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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00703040
Other study ID # ATN 066a
Secondary ID
Status Completed
Phase N/A
First received June 20, 2008
Last updated February 27, 2017
Start date March 2008
Est. completion date March 2010

Study information

Verified date February 2016
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This first phase of a two-phase study involves three components:

1. Review of existing linkage-to-care protocols and sources of referrals for care;

2. Semi-structured telephone or face-to-face interviews with a minimum of two personnel per site who are associated with linkage to medical care. (Preference will be given to personnel with direct experience in linkage to care); and

3. Structured observations of referral sessions.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date March 2010
Est. primary completion date March 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Component 1: Documents identified by clinical site personnel as pertaining to post-test counseling, linkage to care, or standard operating procedures addressing post-test counseling and linkage to care.

- Component 2: Persons employed by one of the AMTUs or an identified linkage-to-care partner and work as clinical staff or a case-manager or is a person familiar to linkage to care; or persons involved in posttest counseling and linkage-to-care processes. Clinical staff and case managers are chosen based on direct experience in the assistance of HIV seropositive youth obtaining medical care. This definition includes, but is not limited to, physicians, nurses, psychologists, social workers, and case managers (who may have diverse professional backgrounds).

- Component 3: All AMTU sites will be included.

Exclusion Criteria:

- Component 1: No a priori exclusions.

- Component 2: No a priori exclusions.

- Component 3: No a priori exclusions.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Montefiore Medical Center Bronx New York
United States Childrens Diagnostic&Treatment Center Fort Lauderdale Florida
United States Mount Sinai Medical Center Manhattan New York
United States St. Jude Childrens Research Hospital Memphis Tennessee
United States University of Miami School of Medicine Miami Florida
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania
United States Children's National Medical Center Washington District of Columbia

Sponsors (3)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill National Institute of Mental Health (NIMH), National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Describe and evaluate community screening standards and practices. 1 year
Primary Describe and evaluate the relationships of screening venues with care-providing venues. 1 year
Primary Describe and evaluate referral and intake protocols. 1 year
Primary Describe and evaluate care adherence support (including support from both clinical and non-clinical sources). 1 year
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