- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02001454
Quality of Pain Management at the Ziv Medical Center
Study Overview
Status
Conditions
Detailed Description
Our belief is that the establishment of a pain protocol at the Ziv Medical Center will improve effectiveness of pain treatment. The present study involves surveying the current knowledge and attitudes of caregivers who are responsible for evaluating pain in patients and subsequent treatment in various departments of the hospital without a pain protocol.
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.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Zefat, Israel, 33100
- Recruiting
- Ziv Medical Center
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Contact:
- Littal Rubin, RN
- Phone Number: +97246828912
- Email: littal.r@ziv.health.gov.il
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Principal Investigator:
- David Rothem, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Staff from the Ziv Medical Center and patients
Exclusion Criteria:
Staff members that do not deal with pain treatment
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Patients in pain
There is no intervention, only questionnaires for the patient
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Attending Physicians and Nurses
The staff physicians and nurses will also fill out a questionnaire
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Improvement of pain treatment for the patient
Time Frame: A 6-month assessment will be performed
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A 6-month assessment will be performed
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 0032-13
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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