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- 21/08/20 - 1 modulo, 1 ItemGroup, 8 elementi, 1 linguaggio
ItemGroup: Postraumatic Stress Screen for the Cognitively Impaired (PTSS-CI)
Carlson, Lauderdale, Hawkins, and Sheikh. (2012). Postraumatic Stress Screen for the Cognitively Impaired (PTSS-CI). Measurement Instrument Database for the Social Science. Retrieved 20.08.2020 from www.midss.ie Key references: Carlson, E. B., Lauderdale, S., Hawkins, J., & Sheikh, J. I. (2008). Posttraumatic stress and aggression among veterans in long-term care. Journal of Geriatric Psychiatry and Neurology, 21, 61-71. Primary use / Purpose: The PTSS-CI is designed to assess posttraumatic stress symptoms in individuals who are cognitively impaired. Background: Posttraumatic stress symptoms can affect an individual's well-being, functioning, and quality of life. Such effects may be exacerbated for individuals who are cognitively impaired and lack the resources to deal with such symptoms or the ability to communicate with, or seek help from, others. The Posttraumatic Stress Screen for the Cognitively Impaired (PTSS-CI) identified symtpoms of posttraumatic stress and is suitable for use with individuals who are elderly and cognitively impaired, brain injured, or developmentally disabled. Both self-report and observer versions are available. Each contains 8 items that assess PTSD symptoms including reexperiencing, avoiding, and hyperarousal. The language used is very simple. Carlson and colleagues (2008) describe the scoring of the instrument. Psychometrics: Preliminary findings on the psychometric properties of the PTSS-CI are discussed in Carlson et al. (2008) Keywords: Anxiety; Family; Stress Other keywords: Posttraumatic Stress Disorder; PTSD; Cognitive Impairment; Stress Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.252 Instructions: This measure can be completed by a health care provider, family member, or friend who has observed the patient’s behavior for at least one week. For each symptom, fill in the number that best reflects the patient’s behavior. Moderate and severe ratings should be given for symptoms that happened many times or for a symptom that happens only once or twice, but is very upsetting. 0 = Not at all 1 = Mild: happened, but was not very upsetting or troublesome 2 = Moderate: clearly noticeable, patient bothered or upset by this problem; patient had to stop what he/she was doing, but only for a few minutes 3 = Severe: patient very upset by this problem; patient had to stop what he/she was doing and took more than 10 minutes to calm down; upset enough for others to notice
- 21/08/20 - 1 modulo, 1 ItemGroup, 8 elementi, 1 linguaggio
ItemGroup: Postraumatic Stress Screen for the Cognitively Impaired (PTSS-CI)
Carlson, Lauderdale, Hawkins, and Sheikh. (2012). Postraumatic Stress Screen for the Cognitively Impaired (PTSS-CI). Measurement Instrument Database for the Social Science. Retrieved 20.08.2020 from www.midss.ie Key references: Carlson, E. B., Lauderdale, S., Hawkins, J., & Sheikh, J. I. (2008). Posttraumatic stress and aggression among veterans in long-term care. Journal of Geriatric Psychiatry and Neurology, 21, 61-71. Primary use / Purpose: The PTSS-CI is designed to assess posttraumatic stress symptoms in individuals who are cognitively impaired. Background: Posttraumatic stress symptoms can affect an individual's well-being, functioning, and quality of life. Such effects may be exacerbated for individuals who are cognitively impaired and lack the resources to deal with such symptoms or the ability to communicate with, or seek help from, others. The Posttraumatic Stress Screen for the Cognitively Impaired (PTSS-CI) identified symtpoms of posttraumatic stress and is suitable for use with individuals who are elderly and cognitively impaired, brain injured, or developmentally disabled. Both self-report and observer versions are available. Each contains 8 items that assess PTSD symptoms including reexperiencing, avoiding, and hyperarousal. The language used is very simple. Carlson and colleagues (2008) describe the scoring of the instrument. Psychometrics: Preliminary findings on the psychometric properties of the PTSS-CI are discussed in Carlson et al. (2008) Keywords: Anxiety; Family; Stress Other keywords: Posttraumatic Stress Disorder; PTSD; Cognitive Impairment; Stress Digital Object Identifier (DOI): http://dx.doi.org/10.13072/midss.252 INTERVIEWER Instructions: This measure is intended for use with patients who have MMSE scores greater than 19. Read the instructions below to the patient. Make sure that the patient understands that the questions are about what happened in the past week. For each symptom, fill in the number that best reflects the patient’s response. Moderate and severe ratings should be given for symptoms that happened many times or for a symptom that happens only once or twice, but is very upsetting. Use the ratings below, but DO NOT read these definitions to the patient. 0 = Not at all 1 = Mild: happened, but was not very upsetting or troublesome 2 = Moderate: clearly noticeable, patient bothered or upset by this problem; patient had to stop what he/she was doing, but only for a few minutes 3 = Severe: patient very upset by this problem; patient had to stop what he/she was doing and took more than 10 minutes to calm down; upset enough for others to notice If the patient seems unsure of how to respond, use prompts such as: “Did that happen last week?” “Did it upset you?” “Did it bother you?”
