Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
400 participants
OBSERVATIONAL
2013-11-30
2015-05-31
Brief Summary
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Detailed Description
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According to the IASP (International Association for the Study of Pain) :" Pain is an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage". According to WHO, assessment is necessary in every situation that involves pain, excluding pain that is life threatening. Valid and reliable assessment is essential for effective pain management. The very nature of pain makes it impossible to measure objectively. There are different types of pain, and as caregivers, we need to diagnose the pain accurately in order that each patient gets the most effective treatment and continued evaluations, as needed. When caregivers decide on a treatment for pain, they are relying on the relatively objective VAS (Visual Analogue Scale.) According to recent studies most patients were dissatisfied with the pain treatment they had received. Approximately eighty percent of patients who present to emergency departments worldwide come because of pain.
Often the patient and the caregiver have different ideas about what pain is and how to treat it. Cultural differences, gender differences, even age differences may affect reactions of both the caretaker and the patient. There are many ways to treat pain, and various reasons for how people react to pain.
The present study is designed to measure the knowledge and attitudes of caregivers and in regard to the pain of their patients. An assessment of patient satisfaction to pain management will be also be performed.
Staff members working in wards involved with pain will be asked to fill out anonymous questionnaires concerning knowledge and attitudes toward pain. Patients will also be asked to fill out anonymous questionnaires in regard to their pain treatment. Informed consent will be requested. Responses will be collated and recorded. A future study is planned using a new pain protocol. The questionnaires will be repeated after the protocol has been in place for 12 months, at which time responses will be compared.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Patients in pain
There is no intervention, only questionnaires for the patient
No interventions assigned to this group
Attending Physicians and Nurses
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No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
25 Years
65 Years
ALL
No
Sponsors
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Ziv Hospital
OTHER_GOV
Responsible Party
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David Eliya Rothem
Orthopedic Joint Specialist
Locations
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Ziv Medical Center
Safed, , Israel
Countries
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Facility Contacts
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Littal Rubin, RN
Role: primary
Other Identifiers
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0032-13
Identifier Type: -
Identifier Source: org_study_id