- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02108873
Factors Associated With Nonattendance at Scheduled Outpatient Appointments in a University General Hospital (AU1)
Study Overview
Status
Detailed Description
Nonattendance at scheduled appointments at outpatient clinics is a common problem in general medical practice, representing a significant cost to the health care system, and resulting in disruption of daily work planning.Nonattendance at medical appointments has consequences not only for doctors (as it requires a greater use of resources and time), but also for patients, because there may be deterioration in the quality of care, and dissatisfaction associated with delays in obtaining a new appointment.
Previous studies have reported that nonattendance at scheduled appointments is most frequently associated with those patients attending follow-up appointments, generally those assigned to another professional, those with appointments on Fridays, and those with appointments assigned 1 - 2 weeks in advance. Nonattendance was also associated with younger patient age, greater psychological problems, and lower socioeconomic status.Furthermore, in patients with chronic diseases, the nonattendance rate was also reported to be lower. Clinical patient characteristics can be important predictors of nonattendance, but they required high quality electronic health records to predict nonattendance accurately In the United States and Europe, the nonattendance rate is estimated to be between 6.5%-55%; there is little evidence regarding nonattendance in Latin America. Many studies have described the prevalence and impact of nonattendance at scheduled medical appointments, and possible strategies to decrease the nonattendance rate. However, few studies have utilized the characteristics associated with nonattendance for building predictive models, which might better identify those patients who may not attend a scheduled appointment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Buenos Aires
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Capital Federal, Buenos Aires, Argentina, C1199ABD
- Hospital Italiano de Buenos Aires
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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:
- Over 17 years.
- Adults who attended, did not attend and cancelled a scheduled appointment at the Outpatient care system at the Italian Hospital of Buenos Aires (HIBA)
Exclusion Criteria:
- The refusal to register or to the informed consent process.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Retrospective Cohort
Adult patients who had scheduled an appointment for outpatient primary care.
Patients were divided into two groups, including those who attended their scheduled appointment and those who missed it.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Prevalence of non attendance, attendance and cancellation
Time Frame: Cohort study of 24 month
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Characterize, describe and compare the clinical and administrative characteristics of outpatients who didn't attend, attended and cancelled an appointment in internal medicine/primary health care, clinical subspecialties and surgical specialties.
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Cohort study of 24 month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical and administrative characteristics
Time Frame: Cohort study of 24 month
|
Characterize, describe and compare the clinical and administrative characteristics of outpatients who didn't attend, attended and cancelled an appointment in internal medicine/primary health care, clinical subspecialties and surgical specialties.
|
Cohort study of 24 month
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Collaborators and Investigators
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
- 2262
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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