- 18/11/20 - 1 modulo, 8 itemgroups, 23 elementi, 2 lingue
Itemgroups: Administrative Documentation, General health, Pain/discomfort, Brain functions, Tasks and activities of daily life, Feelings past 4 weeks, Social activities, Closure
The TOPICS – Short Form 2017 including Casemix forms were developed by the TOPICS-MDS team in collaboration with the Nederlandse Vereniging voor Klinische Geriatrie (NvKG – Dutch Association for Clinical Geriatrics) to use as a Patient Reported Outcome Measure (PROM) in the Dutch outpatient and clinical daily practice. In this version the casemix variables were left out of the Dutch version (with permission by the TOPICS-MDS team), as they are currently not available for the English version. The short forms (including casemix variables for various situations and follow-up in Dutch) can be found on https://topics-mds.eu/topics-short-form/ as pdfs. More information on the public data repository TOPICS-MDS can be found at https://topics-mds.eu/. English Instructions (Dutch Version below): Your experiences as a care receiver are valuable. This list contains questions about your physical and mental health and quality of life. Your answers will be used in research to improve care for the elderly. The more information there is about care for elderly people, the more this can be taken into consideration. Therefore, your experiences are also valuable for other elderly people. Instructions for this questionnaire: - Completing this questionnaire will take approximately 10 minutes. - If you find it difficult to understand or answer the questions, ask your partner, a family member or a friend to help you. - Read each question through completely before selecting an answer. - When you are done, please check that you have not forgotten any questions. Nederlandse Aanwijzingen: Uw ervaringen zijn waardevol. In deze lijst staan vragen over uw lichamelijke en geestelijke gezondheid en kwaliteit van leven. Uw antwoorden worden gebruikt om de zorg voor ouderen in kaart te brengen. Want hoe meer er bekend is over zorg voor ouderen, hoe beter er rekening mee gehouden kan worden. Uw ervaringen zijn dus waardevol, ook voor andere ouderen. Aanwijzingen bij deze vragenlijst: - Het invullen van de vragenlijst kost u ongeveer 10 minuten. - Als u het moeilijk vindt om de vragen te begrijpen of in te vullen, vraag dan hulp aan uw partner, een familielid of vriend. - Lees elke vraag eerst helemaal door voordat u een antwoord kiest. - Bent u klaar, kijk dan of u geen vragen vergeten bent.
- 11/02/21 - 1 modulo, 8 itemgroups, 34 elementi, 2 lingue
Itemgroups: Administrative Documentation, Administrative Documentation of Care Receiver, Relation to your loved one, Your health, Time spent caring for your loved one, How difficult is the care for you, Quality of life for yourself, Closure
The Older Persons and Informal Caregivers Survey Minimum DataSet (TOPICS-MDS) is a public data repository which contains information on the physical and mental health and wellbeing of older persons and informal caregivers across the Netherlands. The database was developed in part to ensure uniform collection of outcomes measures, thus promoting comparability between studies. To date, 53 different research projects have contributed data to this initiative, resulting in a pooled dataset >44,000 older persons and >9,000 informal caregivers. Early 2021, the database will be updated with new data, specifically from older persons with dementia and their informal caregivers. More information can be found at https://topics-mds.eu This form contains the English and Dutch version of TOPICS-MDS 2017 questionnaire for the caregiver for the Baseline and Follow-up measurement. English Instructions for the participant (Dutch version below): Your experiences are valuable. You are caring for your partner, a family member, a friend or a loved one. This list contains questions about what this care means for you as a caregiver. Your answers will be used in research aimed at improving elderly care and informal care. The more information there is about these types of care, the more they can be taken into consideration. For example, when changing the facilities, regulations or legislation for care and wellbeing. Therefore, your experiences are also valuable for other caregivers. Instructions for filling in this questionnaire: Completing this questionnaire will take approximately twenty minutes. If you read ‘your loved one’, then the question refers to the person for whom you are a caregiver. Read each question through completely before answering. Some questions may appear to be ‘repeated’, but please answer all questions. They are intended to view your situation again from a different angle. When you are done, please check that you have not forgotten any questions Nederlandse aanwijzingen: U zorgt voor uw partner, een familielid, een vriend of andere naaste. In deze lijst staan vragen over wat die zorg betekent voor u als mantelzorger. Uw antwoorden worden gebruikt in onderzoek gericht op verbeteringen in de ouderen zorg en mantelzorg. Want hoe meer er bekend is over deze vormen van zorg, hoe beter er rekening mee gehouden kan worden. Bijvoorbeeld bij het veranderen van voorzieningen, regelingen of wetten voor zorgen wel zijn. Uw ervaringen zijn dus waardevol, ook voor andere mantelzorgers. Aanwijzingen bij deze vragenlijst: Het invullen van de vragenlijst kost u ongeveer twintig minuten. Als u leest ‘uw naaste’, dan gaat de vraag over de persoon voor wie u mantelzorger bent. Lees elke vraag eerst helemaal door voordat u een antwoord geeft. Sommige vragen lijken ‘dubbel’, maar we verzoeken u ze toch in te vullen. Ze zijn bedoeld om uw situatie nog eens van een andere kant te bekijken. Bent u klaar? Kijk dan of u geen vragen vergeten bent.
