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Clinical Trials/NCT00703040
NCT00703040
Completed
Not Applicable

HIV-Related Care Engagement: Linkage to Care and Care-Seeking for HIV-Infected Adolescents, Phase I

University of North Carolina, Chapel Hill7 sites in 1 country35 target enrollmentMarch 2008
ConditionsHIV

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
University of North Carolina, Chapel Hill
Enrollment
35
Locations
7
Primary Endpoint
Describe and evaluate community screening standards and practices.
Status
Completed
Last Updated
9 years ago

Overview

Brief 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.
Registry
clinicaltrials.gov
Start Date
March 2008
End Date
March 2010
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Describe and evaluate community screening standards and practices.

Time Frame: 1 year

Describe and evaluate referral and intake protocols.

Time Frame: 1 year

Describe and evaluate care adherence support (including support from both clinical and non-clinical sources).

Time Frame: 1 year

Describe and evaluate the relationships of screening venues with care-providing venues.

Time Frame: 1 year

Study Sites (7)

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