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Recruiting NCT07396623

NCT07396623 Validation of French PHQ-4 and PC-PTSD-5 Screening Scales

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Clinical Trial Summary
NCT ID NCT07396623
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition Mental Illness
Study Type OBSERVATIONAL
Enrollment 90 participants
Start Date 2026-01-26
Primary Completion 2027-08-15

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 90 participants in total. It began in 2026-01-26 with a primary completion date of 2027-08-15.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Mental illness is a major public health issue. It affects one in five people, represents the largest expense for health insurance (14%), is the leading cause of years lived with disability, and suicide is the main cause of death among people aged 15 to 35. Depression affects 15 to 20% of individuals at some point in their lives. Trauma-related disorders affect 4.6% of people, including 1- 2% with post-traumatic stress disorder (PTSD). Screening for mental health problems in primary care is crucial. It enables doctors to provide early treatment, reduces the need for emergency care, and decreases both the number and duration of hospital stays. However, general practitioners and other non-mental health professionals often report lacking the time, training, and tools to conduct such screenings. Fortunately, brief and validated screening tools exist in English: The PHQ-4 (Patient Health Questionnaire-4) for anxiety and depression, and the PC-PTSD-5 (Primary Care PTSD Screen for DSM-5) for PTSD. So far, no French versions of these tools have been validated.

Eligibility Criteria

Inclusion Criteria: * Age ≥ 18 years, * Outpatient or hospitalized for any health-related reason, * Oral and written proficiency in French, * Patient informed and willing to participate in the study, * Patient with health insurance coverage Exclusion Criteria: * Individuals under legal protection measures (guardianship, conservatorship, or legal supervision), * Other factors preventing obtaining non-opposition or conducting the research, such as: limited French proficiency, hearing impairment, or significant cognitive disorders

Contact & Investigator

Central Contact

Vladimir ADRIEN, Doctor

✉ vladimir.adrien@aphp.fr

📞 (+33) 1 48 95 59 37

Frequently Asked Questions

Who can join the NCT07396623 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Mental Illness. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07396623 currently recruiting?

Yes, NCT07396623 is actively recruiting participants. Contact the research team at vladimir.adrien@aphp.fr for enrollment information.

Where is the NCT07396623 trial being conducted?

This trial is being conducted at Bobigny, France.

Who is sponsoring the NCT07396623 clinical trial?

NCT07396623 is sponsored by Assistance Publique - Hôpitaux de Paris. The trial plans to enroll 90 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology