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Measurement Instrument Database for the Social Science (MIDSS) - The Psychosocial Pain Assessment Form (PPAF)

- 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

Measurement Instrument Database for the Social Science (MIDSS) - The Knowledge and Attitudes Survey Regarding Pain (KASRP)

- 1/12/21 - 1 form, 4 itemgroups, 39 items, 1 language
Itemgroups: Pain, Health Surveys, Pain, Health Surveys, Pain, Case, Pain, Case
Ferrell, B. & McCaffery, M. (2012). The Knowledge and Attitudes Survey Regarding Pain (KASRP). Measurement Instrument Database for the Social Science. Retrieved 12.01.2021, from www.midss.ie. Key references: “Knowledge and Attitudes Survey Regarding Pain” developed by Betty Ferrell, RN, PhD, FAAN and Margo McCaffery, RN, MS, FAAN, (http://prc.coh.org), revised 2012. Ferrell, B. R. (2007). Reducing barriers to pain assessment and management: An institutional perspective. Journal of Palliative Medicine, 10(1S), S15-S18. DOI: 10.1089/jpm.2007.9828. McCaffery, M., Ferrell, B. R., Pasero, C. (2000). Nurses' personal opinions about patients' pain and their effect on recorded assessments and titration of opioid doses. Pain Management Nursing, 1(3): 79-87 Primary use / Purpose: The Knowledge and Attitudes Survey Regarding Pain (KASRP) is a 37-item questionnaire. It contains 21 true or false questions and 16 multiple choice ones. Its purpose is to measure the attitudes and knowledge of caregivers on the subject of pain. It is particularly useful as a pre/post test measure and can be used to rate learning outcomes following educational programs on pain. Background: Chronic pain is a debilitating and often incurable problem for many. Palliative care-givers also routinely meet the need for effective treatment of pain in terminally ill patients. Effective care-giving is important in ensuring the wellbeing of these patients. Without sufficient training caregivers will struggle to meet the demands of dealing with chronic pain patients. The Knowledge and Attitudes Survey Regarding Pain (KASRP) is therefore a useful tool for specifically evaluating the knowledge of caregivers on the subject of pain. Psychometrics: The psychometric properties of the Knowledge and Attitudes Survey Regarding Pain (KASRP) are discussed in the introduction to the scale which is attached below. Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.341

Measurement Instrument Database for the Social Science (MIDSS) - The Patient Pain Questionnaire (PPQ)

- 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

Measurement Instrument Database for the Social Science (MIDSS) - The Controlling Pain Vignettes Survey (CPVS) - Patient Vital Signs Vignettes

- 1/12/21 - 4 forms, 3 itemgroups, 17 items, 1 language
Itemgroups: General information qualifier, Health Professional, Patient Information, Patient Information
McCaffery, M., Ferrell, B. R., & O'Neil-Page, E.. (2012) . The Controlling Pain Vignettes Survey (CPVS) . Measurement Instrument Database for the Social Science. Retrieved 12.01.2021, from www.midss.ie Key references: McCaffery, M. & Ferrell, B. R. (1991). How would you respond to these patients in pain? Nursing 91, June, 34-37. McCaffery, M. & Ferrell, B. R. (1991). Patient age: Does it affect your pain-control decisions? Nursing, 91, September, 44-48. McCaffery, M. & Ferrell, B. R. (1992). How vital are vital signs? Nursing 92, January, 43-46. McCaffery, M., Ferrell, B. R., & and O'Neil-Page, E. (1992). Does life style affect your pain-control decisions? Nursing 92, April, 58, 60-61. Primary use / Purpose: The Controlling Pain Vignettes Survey (CPVS) is a four part survey in which nurses are presented with four pairs of patients as hypothetical case studies. The four pairs of patients differ according to four criteria: behaviour, age, vital signs, and lifestyle. The purpose of the survey is to measure the influence of these four criteria on nurse's assessments of patient pain. Background: Nurses are forced to make difficult decisions when presented with patients who are experiencing pain. Ethical dilemmas can also arise around issues such over-medication, under-medication, and opioid side effects to name a few. It is important to gain an understanding of how nurses make these decisions so that more insight can be gained into the factors influencing those decision making processes. This survey is the product of four separate studies, each investigating one specific factor which may be influential during nurses’ assessments of patient pain. Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.330

