Patient-physician communication in the context of persistent pain: validation of a modified version of the patients' Perceived Involvement in Care Scale.

The purpose of this study was to evaluate the psychometric properties of a modified version of the Perceived Involvement in Care Scale (M-PICS), a measure designed to assess pain patients' perceptions of patient health care provider communication during the medical consultation. Eighty-seven breast cancer outpatients with persistent pain completed a battery of questionnaires, including the M-PICS. A factor analysis supported four factors. Factor 1 reflected health care provider information behaviors; Factor 2, health care provider facilitation of patient involvement; Factor 3, patient information provision; and Factor 4, patient participation in decision making. The M-PICS total had an internal consistency of 0.87; alphas for subscales ranged from 0.80 to 0.90. M-PICS scores related to measures of patient characteristics and outcomes, including pain-related communication barriers, psychological status, quality of life, and health care satisfaction, in predicted ways. The M-PICS is a reliable and valid measure of perceived patient-provider communication in the context of persistent pain.

[1]  D. Tripathy,et al.  Randomized clinical trial of the effectiveness of a self-care intervention to improve cancer pain management. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[2]  D. Blake,et al.  Patient non-compliance: deviance or reasoned decision-making? , 1992, Social science & medicine.

[3]  G. Caputo,et al.  Patients’ perceived involvement in care scale: , 2007, Journal of General Internal Medicine.

[4]  M. Weinstein,et al.  A Comparison of Three Psychiatric Screening Tests Using Receiver Operating Characteristic (ROC) Analysis , 1989, Medical care.

[5]  S. Thompson,et al.  Patient-oriented interventions to improve communication in a medical office visit. , 1990 .

[6]  Clotfelter Ce The effect of an educational intervention on decreasing pain intensity in elderly people with cancer. , 1999, Oncology nursing forum.

[7]  R. Elashoff,et al.  Patient Adherence to Cancer Control Regimens: Scale Development and Initial Validation , 1993 .

[8]  M. Fazzari,et al.  Patient and physician factors predict patients' comprehension of health information. , 2003, Patient education and counseling.

[9]  R. Street Analyzing Communication in Medical Consultations: Do Behavioral Measures Correspond to Patients' Perceptions? , 1992, Medical care.

[10]  H. Kraemer,et al.  Mediators and moderators of treatment effects in randomized clinical trials. , 2002, Archives of general psychiatry.

[11]  O. Gureje,et al.  Persistent pain and well-being: a World Health Organization Study in Primary Care. , 1998, JAMA.

[12]  Y. Hwang,et al.  Communication between physicians and older women with localized breast cancer: implications for treatment and patient satisfaction. , 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[13]  S. LeFort,et al.  Randomized controlled trial of a community-based psychoeducation program for the self-management of chronic pain , 1998, Pain.

[14]  T. Bodenheimer,et al.  Patient self-management of chronic disease in primary care. , 2002, JAMA.

[15]  N. Powe,et al.  Race, gender, and partnership in the patient-physician relationship. , 1999, JAMA.

[16]  Gregory Makoul,et al.  The interplay between education and research about patient-provider communication. , 2003, Patient education and counseling.

[17]  C. Cleeland,et al.  Cancer pain management among underserved minority outpatients , 2002, Cancer.

[18]  Sherrie H. Kaplan,et al.  Patients’ participation in medical care , 1988, Journal of General Internal Medicine.

[19]  L. Zandbelt,et al.  A Pain Education Program for chronic cancer pain patients: follow-up results from a randomized controlled trial , 1997, Pain.

[20]  C. Cleeland,et al.  Impact of pain on self-rated health in the community-dwelling older adults , 2002, Pain.

[21]  J. de Haes,et al.  Doctor-patient communication: a review of the literature. , 1995, Social science & medicine.

[22]  S. Dunn,et al.  Patient barriers to optimal cancer pain control , 2003, Psycho-oncology.

[23]  A. Stewart,et al.  Evidence suggesting that a chronic disease self-management program can improve health status while reducing hospitalization: a randomized trial. , 1999, Medical care.

[24]  K. Pargeon,et al.  Barriers to effective cancer pain management: a review of the literature. , 1999, Journal of pain and symptom management.

[25]  Peter Watson,et al.  Do patients benefit from participating in medical decision making? Longitudinal follow‐up of women with breast cancer , 2006, Psycho-oncology.

