French validation of the SAHOT outcome tool after subarachnoid hemorrhage

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, single-centre observational study will validate the French translation of the SAHOT, a patient-reported outcome measure for subarachnoid hemorrhage. Adults seen for follow-up within 12 months of SAH will complete the self-administered French SAHOT, with a proxy version available for accompanying relatives. The primary goal is to assess internal consistency of the French SAHOT; seventy participants are planned, with relatives helping complete proxy assessments when appropriate. The study excludes non-French speakers and individuals with psychiatric conditions that preclude questionnaire completion. The Fondation Ophtalmologique Adolphe de Rothschild sponsors the effort, conducted at Hôpital Fondation Adolphe de Rothschild in Paris.

Why it matters

Who can join: the full rules

Inclusion Criteria (patients):

* Age over 18 years
* Subarachnoid haemorrhage of any aetiology
* Onset less than 12 months before inclusion
* Seen in consultation at the Hôpital Fondation Adolphe de Rothschild
* Judged able to complete a self-administered questionnaire by the evaluating clinician
* Informed and not opposed to participation (or relative's non-opposition if the patient is under guardianship and/or unable to consent)

Inclusion Criteria (relatives):

* Age over 18 years
* Relative / caregiver of a patient with subarachnoid haemorrhage within the previous 12 months
* Attending the follow-up consultation of an included patient
* Informed and not opposed to participation

Exclusion Criteria (patients and relatives):

* Non-French-speaking
* Psychiatric disorder judged incompatible with completion of the questionnaires by the investigator

Where it's running

• Hôpital Fondation Adolphe de Rothschild
  Paris, France Recruiting

Study contacts

• Study coordinator: Emma Gentric
• Email: egentric@for.paris
• Phone: +33 1 48 03 65 00

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.