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Chronic Pain Coping Inventory (CPCI)

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Created 2004 January 15
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Practical Information

Instrument Name:

Chronic Pain Coping Inventory (CPCI)

Instrument Description:

The CPCI originally contained eight subscales consisting of 64 items designed to measure pain coping strategies, and an additional item that asks the patient to list current medications and the number of days per week that it is used. The researchers conceptualized subscales for the coping strategies as being encouraged or wellness-focused [(1) Coping Self Statements, (2) Relaxation, (3) Task Persistence, (4) Exercise/Stretching], discouraged or illness-focused [(5) Guarding, (6) Resting, (7) Asking for Assistance, Medication use], and neither/neutral [(8) Seeking Social Support]. (Ref: 1-3,7) A six-item pacing subscale was later developed and is now included in the CPCI. (Ref: 6) There is a 51-item (+ medications) Significant Other (SO) questionnaire that includes items tapping all subscales except “Coping Self Statements”. (Ref: 2)

Price:

Free; available in developmental article Appendix and the user manual. (Ref: 1-2) Please

Administration Time:

No information found. Based on the number of items, it is estimated at 30 minutes.

Publication Year:

1995

Item Readability:

Items are on average 15 words or less. Sentences are simple and vocabulary seems appropriate for the target audience. The most technical term is “self-hypnosis,” while the most difficult term among items is “distracting.”

Scale Format:

The CPCI has an eight-point scale (0 to 7) representing the number of days in the past week that a patient used a specific coping strategy. (Ref: 1)

Administration Technique:

Self-administered

Scoring and Interpretation:

All items responded to (not including medication use) are summed and divided by the total number of items responded to. To score medication use (item 65), categorize each medication that the patient reported using for pain in the last week as opiods, sedative-hypnotics, and non-steroidal anti-inflammatory medications (NSAID). Any opoid or sedative should be grouped as “opiod and/or sedative,” and any NSAID not containing an opiod or sedative should be grouped as an NSAID. Sum the total number of days each medication category was used; this number may be greater than seven. Subscales are scored by summing the items included in each scale and dividing by the number of items. (Ref: 1)

Forms:

Swedish version. (Ref: Ektor-Anderson J, Orbaek P, Isacsson SO, J of Rehab Med. 2002;34: 33-9) Significant-other version. (Ref: 1-2) One- and two-item versions. (Ref: 8)

Research Contacts

Instrument Developers:

Mark P. Jensen, Judith A. Turner, Joan M. Romano, Susan E. Strom

Instrument Development Location:

University of Washington School of Medicine
Seattle, WA 98195

Instrument Developer Email:

mjensen@u.washington.edu

Instrument Developer Website:

depts.washington.edu/rehab/contacts/jensen.html

Annotated Bibliography

1. Jensen MP, Turner JA, Romano JM, Strom SE. The Chronic Pain Coping Inventory: development and preliminary validation. Pain. 1995 Feb;60(2):203-16. [PMID:7784106]
Purpose: To describe the development and validation of the CPCI.
Sample: Phase 1) N=176 chronic pain patients (mean age=47.43 years, median duration of pain=5.5 years, 57% women, 68% married or living with significant other, 69% not working, 40% not working due to pain, 92% Caucasian) screened for treatment in the University of Washington Multidisciplinary Pain Program. Phase 2) N=78 patients (mean age=42.17 years, 78% married or living with significant other) screened for treatment in the same program and their significant others. The only significant differences between the two samples were age (t=2.82, p<0.01) and marital status (÷2=4.31, p<0.05).
Methods: Phase 1) 103 initial CPCI items were mailed to patients, as well as the Center for Epidemiological Studies Depression Scale (CES-D), Multidimensional Pain Inventory (MPI), and Pain Discomfort Scale (PDS). N=111 patients completed the CPCI two weeks later in order to provide retest data. Phase 2) Seven new items were added to the patient version of the CPCI, and a significant other version was created as well. At the time of screening, patients completed the CPCI and the PDS. Significant others completed their version of the CPCI, along with the PDS, Roland Scale for disability, and MPI-A. Participants were allowed to complete measures at home and mail them in, if necessary.
Implications: Reliability was good for both the patient and significant-other version of the CPCI. Validity of the CPCI was supported with the finding that subscale score correlations with illness-focused scales and measures of dysfunction were in the expected directions in all but one instance (Coping Self-Statements).