- 27/09/21 - 1 modulo, 12 itemgroups, 97 elementi, 2 lingue
Itemgroups: Baseline / Follow-up, Administrative Data, Personal information, Living situation, Health and disease, Tasks and activities of daily life, Mouth care and complaints with mouth, jaws or temples, How you are feeling, Social activities, Quality of life, Your care use, Closure
The Older Persons and Informal Caregivers Survey Minimum DataSet (TOPICS-MDS) is a public data repository which contains information on the physical and mental health and wellbeing of older persons and informal caregivers across the Netherlands. The database was developed in part to ensure uniform collection of outcomes measures, thus promoting comparability between studies. To date, 53 different research projects have contributed data to this initiative, resulting in a pooled dataset >44,000 older persons and >9,000 informal caregivers. Early 2021, the database will be updated with new data, specifically from older persons with dementia and their informal caregivers. More information can be found at https://topics-mds.eu This form contains the English and Dutch version of TOPICS-MDS 2017 questionnaire for the care receiver for the Baseline and Follow-up measurement. For follow-up, please note that for each follow-up measurement separately, all questions containing ‘12 months’ / ‘12 maanden’, the 12 needs to be replaced by the actual follow-up period. For example, when follow-up takes place after 3 months, the 12 is replaced by ‘3’. Additionally some questions are not needed for follow-up: From "Personal Information" only the marital status is needed. From "Health and Disease" the questions about the diseases are optional. They are recommended, if you want to use the frailty index. English Instructions for the participant (Dutch version below): Your experiences as a care receiver are valuable. You receive care. This list contains questions about what this care means for you as a care receiver. Your answers will be used in research to improve care for the elderly. The more information there is about care for elderly people, the more this can be taken into consideration. For example, when changing the facilities, regulations or legislation for care and wellbeing. Therefore, your experiences are also valuable for other elderly people. Instructions for this questionnaire: - Completing this questionnaire will take approximately half an hour. - Read each question through completely before selecting an answer. - If you find it difficult to understand or answer the questions, ask your partner, a family member or a friend to help you. - Some questions may appear to be ‘repeated’, but please answer all questions. They are intended to view your situation again from a different angle. - When you are done, please check that you have not forgotten any questions. Nederlandse aanwijzingen: Uw ervaringen als zorgvrager zijn waardevol. In deze lijst staan vragen over uw lichamelijke en geestelijke gezondheid, kwaliteit van leven en zorggebruik. Uw antwoorden worden gebruikt in onderzoek naar verbetering van de zorg voor ouderen. Want hoe meer er bekend is over wat ouderen zelf vinden, hoe beter er rekening mee gehouden kan worden. Bijvoorbeeld bij het veranderen van voorzieningen, regelingen of wetten voor zorg en welzijn. Uw ervaringen zijn dus waardevol, ook voor andere ouderen. Aanwijzingen bij deze vragenlijst: Het invullen van de vragenlijst kost u ongeveer een half uur. Lees elke vraag eerst helemaal door voordat u een antwoord geeft. Als u het moeilijk vindt om de vragen te begrijpen of in te vullen, vraag dan hulp aan uw partner, een familielid of vriendof vriendin. Sommige vragen lijken ‘dubbel’, maar we verzoeken u ze toch in te vullen. Ze zijn bedoeld om uw situatie nog eens van een andere kant te bekijken. Bent u klaar? Kijk dan of u geen vragen vergeten bent.

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