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  1. 1. Test clinico
  2. 2. Documentazione di routine
  3. 3. Registro / studio di coorte
  4. 4. Garanzia di qualità
  5. 5. Dati Standard
  6. 6. Risultato segnalato dal paziente
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- 12/01/21 - 1 modulo, 4 itemgroups, 39 elementi, 1 linguaggio
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
- 12/01/21 - 1 modulo, 3 itemgroups, 16 elementi, 1 linguaggio
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
- 12/01/21 - 4 moduli, 3 itemgroups, 17 elementi, 1 linguaggio
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
- 01/12/20 - 1 modulo, 2 itemgroups, 9 elementi, 1 linguaggio
Itemgroups: Administrative Data, Subject-completed Rating Scales & Questionnaires
- 11/10/20 - 1 modulo, 15 itemgroups, 69 elementi, 1 linguaggio
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
- 30/09/20 - 1 modulo, 2 itemgroups, 54 elementi, 1 linguaggio
Itemgroups: Instructions, Belief
- 26/08/20 - 1 modulo, 6 itemgroups, 19 elementi, 1 linguaggio
Itemgroups: Administrative, 1. Has there ever been a period of time when you were not your usual self and..., 2. If you checked YES to more than one of the above, have several of these ever happened during the same period of time? Please check 1 response only., 3. How much of a problem did any of these cause you — like being able to work; having family, money, or legal troubles; getting into arguments or fights? Please check 1 response only., 4. Have any of your blood relatives (i.e., children, siblings, parents, grandparents, aunts, uncles) had manic-depressive illness or bipolar disorder?, 5. Has a health professional ever told you that you have manic-depressive illness or bipolar disorder?
- 19/08/20 - 1 modulo, 19 itemgroups, 129 elementi, 1 linguaggio
Itemgroups: General Information, relationship to patient, Whom do you live with?, What types of treatment(s) have you tried for your OCD? (check all that apply), Have any of the following people been diagnosed with OCD? If so, who?, Do any of the following people have suspected OCD or Obsessive Compulsive symptoms? If so, who?, Information, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 2 - Symptom-Specific Impairment, Part 2 - Symptom-Specific Impairment, Part 3 - Family Role-Specific Impairment, Part 3 - Family Role-Specific Impairment
Stewart, Hu, Hezel, Proujansky, Lamstein, Walsh, Ben-Joseph, Gironda, Jenike, Geller & Pauls. (2012). OCD Family Functioning (OFF) Scale. Measurement Instrument Database for the Social Science. Retrieved 19.08.2020 from www.midss.ie Key references: Stewart, E. S., Hu, Y. P., Hezel, D. M., Proujansky, R., Lamstein, A., Walsh, C., … & Pauls, D. L. (2011). Development and psychometric properties of the OCD family functioning (OFF) scale. Journal of Family Psychology, 25, 434-443. Primary use / Purpose: The OFF was developed to explore the content, extent, and perspectives of functional impairment in families affected by OCD. Background: Obsessive Compulsive Disorder (OCD) often has a great impact on family functioning. Parents, and other family members, often become involved in the individual's ritualistic behaviours and family accomodation, either through enabling avoidance or assisting ritualistic behaviours, is very common. The OCD Family Functioning (OFF) Scale is a 42 item self-report questionnaire that consists of three major subscales: family functioning impairment, symptom-specific impairment, and family role-specific impairment. It is designed for use with families of adults and children with OCD. Two versions of the scale are available- a patient version and a relative version. The results of the scale may be used to assess family functioning and to help plan interventions and treatments. Scoring is described in Stewart et al. (2011). Psychometrics: The scale's psychometric properties are examined in Stewart et al. (2011). Keywords: Anxiety, Family, Stress Other keywords: obsessive compulsive disorder, OCD, functional impairment, family Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.231
- 19/08/20 - 1 modulo, 18 itemgroups, 122 elementi, 1 linguaggio
Itemgroups: General Information, Whom do you live with?, What types of treatment(s) have you tried for your OCD? (check all that apply), Have any of the following people been diagnosed with OCD? If so, who?, Do any of the following people have suspected OCD or Obsessive Compulsive symptoms? If so, who?, Information, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 1 - Family Functioning Impairment, Part 2 - Symptom-Specific Impairment, Part 2 - Symptom-Specific Impairment, Part 3 - Family Role-Specific Impairment, Part 3 - Family Role-Specific Impairment
Stewart, Hu, Hezel, Proujansky, Lamstein, Walsh, Ben-Joseph, Gironda, Jenike, Geller & Pauls. (2012). OCD Family Functioning (OFF) Scale. Measurement Instrument Database for the Social Science. Retrieved 19.08.2020 from www.midss.ie Key references: Stewart, E. S., Hu, Y. P., Hezel, D. M., Proujansky, R., Lamstein, A., Walsh, C., … & Pauls, D. L. (2011). Development and psychometric properties of the OCD family functioning (OFF) scale. Journal of Family Psychology, 25, 434-443. Primary use / Purpose: The OFF was developed to explore the content, extent, and perspectives of functional impairment in families affected by OCD. Background: Obsessive Compulsive Disorder (OCD) often has a great impact on family functioning. Parents, and other family members, often become involved in the individual's ritualistic behaviours and family accomodation, either through enabling avoidance or assisting ritualistic behaviours, is very common. The OCD Family Functioning (OFF) Scale is a 42 item self-report questionnaire that consists of three major subscales: family functioning impairment, symptom-specific impairment, and family role-specific impairment. It is designed for use with families of adults and children with OCD. Two versions of the scale are available- a patient version and a relative version. The results of the scale may be used to assess family functioning and to help plan interventions and treatments. Scoring is described in Stewart et al. (2011). Psychometrics: The scale's psychometric properties are examined in Stewart et al. (2011). Keywords: Anxiety, Family, Stress Other keywords: obsessive compulsive disorder, OCD, functional impairment, family Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.231
- 18/08/20 - 1 modulo, 10 itemgroups, 64 elementi, 1 linguaggio
Itemgroups: Information, Section One, Section Two, Section Three, Section Four, Section Five, Section Six, Section Seven, Section Eight, Section Nine

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