2. Jensen MP, Turner JA, Romano JM. Chronic Pain Coping Inventory. 1996 Jan. [No PMID]
Purpose: This packet serves as the user manual. It contains a general description, the patient version and significant-other version of the CPCI, and scoring information.
Sample: Non-applicable.
Methods: Non-applicable.
Implications: Non-applicable.

3. Hadjistavropoulos HD, MacLeod FK, Asmundson GJ. Validation of the Chronic Pain Coping Inventory. Pain. 1999 Apr;80(3):471-81. [PMID:10342409]
Purpose: To examine CPCI validity.
Sample: N=210 patients (over 99% Caucasian, 61% male, 68% married, 11th grade education, mean age=40 years) referred to an interdisciplinary treatment program.
Methods: At pre-admission screening, patients were administered the CPCI, Coping Strategies Questionnaire (CSQ), and Multidimensional Pain Inventory (MPI). Principal components analysis was performed on the first 64 items (not medication use).
Implications: CPCI subscales measure different constructs than the CSQ. The CPCI is valuable for use in pain research and clinical assessment. Factor analysis showed that subscales were supported, with minor modifications suggested.

4. Turner JA, Jensen MP, Romano JM. Do beliefs, coping, and catastrophizing independently predict functioning in patients with chronic pain? Pain. 2000 Mar;85(1-2):115-25.[PMID:10692610]
Purpose: To determine whether coping, catastrophizing, and beliefs can predict functioning in chronic pain patients.
Sample: N=169 patients who completed a multidisciplinary pain clinic evaluation and were entering a pain program. Mean age=43.4 years, 54% female, 34.3% with low back pain as the primary site, median pain duration=2.90 years, 91.7% Caucasian, 36.7% completed some college. Patients in the study, versus those who did not participate, had more post-high school education (p<0.001) and were less likely to report being unemployed due to pain and illness (p<0.05).
Methods: Participants completed several measures: pain intensity (rated average pain over past two weeks on 0-10 scale), beliefs (Survey of Pain Attitudes, Pain Beliefs and Perceptions Inventory), coping and catastrophizing (Coping Strategies Questionnaire, Chronic Pain Coping Inventory), physical disability (Roland Scale), and depression (CES-D).
Implications: The results showed that targeting pain-related beliefs, coping strategies, and catastrophizing is important for modification in treatment of chronic pain patients.

5. Engel JM, Schwartz L, Jensen MP, Johnson DR. Pain in cerebral palsy: the relation of coping strategies to adjustment. Pain. 2000 Dec 1;88(3):225-30. [PMID:11068109]
Purpose: To examine pain coping strategies of patients with pain related to cerebral palsy, and determine the relationship between coping and adjustment.
Sample: N=50 adults (mean age=39.62 years, 52% male, 26% high school graduate or GED, 26% some college, 36% employed, 92% Caucasian) with cerebral palsy and chronic pain, recruited from a previous study.
Methods: Patients were interviewed using a pain severity numerical scale, the Brief Pain Inventory- Pain Interference Scale, CES-D, CSQ, and CPCI.
Implications: Findings support a cognitive-behavioral model of chronic pain as applied to cerebral palsy patients.