[26]  R. Serlin,et al.  Patient-related barriers to pain management: the barriers questionnaire II (BQ-II) , 2002, Pain.

[27]  Sandra E. Ward,et al.  Patient-related barriers to management of cancer pain , 1993, Pain.

[28]  P. Cleary,et al.  Patients evaluate their hospital care: a national survey. , 1991, Health affairs.

[29]  Michael Von Korff,et al.  Graded chronic pain status: an epidemiologic evaluation , 1990, Pain.

[30]  Blair H. Smith,et al.  The epidemiology of chronic pain in the community , 1999, The Lancet.

[31]  R. Kravitz,et al.  Individualized patient education and coaching to improve pain control among cancer outpatients. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[32]  N. Arora,et al.  Interacting with cancer patients: the significance of physicians' communication behavior. , 2003, Social science & medicine.

[33]  Judith A. Hall,et al.  Studies of doctor-patient interaction. , 1989, Annual review of public health.

[34]  R. Portenoy,et al.  Access to care for chronic pain: racial and ethnic differences. , 2005, The journal of pain : official journal of the American Pain Society.

[35]  W. Katon,et al.  Treatment Costs, Cost Offset, and Cost-Effectiveness of Collaborative Management of Depression , 1998, Psychosomatic medicine.

[36]  Psychosocial oncology research. Where we have been, where we are going, and why we will not get there , 1994, Cancer.

[37]  S. Ward,et al.  Patient‐related barriers to cancer pain management in Taiwan , 1995, Cancer nursing.

[38]  K. Teasdale,et al.  Information and anxiety: a critical reappraisal. , 1993, Journal of advanced nursing.

[39]  B. Rimer,et al.  Cancer patients' knowledge, beliefs, and behavior regarding pain control regimens: implications for education programs. , 1984, Patient education and counseling.

[40]  R. Adelman,et al.  Psychosocial concerns in the medical encounter: a comparison of the interactions of doctors with their old and young patients. , 1987, The Gerontologist.

[41]  Sandra E. Ward,et al.  Quality Improvement Guidelines for the Treatment of Acute Pain and Cancer Pain , 1995 .

[42]  Paul Batalden,et al.  General competencies and accreditation in graduate medical education. , 2002, Health affairs.

[43]  J. Lynn,et al.  An outcomes model of medical decision making , 1991, Theoretical medicine.

[44]  J. Ware,et al.  The structure of psychological distress and well-being in general populations , 1983 .

[45]  William H. Rogers,et al.  Functional Status and Well-Being of Patients with Chronic Conditions , 1989 .

[46]  K C Carriere,et al.  Information needs and decisional preferences in women with breast cancer. , 1997, JAMA.

[47]  S. Ward,et al.  Concerns about reporting pain and using analgesics. A comparison of persons with and without cancer. , 1994, Cancer nursing.

[48]  G. Makoul,et al.  Essential Elements of Communication in Medical Encounters: The Kalamazoo Consensus Statement , 2001, Academic medicine : journal of the Association of American Medical Colleges.

[49]  S. Passik,et al.  Patient-related barriers to pain management in ambulatory AIDS patients , 1998, Pain.

[50]  G. Makoul,et al.  Perpetuating passivity: reliance and reciprocal determinism in physician-patient interaction. , 1998, Journal of health communication.

[51]  R. Sanderman,et al.  Structure and Reliability of Ware’s Patient Satisfaction Questionnaire III: Patients’ Satisfaction With Oncological Care in the Netherlands , 2003, Medical care.

[52]  H. Donovan,et al.  The impact on quality of life of patient-related barriers to pain management. , 1998, Research in nursing & health.

[53]  R. Adelman,et al.  Older patient satisfaction with communication during an initial medical encounter. , 1994, Social science & medicine.

[54]  J. Hibbard,et al.  Development of the Patient Activation Measure (PAM): conceptualizing and measuring activation in patients and consumers. , 2004, Health services research.

[55]  R. Street,et al.  Information-giving in medical consultations: the influence of patients' communicative styles and personal characteristics. , 1991, Social science & medicine.

[56]  J. Bensing,et al.  Prevalence of chronic benign pain disorder among adults: a review of the literature , 1998, Pain.

[57]  J. Schaefer,et al.  Collaborative Management of Chronic Illness , 1997, Annals of Internal Medicine.