Typology of quality of life experiences among persons living with HIV

G. J. Huba, Lisa A. Melchior, David A. Cherin, Judith Steinberg, Geoffrey A.D. Smereck, Karen Richardson-Nassif, Peter Reis, Karen L. Meredith, Sandra S. McDonald, Trudy A. Larson, Eustache Jean-Louis, Victor F. German, Tracey Gallagher, Vivian B. Brown, A. T. Panter

Research output: Contribution to journalArticlepeer-review

3 Scopus citations


This article explores the relationships of HIV risk factors, service needs, and vulnerabilities to health-related quality of life in a sample of 1,371 participants newly enrolled into 13 innovative HIV/ AIDS treatment model service demonstration projects. These projects targeted services to traditionally underserved populations. Eight distinct quality of life clusters of HIV patients were used in this analysis along with patient self-identified risk factors. The quality of life clusters were based on patient self-reported quality of life dimensions. The eight clusters were differentiated based on relative strengths and weaknesses in physical functioning, energy levels, and social functioning. Data on patient need-vulnerability factors and demographic characteristics were related to these eight clusters using the data modeling method of Exhaustive CHAID (Chi-squared Automatic Interaction Detector). Through this method, the characteristics most likely to be associated with higher and lower levels of quality of life at the time of enrollment into services were identified. The results provide further support that quality of life assessment is a useful clinical tool for monitoring patient progress.

Original languageEnglish (US)
Pages (from-to)43-63
Number of pages21
JournalHome Health Care Services Quarterly
Issue number3
StatePublished - Dec 23 2000
Externally publishedYes


  • Quality of life

ASJC Scopus subject areas

  • Health Policy
  • Community and Home Care
  • Public Health, Environmental and Occupational Health


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