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Role of Positive Affect in Adjustment to HIV (CHAI)

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT00582023
First received: December 19, 2007
Last updated: November 21, 2013
Last verified: November 2013

December 19, 2007
November 21, 2013
September 2004
June 2012   (final data collection date for primary outcome measure)
  • Well being [ Time Frame: 18 month follow-up ] [ Designated as safety issue: No ]
  • Physical & Mental Health [ Time Frame: 18 months ] [ Designated as safety issue: No ]
  • Coping Response [ Time Frame: 18 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00582023 on ClinicalTrials.gov Archive Site
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Role of Positive Affect in Adjustment to HIV
CHAI Study: Coping, HIV, and Affect Interview Study

The purpose of this study is to examine the role of emotion and mood in the context of HIV.

A growing body of literature indicates that positive affect may have a unique adaptive role in the process of adjustment to chronic stress, independent of the effects of negative affects like depression. The overarching goal of this research is to provide evidence and direction for the development of interventions for people with HIV that include a focus on positive affect. To this end, this study will document the occurrence, predictors, and consequences of positive affect during the 18 months post-notification of HIV+ serostatus.

Observational
Observational Model: Cohort
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Non-Probability Sample

Adults newly diagnosed with HIV in the San Franicsco Bay Area.

HIV Infections
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
160
June 2012
June 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Have been informed they were HIV positive within the past two months
  • Speak English
  • Be 18 years or older
  • Have the ability to provide informed consent to be a research participant

Exclusion Criteria:

  • Severe cognitive impairment
  • Active psychosis
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00582023
CHAI 971423990, R01 MH068170
No
University of California, San Francisco
University of California, San Francisco
National Institute of Mental Health (NIMH)
Principal Investigator: Judith Moskowitz, PhD, MPH University of California, San Francisco
University of California, San Francisco
November 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP