- 1/12/21 - 1 form, 3 itemgroups, 16 items, 1 language
Itemgroups: Instructions, Knowledge, Experience
The City of Hope Pain & Palliative Care Resource Center. (2012) . The Patient Pain Questionnaire (PPQ) . Measurement Instrument Database for the Social Science. Retrieved 12.01.2021, from www.midss.ie Key references: Ferrell, B. R., Ferrell, B., Rhiner, M., Grant, M. (1991). Family Factors Influencing Cancer Pain. Post Graduate Medical Journal, 67 (Suppl 2), 64-69. Ferrell, B. R., Rhiner, M., Cohen, M., Grant, M. (1991). Pain as a Metaphor for Illness. Part I: Impact of Cancer Pain on Family Caregivers. Oncology Nursing Forum, 18(8), 1303-1309. Ferrell, B. R., Cohen, M., Rhiner, M., Rozak, A. (1991). Pain as a Metaphor for Illness. Part II: Family Caregivers' Management of Pain. Oncology Nursing Forum,18(8), 1315-1321. Ferrell, B. R., Rhiner, M., Ferrell, B. (1993). Development and Implementation of a Pain Education Program. Cancer, 72(11), 3426-3432. Primary use / Purpose: The Patient Pain Questionnaire (PPQ) is a 16-item ordinal inventory. Its purpose is to measure the knowledge and experience of a cancer patient in managing chronic pain. Background: Cancer pain is recognised as a serious barrier to mental wellbeing in cancer patients. One of the main aims of palliative care is to buffer patients against pain, both mental and physical. By using the Patient Pain Questionnaire (PPQ) and also the related family pain questionnaire (FPQ) clinicians and researchers can gain a clearer understanding of the patient/caregiver perspective and how this might interact with or even predict wellbeing or adjustment to pain. The PPQ can be used by either clinicans or researchers. Psychometrics: The psychometric properties of the Patient Pain Questionnaire (PPQ) are discussed in the introduction to the instrument itself which is attached below. Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.332
- 1/13/21 - 1 form, 7 itemgroups, 138 items, 1 language
Itemgroups: Pain, Psychosocial assessment, Pain, Psychosocial assessment, Rating scale, Pain, Psychosocial assessment, Economic, Pain, Psychosocial assessment, Social support, Pain, Psychosocial assessment, Activities of Daily Living, Pain, Psychosocial assessment, Emotional support, Pain, Psychosocial assessment, Coping Behavior
Otis-Green, S., & The City of Hope Pain/Palliative Resource Center. (2012) . The Psychosocial Pain Assessment Form (PPAF). Measurement Instrument Database for the Social Science. Retrieved 12.01.2021, from www.midss.ie. Key references: Otis-Green, S. (2006). Psychosocial Pain Assessment Form. In Dow (Ed.), Nursing Care of Women with Cancer. St. Louis, MO: Elsevier Mosby, 556-561. Otis-Green, S. (2005). Psychosocial Pain Assessment Form. In Kuebler, Davis, Moore (Eds.), Palliative Practices: An Interdisciplinary Approach. St. Louis, MO: Elsevier Mosby, 462-467. Primary use / Purpose: The Psychosocial Pain Assessment Form (PPAF) is a comprehensive assessment form for measuring psychosocial pain. It does so under five domains: economic, social support, activities of daily living, emotional impact, and coping style. Additionally, an assessment of prior history is included to help clinicians focus interventions where sexual abuse or other traumatic memories are present. Background: The psychosocial model of pain is now widely accepted. Pain is no longer treated, or thought of, as a purely physiological condition, but instead, one that is the product of a myriad of both psychological and physiological factors. For this reason, there is a need for instruments which measure the full range of outcomes and causes associated with chronic pain, whether they be psychological, economic, or physiological. The Psychosocial Pain Assessment Form (PPAF) was developed to be used in this capacity. Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.344

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