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Recruiting Observational

Quality of Life Related to the Care of Women Living With HIV During the Perinatal Period

NCT06666530 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-06-19
Last updated
2026-01-08

Condition(s) studied

HIV

Investigational drug(s) / intervention(s)

Questionary

Questionary: Three self-questionnaires, either completed independently or with assistance, will be administered at inclusion (between the first obstetric ultrasound and 28 weeks of amenorrhea), during the third trimester of pregnancy, and at 1 year postpartum

Study summary

"The improvement of patient care by assessing the Quality of Life Related to Care (QLRC) in pregnant women living with HIV is of great importance for informing decision-making, resource allocation, and health policy formulation Prospective descriptive survey of women living with HIV followed for a pregnancy in the Infectious diseases department of Bichat-Claude Bernard Hospital, PARIS, France, between the first obstetric ultrasound and the 28th week of amenorrhea.

After recruitment during a follow-up consultation:

Information regarding the prenatal and perinatal management of HIV and the infant's outcomes up to 12 months will be collected retrospectively through the medical records.

Three self-questionnaires, either completed independently or with assistance, will be administered at inclusion (between the first obstetric ultrasound and 28 weeks of amenorrhea), during the third trimester of pregnancy, and at 1 year postpartum."

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
"Inclusion Criteria * Woman living with HIV * Age ≥ 18 years * Pregnant - due date between the first obstetric ultrasound and 28 weeks of amenorrhea * Information provided about the study and the right to refuse participation Exclusion Criteria * Refusal to participate in the study * Non-French speaker"

Primary outcome measure(s)

  • Collection of perceptions of pregnancy care via the Hospital Anxiety and Depression Scale — during the Perinatal Period at 1 Year Postpartum

Trial sites (1)

FacilityCityRegionStatus
Hôpital Bichat-Claude Bernard Paris France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06666530 on ClinicalTrials.gov ↗ ← All trials in France