐‑assisted coping skills training (SA-‐‑CST) programme. Again, this was a three-‐‑arm RCT with control groups attending CST without spousal involvement or 10 group sessions with arthritis education with spousal support (AE-‐‑SS). The participants in this study were diagnosed as having OA, but the diagnostic criteria used were not specified. At the one-‐‑year follow-‐‑up, self-‐‑efficacy and pain coping for the SA-‐‑CST group were significantly better in comparison to the AE-‐‑SS group. Once again, the reduction in pain was out washed during the follow-‐‑
up. Later on, PCST was studied in a four-‐‑arm RCT examining the effects of a 12-‐‑week group-‐‑based spouse-‐‑assisted PCST (SA-‐‑PCST) in combination with exercise training (ET) (Keefe et al. 2004). The participants had been diagnosed with OA of the knees and underwent a physical examination by a rheumatologist. Again, however, no exact information was given on the set of diagnostic criteria used. The combined intervention group (SA-‐‑PCST + ET) demonstrated significant pretest-‐‑posttest differences in self-‐‑efficacy and pain coping in comparison to ET and SC interventions alone. No follow-‐‑up data have been published from this study.
Riddle et al. (2011) performed a quasi-‐‑experimental study among patients scheduled for primary knee arthroplasty and with high initial catastrophizing scores measured with the PC scale (Riddle et al. 2010). The comparison was with a historical cohort scheduled for knee arthroplasty and receiving usual care. The radiological severity of their knee OA was not reported, but considering the setting, one can assume that they were mostly KL3−4.
Two months after the surgery, the study demonstrated significantly better improvements in pain, physical function and pain catastrophizing for the PCST group compared to a historical cohort.
Somers et al. (2012) conducted a four-‐‑arm RCT with a combined PCST and behavioural weight management (BWM) intervention. The PCST intervention in this study was particularly long lasting for one year with 18 group sessions and 6 monthly phone calls.
The participants had to fulfil the ACR clinical criteria for knee OA and have KL1−4 radiological knee OA. The results were analysed with the mixed model and the combined intervention group achieved significantly better results (post-‐‑treatment average) compared to all other study groups for pain improvement, physical function, self-‐‑efficacy and catastrophizing. Comparisons between the single PCST intervention and SC were not reported. However, considering the post-‐‑treatment average levels of different pain and function measures, there were probably no significant differences.
Recent studies using PCST as an intervention have addressed questions of its accessibility. Firstly, the effectiveness of an individual PCST programme held by trained primary care nurse practitioners was tested (Broderick et al. 2014). The participants had to have knee or hip OA confirmed by their physician. Radiographs were evaluated at baseline, but even KL0 was accepted. Follow-‐‑up results revealed significantly better outcomes for the PCST group in pain reduction, physical function, psychological function, pain coping and catastrophizing. In this study, particular emphasis was placed on educating and reaffirming the adherence of the nurse practitioners to the programme. The most recent study by Rini et al. (2015) was an RCT pilot for testing the effectiveness of an
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eight-‐‑week Internet-‐‑based PCST programme in patients with ≥KL2 knee or hip OA. Initial improvements in pain reduction for women and self-‐‑efficacy for the intervention group were reported, but since the study was a pilot, it did not have sufficient statistical power for any further conclusions. Finally, both of these studies included patients with hip or knee OA, and thus the effect of the intervention on knee OA patients is difficult to decipher, since they were not analysed separately.
The remaining study testing a group-‐‑based CB intervention on OA patients was conducted in the early 1990s by Calfas et al. (1992). In this two-‐‑arm RCT, patients could have OA of any joint, and the number of patients with knee OA in the study was not reported. At the 2-‐‑month follow-‐‑up point, a significant difference was detected between the study groups, but the effect was washed out by the 12-‐‑month follow-‐‑up point.
In summary, studies have demonstrated that a plain CB intervention has at most a short-‐‑term impact on pain and function in the conservative treatment of knee OA patients.
Heterogeneity remains in the results concerning psychological function, self-‐‑efficacy and pain coping. From the point of view of knee OA patients, limitations in these studies include the lack of radiological verification of OA or its vagueness, and their inclusion of other OA joint groups.
Table 4.