6. Nielson WR, Jensen MP, Hill ML. An activity pacing scale for the Chronic Pain Coping Inventory: development in a sample of patients with fibromyalgia syndrome. Pain. 2001 Jan;89(2-3):111-5. [PMID: INSERT PMID]
Purpose: To develop and describe the development of a brief pacing scale to be used as part of the CPCI.
Sample: N=110 patients who met American College of Rheumatology criteria for diagnosis of fibromyalgia. Mean age=45.3 years, 89.1% females, 75.5% living with significant other, mean pain duration=80.6 months. A subgroup of 96 patients with pre-admission data was used for test-retest.
Methods: Six items were developed based on clinical observations, and they reflect efforts to pace activities. The CPCI was given, with these items included, as well as the CES-D, Fibromyalgia Impact Questionnaire (FIQ), West Haven-Yale Multidimensional Pain Inventory (WHYMPI), and Marlowe-Crowne Social Desirability Scale (MCSDS). This study examined only the results of the FIQ PI scale, CES-D, and CPCI pacing scale.
Implications: Preliminary results support reliability and validity of the pacing scale.

7. Tan G, Jensen MP, Robinson-Whelen S, Thornby JI, Monga TN. Coping with chronic pain: a comparison of two measures. Pain. 2001 Feb 1;90(1-2):127-33. [PMID:11166978]
Purpose: To use the CPCI and the CSQ to assess coping responses to chronic pain, and compare the measures on prediction of pain severity and patient functioning. In addition, the authors wished to determine the specific subscales on the CPCI and CSQ that accounted for the relationships with pain severity and patient functioning.
Sample: N=564 veterans (mean age=50.8 years, 84.5% high school graduates or received GED, 90.3% male, 62.4% white, 22.6% black, 50.2% married, 57.6% were disabled by pain for >5 years) referred to a chronic pain management program at the Houston VAMC.
Methods: Veterans completed the CPCI, CSQ, CES-D, Sickness Impact Profile-Roland Scale (SIPR), and the Pain Severity scale of the Multidimensional Pain Inventory (MPI). Regression analyses were conducted.
Implications: The CPCI and the CSQ contributed unique but slight variance in predicting pain severity. The CPCI scales do not predict depression as well as the CSQ, but is more effective in predicting disability. The CSQ and CPCI appeared roughly equivalent in predicting pain severity.

8. Jensen MP, Keefe FJ, Lefebvre JC, Romano JM, Turner JA. One- and two-item measures of pain beliefs and coping strategies. Pain. 2003 Aug;104(3):453-69. In press. [PMID:12927618]
Purpose: To develop one- and two-item versions of five common pain belief and coping instruments.
Sample: Two samples of patients from both the University of Washington and Duke University:
University of Washington: N=141 patients from multidisciplinary pain treatment study. Mean age=44.7 years, 51% female, 89.4% Caucasian, primary site low back (34%), median duration of pain=3.2 years, 29% working part- or full-time.
Duke: N=87 patients with osteoarthritis of the knee from a spouse-assisted pain coping skills training intervention trial. Mean age=62.4 years, 61% female, 95.4% Caucasian, median duration of pain=9.5 years.
Methods: Both samples completed measures before and after the respective treatment programs. The University of Washington group completed the CPCI, PBAPI, CES-D, Roland-Morris disability questionnaire, and a 0-10 pain intensity scale during telephone interviews. The Duke sample completed the CSQ, ASES, and subscales (pain, psychological disability, physical disability) of the Arthritis Impact Measurement Scales 1. A series a statistical tests was performed to derive the one- and two-items scales of the CPCI, SOPA, PBAPI, CSQ, and ASES.
Implications: The results support the validity of these scales. The CPCI short versions showed moderate to high correlations with the parent scale. The parent subscales and the 1- and 2-item versions all appeared sensitive to change in coping skills (attributable to coping skills training). The parent subscales were the most sensitive, followed by the 2-itm, then 1-item versions.

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Factors and Norms

Factor Analysis Work:

Principal components factor analysis with oblique rotation was performed. A seven-factor solution was found, which accounted for 48.94% of the variance. There were a number of items that cross-loaded on several factors, therefore, further factor analysis was performed and an eight-factor solution was found. This accounted for 51.53% of the variance, and only six of the items loaded >=0.30 on more than one factor. The final factor structure was: 1) Coping Self Statements, 2) Guarding of Walking/Standing, 3) Exercising/Stretching, 4) Task Persistence, 5) Seeking Social Support, 6) Asking for Assistance, 7) Resting, and 8) Relaxation. Correlations among the final 8 factors were small, ranging from 0.00 to 0.29. (Ref: 3)

