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Predicting Treatment and Care Difficulties Among HIV Infected Patients (PREDIVI)

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ClinicalTrials.gov Identifier: NCT02900599
Recruitment Status : Completed
First Posted : September 14, 2016
Last Update Posted : September 14, 2016
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier de Cayenne

Study Description
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Brief Summary:
Much of HIV is related to behaviour: sexual risk taking, late diagnosis, adherence to antiretroviral therapy, follow up, disclosure of one's HIV status. The project aimed to use various psychometric tools to determine if these scores have a predictive value on late testing, treatment succes, quality of follow up, and disclosure of HIV to sex partners. The expected outcomes would be to be able to stratify patients using a behavioural risk score and allocate targeted ressources to improve the quality of care for the most at risk patients.

Condition or disease Intervention/treatment
HIV Other: Observationnal (no intervention)

Study Design
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Study Type : Observational
Actual Enrollment : 111 participants
Observational Model: Cohort
Time Perspective: Prospective
Study Start Date : February 2015
Actual Primary Completion Date : February 2015
Actual Study Completion Date : July 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS

Groups and Cohorts
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Outcome Measures
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Primary Outcome Measures :
  1. CD4 Count [ Time Frame: 1 year after interview ]
    CD4 count at diagnosis and last recorded measure


Secondary Outcome Measures :
  1. viral load [ Time Frame: 1 year after interview ]
  2. hiv disclosure to partner [ Time Frame: at the time of interview ]
  3. loss to follow up [ Time Frame: one year after interview ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
HIV Cohort
Criteria

Inclusion Criteria:

  • HIV Infected outpatient

Exclusion Criteria:

  • Refusal to participate
Contacts and Locations
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No Contacts or Locations Provided
More Information
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Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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Responsible Party: Centre Hospitalier de Cayenne
ClinicalTrials.gov Identifier: NCT02900599     History of Changes
Other Study ID Numbers: PREDIVI
First Posted: September 14, 2016    Key Record Dates
Last Update Posted: September 14, 2016
Last Verified: September 2016
Keywords provided by Centre Hospitalier de Cayenne:
HIV
Behavior