Pain Relief Satisfaction With New Educational Materials
NCT ID: NCT03698773
Last Updated: 2024-08-27
Study Results
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View full resultsBasic Information
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COMPLETED
NA
106 participants
INTERVENTIONAL
2018-10-01
2020-04-09
Brief Summary
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Detailed Description
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Potential participants will be recruited from the University of New Mexico Hospital (UNMH) Labor \& Delivery floor. Patients will be enrolled following an oral consent process. They will be randomized into either control group or intervention group. Control group participants will have their standard of care visit with an anesthesiologist and routine hospital pain-relief information. Intervention group participants will have their standard of care visit with an anesthesiologist, plus one hour in which to view the patient education website thepainlesspush.com, on an iPad provided by the Anesthesiology department for this purpose. After their delivery and transfer to the mother/baby unit, participants will complete a satisfaction survey brought to them by a study team member. Participants will complete the survey following their delivery and prior to discharge. The primary team will notify us with expected discharge in which we will retrieve the survey from them in their room and answer any last questions. Their active participation in the study will be complete at this time. After a participant completes the satisfaction survey, research team members will collect demographic information and relevant obstetric/medical history information from the electronic medical record.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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Baseline Group
Access to existing educational materials about labor/delivery pain relief options, as well as an opportunity to ask physicians, nurses, and other relevant personnel for more information.
Access to routine information
Access to routine pain-control information
Website Group
Access to a tablet computer set to display an educational website (thepainlesspush.com) with information about labor/delivery pain relief options, as well as an opportunity to ask physicians, nurses, and other relevant personnel for more information.
Access to website
Access to informational website: thepainlesspush.com
Interventions
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Access to routine information
Access to routine pain-control information
Access to website
Access to informational website: thepainlesspush.com
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients unable to provide consent for medical procedures
* Patients who do not speak either English or Spanish
18 Years
FEMALE
No
Sponsors
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University of New Mexico
OTHER
Responsible Party
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Kathleen Reyes
Assistant Professor
Principal Investigators
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Kathleen Reyes, MD
Role: PRINCIPAL_INVESTIGATOR
University of New Mexico Health Sciences Center
Locations
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University of New Mexico Hospital
Albuquerque, New Mexico, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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18-642
Identifier Type: -
Identifier Source: org_study_id
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