- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02578654
Interventions to Improve HIV Care Engagement After Hospital Discharge
April 22, 2016 updated by: Thana Khawcharoenporn, Thammasat University
Interventions to Improve HIV Care Engagement Within 30 Days After Hospital Discharge Among HIV-infected Patients
A quasi-experitmental study of the efficacy interventions, including additional HIV care team daily inpatient round and three telephone calls to remind the upcoming clinic appointment, in improving HIV care engagement within 30 days after hospital discharge among HIV-infected patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
240
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
-
-
-
Pathumthani, Thailand, 12120
- Department of Internal Medicine, Faculty of Medicine, Thammasat University
-
-
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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- HIV-infected patients hospitalized at Thammasat University Hospital during the study period
Exclusion Criteria:
- The patients who die during admission, are readmitted prior to 30 days after discharge or with incomplete data
- Readmission episodes of the same enrolled patients during the study period
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: HEALTH_SERVICES_RESEARCH
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Interventions
Additional HIV care team daily inpatient round and three telephone calls to remind the upcoming clinic appointment.
These interventions are specifically added on "routine care" during the post-intervention period.
The routine care does not include the additional round and the three telephone calls and is assessed during the pre-intervention period.
|
Additional HIV care team daily inpatient round and three telephone calls to remind the upcoming clinic appointment.
These interventions are specifically added on "routine care" during the post-intervention period.
The routine care does not include the additional round and the three telephone calls and is assessed during the pre-intervention period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of HIV-infected patients who come to the designated HIV clinic for follow-up within 30 days after hospital discharge divided by the total number of enrolled HIV-infected patients
Time Frame: 30 days
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Factors associated with no follow-up withing 30 days after hospital discharge(analyzed in multivariable logistic regression)
Time Frame: 30 days
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
November 1, 2012
Primary Completion (ACTUAL)
April 1, 2016
Study Completion (ACTUAL)
April 1, 2016
Study Registration Dates
First Submitted
October 14, 2015
First Submitted That Met QC Criteria
October 15, 2015
First Posted (ESTIMATE)
October 19, 2015
Study Record Updates
Last Update Posted (ESTIMATE)
April 25, 2016
Last Update Submitted That Met QC Criteria
April 22, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
- RNA Virus Infections
- Virus Diseases
- Infections
- Blood-Borne Infections
- Communicable Diseases
- Sexually Transmitted Diseases, Viral
- Sexually Transmitted Diseases
- Lentivirus Infections
- Retroviridae Infections
- Immunologic Deficiency Syndromes
- Immune System Diseases
- Slow Virus Diseases
- HIV Infections
- Acquired Immunodeficiency Syndrome
Other Study ID Numbers
- MTU-EC-IM-2-082/57
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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