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Enrolling by invitation NCT07077642

Validation of a Multidimensional Scale for the Detection of Health Needs in People With HIV

Observational HIV Quality of Life

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: HIV, Quality of Life. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The primary objective is to evaluate the diagnostic performance of the multidimensional screening test in identifying alterations in the domains considered in people with HIV, in order to improve the predictivity of disorders, ensure better care and consequently improve the quality of life of people with HIV

Primary outcome measures

  • Evaluation of the diagnostic performance of multidimensional screening test in identifying alterations in considered domains in patients with hiv [Time frame: At enrollment]

Eligibility criteria

Inclusion criteria

  • Age 18 years and older
  • Confirmed HIV infection
  • Good understanding of the Italian language
  • Signature of informed consent
  • Inclusion of at least 33% women and at least 33% people older than 50 years of age

Exclusion criteria

  • Acute ongoing diseases that, in the opinion of the investigators, may affect the performance of the tests (bacterial or viral infections, neoplasms under active chemotherapy treatment)
  • Dementia or other severe neurodegenerative/neurocognitive disorders.
  • Individuals unable to express consent independently and/or supported by protective legal figures

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Italy · 11 centers
  • Università degli Studi di Genova — Genova
  • ASST Fatebenefratell - Sacco, Ospedale L. Sacco — Milan
  • Clinica delle Malattie Infettive e Tropicali, Dipartimento di Scienze della Salute, Univer — Milan
  • Unità di Malattie Infettive, IRCCS San Raffaele — Milan
  • Ospedale Amedeo di Savoia — Torino
  • UOC Malattie Infettive, Università di Bari "Aldo Moro", AOU Policlinico di Bari — Bari
  • UOC Malattie Infettive, Arnas Garibaldi — Catania
  • Malattie Infettive ed Urgenze Infettivologiche, Presidio Ospedaliero Cotugno - Azienda Osp — Naples
  • … and 3 more centers

Identifiers

NCT: NCT07077642 · MUSA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