Normative Information Availability:

Although normative information was not found, means and standard deviations were provided for a sample of 50 adults with cerebral palsy and chronic pain: (Ref: 5)

CPCI Subscale Mean SD
Guarding 2.46 1.85
Resting 2.82 1.75
Ask for aid 3.40 2.14
Relaxation 2.42 1.55
Task persistence 4.70 1.93
Exercise 2.43 2.04
Coping statements 3.48 2.03
Social support 2.22 1.97

Means and standard deviations were also provided for a sample of veterans in a chronic pain program: (Ref: 7)

CPCI Subscale N Mean SD
Guarding 510 4.50 1.75
Resting 510 4.69 1.63
Ask for aid 508 2.82 2.24
Relaxation 508 2.20 1.68
Task persistence 509 3.13 1.92
Exercise 508 2.20 1.96
Seek Social support 509 2.35 1.68
Coping statements 508 3.33 1.96

Reliability Evidence

Test-retest:

Test-retest for the original eight scales and three medication measures ranged from 0.70 to 0.90, except for the Non-steroidal Medication Use measure, which was r=0.66. The time interval for this retest was two weeks. (Ref: 1) Test-retest (p<0.001), over an average of 12.60 weeks, was performed using the CPCI with the pacing subscale included. Results follow: (Ref: 6)

CPCI Subscale Coefficient
Guarding 0.56
Resting 0.53
Ask for Aid 0.58
Relaxation 0.63
Task Persistence 0.47
Pacing 0.60
Exercise 0.78
Seek Social Support 0.69
Coping Statements 0.66

Inter-rater:

No information found.

Internal Consistency:

In the developmental study, alpha coefficients for the initial eight scales (57 items) ranged from 0.70 to 0.93. During the validation phase of this study, alpha ranged from 0.74 to 0.91 for the 65-item CPCI. A version created for significant others, consisting of seven scales, produced an alpha range of 0.75 to 0.87. (Ref: 1) The reliability of the most recent addition to the CPCI, the pacing subscale, was assessed as well. It showed inter-item correlations from 0.55 to 0.74, item-total correlations from 0.71 to 0.79, and a Cronbach’s alpha of 0.91. (Ref: 6)

Alternate Forms:

No information found.

Validity Evidence

Construct/ Convergent/ Discriminant:

In the developmental sample of 176 chronic pain patients, the CPCI (57 items) was correlated with the Center for Epidemiological Studies Depression Scale (CES-D), Pain Discomfort Scale (PDS), and Multidimensional Pain Inventory-Activity Scale (MPI-A). Significant (p<0.001) correlations were reported as follows: (Ref: 1)

CPCI Scale CES-D PDS MPI-A
Illness-Focused Coping
Guarding 0.35 0.45 -0.36
Resting 0.32 0.43 --
Asking for Assistance -- 0.29 --
Illness-Focused Coping
Task Persistence -0.24 -0.33 --
Coping Self-Statements -- 0.24 --

During the validation phase of the study, the seven scales of the CPCI significant-other version correlated with the CPCI patient-version at 0.13 to 0.65, and the three medication use measures correlated at 0.55, 0.57, and 0.65. These two versions of the CPCI were again compared to the patient-completed (PT) PDS, and the significant-other (SO) completed Roland Scale and MPI-A. Significant (p<0.001) correlations were found between the CPCI scales and the significant-other version of the Roland Scale (r ranged 0.34 to 0.67) and the significant-other version of the MPI-A (r ranged 0.35 to 0.45). However, the patient-completed PDS correlated significantly with only the CPCI patient-completed and significant-other completed Task Persistence scale (-0.33 and –0.43).

Note that, except for the Guarding subscale (r=0.65), correlations between patient and significant-other reports were surprisingly low. Four of the 10 compared subscales had correlations less than 0.40 (Asking for Assistance, Relaxation, Task Persistence, Seeking Social Support).

