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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01726712
Other study ID # 11-0654
Secondary ID 1R34MH097622-01
Status Completed
Phase N/A
First received October 15, 2012
Last updated January 19, 2017
Start date November 2012
Est. completion date August 2015

Study information

Verified date January 2017
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Network Supported Engagement in Care (NSEC) intervention is a brief, theory based and culturally sensitive intervention designed to capitalize on organic yet underutilized social support networks in the lives of young black men who have sex with men (YBMSM) who have been recently diagnosed with HIV. The intervention has been developed with input from clients and their support network members, case managers, social workers, HIV primary care providers and pastoral care at a Federally Qualified Health Center. The goal of the intervention is to improve retention in care for newly diagnosed YBMSM who present for their first HIV primary care clinic appointment.


Recruitment information / eligibility

Status Completed
Enrollment 105
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria:

Index subjects

- Self-identify as African-American and male;

- same gender anal/oral sex in the past 2 years;

- English speaking;

- have at least one SC in their network;

- own a cell phone not shared with other persons;

- agreeable to text-message mini-booster sessions; and

- between the ages of 16-29 years old.

Supportive Contact:

- Index participant has agreed to including the supportive contact;

- Supportive contact is willing to attend face to face and telephone mini-booster sessions;

- 18 years of age or older;

- English speaking; and

- owns a cell phone that is not shared with other persons.

Exclusion Criteria:

Index Subject:

- unable to provide assent/consent;

- plan to move out of the area within the next 12 months;

- are not willing to attend intervention sessions; or

- not willing to return for assessments

Supportive Contact:

- unable to provide informed consent; or

- not willing to return for 3 and 12 month assessments.

Study Design


Related Conditions & MeSH terms

  • HIV
  • Patient Acceptance of Health Care

Intervention

Other:
Supportive Care
Provide emotional support. Provide practical support. Support friend/family by helping him find information or help for those with HIV in the community

Locations

Country Name City State
United States University of Chicago Medical Center Chicago Illinois

Sponsors (3)

Lead Sponsor Collaborator
University of Chicago Access Community Health Network, National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Missed Visit Proportion (MVP) The primary aim is to test for differences in MVP by treatment group across the study time period of 12 months 12 months
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