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OpenTrials
Completed

NCT Number: NCT02900599

Predicting Treatment and Care Difficulties Among HIV Infected Patients

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.

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Key information

Conditions

HIV Behavior

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV Infected outpatient

Exclusion criteria

  • Refusal to participate

Treatment and study plan

Observationnal (no intervention)

Other

Primary outcomes

  1. CD4 Count

    Time frame: 1 year after interview

    CD4 count at diagnosis and last recorded measure

Secondary outcomes

  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

Sponsors and collaborators

Lead sponsor

Centre Hospitalier de Cayenne

Other

Registry information

Acronym: PREDIVI

Important dates

Study start
2015
Primary completion
2015
Study completion
2016
First posted
Sep 14, 2016
Registry last updated
Sep 14, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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