- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01298791
The Impact Of Physician Communication On Family Inpatient Experience
October 7, 2016 updated by: Michael Silverstein, Boston Medical Center
Patient satisfaction is affected by physician communication styles and communication at the bedside.
The investigators are conducting a randomized controlled trial involving both providers and families to determine if providers sitting down while talking with families, will improve one aspect of quality care delivered during an inpatient stay as measured by patient/family satisfaction.
The investigators will additionally study the affects of the intervention on the following outcomes: family assessment of provider communication, readmission rates, and length of stay.
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02118
- Boston Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
No older than 17 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Providers: all attendings, residents, and medical students involved in the care of patients on the pediatric inpatient wards during the study period.
- Families (Parents or legal guardians and children):
- (1) inpatient admissions to the pediatrics medical service at Boston Medical Center
- (2) whose parents or guardian have agreed to participate in family centered walk rounds
- (3) patients age 17 or younger who have family members present at the bedside each morning of hospitalization
- (4) English speaking.
Exclusion Criteria:
- (1) All patients/families that as part of admission justification involves social assessment and concern by the patient care team, including patients with neonatal abstinence syndrome, child maltreatment, and concern for neglect.
- (2) All patients transferred to or from PICU as part of their inpatient care
- (3) All patients transferred from an outside institution to the inpatient ward for further care secondary to progression of disease.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Provider sitting
Providers seated during communication through hospitalization
|
Providers will sit during inpatient family-centered walk rounds throughout the communication during rounds.
The participating members of the care team (attending physician, resident and medical student) will remain seated while communicating with the patient and caregiver.
|
Experimental: Provider standing (control)
Providers standing during communication through hospitalization
|
Providers will stand during inpatient family-centered walk rounds throughout the communication during rounds.
The participating members of the care team (attending physician, resident and medical student) will remain standing while communicating with the patient and caregiver.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient/family satisfaction
Time Frame: 4mo
|
Questionnaire obtains basic provider information
|
4mo
|
Patient/family Satisfaction
Time Frame: 4 mo
|
Caregiver questionnaire obtains baseline information on caregiver and patients
|
4 mo
|
Patient/family satisfaction
Time Frame: 4 months
|
PSQ-18: Assesses parental satisfaction with medical care
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Length of stay
Time Frame: 4 months
|
Chart review of length of inpatient hospitalization during intervention
|
4 months
|
Readmission rate
Time Frame: 5 mo
|
Chart review and parental contact regarding readmission for same reason of initial hospitalization
|
5 mo
|
Family discharge preparedness
Time Frame: 4 mo
|
Brief PREPARED instrument
|
4 mo
|
Follow-up appointment attendance
Time Frame: 5 mo
|
Chart review and communication with caregivers regarding keeping follow-up appointment
|
5 mo
|
Family assessment of doctor-patient communication skills
Time Frame: 4 mo
|
Crossley Communication Questionnaire
|
4 mo
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2011
Primary Completion (Anticipated)
June 1, 2011
Study Completion (Actual)
August 1, 2011
Study Registration Dates
First Submitted
February 16, 2011
First Submitted That Met QC Criteria
February 17, 2011
First Posted (Estimate)
February 18, 2011
Study Record Updates
Last Update Posted (Estimate)
October 10, 2016
Last Update Submitted That Met QC Criteria
October 7, 2016
Last Verified
October 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- 34423
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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