Studies with plain cognitive-behavioural interventions for knee OA patients. Research group, study type, country
Sample size No. of groups Inclusion criteriaInterventionControl Outcome assessment Outcome measures 1) Pain reduction 2) Physical function 3) Psychological function 4) Self-efficacy 5) Pain coping 6) Catastrophizing
Results 1) Pain reduction 2) Physical function 3) Psychological function 4) Self-efficacy 5) Pain coping 6) Catastrophizing Keefe et al. (1990a, 1990b), randomized controlled trial, USA
99, mean age 64 years
3 1) Knee OA diagnosed by medical evaluation and radiographic examination; 2) no other form of arthritis or organic disease significantly affecting function; 3) not receiving disability support payments for OA.
Treatment period: 10 weekly group sessions of PCST (n=32); follow-up (6 months): phone calls at 1, 2 and 4 months 1) 10 weekly AE sessions (n=36); phone calls at 1, 2 and 4 months during the follow-up 2) SC (n=31) Pretest- posttest; follow-up (6 months)
1) AIMS 2) AIMS 3) AIMS 4) NA 5) CSQ 6) NA
Posttest: 1) PCST > AE and SC 2) NS 3) PCST > AE and SC AE > SC 4) NA 5) NR 6) NA Follow-up: 1) NS 2) PCST > AE PCST vs. SC -> NS 3) PCST > AE PCST vs. SC -> NS 4) NA 5) NR 6) NA Calfas et al. (1992), randomized controlled trial (pilot study, not statistically sufficient power), USA
40, mean age 67 years
2 1) Adult; 2) OA (any joint) diagnosed by a physician according to the American Rheumatology Association criteria; 3) at least “modest” functional impairment in one or more functional questions.
10 weekly group sessions of CB modification AE (series of didactic lectures) Pretest- posttest; follow-up (2, 6 and 12 months) 1) AIMS 2) AIMS 3) AIMS, BDI 4) NA 5) NA 6) NA
Follow-up 2 months: 1) NS 2) CB > AE 3) CB > AE (BDI) 4) NA 5) NA 6) NA Follow-up 12 months: 1) NS 2) NS 3) CB > AE (BDI) 4) NA 5) NA 6) NA
Keefe et al. (1996, 1999), randomized controlled trial, USA
88, mean age 63 years
3 1) Married; 2) diagnosed as having OA of the knees; 3) not having any other arthritic disorders other than OA; 3) no other known organic disease that would significantly affect function; 4) not receiving disability payments for OA.
10 weekly group sessions of SA-CST held by a psychologist and a nurse 1) CST without spousal involvement 2) 10 weekly group sessions of AE-SS Pretest- posttest; follow-up (6 and 12 months)
1) AIMS 2) AIMS 3) AIMS 4) ASES 5) CSQ (factors: Coping Attempts, Pain Control and Rational Thinking) 6) NA
Posttest: 1) SA-CST > AE-SS 2) NS 3) SA-CST > AE-SS 4) SA-CST and CST > AE-SS 5) SA-CST > AE-SS 6) NA Follow-up 12 months: 1) NS 2) CST > AE-SS SA-CST vs. AE-SS -> NS 3) NS 4) SA-CST > AE-SS 5) SA-CST > AE-SS 6) NA Keefe et al. (2004), randomized controlled trial, USA
72, mean age 60 years
4 1) Diagnosed as having knee OA; 2) persistent pain due to knee OA; 3) having a spouse.
12 weekly group sessions of SA-PCST + 12 weekly sessions of ET 1) SA-PCST 2) PCST alone 3) ET alone 4) SC Pretest- posttest (week 12) 1) AIMS 2) AIMS 3) AIMS 4) ASES 5) CSQ 6) NA
Posttest: 1) NS 2) NS 3) NS 4) SA-PCST + ET > ET and SC SA-PCT alone > SC 5) SA-PCST + ET > ET and SC SA-PCT alone > ET and SC 6) NA
Riddle et al. (2011), quasi- experimen- tal study, USA
63, mean age 62 years
2 1) Patients scheduled for primary unilateral knee arthroplasty; 2) scored ≥16 on the PC Scale; 3) able to speak and read English.