The Controlling Pain Vignettes Survey (CPVS) - Patient Behavior Vignettes

3 itemgroups 17 items

The Controlling Pain Vignettes Survey (CPVS) - Life Style Vignettes

3 itemgroups 17 items

The Controlling Pain Vignettes Survey (CPVS) - Patient Age Vignettes

3 itemgroups 17 items

Measurement Instrument Database for the Social Science (MIDSS) - The Clinical Decision Making Survey (CDMS)

- 10/11/20 - 1 form, 15 itemgroups, 69 items, 1 language
Itemgroups: Instruction, Pain intensity, Evaluation Method, Pain, Question (Inquiry), Pain intensity (observable entity), rating scale; Pain relief, rating scale, Analgesics, Analgesics, Today, Change of medication, Pain, Evaluation, Documentation, Pain, Prescriptions, Non-drug, Order (action), Pain, Contact with, Physicians, Pain relief, Optimum, Problem, Pain, Decision, Pain management, Conflict (Psychology), Demography, Nurses, Patient
Ferrell, B. R., Eberts, M. T., McCaffery, M., Grant, M.. (2012) . The Clinical Decision Making Survey (CDMS) . Measurement Instrument Database for the Social Science. Retrieved 10.10.2020, from www.midss.ie Key references: Ferrell, B. R., Eberts, M. T., McCaffery, M., Grant, M. (1991). Clinical decision making and pain. Cancer Nurs. 1991 Dec;14(6):289-97. Primary use / Purpose: The Clinical Decision Making Survey (CDMS) is a 14-item survey. Its purpose is to obtain information from nurses relating to their decision making processes when they are dealing with patients who are experiencing pain. Background: Nurses are forced to make difficult decisions when presented with patients who are experiencing pain. Ethical dilemmas can also arise around issues such over-medication, under-medication, and opioid side effects to name a few. It is important to gain an understanding of how nurses make these decisions so that more insight can be gained into the factors influencing those decision making processes. Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.329

Measurement Instrument Database for the Social Science (MIDSS) - Physical Activity and Sport Anxiety Scale (PASAS)

- 5/12/20 - 1 form, 1 itemgroup, 16 items, 1 language
Itemgroup: Statements
Norton, P. J., Hope, D. A., & Weeks, J. W.. (2012). Physical Activity and Sport Anxiety Scale (PASAS). Measurement Instrument Database for the Social Science. Retrieved 11.05.2020 from www.midss.ie Key references: Norton, P. J., Hope, D. A., & Weeks, J. W. (2004). The physical activity and sport anxiety scale (PASAS): Scale development and psychometric analysis. Anxiety, Stress, and Coping, 17, 363-382 Primary use / Purpose: The Physical Activity and Sport Anxiety Scale (PASAS) is a 16-item self-report questionnaire designed to measure social anxiety in physical activities and sports. Background: This test was developed from a need to integrate measures of social anxiety and avoidance into assessment of physical activity and sport. Given the importance of physical exercise to individual health, accounting for psychological moderators of exercise behaviour is crucial. Psychometrics: Psychometric analysis of this scale has been conducted (Norton, Hope, & Weeks, 2004). Keywords: Anxiety, Family *** Scoring Instructions: Items 3, 11, and 14 are reverse scores. Total Scale Score computed by summing all items. *** Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.152

Merkmalskatalog - PHQ - Patient health questionnaires

- 5/11/18 - 1 form, 6 itemgroups, 18 items, 2 languages
Itemgroups: PHQ-9 Depression, PHQ-15 Somatisation, PHQ-15 Somatisation_FUP, PHQ Stress, PHQ Functional, PHQ-PT
PHQ - Patient health questionnaires Merkmalskatalog

ISAR Screening Emergency Admission German Adoption - ISAR Emergency Screening

- 9/27/17 - 1 form, 1 itemgroup, 6 items, 1 language
Itemgroup: ISAR Questionnaire
Emergency Screening „Identification of Seniors at Risk“ (ISAR) Sources:Thiem U, Greuel HW, Reingräber A, Koch-Gwinner P, Püllen R, Heppner HJ, Pfisterer M. [Consensus for the identification of geriatric patients in the emergency care setting in Germany]. Z Gerontol Geriatr. 2012 Jun;45(4):310-4 PubMed PMID: 22622678

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