- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00499161
Effect of Patient-Centered Care (PCC) on Patient Satisfaction at Hospital Discharge (PCC)
The purpose of this randomized clinical trial is to examine the effect of Patient-Centered Care (PCC) on a patient's level of satisfaction on discharge from an acute healthcare setting. Findings from this study will assist in determining if PCC, administered by nurses, should be instituted hospital wide.
SPECIFIC AIMS:
- To examine the effect of Patient-Centered Care on patient satisfaction.
- To examine the effect of Patient-Centered Care on the quality of patient care.
- To examine the effect of patient's perception of nursing care on patient satisfaction.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patient-Centered Care (PCC), also known as individualized patient care or negotiated care, focuses on the patient's right to have his/her values and beliefs respected as an individual.This respect is viewed as part of a commitment to build a deep understanding of the patient as a thinking and feeling individual with the ability to change and develop. A person-centered model of care requires a nurse to work with an individual's beliefs, values, wants, needs and desires.This adaptation to a patient's personal needs requires the nurse to be flexible, respectful, and reciprocal when providing patient care. If the patient's expectations are not appropriate to the type of care needed to heal or if the patient refuses or denies a specific type of treatment that is known as influencing ones quality of care, the nurse must negotiate with the patient. Negotiation incorporates education, which is believed to increase the patient's level of understanding. In addition, negotiation allows the nurse and patient to define a level of treatment that is specific to the patient's needs but still seen as a quality indicator.
The Institute of Medicine (IOM) has listed PCC as one of six national quality aims for improvement. The IOM's vision is that all health professionals will be educated to provide and deliver PCC as part of an interdisciplinary team. In 2001, the IOM report "Crossing the Quality Chasm: A New Health System for the 21st Century" recommends a mixture of approaches to achieve their vision . These approaches include an appropriate training environment, research, public reporting and leadership. At present, there is little evidence to support the critical role nurse clinicians' play in providing PCC and satisfying patient's needs.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15237
- UPMC St. Margaret
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age > 18 years
- Admitted to the service of Dr.RQ and scheduled for bariatric bypass surgery
- Expected length of hospital stay ≥ 2 days.
Exclusion Criteria:
- Any prior admission to the study unit
- Bariatric surgery performed by a surgeon other than Dr.RQ
- Scheduled to have a LAP Band procedure, as this procedure has a different postoperative course.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
NO_INTERVENTION: 1
Control group received usual care
|
|
|
EXPERIMENTAL: 2
Received intervention New model of nursing care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Measure level of overall satisfaction
Time Frame: day of discharge
|
day of discharge
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Measure level of quality of care - 1)Length of stay, 2)infection, 3)falls
Time Frame: day of discharge and 7 days post discharge
|
day of discharge and 7 days post discharge
|
|
measure satisfaction with nursing care
Time Frame: day of discharge
|
day of discharge
|
|
measure level of quality care (unplanned adverse events)
Time Frame: approximately 30 days post discharge
|
approximately 30 days post discharge
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Debra M Wolf, MSN, University of Pittsburh, School of Nursing & UPMC St. Margaret
- Principal Investigator: Lisa Lehman, BSN, University of Pittsburgh
- Principal Investigator: Robert Quinlin, MD, University of Pittsburgh
- Principal Investigator: Jodi Miller, BSN, University of Pittsburgh
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
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
- PRO07030017
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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