8 sessions of PCST (n=18) held by a psychologist: one individual session a month prior and a month following the surgery, 6 telephone- based sessions between them HC (n=45) Baseline; follow-up (2 months after surgery)
1) WOMAC 2) WOMAC 3) NA 4) NA 5) NA 6) PC Scale
Follow-up: 1) PCST > HC 2) PCST > HC 3) NA 4) NA 5) NA 6) PCST > HC Somers et al. (2012), randomized controlled trial, USA
232, mean age 58 years
4 1) Knee pain on most days of the month for at least 6 months; 2) ≥18 years old; 3) BMI ≥25 and ≤42; 4) met the ACR clinical criteria for OA and had radiological evidence (KL 1-4) of knee OA; 5) no other weight- bearing joint affected by OA; 6) knee OA was the primary contributor to the daily function; 7) able to read and speak English.
Treatment period: 18 (12 weekly, 6 every other week) group sessions of PCST and BWM (n=62); follow-up period: 6 monthly phone calls 1) PCT alone (n=60) 2) BWM alone (n=59) 3) SC (n=51)
Pretest- posttest (6 months); follow-up (6 and 12 months) 1) AIMS, WOMAC 2) AIMS, WOMAC 3) AIMS 4) ASES 5) NA 6) CSQ catastrophizing subscale
Baseline – posttreatment average: 1) PCTS + BWM > all other study groups (AIMS, WOMAC) 2) PCTS + BWM > all other study groups (AIMS, WOMAC) 3) NS 4) PCTS + BWM > all other study groups 5) NA 6) PCTS + BWM > all other study groups
Broderick et al. (2014), randomized controlled trial, USA
257, mean age 67 years, knee OA in 77% (n=199)
2 1) Physician- confirmed diagnosis of hip or knee OA (KL 0-4); 2) ≥21 years old; 3) usual pain ≥4 on a 10-point scale of at least 6 months; 4) ability to read, write, understand English; 5) ability to attend 10 intervention sessions; 6) no cognitive/mental impairment; 7) no expected joint replacement surgery.
10 individual weekly sessions of PCST (n=129) held by nurse practitioners SC (n=127) Pretest- posttest; follow-up (6 and 12 months)
1) Composite measure of AIMS, Brief Pain Inventory, WOMAC 2) Composite measure of AIMS, WOMAC 3) Composite measure of AIMS, BDI 4) ASES 5) CSQ subscales excluding the catastrophizing subscale 6) CSQ catastrophizing subscale
Pretest-posttest: 1) PCTS > SC 2) PCTS > SC 3) PCTS > SC 4) PCTS > SC 5) PCTS > SC 6) NS Follow-up 12 months: 1) PCTS > SC 2) PCTS > SC 3) PCTS > SC 4) NS 5) PCTS > SC 6) PCTS > SC Rini et al. (2015), randomized controlled trial (pilot study, not statistically sufficient power), USA
113, mean age 67 years, knee OA 35% (n=40), knee and hip OA 52% (n=59)
2 1) ≥18 years old; 2) with hip or knee OA, confirmed radiographically (KL≥2, with associated pain), with ACR clinical criteria, or by their physician; 3) able to speak English; 4) OA related pain on most days of the month for 3 months.
8-week (8- module) Internet- based PCST programme (n=58) SC (n=55) Pretest- midpoint (5 weeks)- posttest
1) AIMS2 2) AIMS2 3) Pain Anxiety Symptoms Scale, Positive and Negative Affect Scale 4) ASES 5) NA 6) NA
Pretest-posttest: 1) PCST > SC for women 2) NS 3) NS 4) PCST > SC 5) NA 6) NA PCST, pain coping skills training; AE, arthritis education; SC, standard care; AIMS/AIMS2, Arthritis Impact Measurement Scale; NA, not assessed; CSQ, coping skills questionnaire; NS, non-significant; NR, not recorded; CB, cognitive-behavioural; BDI, Beck’s Depression Inventory; SA-CST/-PCST, spouse- assisted coping/pain coping skills training; AE-SS, arthritis education with spousal support; ASES, Arthritis Self-Efficacy Scale; CSQ, Coping Strategies Questionnaire; PC Scale, Pain Catastrophizing Scale; ET, exercise training; HC, historical cohort; BMI, body mass index; BWM, behavioural weight management; ACR, American College of Rheumatology; KL, Kellgren–Lawrence grade.