A second validation study examined the correlation of an eight-factor CPCI with the Coping Strategies Questionnaire (CSQ). Significant (p<0.001) correlations were reported as follows: (Ref: 1)

CPCI Subscale CSQ Praying CSQ Ignoring Pain CSQ Distance from Pain CSQ Catastro- phize CSQ Coping Statement CSQ Distraction
Coping self statements 0.28 0.23 0.31 -- 0.41 0.52
Guarding of walk/stand -- -- -- 0.23 -- --
Exercising/stretching -- -- -- -- -- 0.29
Task persistence -- 0.54 0.25 -- 0.55 --
Seeking social support 0.25 -- -- -- 0.23 0.45
Asking for assistance -- -- -- -- -- 0.27
Resting -- -- -- 0.34 -- 0.30
Structured relaxation -- -- 0.28 -- -- 0.29

Another study looked at correlations between the CPCI, CES-D, Sickness Impact Profile-Roland Scale (SIPR), and Pain Severity Scale of the Multidimensional Pain Inventory (MPIPS). Significant (p<0.05) correlations follow: (Ref: 7)

CPCI Subscale Depression (CES-D) Disability (SIPR) Pain Severity (MPIPS)
Guarding 0.20 0.52 0.23
Resting 0.20 0.35 0.23
Asking for Assistance -- 0.37 0.17
Relaxation -- -- --
Task Persistence -0.24 -0.21 -0.15
Exercise/Stretch -- -- --
Seeking Social Support -- 0.21 --
Coping Self-Statements -- -- --

One other study showed significant (p<0.01) correlations between the CPCI subscales, the Roland Scale, and the CES-D. The CES-D correlated significantly with the Guarding (0.61), Resting (0.29), Asking for Assistance (0.29), and Task Persistence (-0.33) scales, while the Roland Scale correlated significantly with the Guarding (0.31), Task Persistence (-0.32), and Coping Self-Statements (-0.25) scales.

Finally, a correlation of –0.37 (p<0.001) was found between the new pacing subscale of the CPCI and the CES-D. (Ref: 6)

Criterion-related/ Concurrent/ Predictive:

A series of hierarchical regressions was performed to determine the relationship between the CPCI scales, CSQ scales, and depression and disability. Age, education, gender, and pain severity were controlled for. The model, including the control variables and the CPCI scales alone, accounted for 18.3% of the variance in depression. After controlling for demographic variables, pain severity, and the CSQ scales, the CPCI accounted for 20.7% of the variance in disability. (Ref: 7)

Content:

Three of the developmental authors constructed a list of pain coping strategies based on strategies used in the University of Washington Multidisciplinary Pain Treatment Program and strategies found in pain and coping literature reviews. The authors prepared a paragraph description of each strategy, which was then used to create items. An item-writing strategy that included interviews with chronic pain patients would better support the content validity of the scale. Nevertheless, the approach used was disciplined and based on a clear definition of coping, and the method supports the content validity of the instrument. Selection of item content for the subscales also supported the content validity of the instrument. Items were retained if they met both of two criteria: (1) estimated correlation with the parent scale at least 0.40 and (2) estimated correlation at least 0.15 greater than the correlation between the item and all other scales. (Ref: 1)

Responsiveness Evidence:

CPCI subscales appeared responsive to change in coping skills resulting from coping skills training. Full subscales were reported to be more sensitive than their reduced (2-item and 1-item) versions. (Ref: 8)

Scale Application in VA Populations:

Yes. (Ref: 7)

Scale Application in non-VA Populations:

Yes. (Ref: 1,3-6,8)

Comments


The CPCI is well validated, with some evidence of a stable factor structure, good internal consistency, and evidence of responsiveness to change in coping skills. Evidence of stability (test-retest) is marginal, although that may be due to instability in the under-lying constructs. The CPCI appears easy to complete.

Recommendations. The CPCI appears to have different strengths than alternative measures, such as the Coping Strategies Questionnaire (CSQ), which might be used in similar research situations (see Ref: 7). Researchers should evaluate their research objectives carefully, since other measures may be more appropriate for a given situation.