Depression and Anxiety Trial, Recruiting NCT05734768 Sponsor: CHU de Reims Condition: Depression and Anxiety
Printed from Voxsanity (voxsanity.com.au) — NCT05734768 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.
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Depression and Anxiety Trial, Recruiting

NCT05734768
Recruiting Not Applicable

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who may be able to join

For the preterm baby group:

  • The baby was born early, between 32 weeks and 36 weeks + 6 days of pregnancy
  • The baby was born at the maternity ward of Reims University Hospital
  • Both parents are aged 18 or older
  • The parents are covered by social insurance
  • The parents have agreed to take part within 72 hours of the baby's birth

For the full-term baby group:

  • The baby was born at 37 weeks of pregnancy or later
  • The baby was born at the maternity ward of Reims University Hospital
  • Both parents are aged 18 or older
  • The parents are covered by social insurance
  • The parents have agreed to take part within 72 hours of the baby's birth

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • The baby was born as part of a multiple pregnancy (such as twins or triplets)
  • The baby has unstable heart or blood circulation problems
  • More than 72 hours have passed since the baby's birth
  • The baby has a birth defect present from birth
  • The baby has serious brain injury detected by a specialised ultrasound scan done before joining the trial (confirm with trial site for specific details)
  • There are plans for the child to be separated from the parents and placed in care
  • The baby was born anonymously
  • Either parent has a psychiatric condition
  • The mother has serious heart or blood pressure problems
  • Either parent is under legal guardianship
  • The parents do not speak the local language as their native language

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 30 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 3 26 78 94 76

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
CHU de Reims
Registry
ClinicalTrials.gov
Start date
28 November 2023
Est. completion
28 February 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

STAI-Y : State Trait Inventory Anxiety - Y

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

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Data last synced from ClinicalTrials.gov: 30 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov